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Journal of Inherited Metabolic Disease

, Volume 40, Issue 3, pp 325–342 | Cite as

Sweet and sour: an update on classic galactosemia

  • Ana I. Coelho
  • M. Estela Rubio-Gozalbo
  • João B. Vicente
  • Isabel Rivera
Open Access
Review

Abstract

Classic galactosemia is a rare inherited disorder of galactose metabolism caused by deficient activity of galactose-1-phosphate uridylyltransferase (GALT), the second enzyme of the Leloir pathway. It presents in the newborn period as a life-threatening disease, whose clinical picture can be resolved by a galactose-restricted diet. The dietary treatment proves, however, insufficient in preventing severe long-term complications, such as cognitive, social and reproductive impairments. Classic galactosemia represents a heavy burden on patients’ and their families’ lives. After its first description in 1908 and despite intense research in the past century, the exact pathogenic mechanisms underlying galactosemia are still not fully understood. Recently, new important insights on molecular and cellular aspects of galactosemia have been gained, and should open new avenues for the development of novel therapeutic strategies. Moreover, an international galactosemia network has been established, which shall act as a platform for expertise and research in galactosemia. Herein are reviewed some of the latest developments in clinical practice and research findings on classic galactosemia, an enigmatic disorder with many unanswered questions warranting dedicated research.

Keywords

Galactose Aldose Reductase Galactosemia Galactitol Primary Ovarian Insufficiency 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Introduction

Classic galactosemia (type I galactosemia, OMIM #230400) is caused by deficient activity of galactose-1-phosphate uridylyltransferase (GALT, EC 2.7.7.12), the second enzyme of the main pathway of galactose metabolism, the Leloir pathway, and its prevalence is 1:16,000-60,000 live-births (Ashino et al. 1995; Coss et al. 2013; Fridovich-Keil and Walter 2008). It is an autosomal recessive disorder caused by mutations in the GALT gene and over 300 variations have thus far been described (Calderon et al. 2007). Classic galactosemia presents in the neonatal period as a potentially lethal disorder that can lead to chronically debilitating complications (Schweitzer et al. 1993; Waggoner et al. 1990; Waisbren et al. 2012). The only currently available therapeutic strategy is a life-long dietary galactose restriction, which proves insufficient to prevent long-term complications (Bosch et al. 2004b, 2009).

The first description of galactosemia dates back to 1908. Since then, and though a considerable understanding of its molecular, cellular and clinical aspects has been acquired, its exact pathophysiology is not yet fully elucidated.

Galactose importance in health

Galactose is vital for the human body, exhibiting a broad range of functions, as a key energy source in pre-weaning infants and exerting a crucial structural role, being particularly important for early development (Coelho et al. 2015a).

Galactose is a natural aldohexose that occurs mainly in its d-configuration. It is available as free and bound galactose in complex carbohydrates (such as oligosaccharides and polysaccharides, glycoproteins, and glycolipids). Along with glucose, galactose forms the disaccharide lactose, present in most animal milks and a key energy source in infants.

Galactose metabolism

The main dietary source of galactose is lactose present in milk and dairy products. After its ingestion, lactose is hydrolyzed in the intestinal lumen by lactase into glucose and galactose. Galactose is transported across the enterocyte brush border membrane by the sodium/glucose active co-transporter SGLT1, and through facilitated diffusion by the GLUT2 transporter across the enterocyte basolateral membrane. Upon entering the blood stream, it is delivered by the portal blood to the liver, the major site of galactose metabolism, where it is internalized by the low-affinity high-capacity GLUT2 (Wood and Trayhurn 2003).

The main pathway of galactose metabolism

When released from lactose breakdown, galactose is in its beta configuration. Once inside the cells, β-d-galactose is epimerized into its alpha configuration by galactose mutarotase (GALM, EC 5.1.3.3) (Timson and Reece 2003), so that it can enter the Leloir pathway (Fig. 1). This pathway converts α-d-galactose into glucose-1-phosphate (Glc-1-P) by the action of three consecutive enzymes: galactokinase (GALK1) converts α-d-galactose into galactose-1-phosphate (Gal-1-P); galactose-1-phosphate uridylyltransferase (GALT) converts Gal-1-P and uridine diphosphate-glucose (UDP-Glc) into glucose-1-phosphate (Glc-1-P) and uridine diphosphate-galactose (UDP-Gal); and UDP-galactose 4′-epimerase (GALE) is responsible for the interconversion of UDP-Gal to UDP-Glc, as well as of UDP-N-acetylgalactosamine to UDP-N-acetylglucosamine in mammals. UDP-Glc re-enters the pathway so that further galactose is converted into Glc-1-P and UDP-Gal. The Glc-1-P produced by the Leloir pathway is converted by phosphoglucomutase into glucose-6-phosphate, to be further metabolized via i) the glycolytic pathway; ii) the pentose phosphate pathway; or iii) the gluconeogenic pathway. UDP-Gal, in turn, is the galactose donor for glycosylation reactions.
Fig. 1

Galactose metabolism. In the Leloir pathway, galactose is converted to glucose-1-phosphate (Glc-1-P) by the action of three consecutive enzymes: galactokinase (GALK1), galactose-1-phosphate uridylyltransferase (GALT), and UDP-galactose 4′-epimerase (GALE). Alternatively, galactose can be reduced to galactitol by aldose reductase, oxidized to galactonate, presumably by galactose dehydrogenase, or be converted into UDP-Glc, via the pyrophosphorylase pathway, by the sequential activities of GALK1, UDP-glucose/galactose pyrophosphorylase (UGP), and GALE. GALE is also responsible for the interconversion of UDP-N-acetylgalactosamine to UDP-N-acetylglucosamine (not shown). PPi, pyrophosphate

Alternative pathways of galactose metabolism

Besides the Leloir pathway, three accessory pathways of galactose metabolism have been described (Fig. 1): i) the reductive pathway, ii) the oxidative pathway, and iii) the pyrophosphorylase pathway.

Galactose reduction occurs through the polyol pathway, consisting of two enzymatic reactions involving the NADPH-dependent aldose reductase (EC 1.1.1.21) and the NAD+-dependent sorbitol dehydrogenase (EC 1.1.1.14). Aldose reductase has a broad specificity for monosaccharides, and can metabolize glucose and galactose, respectively yielding sorbitol and galactitol. Although both sugars are similarly processed, sorbitol can be further converted to fructose by sorbitol dehydrogenase, whereas galactitol will accumulate in cells and tissues. In the lens, galactitol buildup produces a hyperosmotic effect, leading to swelling of the cells. Additionally, galactitol production depletes the cell of NADPH, decreasing glutathione reductase activity, and consequently free radicals accumulation, yielding oxidative stress and leading to cell death and cataract formation (Lai et al. 2009; Pintor 2012). Elevated galactitol has also been found in the brain of galactosemic children, where it causes edema (Belman et al. 1986; Berry et al. 2001; Quan-Ma et al. 1966).

Galactose can also be oxidized to galactonate, although the respective pathway is still controversial. It is thought to result from a NAD+-dependent galactose dehydrogenase (d-galactose:NAD+ oxidoreductase, EC 1.1.1.48) yielding galactonolactone, which is spontaneously or enzymatically converted to galactonate. Galactonate can be directly excreted in this form or further converted via the pentose phosphate pathway into β-keto-d-galactonate, which subsequently undergoes decarboxylation, liberating carbon C1 to form xylulose (Lai and Klapa 2004; Wehrli et al. 1997).

Neither the reductive nor the oxidative pathways involve any of the Leloir enzymes. The pyrophosphorylase pathway, however, depends on GALK1 and GALE, as it involves the GALK1-catalyzed galactose phosphorylation to Gal-1-P followed by galactose incorporation into UDP-Gal catalyzed by UTP-dependent glucose/galactose pyrophosphorylase (UGP, EC 2.7.7.10). UDP-Gal is then epimerized by GALE into UDP-Glc, from which a second pyrophosphorylase reaction generates Glc-1-P and UTP. This pathway has been suggested as a route of endogenous galactose production (Gitzelmann 1969). The major source of endogenous galactose is, however, the lysosomal hydrolysis of galactose-containing glycoproteins, glycolipids and proteoglycans (Berry et al. 1997).

Several studies have provided quantitative evidence for whole body de novo galactose synthesis in healthy and galactosemic subjects, estimated between 0.48 and 1.71 mg/kg/h in patients and not influenced by short-term exogenous galactose (Berry et al. 2004; Ning et al. 2000; Schadewaldt 2004; Schadewaldt et al. 2014). Notably, it is considerably higher in infants and children, gradually diminishing until adulthood (Berry et al. 2004; Schadewaldt 2004).

The molecular biology of classic galactosemia

GALT protein

GALT is a ubiquitous enzyme with a remarkable degree of conservation throughout evolution. The first insights into GALT structure came from the X-ray crystallographic structure of E. coli GalT, revealing this enzyme is a dimer with two active sites, each formed by amino acids from both subunits (Wedekind et al. 1995). Only recently the crystallographic structure of human GALT was reported (McCorvie et al. 2016) (Fig. 2), confirming the major bacterial GalT structural features, while revealing relevant differences that support a more accurate interpretation and/or prediction of the effect of mutations on GALT structure-function. The human GALT active site contains the H184-P185-H186 sequence, conserved among all known uridylyltransferases (Fig. 2), corresponding in E. coli GalT to residues 164–166 (Field et al. 1989; Wedekind et al. 1995). The Glc-1-P binding site is formed by K334, F335, V337, Y339, E340, and Q346 from one chain, along with Q188 and N173 from the other chain. Uridylylation appears to induce a conformational change of GALT, with UMP-GALT presenting a more compact structure than apo-GALT (McCorvie et al. 2016). The fact that both bacterial and human GALT were crystallized in the uridylylated form supports previous proposals of its catalytic mechanism. GALT catalyzes the transfer of an uridyl group from UDP-Glc to Gal-1-P through a double displacement mechanism involving a transiently uridylylated histidine residue (Fig. 3) (Thoden et al. 1997; Wong and Frey 1974a, b). In the first step of this ‘ping-pong’ mechanism, an electron pair from a histidine side-chain imidazole ring in the active site (H186 in human GALT) attacks the UDP-Glc α-phosphate, resulting in a covalently uridylylated intermediate (UMP-enzyme) and releasing Glc-1-P. In the second reaction step, the UMP moiety is displaced from the enzyme by Gal-1-P, thereby regenerating the active site and yielding the second product, UDP-Gal (Wedekind et al. 1996; Wong and Frey 1974b). GALT is a metalloenzyme, although the role of bound metals is likely structural. Each bacterial GalT monomer harbors one zinc ion (bound to C52, C55, H115, H164) and one iron ion (bound to E182, H281, H299, H301). Whereas zinc has been proposed to stabilize the bacterial GalT active site thereby being essential for activity, iron is thought to play a structural role (Geeganage and Frey 1999). The zinc binding residues in E. coli GalT are poorly conserved in human GALT. However, the structure of human GALT revealed that a zinc ion is bound to residues E202, H301, H319, H321 (Fig. 2) equivalent to the bacterial GalT iron-binding site. Indeed, and similarly to the proposed role of iron in bacterial GalT, this zinc site was shown to structurally stabilize human GALT and prevent its aggregation (McCorvie et al. 2016).
Fig. 2

Crystallographic structure of human GALT. Cartoon representation of uridylylated human GALT crystallographic structure obtained in complex with galactose-1-phosphate (PDB code 5IN3). Each monomer is colored either in cyan or light orange. Active site residues H184-P185-H186 in red sticks; covalently linked UMP in blue sticks; galactose 1-phosphate in yellow sticks; residue Q188, responsible for UMP stabilization and site of the most common mutation (Q188R) in classic galactosemia in green sticks; zinc (purple sphere) binding ligands in gray sticks

Fig. 3

The catalytic mechanism of GALT. In the first step of the reaction, the Nε2 of His186 attacks the α-phosphate of UDP-Glc, releasing Glc-1-P and forming the covalent uridylyl-enzyme intermediate; in the second step, the intermediate reacts with Gal-1-P to produce UDP-Gal

GALT gene—clinically relevant variations

The GALT gene is located in the 9p13 region, it is arranged into 11 exons spanning ≈ 4.0 kb of genomic DNA (NG_009029.1), and is expressed as a housekeeping gene. Analysis of ∼4 kb of the GALT promoter identified three GC-rich Sp1 sites, an imperfect non-palindromic AP-1 site (TCAGTCAG at −126 to −119), a CAAT box, two E-box motifs spaced 23 bp apart (at −146 to −141 bp – CAGGTG and at −117 to −112 bp – CACGTG), and no TATA box sequence (Elsas et al. 2001; Leslie et al. 1992).

An Alu repeat motif with evidence for length variation has been identified in intron 10 (Flanagan et al. 2004). It consists of a polyadenine nucleotide repeat with three length variants, (A)17, (A)24, and (A)29 at frequencies of 47.5, 50.0, and 2.5%, respectively. These length variants have defined associations with particular GALT alleles. The p.Q188R and p.K285N mutant alleles are in linkage disequilibrium with the (A)17 and (A)24 Alu variants, respectively, while (A)29 is only found associated with the p.N314D allele (see below) (Flanagan et al. 2004; Fridovich-Keil and Walter 2008).

At present, there are 336 different variations described at the GALT locus (available at: http://www.arup.utah.edu/database/GALT/GALT_display.php, last surveyed January 2017) (Calderon et al. 2007). A few of these otherwise rare mutations are common, the most frequent being the c.563A>G transition in exon 6 (CAG → CGG), leading to a substitution of a strictly conserved glutamine to an arginine at residue 188 of human GALT (p.Q188R), two residues after the H184-P185-H186 active site. This mutation accounts for ∼64% of all galactosemic alleles in Caucasian populations, being the most common among people of European ancestry. In Europe, p.Q188R shows a gradient of increasing frequency in the North-Western direction, reaching its highest frequency in Ireland, where it accounts for 92–94% of galactosemic alleles. p.Q188R is the sole variant among the Republic of Ireland Traveller population, where its incidence is estimated to be 1 in 430 (Coss et al. 2013; Flanagan et al. 2010; Suzuki et al. 2001). The consideration that p.Q188R is the most prevalent variation could be biased toward non-Asian origins, since both Chinese and Indian populations (contributing to ∼35% of the World’s population) are largely understudied. p.Q188R was identified in 2.7% of a small cohort of Indian galactosemic patients (Singh et al. 2012), whereas it has never been identified in Chinese or Japanese (or descendant) patients (Ashino et al. 1995; Hirokawa et al. 1999; Suzuki et al. 2001). This mutation is described as giving rise to a non-functional variant. Studies on its bacterial homologue revealed the loss of one H-bond established with UDP-Gal (Geeganage and Frey 1998). In human GALT, p.Q188R has been proposed to cause a destabilization of UMP-GALT (Lai et al. 1999), which was further demonstrated by McCorvie et al. who obtained partially uridylylated (∼8%) p.Q188R GALT after over-night incubation with UDP-Glc (McCorvie et al. 2016). This observation contradicted previous hypotheses of an over-stabilization of UMP-GALT based on homology modeling (Coelho et al. 2014a, b; Facchiano and Marabotti 2010; Marabotti and Facchiano 2005). Moreover, McCorvie and co-workers confirmed the increased aggregation propensity of p.Q188R (Coelho et al. 2014b), proposed therein to result from its lower uridylylation (McCorvie et al. 2016). As compared to uridylylated control p.N314D GALT, p.Q188R also presented a less compact and more elongated shape, similarly to control apo-GALT, reinforcing that some misfolding features might be associated with decreased uridylylation (McCorvie et al. 2016).

Patients homozygous for the p.Q188R variant demonstrate essentially no residual RBC GALT activity, and homozygosity for this allele is often associated with a poor outcome (Robertson et al. 2000; Shield et al. 2000). Transformed lymphoblasts from homozygous p.Q188R patients and heterologous expression in bacterial and yeast systems revealed that this variant displays less than 2% of control activity and poorly alleviates galactose toxicity when expressed in a ΔgalT E. coli strain (Coelho et al. 2014b, 2015c; Elsas et al. 1995; Fridovich-Keil and Jinks-Robertson 1993).

The second most common mutation of European origin is c.855G>T in exon 9 (AAG → AAT), leading to a lysine to asparagine substitution at residue 285 of human GALT, p.K285N. This mutation is particularly frequent in countries of Central and Eastern Europe, accounting for 26–34% of galactosemic alleles (Greber-Platzer et al. 1997; Kozák et al. 1999; Lukac-Bajalo et al. 2007; Suzuki et al. 2001; Zekanowski et al. 1999). The Czech, Slovak, Polish, and Austrian galactosemic populations present the highest p.K285N frequencies relatively to other European populations, suggesting a Slavic origin. It has also never been identified in Asian patients (Ashino et al. 1995; Hirokawa et al. 1999; Suzuki et al. 2001). Heterologous expression of this variant revealed essentially null activity (Coelho et al. 2014b; Riehman et al. 2001), and homozygosity in patients is associated with essentially null RBC GALT activity and with a severe clinical phenotype (Zekanowski et al. 1999).

In exon 5, the C→T transition at nucleotide c.404 (TCpG → TTG) leads to a serine to leucine substitution at residue 135 of human GALT, p.S135L. This variant is found almost entirely in individuals of African origin, accounting for approximately 48% of African American and 91% of South African GALT mutant alleles (Lai et al. 1996; Manga et al. 1999). Heterologous expression in bacteria or yeast revealed, respectively, less than 0.1 and 2.7% of control activity (Coelho et al. 2014b; Riehman et al. 2001). Notably, p.S135L appears to exhibit tissue specificity: homozygous patients have essentially no GALT activity in RBC, presenting ∼5.5% of control activity in leukocytes, while liver and intestinal mucosa biopsy specimens display ∼10% of normal GALT activity (Lai et al. 1996). Additionally, homozygous patients are capable of converting galactose to CO2 at a rate comparable to control subjects and homozygosity for this mutation is often associated with milder clinical outcomes (Berry et al. 1997; Lai and Elsas 2001; Lai et al. 1996; Robertson et al. 2000).

Duarte and Los Angeles variants

The first known variant of GALT protein is the Duarte variant, named after the city where it was described. The Duarte allele — Duarte-2, D2 or simply D — is biochemically defined as an isoform with a characteristic isoelectric focusing pattern, and a RBC enzyme activity approximately 50% of the control. Heterozygotes for the Duarte allele present 75% of GALT activity, homozygotes present 50% activity, and compound heterozygotes for the Duarte allele and a classic galactosemia allele present 25% activity in RBC (Elsas et al. 1994).

Later, another variant presenting the same electrophoretic mobility profile as D2 but mildly elevated activity was identified and named as the Los Angeles variant (Duarte-1, D1 or LA) (Langley et al. 1997; Ng et al. 1973). Both variants are now known to be associated with the AAC → GAC transition at nucleotide c.940 in exon 10, leading to an asparagine to aspartate substitution at residue 314 of human GALT (p.N314D). The charge change caused by the substitution of a basic to an acid residue is proposed to be responsible for the resulting specific electrophoretic pattern (Reichardt 1991). The different activities displayed by each variant result from additional base changes: the Los Angeles allele carries p.N314D in linkage disequilibrium exclusively with the synonymous mutation c.652C>T (p.L218L), whereas the Duarte allele carries p.N314D in linkage disequilibrium with c.378-27G>C (IVS4-27G>C), c.507 + 62G>A (IVS5 + 62G>A), c.508-24G>A (IVS5-24G>A) and a 4-bp deletion in the GALT promoter, 116–119 bases upstream the first methionine codon (c.-119_-116delGTCA) (Kozak and Francova 1999; Podskarbi et al. 1996). This deletion removes the first two nucleotides of the −117 to −112 bp E-box motif (CA, located at −117 and −116 bp), which however does not change the E-box motif of CACGTG from −117 to −112 bp, since there are three repeats of GTCA in sequence, and the middle GTCA tetrad fills the deleted CA of the E-box motif (Fig. 4). There is, however, a reduction in the spacing between the two E-box motifs that likely alters trans–acting factors binding, thus impairing positive regulation of GALT expression. Furthermore, this deletion affects the AP-1 site from −124 to −117 bp (TCAGTCAG), as it removes the terminal guanine of this motif, which can also reduce GALT expression. Functional analyses carried out by two independent groups demonstrated that this deletion in the GALT promoter is indeed the major factor contributing to the diminished expression and activity of the Duarte variant (Elsas et al. 2001; Trbušek et al. 2001).
Fig. 4

The GALT promoter deletion of the Duarte allele. The GALT promoter presents an AP-1 site from −126 to −119 bp (TCAGTCAG) and two E-box motifs from −146 to −141 bp (CAGGTG) and from −117 to −112 bp (CACGTG). The −119 to −116 GTCA deletion removes the first two nucleotides (CA, in bold) of the −117 to −112 bp E-box motif. The middle tetrad GTCA fills the deleted CA of the E-box motif; however, the spacing between the two E-box motifs is reduced, and the terminal G of the AP-1 site is removed. Nucleotide +1 is the A of the ATG-translation initiation codon

At present, p.N314D is a common allele with a frequency of approximately 11% in European populations and lower frequencies in other populations, with an 8.3% pan-ethnic frequency (Carney et al. 2009; Suzuki et al. 2001). Interestingly, a study on the origin and distribution of the Duarte allele suggested that p.D314 is in fact the ancestral allele and that p.N314 only arose early in human evolution once humans migrated out of Africa (Carney et al. 2009).

Functional and structural characterization of the p.N314D variant confirmed that, in vitro, it displays enzymatic activity essentially identical to control, although with impaired conformational stability (Coelho et al. 2014b). This variant was recently used for the first description of the crystallographic structure of human GALT (McCorvie et al. 2016).

Biochemical features and follow-up

Severe impairment of GALT activity results in the accumulation of metabolites such as galactose, Gal-1-P, galactitol, and galactonate, and in deficiency of UDP-Gal and UDP-Glc.

Galactose only differs from glucose in the hydroxyl moiety configuration at the carbon-4 position. However, galactose is less stable and more susceptible to the formation of nonspecific glycoconjugates (Decombaz et al. 2011). The human body is able to metabolize large galactose amounts, as evidenced by its rapid clearance from blood: 50% of radiolabeled galactose is found in glucose pools within 30 min after intravenous administration. For nursing infants, galactose conversion to glucose is crucial to maintain euglycemia, since 40% of calories derive from lactose hydrolysis into galactose and glucose (Coelho et al. 2015a). In contrast to healthy infants, galactosemic newborns accumulate galactose in the blood, as well as in other cells and tissues, and they present high urinary galactose concentrations, whereas blood glucose levels can fall to hypoglycemic levels. Upon initiation of dietary galactose restriction—the current standard of care—blood galactose levels fall quickly, but always remain elevated. Additionally, patients also present high RBC Gal-1-P concentrations which, despite falling dramatically upon diet implementation, never normalize (Gitzelmann 1995). Gal-1-P accumulation has been widely pointed out as a key pathogenic agent (Gitzelmann 1995; Lai et al. 2009; Leslie 2003; Tang et al. 2010). Gal-1-P has been described to inhibit in vitro enzymes involved in carbohydrate metabolism, such as UDP-glucose pyrophosphorylase, glucose-6-phosphatase, glucose-6-phosphate dehydrogenase, phosphoglucomutase, and glycogen phosphorylase (Gitzelmann 1995). Additionally, Gal-1-P has been described to inhibit inositol monophosphatase, which could lead to a reduced inositol pool. Brain autopsy of two newborn patients showed a reduction of up to 80% free inositol (Ins) and phosphatidyl-inositol (PtdIns) comparatively with healthy controls, and rats with a high-galactose diet exhibited a reduction of up to 30% of free Ins and PtdIns (Bhat 2003). There is also evidence that high levels of Gal-1-P inhibit galactosyltrans-ferases, which may disturb glycosylation (Charlwood et al. 1998; Jaeken et al. 1992). Additionally, UDP-Gal and UDP-Glc levels have been found decreased in a number of studies (Coss et al. 2012, 2014; Lai et al. 2003a; Ng et al. 1989). These UDP-hexoses are the galactose and glucose donors in glycosylation reactions, and several studies have indeed reported glycosylation abnormalities in classic galactosemia (Charlwood et al. 1998; Coman et al. 2010; Coss et al. 2012, 2014; Lebea and Pretorius 2005; Liu et al. 2012; Maratha et al. 2016; Petry 1991; Sturiale et al. 2005).

High galactitol levels have been found in blood, tissues, and urine of galactosemic patients (Berry et al. 2001; Jakobs et al. 1995; Palmieri et al. 1999). When dietary treatment is implemented, most galactitol is cleared via urine, but does not entirely disappear, likely because of endogenous galactose production.

Galactonate has been detected in urine and in several tissues of galactosemic patients. However, galactonate in patients’ plasma is below the detection level, and is not elevated in the RBC of all galactosemic patients (Ning and Segal 2000; Wehrli et al. 1997; Yager et al. 2003).

Diagnosis

Acute clinical presentation and diagnosis

Infants with classic galactosemia generally appear asymptomatic at birth. However, after a few days of galactose ingestion through breast and/or formula feeding, children start developing life-threatening symptoms that, if undiagnosed and untreated, may lead to death. Initial symptoms include poor feeding with poor weight gain, vomiting and diarrhea, hepatocellular damage, lethargy, and hypotonia. Progression of this acute neonatal toxicity syndrome may include the development of Gram negative sepsis, cataracts, and pseudotumor cerebri causing a bulging fontanel (Berry and Walter 2012).

There are several tests to diagnose classic galactosemia. Screening for reducing substances in urine can be informative; however, it is not sensitive or specific, leading to false positives due to fructosuria, lactosuria (from intestinal lactase deficiency), or to conditions that impair blood galactose clearance, such as severe liver disease or antibiotic treatment. In contrast, if the child is on intravenous feeding, galactosuria may no longer be present, thus leading to false negatives (Berry and Walter 2012; Bosch 2006).

A more specific approach is the measurement of galactose metabolites, such as galactose, Gal-1-P and/or galactitol, in blood and/or urine. Galactosemic patients present invariably high RBC Gal-1-P levels. However, benign variants can also originate increased Gal-1-P levels and diagnosis should not be done based exclusively on it (Berry 2012; Berry and Walter 2012). Hemolysate Gal-1-P can be measured by different methods: spectrophotometric coupled enzymatic assay, isotope-dilution gas chromatography–mass spectrometry (GC/MS), or tandem MS (MS/MS) (Chen et al. 2002a; Jensen et al. 2001; Schadewaldt et al. 2003). Another approach is the Paigen test, which quantifies total galactose through a microbiological assay which is, however, not suitable for automation and is sensitive to antibiotic therapy taken by newborns or their mothers (Beutler 1991). Nursing infants with galactosemia also present high galactitol amounts in their urine and plasma, which stay higher than in controls, even upon diet implementation. Galactitol in urine can be measured by nuclear magnetic resonance (NMR) or GC/MS, whereas in RBC GC/MS is required due to its higher sensitivity (Chen et al. 2002b; Palmieri et al. 1999; Wehrli et al. 1997; Yager et al. 2003, 2006).

The gold standard for diagnosis is the GALT activity measurement in RBC, which can be done by the semi-quantitative Beutler fluorescent spot test or by a preferable quantitative assay. It can be done indirectly by a coupled enzymatic assay, or directly by quantifying radioactively labeled Gal-1-P conversion to UDP-Gal or, alternatively, by quantifying unlabeled substrates and products by HPLC (Cuthbert et al. 2008; Lindhout et al. 2010). Classic galactosemic patients usually present undetectable or less than 1% of control GALT activity (Elsas 2010). RBC GALT activity analysis is, however, not suitable for children that have been subjected to blood transfusion within the last 3 to 4 months, since a false-negative might result.

GALT mutational analysis is currently available in many laboratories for the most common variations, and has been used in some newborn screening programs to refine the screening process. A negative result does not exclude the disease, and full gene sequencing, including deep intronic regions, may be required (Coelho et al. 2015b; Wadelius et al. 1993).

Newborn screening

Neonatal screening for classic galactosemia has been debated for years, but no consensus has been reached. The principles originally articulated by Wilson and Jungner for screening and later expanded by Pollitt et al. have been accepted as the criteria for neonatal screening (Clarke 2005; Pollitt et al. 1997). Galactosemia has been excluded from some newborn screening programs based on two major arguments: it can be diagnosed clinically and long-term complications still develop despite early treatment. Despite Pollitt et al. recognizing that effective treatment availability was not an absolute prerequisite for a disease to be included in newborn screening programs, galactosemia-specific screening was still not recommended. Nevertheless, there were recommendations for all samples with increased phenylalanine to be screened for galactosemia as a secondary test. A later study compared 139 children with metabolic diseases identified by neonatal screening (17 galactosemic) to 124 children identified on the basis of clinical symptoms (9 galactosemic), and concluded that, despite the similar rate of hospitalization, 47% of the clinically identified children had mental retardation compared to only 14% of those identified by newborn screening, and that parental stress tended to be greater in families of children identified clinically (Waisbren et al. 2002).

Newborn screening for galactosemia is included in several European countries—Austria, Germany, Hungary, Ireland, Sweden, Switzerland, The Netherlands—while others—Turkey, Italy, and Belgium—present pilot programs (EGS 2003; Karadag et al. 2013; Ohlsson et al. 2012). Ireland presents a high classic galactosemia incidence (1:16,476), especially in the Traveller population (1:430), and newborn screening for classic galactosemia has been performed since 1972 (Coss et al. 2013). Irish newborns undergo screening within 72 to 120 h after birth, while all high-risk Traveller neonates are evaluated at day 1 or 2. On the other hand, Sweden presents a relatively low frequency (1:100,000) and yet newborn screening program includes galactosemia (Ohlsson et al. 2012). Other countries, such as France and Portugal do not offer neonatal screening and some, like Norway, Denmark, and Scotland, have stopped their programs (EGS 2003; Hansen and Lie 1988; Lund et al. 2012; Shah et al. 2001). In the USA, screening for galactosemia is currently offered in all states, and in Canada only two out of ten provinces offer universal screening (Fridovich-Keil and Walter 2008; Shah et al. 2001).

Standard of care

Lifelong dietary restriction of galactose has been the therapeutic basis for classic galactosemia since Mason and Turner described in 1935 how removing galactose from the diet eliminated the acute clinical presentation.

After the initial symptoms and upon the first suspicion of galactosemia, patients should be put immediately on a galactose-restricted diet (Berry and Walter 2012). Commercial infant formulas appropriate for use in galactosemia management include elemental and soy formulas. Despite elemental formulas containing no galactose, there is insufficient evidence that supports their added value comparatively with soy formulas. In fact, the latter are most often recommended, except for premature infants, in which case an elemental formula is preferable (Van Calcar et al. 2014a).

With the introduction of solid foods, some galactose is inevitably introduced into the diet. While there is consensus regarding the restriction of most dairy products, cheese consumption has always been a matter of debate. Some studies have been developed to elucidate the galactose content in several cheeses, revealing that most mature cheeses are adequate for galactosemia diet (Portnoi and MacDonald 2009; Portnoi and MacDonald 2011; Portnoi and MacDonald 2016; Van Calcar et al. 2014b). Galactose is also naturally found in cereals, offal meats, pulses, fruits, and vegetables; their galactose content, however, is considerably lower than in lactose-rich foods (Gropper et al. 2000; Gross et al. 1995; Gross and Acosta 1991; Kim et al. 2007; Van Calcar et al. 2014b). In addition, galactose can also be found in its complex form, which is presumably hydrolyzed in the gastrointestinal tract, rendering galactose available for absorption. However, presently it is considered that most galactose is actually not available for digestion (Van Calcar et al. 2014a).

Concerning galactosemia outcome, the significance of non-dairy foods to the total galactose intake has long been questioned. Berry et al. demonstrated that a lactose-free diet highly enriched in fruits and vegetables resulted in a mean galactose intake of 54 mg per day, and further demonstrated that the daily ingestion of 200 mg of fruit-derived galactose (50 mg of pure galactose in fruit juice 4 times per day) during 3 weeks had no impact on RBC Gal-1-P values and relatively little effect on urinary galactitol levels, despite the patients having null RBC GALT activity (Berry et al. 1993). In another study, Bosch et al. demonstrated that galactose supplementation for 6 weeks up to a maximum of 600 mg per day—corresponding to the amount of galactose in 7 kg of apples, 2.5 kg of tomatoes or 12 kg of peas—did not result in any physical, ophthalmological, or biochemical abnormalities (Bosch et al. 2004a). These data suggest that reducing the daily dietary galactose intake by restricting fruit and vegetables is negligible and, in the short-term, does not seem to have a significant impact on the clinical outcome. In a retrospective study, Hughes et al. reported no difference in long-term complications of siblings from 14 families (total of 30 subjects) with lower (<20 mg/day) and higher galactose intake (>20 mg/day) (Hughes et al. 2009). Another study reported that the ingestion of galactose, gradually increased from 300 to 4000 mg/day for a period of 16 weeks, improved the abnormalities in plasma IgG N-glycan profiles (Coss et al. 2012). Furthermore, the realization that galactosemic patients endogenously synthesize galactose to an extent that far exceeds that from non-dairy foods has minimized this concern. Accordingly, some countries have liberalized the therapy, currently advising a lactose-free diet (Bosch et al. 2004a; Van Calcar et al. 2014a). The international clinical guideline for the management of classic galactosemia recommends a life-long galactose-restricted diet that only eliminates sources of lactose and galactose from dairy products, allowing mature cheeses, caseinates, and non-milk foods (Welling et al. 2016).

Pathophysiology and long-term outcome

While the success of early treatment on the acute neonatal symptoms is unquestioned, the long-term outcome can be extremely disappointing since many patients develop burdensome complications.

Cognitive impairment

One of the most frequent and well-established long-term complications is cognitive impairment. Across most studies, IQ standard scores have been found to be in the low average (85–100) to borderline-low (<85) range, with considerable inter-individual variability (Antshel et al. 2004; Doyle et al. 2010; Kaufman et al. 1995; Potter et al. 2008; Waggoner et al. 1990; Waisbren et al. 1983). Motor disturbances, such as coordination, gait, balance, fine motor tremors, and severe ataxia are quite frequent, as well as memory, speech, and language problems (Antshel et al. 2004; Hughes et al. 2009; Kaufman et al. 1995; Potter 2011; Potter et al. 2008, 2013; Robertson et al. 2000; Schweitzer et al. 1993; Timmers et al. 2011, 2012; Waggoner et al. 1990; Waisbren et al. 1983, 2012). Speech and language impairment has been estimated to affect 38–88% of patients and cannot be solely explained by lower cognitive abilities in general (Hughes et al. 2009; Potter et al. 2008; Robertson et al. 2000; Schweitzer et al. 1993; Timmers et al. 2011, 2012; Waggoner et al. 1990; Waisbren et al. 1983). Expressive language is mainly affected, with receptive language or comprehension being relatively preserved (Potter et al. 2008; Timmers et al. 2011). Patients exhibit speech motor abnormalities such as childhood dyspraxia of speech and voice dysfunction (Potter 2011; Potter et al. 2013), besides impaired cognitive planning of language at several stages, from conceptualization to lexical and syntactic planning (Timmers et al. 2012), showing altered neural activity and connectivity patterns (Timmers et al. 2015a).

Studies on galactosemic patients’ brains have reported structural abnormalities, such as cerebral and cerebellar atrophy, and white matter abnormalities possibly due to altered myelination (Crome 1962; Haberland et al. 1971; Hughes et al. 2009; Koch et al. 1992; Krabbi et al. 2011; Lo et al. 1984; Nelson et al. 1992; Wang et al. 2001). A recent study on the white matter microstructure in galactosemic patients revealed increased neurite dispersion (i.e., less organized axons) and lower neurite density (Timmers et al. 2015b). Impaired galactosylation of glycoconjugates in the brain has been suggested as the underlying pathogenic mechanism (Coss et al. 2012; Petry 1991).

Visual and perceptual impairments also occur in galactosemic patients and seem to be independent of the IQ (Antshel et al. 2004; Kaufman et al. 1995; Schweitzer et al. 1993). Handwriting, reading, and difficulties in mathematics are also common, and galactosemic children are often academically retained (Antshel et al. 2004; Schweitzer et al. 1993). School achievements are below the grades reached by healthy siblings and/or parents. Whereas a comprehensive multidisciplinary study on galactosemic adults reported an average schooling of 1 to 2 years of college, with an occupational level of skilled manual laborer (Waisbren et al. 2012), another revealed that many patients lacked educational qualifications and were unemployed (Bhat et al. 2005). Patients are often described as shy and reserved but generally do not present behavioral dysregulation (Antshel et al. 2004), and are single and live with their parents, as only a minority is able to build up strong partnerships outside the family core (Waisbren et al. 2012). Approximately 40% of patients recognize that galactosemia impairs their relationships with other people (Hoffmann et al. 2012). Bosch and colleagues reported that galactosemia is seen as a burden by a significant number of patients (39%), with many feeling different because of the disease (34%), and believing they are not well understood (22%). Furthermore, many parents feel the disorder influenced their contact with the child (73%) and that taking care of a galactosemic child represents a burden (60%), despite raising their child the same way as their healthy children (69 and 77%, respectively) (Bosch et al. 2004b). This study concluded that galactosemia negatively influences the health-related quality of life (HRQoL) on the communication, social and, most strikingly, cognitive domains. In another study, Bosch et al. compared the course of life of galactosemic patients with that of the general population and with phenylketonuric patients (Bosch et al. 2009). Galactosemic patients achieved fewer social and psychosexual developmental milestones as compared to healthy or phenylketonuric controls, suggesting that these differences result from specific complications of classic galactosemia and not from the burden of a chronic disease or lifelong dietary restrictions. The social and psychosexual development milestones of men studied in a small cohort appeared severely delayed, leading to the suggestion that early intervention (e.g., social skills training) might improve the patients’ psychosocial competences (Gubbels et al. 2011).

Bone health

Because of their galactose-restricted diet, patients are at risk for nutritional deficiencies, particularly regarding calcium, since dairy products are considered its best source for their high calcium content in casein-micelles (Lewis 2011). Decreased height and growth rate have been reported. However, growth often continues through the late teens, so that the target height can be reached by children who grow beyond the age of 18 (Panis et al. 2007; Waggoner et al. 1990). Treated galactosemic patients are at risk for diminished bone mineral density (BMD) (Batey et al. 2013; Kaufman et al. 1993; Panis et al. 2004; Rubio-Gozalbo 2002; van Erven et al. 2017). A patient group with no evidence of nutritional deficiencies exhibited decreased levels of bone formation and resorption markers (Panis et al. 2004). Since carboxylated osteocalcin is a marker for the vitamin K nutritional status, Panis et al. developed a 2-year randomized clinical trial to investigate whether vitamin K, given in combination with calcium and vitamin D, could play a role in the pathophysiology of this complication. In fact, they found a statistically significant increase in osteocalcin carboxylation in both prepubertal and pubertal children receiving supplementation (Panis et al. 2006).

Batey et al. reported that out of 32 evaluated adult patients, only 10% were followed by a nutritionist, suggesting nutritional counseling as a strategy to optimize bone accrual during adolescence and to maintain bone mass during adulthood (Batey et al. 2013). Nevertheless, several studies have excluded major nutritional deficiencies, and concluded that other intrinsic factors must be involved (Batey et al. 2013; Kaufman et al. 1993; Panis et al. 2005, 2006).

Gonadal impairment

The most common complication reported for girls and women with classic galactosemia is primary ovarian insufficiency (POI), with an incidence above 80% (Berry 2008; Fridovich-Keil et al. 2011; Kaufman et al. 1981; Rubio-Gozalbo et al. 2010; Waggoner et al. 1990). POI clinical manifestations range from absent or delayed pubertal development, primary amenorrhea, secondary amenorrhea or oligomenorrhea, and premature menopause. Many female patients do not spontaneously reach puberty, which has to be induced to reach a normal pubertal development and prevent sequelae (Gubbels et al. 2008; Spencer et al. 2013). The proposed pathogenic mechanisms include ovarian damage due to elevated Gal-1-P and galactitol; UDP-Gal deficiency causing aberrant glycosylation of glycoconjugates involved in ovarian function; increased apoptosis of maturing follicles, with accelerated follicle atresia; and possible abnormalities of the immune system, such as unrecognized auto-ovarian antibodies (Forges et al. 2006; Lai et al. 2003b; Liu et al. 2000; Rubio-Gozalbo et al. 2010). Two neonates have been reported to have morphologically normal ovaries and abundant oocytes (Levy 1996; Levy et al. 1984), whereas young adult females’ ovaries have been reported to have a severely decreased number of normal primordial follicles (Rubio-Gozalbo et al. 2010). Follicle-stimulating hormone (FSH)—an indirect marker of ovarian reserve—has been found elevated in patients very early in life up to the onset of puberty (4 months to 12 years) (Berry 2008; Fridovich-Keil et al. 2011; Rubio-Gozalbo et al. 2010; Sanders et al. 2009). Anti-Mullerian hormone (AMH)—a direct marker for ovarian reserve that is produced by granulosa cells in the developing ovarian follicle—has been found low in female patients (Sanders et al. 2009; Spencer et al. 2013). However, low AMH levels in galactosemia patients might be not only due to follicle depletion, but might also reflect an impaired follicle maturation (Rubio-Gozalbo et al. 2010). Indeed, extremely low AMH levels do not preclude spontaneous pregnancy (Gubbels et al. 2009). In fact, spontaneous pregnancies occur (Briones et al. 2001; De Jongh et al. 1999; Gubbels et al. 2009; Kimonis 2001; Ohlsson et al. 2007; Roe et al. 1971; Samuels et al. 1976; Tedesco et al. 1972). And, whereas in the past women were told to be infertile, presently women are informed that spontaneous pregnancies may occur. The term subfertility is more accurate than infertility. Nevertheless, subfertility remains a major concern for patients and parents, and physicians are often asked about fertility preservation options (Spencer et al. 2013; van Erven et al. 2013).

Few studies have examined the male reproductive system and, until recently, male fertility was believed not to be impaired (Gubbels et al. 2013; Rubio-Gozalbo et al. 2010). A study on cryptorchidism in galactosemic individuals revealed a 25% prevalence (three of the 12 males), compared with ≤1% in the healthy age-matched population (Rubio-Gozalbo et al. 2006). A more recent investigation on the reproductive system of 26 galactosemic patients demonstrated an increased prevalence of cryptorchidism (11.6%), with low semen volume, and lower testosterone, inhibin B and sperm concentrations than in control subjects—although within the normal range on average—which might indicate mild defects in Sertoli and Leydig cell functions (Gubbels et al. 2013). With the exception of cryptorchidism, these abnormalities are expected to have little impact on fertility (Gubbels et al. 2013; Rubio-Gozalbo et al. 2006). Besides the three fathered pregnancies in the literature, there are no data on paternity in galactosemic patients other than anecdotal cases which may be related to a publication bias and to difficulty in documenting paternity, or to the known social interaction problems and delayed psychosocial development documented in these men (Gubbels et al. 2013; Waisbren et al. 2012).

Models of classic galactosemia: toward the understanding of the underlying pathophysiology

Different cellular and animal models have been developed to understand the pathogenic mechanisms of classic galactosemia.

Yeast model

Saccharomyces cerevisiae deleted in the GAL7 gene (the yeast orthologue of human GALT) shows a growth arrest upon galactose addition to the medium despite the presence of other carbon sources (Douglas and Hawthorne 1964, 1966). Using GALT-deficient yeast, Fridovich-Keil’s group has studied several human GALT mutations (Crews et al. 2000; Fridovich-Keil and Jinks-Robertson 1993; Fridovich-Keil et al. 1995; Mumma et al. 2008; Ross et al. 2004; Wells and Fridovich-Keil 1997). Furthermore, the yeast model has been used to provide new insights on the metabolic role of each of the Leloir pathway enzymes and galactose metabolites (Riehman et al. 2001; Ross et al. 2004). Interestingly, GAL1- (orthologue for the human GALK1 gene) deficient yeast does not cease to grow upon galactose addition to the growth medium (Ross et al. 2004; Slepak et al. 2005). Additionally, the yeast model of classic galactosemia has been used to study gene expression upon galactose exposure (De-Souza et al. 2014; Slepak et al. 2005), revealing that galactose induces metabolic and endoplasmic reticulum (ER) stress and triggers the unfolded protein response (UPR).

Bacterial model

Bacterial expression systems have been used to study several human GALT mutations, by expressing recombinant human GALT variants (Coelho et al. 2014b; Lai and Elsas 2001; Lai et al. 1999). Most recombinant human GALT variants displayed a severely impaired catalytic activity and/or decreased stability, establishing GALT misfolding and/or aggregation as the pathogenic mechanism underlying several variants, leading to the classification of classic galactosemia as a conformational disorder (Coelho et al. 2014b; McCorvie et al. 2013).

A prokaryotic model with a deletion of the endogenous galT gene has been employed to evaluate the functional impact of several human GALT mutations in a cellular context. Expression of the p.Q188R, p.K285N, p.G175D, and p.P185S variants failed to alleviate galactose toxicity (Coelho et al. 2015c).

Mouse model

Two decades ago, the first animal model of classic galactosemia—a Galt-knockout mouse—was developed (Leslie et al. 1996), displaying a complete loss of Galt activity and accumulating Gal-1-P at levels comparable to those in galactosemic humans. However, the mouse was described to remain healthy despite dietary exposure to galactose. More recently, another Galt-deficient mouse model was developed by Lai’s group, using a Galt gene-trapping approach, which exhibited null Galt activity and Gal-1-P accumulation in RBC (Tang et al. 2014). Despite some resistance to galactose toxicity, expanded characterization of the model revealed subtle phenotypic differences to wild-type mice. Histological examination of galactose-fed pups revealed hepatic and brain (cerebral and cerebellar) alterations. Additionally, excess galactose also led to manifestation of oxidative stress in mutant pups (lower GSH/GSSG ratio) comparatively to wild-type or non-challenged mutant pups. In the long-term, some degree of growth and fertility impairments also became evident. The newborn intoxicated pups that survived the galactose insult manifested a decreased growth rate and weight, even when normal chow resumed after the weaning period ended, that was only recovered with puberty. Additionally, mutant mice exhibited a smaller litter size and a longer time to achieve pregnancy, suggestive of subfertility.

Fruit fly model

A Galt-deficient Drosophila melanogaster model has also been developed, which showed a null GALT activity and Gal-1-P accumulation (Kushner et al. 2010). If exposed to galactose, these flies succumbed during development; however, they lived when maintained on a galactose-restricted diet. In the long-term, Galt-deficient adult flies under a galactose-restricted diet demonstrated an impaired negative geotaxic response, suggesting the development of movement impairments. Both galactose lethality and motor impairments could be rescued by the expression of a wild-type human GALT transgene (accounting for ≈ 4% of wild-type GALT activity). A more recent study has shown that GALT deficiency results in structural synaptic overelaboration and glycosylation abnormalities of the flies neuromuscular junction (NMJ), namely reductions in the galactosyl, N-acetylgalactosamine, and fucosylated moieties (Jumbo-Lucioni et al. 2014a). Mutant flies on restricted-galactose and high-galactose diets showed identical movement impairments and overelaborated NMJ architecture, reinforcing the notion that classic galactosemia’s long-term phenotype is independent of dietary galactose. Additionally, the Wnt trans-synaptic co-receptor and ligand abundance were shown to be altered. Since signaling of the Wnt protein Wingless (Wg) is regulated by the heparan sulfate proteoglycan (HSPG) co-receptor Dally-like protein (Dlp) and known to drive the NMJ synaptogenesis, the authors hypothesized that UDP-sugar deficiency triggered changes in the NMJ synaptomatrix glycosylation, including levels of HSPG Dlp, which subsequently affected the Wnt signaling, causing an excessive growth and overelaborated architectural complexity. Mutations in the GALK1- or UDP-glucose dehydrogenase-encoding genes were identified, respectively, as critical environmental and genetic modifiers of behavioral and cellular defects. Double GALT and GALK mutants or overexpression of UDP-Glc dehydrogenase corrected the glycosylation defects, the NMJ architectural alterations and the movement impairments associated with the Drosophila classic galactosemia model. Recently, Daenzer and co-workers reported that the Drosophila model did not show phenotypic rescue by knocking out the GALK1 gene (Daenzer et al. 2016). Additionally, double GALT and GALE mutants as well as GALT and UGP mutants displayed severe abnormalities in the coordinated locomotor movement, in NMJ formation, in the synaptomatrix glycosylation and in the Wnt trans-synaptic signaling (Jumbo-Lucioni et al. 2016).

These animal models are able to recapitulate many pathophysiological aspects of classic galactosemia and expand the molecular insights from bacterial and yeast models, bringing new important insights of the underlying pathogenesis.

Therapeutic approaches in classic galactosemia

In 1935, Mason and Turner described how removing galactose from the diet eliminated the neonatal toxicity and thereafter, dietary galactose restriction became the first recommended therapy for galactosemia that still prevails nowadays.

Considering that classic galactosemia is characterized by deficiency in UDP-hexoses, the potential therapeutic role of uridine was evaluated in a 5-year longitudinal study of galactosemic patients (Manis et al. 1997). Despite no improvements in cognitive function, it remains to be clarified whether uridine was able to enter the cells (Tang et al. 2012).

Aldose reductase inhibition has also been suggested as a therapeutic option, since galactitol is an important pathogenic agent. However, the fact that patients with GALK1 deficiency experience galactitol accumulation but not the broad range of severe long-term complications of classic galactosemia strongly suggests a limited efficacy of aldose reductase inhibitors (Berry 1995).

Another ongoing therapeutic strategy under study concerns the conversion of classic galactosemia into GALK1 deficiency, a milder form of galactosemia in which patients do not accumulate Gal-1-P. GALK1-deficient patients may present cataracts (attributed to galactitol accumulation) and neurological sequelae. In a review from the literature, Bosch et al. reported a frequency of mental retardation in 7% of patients (three out of 43) (Bosch et al. 2003). In a more recent study, approximately 30% of patients (five out of 16) were described as presenting mental retardation, which the authors could not unambiguously attribute to GALK1 deficiency and hypothesized that secondary factors could also take a toll (consanguinity was excluded as a causative agent) (Hennermann et al. 2011). Using recombinant human GALK1 protein, a quantitative high-throughput screening identified a number of small-molecule GALK1 inhibitors, of which the spiro-benzoxazole containing series emerged as lead compounds. These compounds have been further optimized and validated in primary patient fibroblasts, exhibiting reasonable pharmacokinetic properties (Liu et al. 2015; Odejinmi et al. 2011; Tang et al. 2010; Wierenga et al. 2008).

Increased oxidative stress has been reported in the fruit fly model of classic galactosemia, and superoxide dismutase-mimicking manganese-based compounds proved beneficial to GALT-null larvae and adult flies (Jumbo-Lucioni et al. 2014b). Moreover, it has been hypothesized that acetylated anthocyanins derived from purple sweet potato color, previously shown to have a protective effect against galactose toxicity in mice on a high galactose diet (Lu et al. 2010; Zhang et al. 2010), may alleviate galactosemia’s oxidative damage (Timson 2014).

Until recently, the effect of a mutation was assumed to affect only its coding potential. In recent years, however, there has been increasing evidence that both exonic and deep intronic mutations may affect splicing. Mutational analysis of Portuguese patients revealed an intronic variation, c.820 + 13A>G (IVS8 + 13A>G), as the second most frequent mutation. Functional characterization of c.820 + 13A>G revealed it activates the cryptic donor site c.820 + 14_820 + 15, leading to the exonization of the first 13 nucleotides of intron 8, thereby confirming that this intronic variation is actually a disease-causing mutation. Coelho and coworkers employed two locked nucleic acid (LNA) oligonucleotides and the mini-gene approach to successfully restore the splicing profile, thus establishing a proof of concept for the application of antisense therapy for mis-splicing mutations in classic galactosemia (Coelho et al. 2015b).

Classic galactosemia: where do we stand?

After more than 100 years since the first description of galactosemia, there are still many “clouds gathering over galactosemia” (Anonymous 1982):
  • The only currently available treatment, though very effective at preventing or resolving acute and potentially lethal sequelae in the neonatal period, is ineffective in preventing long-term sequelae. Despite early diagnosis and early implementation of therapy, patients still go on to develop burdensome chronic complications.

  • Younger siblings of galactosemic patients put on a galactose-restricted diet immediately after birth fail to show a better clinical outcome than the older siblings later in life.

  • The reduction in galactose intake by restricting fruit and vegetables seems to be negligible and it has been described that a slightly higher galactose intake may actually improve glycosylation abnormalities. Many countries have now liberalized the therapy, currently advising a lactose-free diet.

  • Severe impairment of GALT activity results in the accumulation of galactose metabolites and in UDP-hexoses deficiency. As GALT substrate, Gal-1-P accumulation has been widely pointed out as a key pathogenic agent. Glycosylation abnormalities are extensively reported in classic galactosemia and have also been suggested as an important pathogenic factor.

  • Small-molecule GALK1 inhibitors that mitigate Gal-1-P accumulation are being explored as possible therapeutic agents for classic galactosemia and studies on patients’ fibroblasts have shown encouraging results.

  • The pathogenic mechanism underlying the severe impairment of GALT activity is protein misfolding and/or aggregation, leading to the recognition of classic galactosemia as a conformational disorder. In recent years, the paradigm that the great majority of inherited diseases are conformational disorders has emerged, which has provided a common framework for the analysis of rather diverse diseases, including Alzheimer’s and Parkinson’s diseases, and many other proteinopathies.

  • The most suitable therapeutic strategy for conformational disorders focuses on pharmacological/chemical chaperones, which support the proper folding of protein variants and improve their stability and consequently their activity above a functional threshold. In the specific case of classic galactosemia, a chaperone-based therapy would aim to mitigate GALT misfolding and aggregation, thereby enhancing GALT activity/stability. Considering the molecular heterogeneity of the GALT locus, which leads to a high number of protein variants, ideally pharmacological/chemical chaperones should act in a non-mutation-specific way.

  • The recently reported crystallographic structure of human GALT provides new insights on the mutations’ effect on GALT structure and function, and will support the design of compounds with pharmacological interest.

  • The improvement of patients’ outcome is also hindered by differences in care provided worldwide to galactosemic patients (Jumbo-Lucioni et al. 2012).

  • In 2012, an international network of galactosemia—GalNet —was established, aiming at the harmonization and improvement of patients’ outcome and care (Rubio-Gozalbo et al. 2016). It includes professionals from centers in 18 European countries, Israel, Australia, and the USA (www.galactosemianetwork.org). Thus far, a patient Registry has been developed and is currently being implemented across countries; expert- and evidence-based guidelines for treatment and follow-up have been devised, and collaborative research is taking place.

In conclusion, although the outcome for classic galactosemia is still very disappointing at present, there have been encouraging developments in recent years. With the recent growth of knowledge on the molecular basis of galactosemia, there is now a new hope for the development of a truly effective therapy, possibly combining different yet complementary approaches.

Notes

Acknowledgements

Support of the European Union’s Horizon 2020 research and innovation program under Marie Skłodowska-Curie Actions Individual Fellowship (MSCA-IF; project ID: 658967), and of iNOVA4Health - UID/Multi/04462/2013, a program financially supported by Fundação para a Ciência e a Tecnologia/Ministério da Educação e Ciência, through national funds and co-funded by FEDER under the PT2020 Partnership Agreement, are acknowledged.

Compliance with ethical standards

Conflict of interest

None.

Informed consent/animal rights

This article does not contain any studies with human or animal subjects performed by the any of the authors.

Funding

iNOVA4Health - UID/Multi/04462/2013, a program financially supported by FCT/Ministério da Educação e Ciência, through national funds and co-funded by FEDER under the PT2020 Partnership Agreement, is acknowledged. The authors confirm independence from the sponsors; the content of the article has not been influenced by the sponsors.

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Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  • Ana I. Coelho
    • 1
  • M. Estela Rubio-Gozalbo
    • 1
  • João B. Vicente
    • 2
  • Isabel Rivera
    • 3
    • 4
  1. 1.Department of Pediatrics and Department of Clinical GeneticsMaastricht University Medical CentreMaastrichtThe Netherlands
  2. 2.Instituto de Tecnologia Química e Biológica António XavierUniversidade Nova de LisboaOeirasPortugal
  3. 3.Metabolism & Genetics Group, Research Institute for Medicines (iMed.ULisboa), Faculty of PharmacyUniversidade de LisboaLisbonPortugal
  4. 4.Department of Biochemistry and Human Biology, Faculty of PharmacyUniversidade de LisboaLisbonPortugal

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