Glutaric aciduria type I (synonym, glutaric acidemia type I) is a rare organic aciduria. Untreated patients characteristically develop dystonia during infancy resulting in a high morbidity and mortality. The neuropathological correlate is striatal injury which results from encephalopathic crises precipitated by infectious diseases, immunizations and surgery during a finite period of brain development, or develops insidiously without clinically apparent crises. Glutaric aciduria type I is caused by inherited deficiency of glutaryl-CoA dehydrogenase which is involved in the catabolic pathways of L-lysine, L-hydroxylysine and L-tryptophan. This defect gives rise to elevated glutaric acid, 3-hydroxyglutaric acid, glutaconic acid, and glutarylcarnitine which can be detected by gas chromatography/mass spectrometry (organic acids) or tandem mass spectrometry (acylcarnitines). Glutaric aciduria type I is included in the panel of diseases that are identified by expanded newborn screening in some countries. It has been shown that in the majority of neonatally diagnosed patients striatal injury can be prevented by combined metabolic treatment. Metabolic treatment that includes a low lysine diet, carnitine supplementation and intensified emergency treatment during acute episodes of intercurrent illness should be introduced and monitored by an experienced interdisciplinary team. However, initiation of treatment after the onset of symptoms is generally not effective in preventing permanent damage. Secondary dystonia is often difficult to treat, and the efficacy of available drugs cannot be predicted precisely in individual patients. The major aim of this revision is to re-evaluate the previous diagnostic and therapeutic recommendations for patients with this disease and incorporate new research findings into the guideline.
Glutaric aciduria type I (synonym, glutaric acidemia type I) is an autosomal recessive disease caused by inherited deficiency of glutaryl-CoA dehydrogenase (GCDH, EC 184.108.40.206). It has an estimated prevalence of 1 in 100,000 newborns (Lindner et al. 2004). The GCDH gene is localized on chromosome 19p13.2 and encodes a flavin adenine dinucleotide-dependent mitochondrial matrix protein that is involved in the degradative metabolism of L-lysine, L-hydroxylysine and L-tryptophan (Fu et al. 2004; Greenberg et al. 1995). More than 200 disease-causing mutations are known (Goodman et al. 1998; Zschocke et al. 2000). Biochemically, GA-I is characterized by an accumulation of glutaric acid (GA), 3-hydroxyglutaric acid (3-OH-GA), glutaconic acid (less frequently), and glutarylcarnitine (C5DC). These can be detected in body fluids (urine, plasma, CSF) and tissues by gas chromatography/mass spectrometry (GC/MS) or electrospray-ionization tandem mass spectrometry (MS/MS; Baric et al. 1999; Chace et al. 2003). Two biochemically defined subgroups of patients have been described based on urinary metabolite excretion of GA, i.e., low and high excretors (Baric et al. 1999). The low excreting patients have the same risk of developing striatal injury as the high excretors (Christensen et al. 2004; Kölker et al. 2006) and must not be considered to have a “mild” clinical phenotype.
Since the description of two index patients in 1975 (Goodman et al. 1975) more than 500 patients have been reported worldwide. Four genetic isolates with a high carrier frequency (up to 1:10) and over-representation of this disease have been identified, the Amish Community (Morton et al. 1991), Canadian Oji-Cree natives (Haworth et al. 1991), the Irish travellers (Naughten et al. 2004), and the Lumbee in North Carolina (Basinger et al. 2006). Untreated, approximately 90% of patients will develop neurological disease during a finite period of brain development (age 3-36 months) following an acute encephalopathic crisis often precipitated by gastroenteritis, intercurrent febrile illness, immunization, or surgical intervention (Hoffmann et al. 1991; Kölker et al. 2006). The characteristic neurological sequela of these crises is acute bilateral striatal injury and, subsequently, a complex movement disorder. Dystonia is the dominant extrapyramidal symptom, usually superimposed on axial hypotonia (Hoffmann et al. 1991; Kyllerman et al. 1994; Heringer et al. 2010). With aging, there is a tendency for a fixed dystonia and akinetic-rigid parkinsonism to develop (Gitiaux et al. 2008). Morbidity and mortality is high in patients who have had a crisis (Kyllerman et al. 2004; Kölker et al. 2006). In 10-20% of patients, neurologic disease has been demonstrated in the absence of any documented encephalopathic crisis and has been termed insidious-onset (Busquets et al. 2000; Hoffmann et al. 1996) and late-onset (Bähr et al. 2002; Külkens et al. 2005). Two patients with insidious-onset type were reported in whom striatal injuries had occurred before or shortly after birth, followed by latent periods of several months before disability was apparent (Strauss et al. 2007). This study suggests that catabolism in the postnatal transition period may contribute to the manifestation of neurological impairment.
During the last three decades therapeutic concepts have been established and optimized for GA-I. Dietary treatment in combination with oral supplementation of L-carnitine and riboflavin (less frequently) during maintenance treatment, and an intensified emergency treatment during episodes of intercurrent illness are used for the majority of patients. This treatment strategy has considerably reduced the frequency of acute encephalopathic crises and thus morbidity and mortality in early diagnosed patients (Kölker et al. 2006; Kölker et al. 2007a; Monavari and Naughten 2000; Strauss et al. 2003; Strauss et al. 2007). Indeed a recent study has confirmed the effectiveness of emergency and maintenance therapy (Heringer et al. 2010). Therefore, GA-I is now considered to be a treatable condition. Furthermore, studies in Gcdh-deficient mice, an animal model for GA-I, has provided evidence that low lysine diet and increased glucose intake reduces the accumulation of putatively neurotoxic GA and 3-OH-GA in the brain, and that carnitine supplementation increases the formation of C5DC and the brain, liver and plasma concentrations of free carnitine (Sauer et al. 2010; Zinnanti et al. 2007).
Early clinical diagnosis is hampered by the lack of characteristic or even pathognomonic signs and symptoms before an encephalopathic crisis. Macrocephaly is found in 75% of patients during infancy (Bjugstad et al. 2000), but is non-specific. Therefore GA-I has been included in the disease panel of newborn screening in some countries. DNA-based mutation analysis is used for the high-risk screening in one cohort of low excretors (Greenberg et al. 2002).
Significant differences still exist in the approaches used to diagnose and manage affected patients, and there is a wide variation in the outcome, particularly in patients diagnosed presymptomatically (Kölker et al. 2006). The major aim of this guideline is to re-assess the common practice and to formulate recommendations for diagnosis and management of GA-I based on the best evidence available.
The guideline development process was initiated following the 3rd International Workshop on Glutaryl-CoA Dehydrogenase Deficiency in Heidelberg, Germany (October 2003). Three further meetings were held in Rimini (May 2004), Amsterdam (August 2004), and Prague (May 2005). Working groups were established focusing on the guideline topics. The members of the guideline development group (GDG) performed systematic literature review, drafted the guideline, and discussed it with the GDG members and external consultants. The guideline draft was reviewed by external consultants (J. V. Leonard, M. Dixon, R. Surtees†, M. Kyllerman, B. Wilcken). The final guideline was published in 2007 (Kölker et al. 2007b) and, subsequently, it was revised including new literature and feedback from metabolic experts. The 1st revision was based on discussions during the 5th guideline meeting in Hamburg (September 2007). The recent 2nd revision is based on the 6th guideline meeting in San Diego (September 2009). The GDG consists of Pediatric metabolic specialists and child neurologists (A. Boneh, A. B. Burlina, S. I. Goodman, A. Garcia Cazorla, C. R. Greenberg, G. F. Hoffmann, D. M. Koeller, S. Kölker [chairman], C. Mühlhausen, E. R. Naughten), chemists (E. Christensen, M. Duran, J. G. Okun [secretary]), a psychologist (P. Burgard), specialist metabolic dietitians (E. Müller, M. Dixon), and an adult neurologist (A. P. Burlina).
Systematic literature review
The evidence base for this guideline was similar to the methodology used by SIGN (Scottish Intercollegiate Guideline Network; URL: http://www.sign.ac.uk). A systematic review of the literature on GA-I was carried out using Medline, Embase, the Cochrane Library, MedLink, and Orphanet. The years covered were 1975-2010. Internet searches were also performed on various websites including international and national societies for inborn errors of metabolism and those of parent groups. The main searches were selected and evaluated by a minimum of two members of the GDG before conclusions were considered as evidence (Suppl. Tables 1–3).
Prospective follow-up study evaluating the guideline
To evaluate whether the use of the guideline improves the outcome of affected individuals with GA-I, some of the GDG members (S. K., G. F. H., P. B., C. M., E. M.) performed a prospective follow-up study in Germany including 52 patients. This study has confirmed that the use of therapy recommendations (see statements #7-9 of this guideline) significantly improves the outcome of patients diagnosed by newborn screening (Heringer et al. 2010). It showed for the first time that both basic metabolic treatment (low lysine diet, carnitine supplementation) and emergency treatment were clearly beneficial for patients diagnosed by newborn screening. The beneficial effect of emergency treatment was more pronounced than that of maintenance treatment. Furthermore, this study confirmed that follow-up by a metabolic center is beneficial, highlighting that treatment and follow-up of these patients should be performed by an interdisciplinary team of specialists (see statement #6).
To the best of our knowledge, none of the recommendations in the previously published guideline (Kölker et al. 2007b) have been proven invalid. However, based on clinical studies published in the interim the level of evidence on which recommendations are based has changed in some areas. To improve the clarity of the text, the wording of some statements has been revised and age-adapted recommendations have been included for metabolic maintenance and emergency treatment. Furthermore, we have removed six good clinical practice (GCP) statements and four low grade recommendations (previous statements #7, 9-11, 13-16, 21, and 26) reducing the total number of statements from 31 to 21. This has been made to improve the readability by providing this information in the text only and to focus on statements with defined level of evidence. Five GCP statements with high practical relevance (#1, 10, 11, 17, and 21) have been left in the revised version.
Figure 1 summarizes the diagnostic procedure for GA-I.
GA-I is defined as inherited deficiency of GCDH confirmed by enzyme analysis and/or demonstration of two disease-causing mutations. All other signs, symptoms and laboratory abnormalities that are found in affected patients are not pathognomonic so that the diagnosis should be suspected, but is not confirmed. These include macrocephaly, acute encephalopathy, basal ganglia injury, white matter disease, movement disorders, subdural and retinal hemorrhage, and isolated elevation of GA, 3-OH-GA, and C5DC in body fluids. Most of these in isolation have a wide differential diagnosis, whereas a combination of two or more abnormalities increases the probability for GA-I.
Statement #1. The accurate diagnosis of GA-I has important practical implications when devising treatment plans and giving appropriate information to children and their families. The diagnostic work-up should be done by metabolic specialists (GCP).
Newborn and high-risk screening
Newborn screening disease panel
GA-I has been widely considered a disorder for which newborn screening should be offered (Pollitt et al. 1997; Thomason et al. 1998; Watson et al. 2006). It has already been included in the disease panels of expanded newborn screening in some countries.
Timely diagnosis and start of treatment, i.e., before irreversible neurological symptoms occur, results in a better outcome than start of treatment after the onset of neurological disease (Bijarnia et al. 2008; Boneh et al. 2008; Heringer et al. 2010; Hoffmann et al. 1996; Kölker et al. 2006; Kölker et al. 2007a; Naughten et al. 2004; Strauss et al. 2003; Strauss et al. 2007). The aim of newborn and high-risk screening is to reduce the incidence of neurological disease.
Population-wide newborn mass screening for GA-I is performed by MS/MS analysis of acylcarnitines in newborn blood spots. High-risk screening for GA-I is performed in neonates with an increased a priori risk.
Summarizing results from international screening laboratories the overall prevalence of GA-I is approximately 1 in 100,000 newborns but varies considerably in different countries. The diagnostically relevant metabolite is C5DC in dried blood spots (DBS). In addition, some laboratories are also using ratios to other measured acylcarnitines (Lindner et al. 2006) and others repeat the analysis on another bloodspot from the same DBS as an internal quality control, but this is a matter for individual laboratories and no recommendations are given in this guideline. In comparison to DBS, cord blood testing is of limited value in detecting many inherited metabolic diseases (Walter et al. 2009). However, this has not yet been studied systematically in GA-I.
A C5DC value above the cut-off is considered positive and requires follow-up. The cut-off level for C5DC has to be set by each laboratory as it will be influenced by many factors. Cut-off levels are typically adjusted with more experience of screening, a process that is likely to continue. At present, there is no general recommendation for the establishment and setting of cut-off levels.
Not all patients can be diagnosed by this method, as there are patients with a normal or only slightly increased C5DC concentration in DBS. Patients with GA-I have been missed by newborn screening (Heringer et al. 2010; Smith et al. 2001; Wilcken et al. 2003) or by retrospective analysis of the newborn blood spots (Gallagher et al. 2005; Treacy et al. 2003), particularly those with a low excreting phenotype. To circumvent this problem most laboratories are now using additional tests for follow-up investigations of initially positive screening results such as analysis of urinary GA and 3-OH-GA. Apparent increases in C5DC have also been demonstrated in medium-chain acyl-CoA dehydrogenase deficiency, most probably because of acylcarnitines of identical mass, such as hydroxydecanoylcarnitine (Napolitano et al. 2004). In patients with multiple acyl-CoA dehydrogenase deficiency, C5DC can also be elevated but is accompanied by increased concentrations of other acylcarnitines. In patients with renal insufficiency due to acquired or congenital renal disease, C5DC can also be increased (Hennermann et al. 2009). Since newborn screening in the child reflects the metabolic state of the mother and infant, newborn screening laboratories should be aware that elevated C5DC concentrations may indicate maternal GA-I (Crombez et al. 2008; Garcia et al. 2008).
Statement #2. For mass newborn screening for glutaric aciduria type I determination of C5DC in DBS by MS/MS should be used (grade B, see Suppl. Table 2).
Alternative methods for high-risk population screening
Clusters of affected patients from genetic isolates with high carrier frequencies have been identified. The Amish, Irish travellers and Lumbees have a high excretor phenotype (Basinger et al. 2006; Naughten et al. 2004; Strauss et al. 2003), whereas the Oji-Cree natives are low excretors (Greenberg et al. 2002). High-risk screening in the Amish and the Irish travellers was first performed by organic acid analysis but detection of C5DC in DBS is now used. There have been no documented false negatives in the Amish and the Irish travellers populations, whereas false negatives in the Oji-Cree natives were common when MS/MS was used. As a consequence, high-risk screening using DBS and a DNA-based technique specific for the DNA mutation present in this population has been implemented (Greenberg et al. 2002).
Statement #3. In a cohort with a high disease incidence due to a single common GCDH mutation and a low excretor phenotype, DNA based methods should be considered for newborn screening. The use of MS/MS-based screening in such populations will likely lead to false negative results (grade D).
Confirmation of a positive screening result
A positive MS/MS screening result should be confirmed by one or more alternative techniques, including a sensitive method for quantitative determination of GA and 3-OH-GA in urine or blood such as GC/MS (Al-Dirbashi et al. 2005; Baric et al. 1999; Shigematsu et al. 2005), mutation analysis of the GCDH gene, and/or GCDH enzyme analysis (Christensen 1983; Goodman et al. 1998). A normal urine or blood 3-OH-GA level will make the diagnosis unlikely, whereas an elevated urine or blood level of 3-OH-GA should be followed by mutation analysis and start of treatment. The finding of two known disease-causing mutations will establish the diagnosis. If only one or no known disease-causing mutation or no mutations are found, GCDH activity should be determined. Low enzyme activity will again establish the diagnosis, while a normal activity will exclude it (Fig. 1). Since GCDH gene analysis is more broadly available than GCDH enzyme analysis and since the identification of two disease-causing mutations is also important for prenatal diagnosis and genetic counselling, we recommend starting with GCDH gene analysis. According to local availability and experience, however, GCDH enzyme analysis could be performed first.
Statement #4. For the confirmation of a positive newborn screening result, a specific diagnostic work-up is required, including a quantitative analysis of GA and 3-OH-GA in urine or blood, mutation analysis, and, if feasible, enzyme analysis (grade D).
If an infant or child presents with clinical signs or symptoms, or neuroradiologic findings (Suppl. Table 4) of GA-I, a diagnostic evaluation should be undertaken regardless of whether the child was previously evaluated in a newborn screening programme. The major disadvantage of relying on clinical suspicion before initiating testing is that there is no single pathognomonic sign or symptom that will reliably identify affected patients before irreversible neurological damage occurs. A few asymptomatic patients have been diagnosed in the course of a diagnostic work-up for macrocephaly (Kölker et al. 2006), but this is a non-specific sign and has a low predictive value. The only effective way to identify patients with a low a priori risk is via newborn screening.
Quantitative organic acid analysis has some advantages for selective screening compared to MS/MS analysis of acylcarnitines in DBS or plasma (higher sensitivity and specificity), particularly in patients with secondary carnitine depletion, and is therefore usually the first line method for selective screening (Baric et al. 1999). False positive test results have been observed (Suppl. Table 5); the separation of 3-OH-GA from 2-hydroxyglutaric acid may be cumbersome. The analysis of urinary C5DC is also helpful since it may remain elevated in patients with secondary carnitine depletion, and in low excretors (Tortorelli et al. 2005). Analysis of GCDH enzyme activity in fibroblasts or leukocytes is the ‘gold standard’ for confirming the diagnosis (Christensen 1983). Mutation analysis of the GCDH gene has a sensitivity of 98-99% (Zschocke et al. 2000). The use of in vivo loading tests using lysine or prolonged fasting tests is not recommended as age-matched controls are usually not available and the tests are potentially harmful.
Statement #5. In patients with signs and symptoms of glutaric aciduria type I, a specific diagnostic work-up should include quantitative analysis of GA and 3-OH-GA in urine or blood, GCDH gene mutation analysis, and/or enzyme analysis (grade D).
Cascade screening is the systematic programme of approaching relatives of index patients enabling the identification of asymptomatic patients and of carriers. It is most likely to be valuable in inbred communities and may prevent the manifestation of neurologic disease in patients born before the start of, or missed by, C5DC screening. However, cascade screening may not be necessary once newborn mass screening has been established in a country. Despite the preventive value of the information, relatives may object to cascade screening insisting on their right ‘not to know’ that they are at risk (de Wert 2005). However, it is important to screen siblings of identified patients.
Metabolic maintenance treatment
Table 1 summarizes recommended best practice on metabolic maintenance treatment in GA-I based on the clinical experience of the GDG.
Treatment should be started before confirmation of the diagnosis by enzyme and/or mutation analysis where there is strong suspicion of GA-I (Fig. 1). It has been demonstrated recently that implementation of metabolic treatment and regular follow-up by specialized metabolic centers improves the outcome of patients with GA-I (Heringer et al. 2010).
Statement #6. Metabolic treatment should be implemented by an interdisciplinary team that includes metabolic pediatricians, dietitians, and nurses. Parents and patients should have regular training and written treatment protocols (grade C).
Treatment and outcome
Most patients remain asymptomatic if treatment is started in the newborn period (Bijarnia et al. 2008; Boneh et al. 2008; Heringer et al. 2010; Kölker et al. 2007a; Naughten et al. 2004; Strauss et al. 2003). Dietary treatment in combination with carnitine and emergency treatment has been demonstrated to be effective in preventing neurological disease (Kölker et al. 2007b). Recently the relative efficacy of each single component of this therapy has been evaluated, demonstrating that outcome was best in patients who received all three interventions (low lysine diet, carnitine, and emergency treatment), and that deviations from basic metabolic treatment (low lysine diet, carnitine) resulted in an intermediate outcome. Disregard of emergency treatment recommendations was associated with a poor outcome (Heringer et al. 2010). The results of this study are supported by the highest level of evidence available regarding GA-I (i.e., 2++), and confirm previous observations suggesting that emergency treatment is the most important component of this treatment strategy (Kölker et al. 2007a, b; Naughten et al. 2004; Strauss et al. 2007). Since striatal injury occurs acutely or insidiously until age 6 years, treatment recommendations for maintenance and emergency treatment are strict for patients at ages 0-6 years and relaxed for patients older than 6 years of life.
In contrast to patients identified presymptomatically, outcome in GA-I is poor when diagnosed after the manifestation of neurological disease (Busquets et al. 2000; Bjugstad et al. 2000; Hoffmann et al. 1996; Kyllerman et al. 2004). The value of metabolic treatment is unclear in patients with severe neurological symptoms, but individual patients may benefit by prevention of progressive neurological deteroriation (Bjugstad et al. 2000; Hoffmann et al. 1996; Kölker et al. 2006; Strauss et al. 2003).
Use of dietary recommendations and individualization of treatment
Dietary recommendations outlining the age-dependent needs of a growing child have been developed by international organizations (Suppl. Tables 6, 7). They are usually set to the safe level. Note that in Suppl. Table 6 protein recommendations for infants and children may vary significantly between the recommendations due to the use of different reference proteins and the use of average versus safe levels. Standard dietary recommendations can form the basis for dietary treatment in GA-I but due to discrepant and varying requirements for nutrients and energy in symptomatic children they should be adjusted to the individual (Müller and Kölker 2004; Yannicelli et al. 1994). There is still limited practical experience with the use of more recent recommendations such as the report of the joint WHO/FAO/UNU expert consultation (World Health Organization 2007).
Low lysine diet
Dietary treatment for GA-I aims to reduce the intake of lysine, the quantitatively most relevant amino acid precursor of neurotoxic GA and 3-OH-GA, while maintaining sufficient intake of essential nutrients and energy substrates. Many metabolic centers limit the total protein intake to reduce lysine intake rather than limiting lysine intake per se. This is often for practical reasons such as the lack of precise or recent data on lysine contents of foods in their country. However, since the lysine content varies considerably in different natural proteins, eg 2-4% (lysine/protein) in cereals and 9% (lysine/protein) in fish, the daily lysine intake may be less well controlled by calculation of protein intake rather than lysine intake (Suppl. Table 8). This may also increase the risk of essential amino acid deficiencies, including tryptophan, which is associated with neurological dysfunction such as irritability and sleep irregularity (Hoffmann et al. 1991). Low lysine diet is often combined with the use of lysine-free, tryptophan-reduced amino acids (AA) supplements. These supplements are given with the aim of preventing malnutrition by providing essential amino acids and (depending on the product) also minerals, trace elements and vitamins. Although in some studies (Busquets et al. 2000; Kölker et al. 2006; Kölker et al. 2007a; Heringer et al. 2010; Naughten et al. 2004) the majority of patients on a low lysine diet also received lysine-free, tryptophan-reduced amino acids supplements, whether a low lysine diet is more effective and safer if it is combined with these supplements has not been systematically studied.
The use of a diet based on lysine intake combined with lysine-free, tryptophan-reduced AA supplements to maintain adequate total protein intake has been associated with the most favorable neurologic outcome and normal growth in some studies (Heringer et al. 2010; Kölker et al. 2006; Kölker et al. 2007a), whereas other studies in smaller cohorts have not found a significant effect of dietary treatment on the outcome (Strauss et al. 2007; Boneh et al. 2008). A possible explanation for this discrepancy is that larger patient groups are required for the delineation of a beneficial effect of dietary treatment from the somewhat stronger effect of emergency treatment. The prescription of dietary treatment should be adjusted to the experience of metabolic centers. For instance, prescribing a total amount of natural protein based on international dietary recommendations in combination with an exchange system (i.e., one exchange is the amount of food which provides 1 g protein) may be used instead of calculation of lysine intake. This method will reduce overall lysine intake but is likely to be associated with more day to day variability.
Breast feeding has proven benefits for infants but, with the exception of phenylketonuria (PKU), there are few published reports for inherited metabolic diseases (Huner et al. 2005; MacDonald et al. 2006). However, breast feeding in infants with GA-I should be encouraged. It can be performed in analogy to PKU (Francis and Smith 1981) using breastfeeding on demand with special lysine-free and tryptophan-reduced infant formula given prior to breastfeeds thus limiting lysine intake. Although other safe methods for incorporation of breastfeeding into treatment of PKU have been established (van Rijn et al. 2003), they have not been systematically studied in GA-I. Since the amount of lysine in breastmilk is known (86 mg per 100 mL, “Bundeslebensmittelschlüssel II.3”; www.bls.nvs2.de), daily lysine intake can be estimated when breast milk is the only source of natural protein. Bottle feeding can be based on actual lysine intake as the lysine content of infant formula is known. However, limiting lysine intake via exclusive use of standard infant formula may increase the risk for nutritional deficiencies.
Statement #7. A low lysine diet (i.e., reducing lysine intake to a safe requirement) with or without additional administration of lysine-free, tryptophan-reduced amino acids supplements should be used for dietary treatment, in particular in asymptomatic patients up to age 6 years (grade C).
Dietary treatment after age 6 years
The long-term outcome in patients with GA-I is not well documented. Besides the injury associated with acute encephalopathic crises, there is also evidence of chronic neurologic deterioriation in late-onset and insidious-onset patients with no documented crisis (Bähr et al. 2002; Harting et al. 2009; Külkens et al. 2005). With the exception of single case reports that have suggested a potential benefit to dietary treatment after age 6 years, its efficacy has not been systematically evaluated. However, there is evidence for ongoing extrastriatal neuroradiological changes after age 6 years (Harting et al. 2009), and though the clinical relevance of these changes is unclear, it may be advisable to continue dietary treatment using a less stringent protocol than that used prior to age 6 years.
Children with feeding problems
Dystonic children are at increased risk for malnutrition (Müller and Kölker 2004; Yannicelli et al. 1994), mobility and feedings skills are important prognostic parameters (Kölker et al. 2006). Children with feeding problems therefore need skilled metabolic dietetic supervision. They often require tube and overnight feeding and pharmacotherapy or surgery (i.e., fundoplication, gastrostomy, jejunostomy) to maintain adequate nutrition.
The efficacy of the low lysine diet critically depends upon adequate provision of information and education of parents, patients and caregivers. It is essential they receive continued support and education.
Secondary carnitine depletion in plasma is common in untreated patients (Lipkin et al. 1988; Seccombe et al. 1986), whereas the concomitant intracellular carnitine concentrations are unknown. Conjugation of glutaryl-CoA to form non-toxic C5DC is considered a physiological detoxification, and proposed to replenish the intracellular CoA pool (Seccombe et al. 1986). L-Carnitine supplementation alone or in combination with a low lysine diet is thought to contribute to improved outcome in patients identified during the newborn period (Heringer et al. 2010; Kölker et al. 2007a; Strauss et al. 2003). However, no randomized controlled studies are available (Nasser et al. 2009; Walter 2003). To prevent or reverse secondary carnitine depletion, an initial oral dosage of 100 mg L-carnitine/kg per day is commonly used (Kölker et al. 2007a; Strauss et al. 2003). The dosage is then adjusted to maintain the plasma free L-carnitine concentration in the normal range. Usually, oral L-carnitine supplementation can be reduced to 50 mg/kg per day in children at age 6 years, and further reduced in adolescents and adults. A reduction of L-carnitine can be considered if side effects, such as diarrhoea and fish odor, occur.
Statement #8. L-Carnitine should be supplemented in patients with glutaric aciduria type I and should be continued lifelong (grade C).
Although an improvement of biochemical parameters has been suggested in single patients (Brandt et al. 1979; Lipkin et al. 1988), there is no firm evidence that riboflavin improves the neurological outcome of this disease (Kölker et al. 2006). Riboflavin responsiveness in GA-I appears to be exceedingly rare (Chalmers et al. 2006). There is no standardized protocol of how to assess riboflavin sensitivity, or means to predict it based on GCDH gene mutation analysis.
There is no firm evidence that administration of other drugs, such as phenobarbitone, N-acetylcysteine, creatine monohydrate, topiramate, glutamate receptor antagonists and antioxidants are beneficial (Greenberg et al. 2002; Kyllerman et al. 1994; Kyllerman et al. 2004; Strauss et al. 2003), though theoretically they may appear to be of value.
Routine treatment does not protect against encephalopathic crises, so it is crucial to use an intensified emergency treatment protocol when the patient is thought to be at risk (Heringer et al. 2010; Monavari and Naughten 2000; Strauss et al. 2007). The decision to institute emergency treatment should be made very freely with a low index of suspicion.
Basic principles of emergency treatment
Emergency treatment follows the basic treatment principles of metabolic diseases of the intoxication type (Dixon and Leonard 1992; Prietsch et al. 2002): (1) the prevention or reversal of a catabolic state by administration of a high-energy intake (plus insulin to control for hyperglycemia if required); (2) reduction of GA and 3-OH-GA production by transient reduction or omission of natural protein for 24 (-48) hours; (3) amplification of physiological detoxification mechanisms and prevention of secondary carnitine depletion by L-carnitine supplementation and (4) maintenance of normal fluid, electrolytes, and pH status via enteral of IV fluids. Non-adherence to previously described emergency treatment recommendations (Kölker et al. 2007b) has been associated with a high probability of developing striatal injury (Heringer et al. 2010).
Management of emergency treatment
Delayed start of the emergency regimen can have serious consequences. The causes of delay are many and varied; all of these should be identified systematically (Table 2). For example, plans for metabolic management during and after elective surgery should be made ahead in consultation with the surgical team prior to the procedure.
Start of emergency treatment
The possibility of a crisis should be suspected during each infectious disease, immunization, or surgical intervention during the vulnerable period (age 0-6 years). In particular, conditions accelerating catabolism, such as repeated vomiting and diarrhoea (with or without fever), and the manifestation of severe neurological symptoms (i.e., hypotonia, irritability, rigor, dystonia, reduced consciousness) should be considered as alarming symptoms. With increasing age, and in particular after age 6 years, the risk of acute neurological insult appears to be much reduced (Bjugstad et al. 2000; Kölker et al. 2006; Strauss et al. 2003). Emergency treatment should aim to start before the onset of alarming neurological symptoms (Heringer et al. 2010; Strauss et al. 2007).
Statement #9. Emergency treatment should start without delay and should be performed aggressively during febrile illness, surgery and immunization within the vulnerable period for acute encephalopathic crises (up to age 6 years) (grade B).
Emergency treatment at home
If the body temperature is less than 38.5°C and the child is not vomiting, is tolerating the formulae and if there is no alteration in level of consciousness or any other alarming neurological symptoms, a trial treatment period at home of up to 12 hours is recommended. During this time period patients should be reassessed every two hours regarding state of consciousness, fever, and feed tolerance. If parents are adequately trained, maltodextran solutions can be applied via nastrogastric, gastrostomy, or jejunostomy tube to achieve overnight and optimal energy intakes. If body temperature rises above 38.5°C, antipyretics such as ibuprofen or paracetamol should be administered. If emergency treatment at home is successful and no worrying signs or symptoms occur during this period, maintenance treatment should be reintroduced stepwise during the next 48 (-72) h. Table 3 summarizes recommended best practice based on the clinical experience of the GDG.
Emergency treatment at hospital
If the patient has recurrent vomiting, recurrent diarrhoea, reduced intake of nutrients, spiking temperature or concerning neurological signs, emergency therapy at home is not safe and the patient should be transferred immediately to a metabolic center or the closest hospital (preferably under the guidance of a metabolic center). At hospital the child should be seen immediately, assessed and treatment begun. Table 4 summarizes recommended best practice based on the clinical experience of the GDG.
Emergency treatment after age 6 years
Although encephalopathic crises are extremely rare if they occur at all after age 6 years (Bjugstad et al. 2000; Kölker et al. 2006; Strauss et al. 2003), it cannot be concluded that febrile illness, surgery and immunization are completely harmless at this age group.
Statement #10. Emergency treatment in children after age 6 years should be considered at least during severe illness. It should be performed similarly to that in the age group 0-6 years with adaptation to the individual (GCP).
Management of neurologic complications
The major neurological complications in GA-I are the manifestation of a complex movement disorder and subdural hemorrhage. Epileptic seizures and arachnoid cysts may also be observed.
Management of movement disorders
Striatal injury induces a variable clinical picture. Dystonia superimposed on axial hypotonia is usually the dominant extrapyramidal symptom (Hoffmann et al. 1996; Kyllerman et al. 1994). With aging, it tends to evolve from mobile to fixed dystonia and to be associated with akinetic-rigid parkinsonism (Gitiaux et al. 2008). Prevention of fixed dystonia and joint deformities can be done by means of physical and occupational therapy as well as with pharmacological and surgical treatments.
Statement #11. In all patients with GA-I, expert neurological evaluation should be performed by a neuropediatrician and/or later on by a neurologist to identify clearly the kind and severity of movement disorder. In addition, dietitians, physicotherapists, occupational therapists, orthopedists, seating and speech specialists and providers of communication aids, should be consulted to provide multi-disciplinary support for children with movement disorders (GCP).
Dystonia rating scales
Objective assessment of the complex movement disorder in symptomatic patients is important to evaluate the efficacy of treatment and to adjust the dosage of medications. One study (Heringer et al. 2010) however has identified limitations in the use of the Barry-Albright dystonia rating scale (Monbaliu et al. 2010; Barry et al. 1999) since it likely underestimated the severity of the movement disorder in infants and young children.
Movement disorders in GA-I are very difficult to treat, and many of the drugs used have not been studied systematically (Burlina et al. 2004). Previous studies have shown that baclofen and benzodiazepines are benefical in the majority of symptomatic patients and are recommended for first-line treatment.
Baclofen is generally used for symptomatic treatment of spasticity and also for the long-term treatment of dystonia in GA-I. Together with diazepam it is the most widely used and efficacious drug in GA-I (Hoffmann et al. 1996) and with beneficial effects in 85% of symptomatic patients (Kyllerman et al. 1994). Oral baclofen should be used in dosages according to general recommendations. Intrathecal baclofen administration has been used with success in a few children with severe dystonia (Kyllerman et al. 2004), and reduces the risk of over-sedation.
Diazepam (positive effect in more than 90% of symptomatic patients) and clonazepam have been successfully used in treating dystonia (Hoffmann et al. 1996; Kyllerman et al. 1994; Kyllerman et al. 2004). Dosages should be administered according to general recommendations. In patients in whom the severity of symptoms is highly variable the dosage can be adjusted daily within a given range. Intermittent treatment may be required to prevent tachyphylaxis.
If patients do not benefit from treatment with baclofen and/or benzodiazepines or adverse effects occur, anticholinergic drugs should be considered as second line medication.
Trihexyphenidyl can be effective in treating dystonic symptoms but there are few reports on its use in GA-I (Burlina et al. 2004). In children, trihexiphenidyl has been mainly used as a symptomatic treatment for dystonic cerebral palsy. Although the response to trihexiphenidyl treatment seems best in adolescents and adults, it may also be safe and effective in children if sufficient time is given to respond and the dosage is increased slowly. However, secondary effects are common, and it may worsen symptoms in patients with hyperkinetic forms of dystonia, as seen in GA-I (Rice and Waugh 2009; Sanger et al. 2007). Adverse effects such as blurred vision and dry mouth are usually temporary. Memory deficit and confusion usually persist and require a reduction of the dosage. Periodic ocular tonometry is recommended for adult patients.
Botulinum toxin type A may be useful to prevent hip dislocation and disabling limb dystonia (Burlina et al. 2004). Some patients may develop immunity against the toxin, precluding further therapy; therefore, botulinum toxin is usually administered every three to six months to minimize the formation of antibodies against the toxin.
Drugs for the movement disorder of no proven benefit or with adverse effects
Some antiepileptic drugs have been used in the past (Hoffmann et al. 1996; Kyllerman et al. 1994; Kyllerman et al. 2004; Yannicelli et al. 1994): Vigabatrin and valproate had little effect (i.e., 10-25% symptomatic patients showed a therapeutic benefit). Vigabatrin has putatively severe adverse effects (peripheral visual field defects). Valproate effectively may promote disturbances in the mitochondrial acetyl-CoA/CoA ratio. Therefore, valproate and vigabatrin should not be used for the treatment of movement disorder in GA-I. Carbamazepine was always unequivocally ineffective. There is no improvement of the extrapyramidal syndrome with L-DOPA. In a few patients, amantadine was used but there was no improvement in dystonic movement disorder.
Statement #12. Baclofen and benzodiazepines as monotherapy or in combination should be used as first line drug treatment for focal and generalized dystonia. Intrathecal baclofen should be considered as additional therapy for generalized dystonia and spasticity. Trihexyphenidyl should be considered as second line treatment for dystonia, particularly in adolescents and adults. Botulinum toxin A should be considered as additional therapy for severe focal dystonia (grade D).
Stereotactic surgery (pallidotomy) for severe generalized dystonia has been reported for three patients. The results reported in two patients were unsatisfactory (Strauss et al. 2003), whereas short-term improvement in dystonic symptoms were described in one (Rakocevic et al. 2004). The results of deep brain stimulation of the globus pallidus internus has not yet been reported in patients with dystonia due to GA-I.
Epilepsy is not a major symptom in GA-I, whereas single seizures may be observed during an acute encephalopathic crisis (Greenberg et al. 2002; Kölker et al. 2006; Kyllerman et al. 2004; Strauss et al. 2003). In one child, however, epileptic seizures were the sole presenting feature (McClelland et al. 2009), but dystonic movements may be mistaken as seizures (Cerisola et al. 2009). No study has compared the relative efficacy of antiepileptic agents in GA-I. However, as mentioned before valproate should not be used because of potential effects on mitochondrial function.
Statement #13. Diagnosis, choice of antiepileptic drug therapy and management of seizures in GA-I should follow existing guidelines – except for the use of valproate which should be avoided in this condition. The diagnosis of epilepsy and choice of antiepileptic drugs should be made by a pediatric neurologist or pediatrician with expertise in childhood epilepsy. In adulthood, patients with epilepsy should be followed and antiepileptic therapy should be monitored by an adult neurologist (GCP).
Subdural haemorrhage and arachnoid cysts
Subdural haemorrhage may occur at any age in GA-I but peaks during the age of maximal extent of macrocephaly, i.e., late infancy (Brismar and Ozand 1995; Köhler and Hoffmann 1998; Woelfle et al. 1996). Minor head traumas with disruption of elongated bridging veins have been suggested as underlying mechanisms. The exact frequency of subdural bleeding is unknown, since affected patients may remain asymptomatic. Subdural haemorrhage in GA-I may be mistaken with shaken baby syndrome and vice versa (Hartley et al. 2000; Morris et al. 1999). Bitemporal arachnoid cysts have been described in some affected patients and should result in a high suspicion for GA-I (Hald et al. 1991; Jamjoom et al. 1995; Lücherath et al. 2000; Martinez-Lage et al. 1994), whereas unilateral arachnoid cysts are a rare occurence in this disease.
Statement #14. Children with subdural haemorrhage and/or bitemporal arachnoid cysts should be investigated for glutaric aciduria type I, in particular if occuring in combination with macrocephaly and/or a movement disorder (grade D).
Statement #15. Glutaric aciduria type I should be excluded in children with suspected shaken baby syndrome using the recommendations for selective screening (see also statement #5, Fig. 1) (grade D).
Neurosurgical interventions have been performed in a small number of affected patients with arachnoid cysts and subdural haemorrhage (Hald et al. 1991; Lütcherath et al. 2000; Martinez-Lage et al. 1994; Woelfle et al. 1996). The majority of these patients had a poor neurological outcome or sometimes with significant worsening of the neurological symptoms in the context of the neurosurgical intervention. In particular, neurosurgical interventions in undiagnosed patients who do not receive specific metabolic treatment neurosurgical interventions can precipitate an encephalopathic crisis. Subdural haemorrhage may regress without neurosurgical intervention.
Statement #16. Neurosurgical intervention for arachnoid cysts and subdural haemorrhages in affected patients should be undertaken very cautiously in close consultation with the pediatric neurosurgeon (grade D).
The metabolic management during and after any surgical interventions should be based on recommendations for metabolic treatment and should be supervised by a metabolic specialist (see also statements #6-10).
The aim of regular therapy monitoring is to assess the efficacy of treatment and to identify complications or side effects. In children, it should also include an evaluation of psychomotor development and growth. In general, monitoring should include those tests that influence therapeutic decisions and should be preventive in its overall approach. However at present, there is no reliable marker that predicts the outcome of GA-I.
Clinical monitoring should be frequent, and consist of a wide variety of investigations, including general pediatric parameters (e.g., anthropometrics, developmental milestones), neurological assessment, and specific psychological tests. Although overall average cognitive outcomes may be normal, subtle deficits, mainly in speech development and fine motor function, may be observed in individual patients (Beauchamp et al. 2009; Harting et al. 2009). Expertise from general pediatricians, metabolic specialists, and dietitians from metabolic centers should be included into the evaluation of patients in an integrative way. In addition, consultations from other specialties (e.g., child neurologists, psychologists, physiotherapists) should be considered as necessary.
Statement #17. Therapy should be accompanied by regular professional monitoring. Monitoring should be intensified at any age if there are new complications (disease- or therapy-related) or non-adherence to treatment (GCP).
Routine biochemical monitoring
Table 5 summarizes recommended best practice based on the clinical experience of the GDG on routine laboratory monitoring in GA-I. At present, there is no reliable biochemical marker that is useful for the monitoring of maintenance treatment in GA-I and there is considerable variation in expert opinion (Mühlhausen et al. 2004).
A decrease in the urinary concentrations of GA and 3-OH-GA has been demonstrated in high excretors following dietary treatment (Hoffmann et al. 1991; Hoffmann et al. 1996; Strauss et al. 2003), whereas this biochemical response is usually not found in the urine of low excretors (Greenberg et al. 2002). At present, there is no evidence that urinary concentrations of GA and 3-OH-GA correlate with the long-term clinical outcome (Christensen et al. 2004; Kölker et al. 2006).
Statement #18. Urine analysis of GA and 3-OH-GA is not informative for therapy monitoring (grade D).
Analysis of all essential amino acids in plasma is useful to ensure that nutrition is not being compromised in patients receiving dietary treatment and in children with feeding problems (Müller and Kölker 2004; Yannicelli et al. 1994). Tryptophan should be assayed by specific HPLC analysis (or MS/MS analysis) as conventional amino acid analysis is not satisfactory (Krstulovic et al. 1977; Laich et al. 2002).
Statement #19. Amino acids in plasma (ideally 3-4 h postprandially) should be monitored during dietary treatment (grade D).
L-Carnitine supplementation prevents secondary depletion of free carnitine and is thought to contribute to improved outcome (Heringer et al. 2010; Kölker et al. 2006; Seccombe et al. 1986). Carnitine status in plasma can be assessed using HPLC or MS/MS analysis, and gives valuable information on compliance. MS/MS analysis in dried blood spots is also useful to detect secondary carnitine depletion, although less accurately than plasma analysis.
Statement #20. Carnitine status in plasma should be monitored in all patients to detect secondary carnitine depletion (grade D).
Assessment of C5DC and other acylcarnitines in dried blood spots is of little value in regular biochemical monitoring. C5DC will increase markedly with the start of L-carnitine supplementation.
Additional biochemical monitoring
Analysis of other parameters, such as complete blood cell count, albumin, calcium, phosphate, vitamin D status, ferritin, and serum transaminases may be helpful for routine surveillance (Yannicelli et al. 1994).
Biochemical monitoring during acute illness
Vomiting, diarrhoea and reduced intake of nutrients and fluids increase the risk of dehydration, electrolyte abnormalities, acidosis, and subsequently acute encephalopathic crises (Bjugstad et al. 2000; Hoffmann et al. 1996; Kölker et al. 2006; Kyllerman et al. 2004; Strauss et al. 2003). Imbalances in the metabolic state, hydration and serum electrolytes, and complications should be identified on admission and emergency treatment adjusted accordingly.
Cranial MRI in affected patients often demonstrates a characteristic pattern of gray and white matter changes and abnormalities of CSF spaces that should prompt a high suspicion for the diagnosis of GA-I (Suppl. Table 4). However, striatal and extrastriatal MR abnormalities may be highly variable and may progress in a different way and with discrepant velocity (Harting et al. 2009). MRI studies, in particular those using echo-planar imaging spin-echo or apparent diffusion coefficient maps, detect striatal lesions earlier and more reliably than CT scans (Brismar and Ozand 1995; Desai et al. 2003; Elster 2004; Neumaier-Probst et al. 2004; Oguz et al. 2005; Strauss et al. 2007; Twomey et al. 2003). Some of these neuroradiological changes can also be detected by ultrasound (Forstner et al. 1999), even already during the last trimester of pregnancy (Lin et al. 2002; Mellerio et al. 2008). The benefit of serial MRI investigations is unclear and is not considered essential for regular monitoring. As long as the fontanelle is open, cranial ultrasound can be used instead (but may miss hygromas).
Statement #21. Neuroradiologic investigations should be performed in case of neurologic deteroriation but are not generally recommended for regular follow-up monitoring (GCP).
Although many questions remain regarding the pathogenesis and treatment of GA-I, much has been learned since publication of the initial version of this guideline. Basic and clinical research, as well as the diligent recording of the natural history of the disease in many patients, has led to improvements in patient outcomes. These advances in our knowledge and the quality of evidence regarding treatment of GA-I have been incorporated into these revised guidelines. However, in spite of recent advances, future studies will be required to evaluate long-term outcome, better characterize atypical patients, and develop reliable diagnostic algorithms for patients with a low excretor phenotype. Further evidence regarding dietary management and therapy monitoring is also needed. The results of these and other studies will increase the level of evidence of future guidelines, which in the long-term we hope will improve the outcome of all patients with GA-I.
Dried blood spots
Glutaric aciduria type I
Good clinical practice
Gas chromatography/mass spectrometry
Guideline developmental group
Tandem mass spectrometry
Scottish Intercollegiate Guidelines Network
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We thank Eileen R. Naughten for her valuable contribution to the guideline development.
Details of funding
This publication arises from the project "E-IMD" (to S. Kölker, G. F. Hoffmann, E. Christensen, A. B. Burlina and A. Garcia Cazorla) which has received funding from the European Union, in the framework of the Health Programme. Guideline development for glutaric aciduria type I (GA-I) has also been supported by the German Federal Ministry of Education and Science (BMBF # 01GM0305; to S. Kölker and G. F. Hoffmann) and the “Kindness for Kids” Foundation, Munich, Germany (to S. Kölker and G. F. Hoffmann). Milupa Metabolics, SHS International, Applied Nutrition, Nutricia, and Vitaflo have sponsored the guidelines meetings. The authors confirm independence from the sponsors; the content of the article has not been influenced by the sponsors.
This guideline is not intended to serve as a standard of care. Standards of care are determined on the basis of all clinical data available for an individual case and are subject to change as scientific knowledge and technology advance and patterns of care evolve. Adherence to guideline recommendations will not ensure the correct diagnosis and satisfactory outcome in every case, nor should they be construed as including all proper methods of diagnostic work-up and care, or excluding other acceptable methods aimed at the same results. The ultimate judgement must be made by the appropriate healthcare professional(s) responsible for clinical decisions regarding a particular clinical procedure or treatment plan. The judgement should only be arrived at following discussions of the options with the patient and their family, covering the diagnostic and treatment choices available.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
References to electronic databases:
Glutaric aciduria type I: OMIM # 231670. Glutaryl-CoA dehydrogenase: EC 220.127.116.11.
Competing interest: None declared.
Communicated by: Ertan Mayatepek
Electronic supplementary materials
Below is the link to the electronic supplementary material.
Levels of evidence (DOC 38 kb)
Grades of recommendations (DOC 38 kb)
Evidence table of systematic literature review (DOC 195 kb)
Neuroradiologic findings in glutaric aciduria type I (DOC 40 kb)
Pitfalls of organic acid analysis in urine. (DOC 40 kb)
International dietary recommendations (DOC 73 kb)
a. Recommended dietary allowances for amino acids. b. Estimates of amino acid requirements (DOC 55 kb)
Estimation of lysine intake. a. Average lysine content in protein from different kinds of food. b. Estimation of the lysine content of manufactured food (DOC 54 kb)
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Kölker, S., Christensen, E., Leonard, J.V. et al. Diagnosis and management of glutaric aciduria type I – revised recommendations. J Inherit Metab Dis 34, 677 (2011). https://doi.org/10.1007/s10545-011-9289-5
- Newborn Screening
- Arachnoid Cyst
- Glutaric Acid
- Glutaric Aciduria Type