Skip to main content

Systematic Review and Meta-analysis of Intelligence Quotient in Early-Treated Individuals with Classical Galactosemia

  • Research Report
  • Chapter
  • First Online:
JIMD Reports, Volume 37

Abstract

Introduction: Cognitive impairment is a well-known complication of classical galactosemia (CG). Differences in patient characteristics and test methods have hampered final conclusions regarding the extent of intellectual disabilities in CG. The primary aim of this systematic review was to assess intellectual performance in early-treated (≤4 weeks of life) individuals with confirmed CG (defined by absent or barely detectable GALT enzyme activity and/or the presence of two null or severe missense variations), assessed with comparable test instruments. The full-scale IQ (FSIQ) was the variable of interest.

Methods: A clinical librarian developed search strategies, and two independent investigators performed the study selection, risk of bias assessment and data extraction. Individual patient data were pooled for meta-analysis using linear mixed-effect models with a random intercept per study and including covariates (age or gender) as fixed effects where appropriate.

Results: Four articles were included in this meta-analysis. Data of 87 individuals (median age 13 years, range 3–38 years) were used to assess mean FSIQ in CG. The FSIQ ranged from 47 to 122, and the mean score was 87 (95% CI, 81–94). Forty-five percent of individuals attained scores <85, almost 40% attained scores of 85–100, and a minority (15%) attained scores above 100. There was no significant correlation between FSIQ and age.

Conclusions: Results from this meta-analysis fortify conclusions from previous studies that early-treated individuals with CG are at risk for having impaired cognitive abilities. However, IQ varies considerably between affected individuals.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Institutional subscriptions

References

  • Antshel KM, Epstein IO, Waisbren SE (2004) Cognitive strengths and weaknesses in children and adolescents homozygous for the galactosemia Q188R mutation: a descriptive study. Neuropsychology 18:658–664

    Article  PubMed  Google Scholar 

  • Badawi N, Cahalane SF, McDonald M et al (1996) Galactosaemia – a controversial disorder. Screening & outcome. Ireland 1972-1992. Ir Med J 89:16–17

    CAS  PubMed  Google Scholar 

  • Bates D, Maechler M, Bolker B, Walker S (2014) lme4: linear mixed-effects models using Eigen and S4. R package version 1.1-6. http://CRAN.R-project.org/package=lme4

  • Borenstein M, Hedges LV, Higgins JPT, Rothstein HR (2009) Introduction to meta-analysis. Wiley, London, pp 83–84

    Book  Google Scholar 

  • Bosch AM (2006) Classical galactosaemia revisited. J Inherit Metab Dis 29:516–525

    Article  CAS  PubMed  Google Scholar 

  • The Cochrane Collaboration (2011) Cochrane handbook for systematic reviews of interventions version 5.1.0 [updated March 2011]

    Google Scholar 

  • Coss KP, Doran PP, Owoeye C et al (2013) Classical Galactosaemia in Ireland: incidence, complications and outcomes of treatment. J Inherit Metab Dis 36:21–27

    Article  CAS  PubMed  Google Scholar 

  • Coss KP, Treacy EP, Cotter EJ et al (2014) Systemic gene dysregulation in classical Galactosaemia: is there a central mechanism? Mol Genet Metab 113:177–187

    Article  CAS  PubMed  Google Scholar 

  • Donnell GN, Collado M, Koch R (1961) Growth and development of children with galactosemia. J Pediatr 58:845–851

    Article  Google Scholar 

  • Doyle CM, Channon S, Orlowska D, Lee PJ (2010) The neuropsychological profile of galactosaemia. J Inherit Metab Dis 33:603–609

    Article  PubMed  Google Scholar 

  • Fishler K, Koch R, Donnell G, Graliker BV (1966) Psychological correlates in galactosemia. Am J Ment Defic 71:116–125

    CAS  PubMed  Google Scholar 

  • Fishler K, Donnell GN, Bergren WR, Koch R (1972) Intellectual and personality development in children with galactosemia. Pediatrics 50:412–419

    CAS  PubMed  Google Scholar 

  • Haidich AB (2010) Meta-analysis in medical research. Hippokratia 14:29–37. doi:10.5005/jp/books/10519

    CAS  PubMed  PubMed Central  Google Scholar 

  • Hansen TW, Henrichsen B, Rasmussen RK et al (1996) Neuropsychological and linguistic follow-up studies of children with galactosaemia from an unscreened population. Acta Paediatr 85:1197–1201

    Article  CAS  PubMed  Google Scholar 

  • Hoffmann B, Wendel U, Schweitzer-Krantz S (2011) Cross-sectional analysis of speech and cognitive performance in 32 patients with classic galactosemia. J Inherit Metab Dis 34:421–427

    Article  CAS  PubMed  Google Scholar 

  • Hughes J, Ryan S, Lambert D et al (2009) Outcomes of siblings with classical galactosemia. J Pediatr 154:721–726

    Article  PubMed  Google Scholar 

  • Jones NL, Leak D (1959) The treatment of congenital galactosaemia. Arch Dis Child 34:307–311

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kaufman FR, Reichardt JK, Ng WG et al (1994) Correlation of cognitive, neurologic, and ovarian outcome with the Q188R mutation of the galactose-1-phosphate uridyltransferase gene. J Pediatr 125:225–227

    Article  CAS  PubMed  Google Scholar 

  • Kaufman FR, McBride-Chang C, Manis FR et al (1995) Cognitive functioning, neurologic status and brain imaging in classical galactosemia. Eur J Pediatr 154:S2–S5

    Article  CAS  PubMed  Google Scholar 

  • Komrower GM, Lee DH (1970) Long-term follow-up of galactosaemia. Arch Dis Child 45:367–373

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lee DH (1972) Psychological aspects of galactosaemia. J Ment Defic Res 16:173–191

    CAS  PubMed  Google Scholar 

  • Maas CJM, Hox JJ (2005) Sufficient sample sizes for multilevel modeling. Methodology 1:86–92

    Article  Google Scholar 

  • Manis FR, Cohn LB, McBride-Chang C et al (1997) A longitudinal study of cognitive functioning in patients with classical galactosaemia, including a cohort treated with oral uridine. J Inherit Metab Dis 20:549–555

    Article  CAS  PubMed  Google Scholar 

  • Ounap K, Joost K, Temberg T et al (2010) Classical galactosemia in Estonia: selective neonatal screening, incidence, and genotype/phenotype data of diagnosed patients. J Inherit Metab Dis 33:175–176

    Article  PubMed  Google Scholar 

  • R Core Team (2014) A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. http://www.R-project.org/

    Google Scholar 

  • Rasmussen RK, Andreassen AB, Stromme P, Hansen TW (1996) Learning disabilities and language pathology in patients with galactosemia. Logoped Phoniatr Vocol 21:157–162

    Article  CAS  PubMed  Google Scholar 

  • Rizzo M, Székely G (2010) DISCO analysis: a nonparametric extension of analysis of variance. Ann Appl Stat 4:1034–1055

    Article  Google Scholar 

  • Rizzo M, Székely G (2014) Energy: e-statistics (energy statistics). R package version 1.6.2. http://CRAN.R-project.org/package=energy

  • Rubio-Agusti I, Carecchio M, Bhatia KP et al (2013) Movement disorders in adult patients with classical galactosemia. Mov Disord 28:804–810

    Article  PubMed  Google Scholar 

  • Schadewaldt P, Hoffmann B, Hammen HW et al (2010) Longitudinal assessment of intellectual achievement in patients with classical galactosemia. Pediatrics 125:e374–e381

    Article  PubMed  Google Scholar 

  • Schweitzer S, Shin Y, Jakobs C, Brodehl J (1993) Long-term outcome in 134 patients with galactosaemia. Eur J Pediatr 152:36–43

    Article  CAS  PubMed  Google Scholar 

  • Shield JP, Wadsworth EJ, MacDonald A et al (2000) The relationship of genotype to cognitive outcome in galactosaemia. Arch Dis Child 83:248–250

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Waggoner DD, Buist NRM (1993) Long-term complications in treated galactosemia. 175 US cases. Int Pediatr 8:97–100

    Google Scholar 

  • Waggoner DD, Buist NR, Donnell GN (1990) Long-term prognosis in galactosaemia: results of a survey of 350 cases. J Inherit Metab Dis 13:802–818

    Article  CAS  PubMed  Google Scholar 

  • Waisbren SE, Norman TR, Schnell RR, Levy HL (1983) Speech and language deficits in early-treated children with galactosemia. J Pediatr 102:75–77

    Article  CAS  PubMed  Google Scholar 

  • Waisbren SE, Potter NL, Gordon CM et al (2012) The adult galactosemic phenotype. J Inherit Metab Dis 35:279–286

    Article  PubMed  Google Scholar 

  • Widhalm K, Miranda-Da-Cruz B, De Sonneville LMJ (2002) Information processing characteristics and uridine treatment in children with classical galactosemia. Nutr Res 22:257–270

    Article  CAS  Google Scholar 

  • Wilkin A, Derrington C, White R, et al (2010) Improving the outcomes for Gypsy, Roma and traveller pupils: final report: research brief. Department of Education 138

    Google Scholar 

  • Zuur A, Ieno EN, Walker N et al (2009) Mixed effects modelling for nested data. In: Mixed effects models and extensions in ecology with R. Springer, New York. Chapter 5

    Chapter  Google Scholar 

Download references

Acknowledgements

The authors would like to thank Arnold G. E. Leenders for creating the search strategies.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Annet M. Bosch .

Editor information

Editors and Affiliations

Additional information

Communicated by: Ivo Bari, M.D., Ph.D., Professor of Pediatrics

Take-Home Message

Early-treated individuals with classical galactosemia are at risk for having impaired cognitive abilities, but FSIQ scores vary considerably between affected individuals.

Contributions of Individual Authors

All authors participated in analysis and interpretation of data and drafting the article and revising it critically for important intellectual content. Annet M. Bosch, Johanna H. van der Lee, Susan E. Waisbren and Lindsey Welling participated additionally in conception and design of the study.

Guarantor

Annet M. Bosch.

Conflict of Interest

Annet M. Bosch is in receipt of research grants from Nutricia and was a member of an advisory board for Nutricia, Merck Serono and BioMarin.

Kevin M. Antshel declares that he has no conflict of interest.

Hugh-Owen Colhoun declares that he has no conflict of interest.

Matthias Gautschi declares that he has no conflict of interest.

Stephanie Grünewald declares that she has no conflict of interest.

Rebecca Holman declares that she has no conflict of interest.

Johanna H. van der Lee declares that she has no conflict of interest.

Eileen P. Treacy declares that she has no conflict of interest.

Susan E. Waisbren declares that she has no conflict of interest.

Lindsey Welling declares that she has no conflict of interest.

Details of Funding

This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors.

Details of Ethics Approval

Not required for this research study. This article does not contain any studies with human or animal subjects performed by any of the authors.

Electronic Supplementary Material

Supplementary Data 1

Search strategies (DOCX 22 kb)

Supplementary Data 2

Data retrieval (DOCX 52 kb)

Supplementary Data 3

Raw data FSIQ scores classical galactosemia patients (PDF 53 kb)

Rights and permissions

Reprints and permissions

Copyright information

© 2017 SSIEM and Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Welling, L. et al. (2017). Systematic Review and Meta-analysis of Intelligence Quotient in Early-Treated Individuals with Classical Galactosemia. In: Morava, E., Baumgartner, M., Patterson, M., Rahman, S., Zschocke, J., Peters, V. (eds) JIMD Reports, Volume 37. JIMD Reports, vol 37. Springer, Berlin, Heidelberg. https://doi.org/10.1007/8904_2017_22

Download citation

  • DOI: https://doi.org/10.1007/8904_2017_22

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-56358-8

  • Online ISBN: 978-3-662-56359-5

  • eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)

Publish with us

Policies and ethics