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Disturbed visual system function in methionine synthase deficiency

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Abstract

Background

Isolated functional methionine synthase deficiency occurs in the cblE and cblG defects of methylcobalamin metabolism and is one of a number of causes of severely elevated plasma homocysteine. Clinical features are predominantly of a neurological nature but also include functional restriction of the visual system manifesting as loss of visual acuity and nystagmus. As yet, the origin and pathogenesis of impaired vision have not been explained.

Materials and methods

We investigated a patient who was proven by complementation analysis in cultured fibroblasts to belong to the cblG complementation group. Ganzfeld electroretinograms (ERG) and flash visual evoked potentials (VEP) were recorded over a period of 4 years.

Results

Amplitudes of all International Society for Clinical Electrophysiology of Vision (ISCEV) standard responses were below normal. The greatest reductions were of rod response to 24 μV, of standard combined response (SC) b-wave to 120 μV, of oscillatory potentials (OP) to 5 μV, of cone response b-wave to 35 μV, and of 30 Hz flicker response to 8 μV. Except for SC and cone a-waves at age 2.5 and 3.5 years, as well as cone b-wave at 3.5 years, amplitudes remained at a subnormal level at follow-up examinations. Implicit times were slightly prolonged (SC b-wave 6 ms, OPs 2 ms, cone b-wave 2 ms, 30 Hz flicker 4 ms) or fell within the normal range. Responses of the flash VEP were severely deformed but reproducible.

Conclusions

This is the first report of detailed investigations of the visual system in a patient with isolated methionine synthase deficiency. Reduced oscillatory potentials suggest microvascular damage to the retina through homocysteine. Decreased photoreceptor function as well as ganglion cell loss as indicated by pathological flash VEPs may reflect a cytotoxic impact of homocysteine on neurons of the visual pathway.

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References

  1. Carmel R, Green R, Rosenblatt DS, Watkins D (2003) Update on cobalamin, folate, and homocysteine. Hematology 1:62–81

    Article  Google Scholar 

  2. Fowler B (1998) Genetic defects of folate and cobalamin metabolism. Eur J Pediatr 157:60–66

    Google Scholar 

  3. Fowler B, Jakobs C (1998) Post- and prenatal diagnostic methods for the homocystinurias. Eur J Pediatr 157:88–93

    Google Scholar 

  4. Fowler B, Whitehouse C, Wenzel F, Wraith JE (1997) Methionine and serine formation in control and mutant human cultured fibroblasts: evidence for methyl trapping and characterization of remethylation defects. Pediatr Res 41:145–151

    Google Scholar 

  5. Hofmann MA, Kohl B, Zumbach M, Borcea V, Bierhaus A, Henkels M, Amiral J, Schmidt AM, Fiehn W, Ziegler R, Wahl P, Nawroth PP (1998) Hyperhomocyst(e)inemia and endothelial dysfunction in IDDM. Diabetes Care 21:841–848

    CAS  PubMed  Google Scholar 

  6. Iohom G, Whyte A, Flynn T, O’Connor G, Shorten G (2004) Postoperative changes in the full-field electroretinogram following sevoflurane anaesthesia. Eur J Anaesthesiol 21:272–278

    CAS  PubMed  Google Scholar 

  7. Li YN, Gulati S, Baker PJ, Brody LC, Banerjee R, Kruger WD (1993) Cloning, mapping and RNA analysis of the human methionine synthase gene. Hum Mol Genet 5:1851–1855

    Article  Google Scholar 

  8. Maestro de las Casas C, Epeldegui M, Tudela C, Varela-Moreiras G, Perez-Miguelsanz J (2003) High exogenous homocysteine modifies eye development in early chick embryos. Birth Defects Res, Part A Clin Mol Teratol 67:35–40

    Google Scholar 

  9. Moore P, El-Sherbeny A, Roon P, Schoenlein PV, Ganapathy V, Smith SB (2001) Apoptotic cell death in the mouse retinal ganglion cell layer is induced in vivo by the excitatory amino acid homocysteine. Exp Eye Res 73:45–57

    Article  CAS  PubMed  Google Scholar 

  10. Naggar H, Fei YJ, Ganapathy V, Smith SB (2003) Regulation of reduced-folate transporter-1 (RFT-1) by homocysteine and identity of transport systems for homocysteine uptake in retinal pigment epithelial (RPE) cells. Exp Eye Res 77:687–697

    Article  CAS  PubMed  Google Scholar 

  11. Watkins D, Ru M, Hwang HY, Kim CD, Murray A, Philip NS, Kim W, Legakis H, Wai T, Hilton JF, Ge B, Dore C, Hosack A, Wilson A, Gravel RA, Shane B, Hudson TJ, Rosenblatt DS (2002) Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L. Am J Hum Genet 71:143–153

    Article  CAS  PubMed  Google Scholar 

  12. Watkins D, Rosenblatt DS (1989) Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity. Am J Med Genet 34:427–434

    CAS  PubMed  Google Scholar 

  13. Watkins D, Rosenblatt DS (1988) Genetic heterogeneity among patients with methylcobalamin deficiency: definition of two complementation groups, cblE and cblG. J Clin Invest 81:1690–1694

    CAS  PubMed  Google Scholar 

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Acknowledgements

We are grateful to Dr. T. Suormala (Basel) for performing the complementation study. This work was supported by the Deutsche Forschungsgemeinschaft (DFG Lo 457/3-3).

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Correspondence to Charlotte M. Poloschek.

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The authors have no competing interests

The authors have full control of all primary data and they agree to allow Graefe’s Archives of Clinical and Experimental Ophthalmology to review their data if requested

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Poloschek, C.M., Fowler, B., Unsold, R. et al. Disturbed visual system function in methionine synthase deficiency. Graefe's Arch Clin Exp Ophthalmol 243, 497–500 (2005). https://doi.org/10.1007/s00417-004-1044-2

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  • DOI: https://doi.org/10.1007/s00417-004-1044-2

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