Effects of APOE and CHRNA4 genotypes on retinal nerve fibre layer thickness at the optic disc and on risk for developing exfoliation syndrome

Acta Ophthalmol Scand. 2007 May;85(3):257-61. doi: 10.1111/j.1600-0420.2006.00824.x.

Abstract

Purpose: To investigate whether CHRNA4 and APOE genotypes influence retinal nerve fibre layer (RNFL) thickness at the optic disc, intraocular pressure (IOP) and the development of exfoliation syndrome (XFS).

Methods: A sample of 88 healthy adults (aged 50-75 years) genotyped for polymorphisms of APOE and CHRNA4 underwent an eye examination including slit-lamp examination and fundus photography, as well as measurements of visual acuity, refraction, IOP and RNFL thickness at the optic disc by optical coherence tomography. The Fisher-Boschloo unconditional full multinomial test and two sample t-tests were used in the statistical analyses.

Results: There was no correlation between CHRNA4 and APOE genotypes and average RNFL thickness at the optic disc in the two eyes. Mean IOP in the eyes of APOE2 carriers was 13.18 mmHg, whereas that in the eyes of non-APOE2 carriers, at 14.82 mmHg, was significantly higher (p = 0.014). Exfoliation syndrome was found in one or both eyes in 15 persons. The presence of XFS was less likely in CC carriers of the CHRNA4 gene than in TT and TC carriers (p = 0.049).

Conclusions: We found no significant difference in RNFL thickness at the optic disc in the different genotype carriers of the APOE and CHRNA4 genes, and thereby no evidence for increased loss of ganglion cells in the retina as an effect of these genes. APOE2 carriers had significantly lower IOP than non-APOE2 carriers. However, both values are within the normal range and RNFL thickness measurements at the optic disc showed no difference between these two groups. In our study population, CC carriers of the CHRNA4 gene were less likely to develop XFS.

MeSH terms

  • Aged
  • Apolipoproteins E / genetics*
  • Exfoliation Syndrome / diagnosis*
  • Exfoliation Syndrome / genetics
  • Female
  • Genotype
  • Humans
  • Intraocular Pressure
  • Male
  • Middle Aged
  • Nerve Fibers / pathology*
  • Optic Disk / pathology*
  • Polymerase Chain Reaction
  • Polymorphism, Genetic
  • Receptors, Nicotinic / genetics*
  • Retinal Ganglion Cells / pathology*
  • Risk Factors
  • Tomography, Optical Coherence
  • Visual Acuity

Substances

  • Apolipoproteins E
  • Receptors, Nicotinic
  • nicotinic acetylcholine receptor alpha4 subunit