The -174G/C interleukin-6 promoter polymorphism influences the development of macular oedema following uncomplicated phacoemulsification surgery

Eye (Lond). 2007 Nov;21(11):1412-5. doi: 10.1038/sj.eye.6702610. Epub 2006 Oct 6.

Abstract

Aim: To determine whether the functional -174 G/C interleukin-6 gene polymorphism is a risk factor for the development of cystoid macular oedema (CMO) following routine uncomplicated phacoemulsification surgery in patients with no established risk factors.

Methods: A total of 40 patients who underwent routine phacoemulsification surgery as part of a randomised controlled trial comparing the use of postoperative steroid drops against a single sub-tenon injection of triamcinolone were genotyped for the IL-6 -174G/C polymorphism. All patients underwent fluorescein angiography at 30 days and anterior chamber flare measurements pre-operatively and at day 1, 7, and 30.

Results: Angiographic CMO developed in 14 patients of the 40 studied. 9 out of the 14 patients carried the GG genotype (Fisher's exact test P=0.05, Hazard ratio for GG genotype; 4.05 (1.02-16.00)). There was no difference in flare measurements between the GG and Non-GG (GC/CC) group. The two groups were otherwise well matched in terms of age, sex, phacoemulsification energy used intraoperatively, and proportion of patients receiving postoperative triamcinolone or steroid drops.

Conclusion: The -174G/C interleukin-6 promoter gene variant appears to modulate the response to phacoemulsification surgery and to influence the development of postoperative CMO. These data suggest a genetic predisposition to this complication.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Glucocorticoids / administration & dosage
  • Humans
  • Interleukin-6 / genetics*
  • Macular Edema / etiology
  • Macular Edema / genetics*
  • Male
  • Middle Aged
  • Phacoemulsification / adverse effects*
  • Polymorphism, Genetic*
  • Postoperative Care / methods
  • Promoter Regions, Genetic / genetics
  • Risk Factors
  • Triamcinolone / administration & dosage

Substances

  • Glucocorticoids
  • Interleukin-6
  • Triamcinolone