» Articles » PMID: 29335418

Gender-specific Association of Early Age-related Macular Degeneration with Systemic and Genetic Factors in a Japanese Population

Overview
Journal Sci Rep
Specialty Science
Date 2018 Jan 17
PMID 29335418
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

The Tsuruoka Metabolomics Cohort Study included subjects aged 35-74 years from participants in annual health check-up programs in Tsuruoka, Japan. The gender-specific associations of early age-related macular degeneration (AMD) with systemic and genetic factors was assessed cross-sectionally. Of these, 3,988 subjects had fundus photographs of sufficient quality, and early AMD was present in 12.3% and 10.3% of men and women, respectively. In men, higher levels of high-density lipoprotein cholesterol and lower levels of triglycerides were associated with increased odds of having early AMD after adjusting for potential risk factors (for each 1 mmol/L increase, odds ratio [OR]: 1.61 and 0.78, 95% confidence interval [CI]: 1.17-2.23 and 0.64-0.96, respectively). In women, higher levels of total cholesterol and low-density lipoprotein cholesterol were associated with increased risk of having early AMD (OR: 1.21 and 1.26, 95% CI: 1.01-1.44 and 1.03-1.53, respectively). Sub-analysis demonstrated that women with ARMS2 A69S polymorphisms had a stronger risk for early AMD (OR: 3.25, 95% CI: 2.10-5.04) than men (OR: 1.65, 95% CI: 1.02-2.69). Differential associations of early AMD with both systemic and genetic factors by sex were demonstrated in a Japanese cohort, which suggests that disease process of early AMD could be different by sex.

Citing Articles

Sex-specific and cell-type-specific changes in chaperone-mediated autophagy across tissues during aging.

Khawaja R, Martin-Segura A, Santiago-Fernandez O, Sereda R, Lindenau K, McCabe M Nat Aging. 2025; .

PMID: 39910244 DOI: 10.1038/s43587-024-00799-6.


A high-fat plus high-sucrose diet induces age-related macular degeneration in an experimental rabbit model.

Wang Y, Lv Z, Chen Y, Cen X, Zhang H, Chen D Dis Model Mech. 2024; 17(11).

PMID: 39463155 PMC: 11625886. DOI: 10.1242/dmm.052015.


Sex-dependent regulation of retinal pigment epithelium and retinal function by .

Taskintuna K, Bhat M, Shaikh T, Hum J, Golestaneh N Front Cell Neurosci. 2024; 18:1442079.

PMID: 39285939 PMC: 11403373. DOI: 10.3389/fncel.2024.1442079.


Female sex hormones exacerbate retinal neurodegeneration.

Rowe A, Reyes S, Velasquez M, Yee T, Nettesheim E, McDonald J bioRxiv. 2024; .

PMID: 39071341 PMC: 11275730. DOI: 10.1101/2024.07.11.603104.


Correlations Between the Neutrophil-Lymphocyte Ratio, Platelet-Lymphocyte Ratio, and Serum Lipid Fractions With Neovascular Age-Related Macular Degeneration.

Tricorache D, Dascalu A, Alexandrescu C, Bobirca A, Grigorescu C, Tudor C Cureus. 2024; 16(6):e62503.

PMID: 39022525 PMC: 11252630. DOI: 10.7759/cureus.62503.


References
1.
Klein R, Klein B, Marino E, Kuller L, Furberg C, Burke G . Early age-related maculopathy in the cardiovascular health study. Ophthalmology. 2003; 110(1):25-33. DOI: 10.1016/s0161-6420(02)01565-8. View

2.
Tserentsoodol N, Sztein J, Campos M, Gordiyenko N, Fariss R, Lee J . Uptake of cholesterol by the retina occurs primarily via a low density lipoprotein receptor-mediated process. Mol Vis. 2006; 12:1306-18. View

3.
Spaide R, Armstrong D, Browne R . Continuing medical education review: choroidal neovascularization in age-related macular degeneration--what is the cause?. Retina. 2003; 23(5):595-614. DOI: 10.1097/00006982-200310000-00001. View

4.
Delcourt C, Michel F, Colvez A, Lacroux A, Delage M, Vernet M . Associations of cardiovascular disease and its risk factors with age-related macular degeneration: the POLA study. Ophthalmic Epidemiol. 2001; 8(4):237-49. DOI: 10.1076/opep.8.4.237.1613. View

5.
Upston J, Niu X, Brown A, Mashima R, Wang H, Senthilmohan R . Disease stage-dependent accumulation of lipid and protein oxidation products in human atherosclerosis. Am J Pathol. 2002; 160(2):701-10. PMC: 1850639. DOI: 10.1016/S0002-9440(10)64890-0. View