Division of Vitreous and Retina, Department of Ophthalmology, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon 16247, Korea.
Food and Nutrition, Obesity/Diabetes Research Center, Hoseo University, Asan 31499, Korea.
Nutrients. 2020 Oct 26;12(11):3282. doi: 10.3390/nu12113282.
Glaucoma, a leading cause of blindness, has multifactorial causes, including environmental and genetic factors. We evaluated genetic risk factors of glaucoma with gene-gene interaction and explored modifications of genetic risk with gene-lifestyles interaction in adults >40 years. The present study included 377 subjects with glaucoma and 47,820 subjects without glaucoma in a large-scale hospital-based cohort study from 2004 to 2013. The presence of glaucoma was evaluated by a diagnostic questionnaire evaluated by a doctor. The genome-wide association study was performed to identify genetic variants associated with glaucoma risk. Food intake was assessed using a semiquantitative food frequency questionnaire. We performed generalized multifactor dimensionality reduction analysis to construct polygenetic-risk score (PRS) and explored gene × nutrient interaction. PRS of the best model included LIM-domain binding protein () rs3763969, cyclin-dependent kinase inhibitor 2B () rs523096, rs2073823, phosphodiesterase-3A () rs12314390, and cadherin 13 () rs12449180. Glaucoma risk in the high-PRS group was 3.02 times that in the low-PRS group after adjusting for confounding variables. For those with low serum glucose levels (<126 mg/dL), but not for those with high serum glucose levels, glaucoma risk in the high-PRS group was 3.16 times that in the low-PRS group. In those with high carbohydrate intakes (≥70%), but not in those with low carbohydrate intakes, glaucoma risk was 3.74 times higher in the high-PRS group than in the low-PRS group. The glaucoma risk was 3.87 times higher in the high-PRS group than in the low-PRS group only in a low balanced diet intake. In conclusion, glaucoma risk increased by three-fold in adults with a high PRS, and it can be reduced by good control of serum glucose concentrations and blood pressure (BP) with a balanced diet intake. These results can be applied to precision nutrition to reduce glaucoma risk.
青光眼是导致失明的主要原因之一,其发病原因具有多因素性,包括环境和遗传因素。我们评估了基因-基因相互作用与基因-生活方式相互作用对 40 岁以上成年人青光眼的遗传风险因素,并探讨了遗传风险的修饰作用。本研究纳入了 2004 年至 2013 年一项大型基于医院的队列研究中 377 例青光眼患者和 47820 例非青光眼患者。通过医生评估的诊断问卷来评估青光眼的存在。采用全基因组关联研究来鉴定与青光眼风险相关的遗传变异。通过半定量食物频率问卷来评估食物摄入情况。我们进行广义多因子降维分析构建多基因风险评分(PRS),并探讨基因-营养物相互作用。最佳模型的 PRS 包含 LIM 结构域结合蛋白()rs3763969、细胞周期蛋白依赖性激酶抑制剂 2B()rs523096、rs2073823、磷酸二酯酶-3A()rs12314390 和钙黏蛋白 13()rs12449180。在调整混杂因素后,高 PRS 组的青光眼风险是低 PRS 组的 3.02 倍。对于血清葡萄糖水平较低(<126mg/dL)的患者,高 PRS 组的青光眼风险是低 PRS 组的 3.16 倍,但对于血清葡萄糖水平较高的患者则无此相关性。对于高碳水化合物摄入(≥70%)的患者,高 PRS 组的青光眼风险是低 PRS 组的 3.74 倍,但对于低碳水化合物摄入的患者则无此相关性。仅在低均衡饮食摄入时,高 PRS 组的青光眼风险比低 PRS 组高 3.87 倍。总之,在成年人中,高 PRS 组的青光眼风险增加了三倍,可以通过良好的血清葡萄糖浓度和血压(BP)控制以及均衡饮食摄入来降低。这些结果可应用于精准营养以降低青光眼风险。