Plasma lipid levels and risk of primary open angle glaucoma: a genetic study using Mendelian randomization

被引:18
|
作者
Xu, Mengqiao [1 ,2 ]
Li, Shengguo [3 ]
Zhu, Jundong [4 ]
Luo, Dawei [1 ,2 ]
Song, Weitao [5 ,6 ]
Zhou, Minwen [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai First Peoples Hosp, Dept Ophthalmol, 100 Haining Rd, Shanghai 200080, Peoples R China
[2] Shanghai Key Lab Fundus Dis, Shanghai, Peoples R China
[3] Cent South Univ, Dept Ophthalmol, Second Xiangya Hosp, Changsha, Peoples R China
[4] Southern Med Univ, First Peoples Hosp Chenzhou, Dept Ophthalmol, Chenzhou, Peoples R China
[5] Cent South Univ, Eye Ctr Xiangya Hosp, Changsha, Peoples R China
[6] Hunan Key Lab Ophthalmol, Changsha, Peoples R China
基金
中国国家自然科学基金;
关键词
Primary open angle glaucoma; Plasma lipid; Mendelian randomization; NATIONAL-HEALTH; PREVALENCE; INSTRUMENTS; HYPOTHYROIDISM;
D O I
10.1186/s12886-020-01661-0
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background The causal effects of plasma lipid concentrations and the risk of primary open angle glaucoma (POAG) are still unclear. Thus, the purpose of this study was to identify, applying a two-sample Mendelian randomization (MR) analysis, whether plasma lipid concentrations are causally associated with the risk of POAG. Methods Two-sample MR analysis of data from a genome-wide association study (GWAS) was performed to investigate the causal role of plasma lipid levels and POAG. A total of 185 independent single-nucleotide polymorphisms (SNPs) associated with plasma lipid levels were selected as instrumental variables (IVs). The SNPs were obtained from a meta-analysis of GWAS based on 188,577 European-ancestry individuals for MR analyses. Association with POAG for the SNPs was obtained from a GWAS conducted among the United Kingdom (UK) Biobank study participants with a total of 463,010 European-ancestry individuals. Four MR methods (inverse variance weighted [IVW], weighted mode, weighted median, and MR-Egger regression) were applied to obtain the overall causal estimate for multiple, instrumental SNPs. Results Using the IVW analysis method, no evidence was found to support a causal association between plasma LDL-C level and POAG risk (beta = - 0.00026; 95% CI = -0.00062, 0.00011;P = 0.165) with no significant heterogeneity among SNPs. The overall causal estimate between plasma LDL-C level and POAG was consistent using the other three MR methods. Using the four MR methods, no evidence of an association between plasma HDL-C (beta = 0.00023; 95% CI = -0.00015, 0.00061;P = 0.238; IVW method) or TG levels (beta = - 0.00028; 95% CI = -0.00071, 0.00015;P = 0.206; IVW method) and POAG risk was found. Sensitivity analyses did not reveal any sign of directional pleiotropy. Conclusions The present study did not find any evidence for a causal association between plasma lipid levels and POAG risk. Further research is needed to elucidate the potential biological mechanisms to provide a reasonable interpretation for these results.
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页数:11
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