孟德尔随机化
医学
内科学
骨矿物
全基因组关联研究
单核苷酸多态性
置信区间
骨质疏松症
血压
股骨颈
肿瘤科
内分泌学
混淆
遗传学
生物
遗传变异
基因型
基因
作者
Bin He,Lifeng Yin,Muzi Zhang,Qiong Lyu,Zhengxue Quan,Yunsheng Ou
标识
DOI:10.3389/fendo.2021.716681
摘要
Hypertension may have some association with osteoporosis. This Mendelian randomization (MR) study aimed to explore the causal effect of blood pressure (BP) on bone mineral density (BMD), fall, and fracture.We used the genome-wide association study (GWAS) summary data among 330,956 European-descent individuals to identify 107 single-nucleotide polymorphisms (SNPs) as the instrumental variables of BP. MR analyses of these instruments were performed on 53,236 European individuals for the association with forearm BMD (FA-BMD), femoral neck BMD (FN-BMD), and lumbar spine BMD (LS-BMD); 451,179 European individuals for fall susceptibility; and up to 1.2 million individuals from European descent for fracture. Conventional inverse variance weighted (IVW) method was adopted to obtain the causal estimates of BP on different outcomes, while weighted median, MR-egger, and MR pleiotropy residual sum and outlier (MR-PRESSO) test were used for sensitivity analyses.Genetically high pulse pressure (PP) could significantly improve FA-BMD (beta-estimate: 0.038, 95% confidence interval [CI]: 0.013 to 0.063, SE:0.013, P-value=0.003
科研通智能强力驱动
Strongly Powered by AbleSci AI