Afzal Shoaib, Nordestgaard Børge G
From the Department of Clinical Biochemistry and the Copenhagen General Population Study, Herlev and Gentofte Hospital (S.A., B.G.N.) and the Copenhagen City Heart Study, Frederiksberg Hospital (B.G.N.), Copenhagen University Hospital, Herlev, Denmark; and Faculty of Health and Medical Sciences, University of Copenhagen, Denmark (S.A., B.G.N.).
Hypertension. 2017 Jul 31. doi: 10.1161/HYPERTENSIONAHA.117.09411.
Observational studies indicate that low concentrations of plasma 25-hydroxyvitamin D (25(OH)D) are associated with high blood pressure, hypertension, and ischemic stroke. However, whether these associations are causal remain unknown. A total of 116 655 white individuals of Danish descent from the general population were genotyped for genetic variants in and affecting plasma 25(OH)D concentrations; 35 517 had plasma 25(OH)D measurements. Primary outcomes were blood pressure, hypertension, and ischemic stroke. Median follow-up for incident ischemic stroke was 9.3 years (range, 1 day-33.6 years). allele score was as expected associated with lower 25(OH)D concentration (F=328 and =1.0%). A genetically determined 10 nmol/L lower 25(OH)D concentration was associated with a 0.68 (95% confidence interval [CI], 0.20-1.17) mm Hg higher systolic blood pressure and a 0.36 (95% CI, 0.08-0.63) mm Hg higher diastolic blood pressure with corresponding observational estimates of 0.58 (95% CI, 0.50-0.68) and 0.40 (95% CI, 0.35-0.45) mm Hg. The odds ratio for hypertension was 1.02 (95% CI, 0.97-1.08) for a genetically determined 10 nmol/L lower 25(OH)D with a corresponding observational odds ratio of 1.06 (95% CI, 1.05-1.07). The odds ratio for ischemic stroke was 0.98 (95% CI, 0.86-1.13) for a genetically determined 10 nmol/L decrease in 25(OH)D with a corresponding observational odds ratio of 1.03 (95% CI, 1.01-1.05). Genetic and observational low 25(OH)D concentrations were associated with higher blood pressure, as well as with hypertension consistent with causal relationships. Because observational but not genetic low 25(OH)D concentration was associated with ischemic stroke, and as the CIs overlapped, we can neither support nor exclude a causal relationship.
观察性研究表明,血浆25-羟维生素D(25(OH)D)浓度较低与高血压、高血压病和缺血性卒中相关。然而,这些关联是否为因果关系尚不清楚。对来自普通人群的116655名丹麦裔白人个体进行基因分型,检测影响血浆25(OH)D浓度的基因变异;其中35517人进行了血浆25(OH)D测量。主要结局为血压、高血压病和缺血性卒中。缺血性卒中发病的中位随访时间为9.3年(范围1天至33.6年)。等位基因评分与较低的25(OH)D浓度相关,正如预期(F=328,P=1.0%)。基因决定的25(OH)D浓度降低10 nmol/L与收缩压升高0.68(95%置信区间[CI],0.201.17)mmHg及舒张压升高0.36(95%CI,0.080.63)mmHg相关,相应的观察性估计值分别为0.58(95%CI,0.500.68)和0.40(95%CI,0.350.45)mmHg。基因决定的25(OH)D浓度降低10 nmol/L时,高血压病的比值比为1.02(95%CI,0.971.08),相应的观察性比值比为1.06(95%CI,1.051.07)。基因决定的25(OH)D浓度降低10 nmol/L时,缺血性卒中的比值比为0.98(95%CI,0.861.13),相应的观察性比值比为1.03(95%CI,1.011.05)。基因和观察性低25(OH)D浓度均与较高血压相关,也与高血压病相关,符合因果关系。由于观察性而非基因低25(OH)D浓度与缺血性卒中相关,且置信区间有重叠,因此我们既不能支持也不能排除因果关系。