Department of Psychiatry, Oxford University, Oxford, United Kingdom.
Department of Psychiatry, Oxford University, Oxford, United Kingdom.
Biol Psychiatry. 2021 Apr 15;89(8):817-824. doi: 10.1016/j.biopsych.2020.12.015. Epub 2020 Dec 27.
Findings from randomized controlled trials have yielded conflicting results on the association between blood pressure (BP) and dementia traits. We tested the hypothesis that a causal relationship exists between systolic BP (SBP) and/or diastolic BP (DBP) and risk of Alzheimer's disease (AD).
We performed a generalized summary Mendelian randomization (GSMR) analysis using summary statistics of a genome-wide association study meta-analysis of 299,024 individuals of SBP or DBP as exposure variables against three different outcomes: 1) AD diagnosis (International Genomics of Alzheimer's Project), 2) maternal family history of AD (UK Biobank), and 3) paternal family history of AD (UK Biobank). Finally, a combined meta-analysis of 368,440 individuals that included these three summary statistics was used as final outcome.
GSMR applied to the International Genomics of Alzheimer's Project dataset revealed a significant effect of high SBP lowering the risk of AD (β = -0.19, p = .04). GSMR applied to the maternal family history of AD UK Biobank dataset (SBP [β = -0.12, p = .02], DBP [β = -0.10, p = .05]) and to the paternal family history of AD UK Biobank dataset (SBP [β = -0.16, p = .02], DBP [β = -0.24, p = 7.4 × 10]) showed the same effect. A subsequent combined meta-analysis confirmed the overall significant effect for the other SBP analyses (β = -0.14, p = .03). The DBP analysis in the combined meta-analysis also confirmed a DBP effect on AD (β = -0.14, p = .03).
A causal effect exists between high BP and a reduced late-life risk of AD. The results were obtained through careful consideration of confounding factors and the application of complementary MR methods on independent cohorts.
随机对照试验的结果表明,血压(BP)与痴呆特征之间的关联存在矛盾。我们检验了这样一个假设,即收缩压(SBP)和/或舒张压(DBP)与阿尔茨海默病(AD)风险之间存在因果关系。
我们使用 299024 名个体的全基因组关联研究荟萃分析的汇总统计数据,进行了广义汇总孟德尔随机化(GSMR)分析,将 SBP 或 DBP 作为暴露变量,针对三个不同的结局进行分析:1)AD 诊断(国际阿尔茨海默病基因组学项目),2)AD 家族史(英国生物库),和 3)AD 家族史(英国生物库)。最后,使用包含这三个汇总统计数据的 368440 名个体的综合荟萃分析作为最终结局。
应用于国际阿尔茨海默病基因组学项目数据集的 GSMR 显示,高 SBP 降低 AD 风险具有显著效果(β=-0.19,p=0.04)。应用于 AD 家族史英国生物库数据集的母体(SBP [β=-0.12,p=0.02],DBP [β=-0.10,p=0.05])和 AD 家族史英国生物库数据集的父体(SBP [β=-0.16,p=0.02],DBP [β=-0.24,p=7.4×10)的 GSMR 显示出相同的效果。随后的综合荟萃分析证实了其他 SBP 分析的总体显著效果(β=-0.14,p=0.03)。综合荟萃分析中的 DBP 分析也证实了 DBP 对 AD 的影响(β=-0.14,p=0.03)。
高 BP 与晚年 AD 风险降低之间存在因果关系。这些结果是通过仔细考虑混杂因素和在独立队列中应用互补 MR 方法获得的。