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多基因相互作用与血压调节中的环境暴露:HUNT 研究。

Polygenic Interactions With Environmental Exposures in Blood Pressure Regulation: The HUNT Study.

机构信息

HUNT Center for Molecular and Clinical Epidemiology (MCE), Department of Public Health and Nursing Norwegian University of Science and Technology (NTNU) Trondheim Norway.

Cardiac Exercise Research Group (CERG), Department of Circulation and Medical Imaging Norwegian University of Science and Technology (NTNU) Trondheim Norway.

出版信息

J Am Heart Assoc. 2024 Oct;13(19):e034612. doi: 10.1161/JAHA.123.034612. Epub 2024 Sep 18.

Abstract

BACKGROUND

The essential hypertension phenotype results from an interplay between genetic and environmental factors. The influence of lifestyle exposures such as excess adiposity, alcohol consumption, tobacco use, diet, and activity patterns on blood pressure (BP) is well established. Additionally, polygenic risk scores for BP traits are associated with clinically significant phenotypic variation. However, interactions between genetic and environmental risk factors in hypertension morbidity and mortality are poorly characterized.

METHODS AND RESULTS

We used genotype and phenotype data from up to 49 234 participants from the HUNT (Trøndelag Health Study) to model gene-environment interactions between genome-wide polygenic risk scores for systolic BP and diastolic BP and 125 environmental exposures. Among the 125 environmental exposures assessed, 108 and 100 were independently associated with SBP and DBP, respectively. Of these, 12 interactions were identified for genome-wide PRSs for systolic BP and 4 for genome-wide polygenic risk scores for diastolic BP, 2 of which were overlapping ( < 2 × 10). We found evidence for gene-dependent influence of lifestyle factors such as cardiorespiratory fitness, dietary patterns, and tobacco exposure, as well as biomarkers such as serum cholesterol, creatinine, and alkaline phosphatase on BP.

CONCLUSIONS

Individuals that are genetically susceptible to high BP may be more vulnerable to common acquired risk factors for hypertension, but these effects appear to be modifiable. The gene-dependent influence of several common acquired risk factors indicates the potential of genetic data combined with lifestyle assessments in risk stratification, and gene-environment-informed risk modeling in the prevention and management of hypertension.

摘要

背景

原发性高血压表型是遗传和环境因素相互作用的结果。生活方式暴露,如肥胖、饮酒、吸烟、饮食和活动模式对血压(BP)的影响已得到充分证实。此外,BP 特征的多基因风险评分与临床显著的表型变异相关。然而,高血压发病率和死亡率中遗传和环境风险因素之间的相互作用尚未得到充分描述。

方法和结果

我们使用了来自 HUNT(特隆德拉格健康研究)的多达 49234 名参与者的基因型和表型数据,以对全基因组收缩压和舒张压多基因风险评分与 125 种环境暴露之间的基因-环境相互作用进行建模。在所评估的 125 种环境暴露中,有 108 种和 100 种分别与 SBP 和 DBP 独立相关。其中,有 12 个与全基因组 PRS 相关的收缩压交互作用,4 个与全基因组 PRS 相关的舒张压交互作用,其中 2 个重叠(<2×10)。我们发现了生活方式因素(如心肺适应能力、饮食模式和烟草暴露)以及生物标志物(如血清胆固醇、肌酐和碱性磷酸酶)对 BP 的基因依赖性影响的证据。

结论

遗传上易患高血压的个体可能更容易受到常见的高血压获得性危险因素的影响,但这些影响似乎是可改变的。一些常见获得性危险因素的基因依赖性影响表明,遗传数据与生活方式评估相结合在风险分层、基因-环境信息风险模型在高血压的预防和管理中具有潜在的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e24a/11681455/3d120277d1aa/JAH3-13-e034612-g001.jpg

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