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The Interplay of Epigenetic, Genetic, and Traditional Risk Factors on Blood Pressure: Findings from the Health and Retirement Study.
Zhang, Xinman; Ammous, Farah; Lin, Lisha; Ratliff, Scott M; Ware, Erin B; Faul, Jessica D; Zhao, Wei; Kardia, Sharon L R; Smith, Jennifer A.
Affiliation
  • Zhang X; Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Ammous F; Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Lin L; Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Ratliff SM; Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Ware EB; Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI 48104, USA.
  • Faul JD; Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI 48104, USA.
  • Zhao W; Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Kardia SLR; Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI 48104, USA.
  • Smith JA; Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
Genes (Basel) ; 13(11)2022 10 27.
Article in En | MEDLINE | ID: mdl-36360196
ABSTRACT
The epigenome likely interacts with traditional and genetic risk factors to influence blood pressure. We evaluated whether 13 previously reported DNA methylation sites (CpGs) are associated with systolic (SBP) or diastolic (DBP) blood pressure, both individually and aggregated into methylation risk scores (MRS), in 3070 participants (including 437 African ancestry (AA) and 2021 European ancestry (EA), mean age = 70.5 years) from the Health and Retirement Study. Nine CpGs were at least nominally associated with SBP and/or DBP after adjusting for traditional hypertension risk factors (p < 0.05). MRSSBP was positively associated with SBP in the full sample (ß = 1.7 mmHg per 1 standard deviation in MRSSBP; p = 2.7 × 10-5) and in EA (ß = 1.6; p = 0.001), and MRSDBP with DBP in the full sample (ß = 1.1; p = 1.8 × 10-6), EA (ß = 1.1; p = 7.2 × 10-5), and AA (ß = 1.4; p = 0.03). The MRS and BP-genetic risk scores were independently associated with blood pressure in EA. The effects of both MRSs were weaker with increased age (pinteraction < 0.01), and the effect of MRSDBP was higher among individuals with at least some college education (pinteraction = 0.02). In AA, increasing MRSSBP was associated with higher SBP in females only (pinteraction = 0.01). Our work shows that MRS is a potential biomarker of blood pressure that may be modified by traditional hypertension risk factors.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retirement / Hypertension Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limits: Aged / Female / Humans Language: En Journal: Genes (Basel) Year: 2022 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retirement / Hypertension Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limits: Aged / Female / Humans Language: En Journal: Genes (Basel) Year: 2022 Document type: Article Affiliation country: Estados Unidos