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Examining Individual and Synergistic Contributions of PTSD and Genetics to Blood Pressure: A Trans-Ethnic Meta-Analysis

Authors :
Jennifer A. Sumner
Adam X. Maihofer
Vasiliki Michopoulos
Alex O. Rothbaum
Lynn M. Almli
Ole A. Andreassen
Allison E. Ashley-Koch
Dewleen G. Baker
Jean C. Beckham
Bekh Bradley
Gerome Breen
Jonathan R. I. Coleman
Anders M. Dale
Michelle F. Dennis
Norah C. Feeny
Carol E. Franz
Melanie E. Garrett
Charles F. Gillespie
Guia Guffanti
Michael A. Hauser
Sian M. J. Hemmings
Tanja Jovanovic
Nathan A. Kimbrel
William S. Kremen
Bruce R. Lawford
Mark W. Logue
Adriana Lori
Michael J. Lyons
Jessica Maples-Keller
Matig R. Mavissakalian
Regina E. McGlinchey
Divya Mehta
Rebecca Mellor
William Milberg
Mark W. Miller
Charles Phillip Morris
Matthew S. Panizzon
Kerry J. Ressler
Victoria B. Risbrough
Barbara O. Rothbaum
Peter Roy-Byrne
Soraya Seedat
Alicia K. Smith
Jennifer S. Stevens
Leigh Luella van den Heuvel
Joanne Voisey
Ross McD Young
Lori A. Zoellner
Caroline M. Nievergelt
Erika J. Wolf
Source :
Frontiers in Neuroscience, Vol 15 (2021), Frontiers in Neuroscience
Publication Year :
2021
Publisher :
eScholarship, University of California, 2021.

Abstract

Growing research suggests that posttraumatic stress disorder (PTSD) may be a risk factor for poor cardiovascular health, and yet our understanding of who might be at greatest risk of adverse cardiovascular outcomes after trauma is limited. In this study, we conducted the first examination of the individual and synergistic contributions of PTSD symptoms and blood pressure genetics to continuous blood pressure levels. We harnessed the power of the Psychiatric Genomics Consortium-PTSD Physical Health Working Group and investigated these associations across 11 studies of 72,224 trauma-exposed individuals of European (n = 70,870) and African (n = 1,354) ancestry. Genetic contributions to blood pressure were modeled via polygenic scores (PGS) for systolic blood pressure (SBP) and diastolic blood pressure (DBP) that were derived from a prior trans-ethnic blood pressure genome-wide association study (GWAS). Results of trans-ethnic meta-analyses revealed significant main effects of the PGS on blood pressure levels [SBP: β = 2.83, standard error (SE) = 0.06, p < 1E-20; DBP: β = 1.32, SE = 0.04, p < 1E-20]. Significant main effects of PTSD symptoms were also detected for SBP and DBP in trans-ethnic meta-analyses, though there was significant heterogeneity in these results. When including data from the largest contributing study – United Kingdom Biobank – PTSD symptoms were negatively associated with SBP levels (β = −1.46, SE = 0.44, p = 9.8E-4) and positively associated with DBP levels (β = 0.70, SE = 0.26, p = 8.1E-3). However, when excluding the United Kingdom Biobank cohort in trans-ethnic meta-analyses, there was a nominally significant positive association between PTSD symptoms and SBP levels (β = 2.81, SE = 1.13, p = 0.01); no significant association was observed for DBP (β = 0.43, SE = 0.78, p = 0.58). Blood pressure PGS did not significantly moderate the associations between PTSD symptoms and blood pressure levels in meta-analyses. Additional research is needed to better understand the extent to which PTSD is associated with high blood pressure and how genetic as well as contextual factors may play a role in influencing cardiovascular risk.

Details

ISSN :
16624548
Database :
OpenAIRE
Journal :
Frontiers in Neuroscience, Vol 15 (2021), Frontiers in Neuroscience
Accession number :
edsair.doi.dedup.....b015803a21cfe71216d19291b4677701