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GWAS Study

Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.

Wenric S, Jeff JM, Joseph T et al.

33168928 PubMed ID
GWAS Study Type
3699 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WS
Wenric S
JJ
Jeff JM
JT
Joseph T
YM
Yee MC
BG
Belbin GM
OO
Owusu Obeng A
ES
Ellis SB
BE
Bottinger EP
GO
Gottesman O
LM
Levin MA
KE
Kenny EE
Chapter II

Abstract

Summary of the research findings

The emergence of genomic data in biobanks and health systems offers new ways to derive medically important phenotypes, including acute phenotypes occurring during inpatient clinical care. Here we study the genetic underpinnings of the rapid response to phenylephrine, an α1-adrenergic receptor agonist commonly used to treat hypotension during anesthesia and surgery. We quantified this response by extracting blood pressure (BP) measurements 5 min before and after the administration of phenylephrine. Based on this derived phenotype, we show that systematic differences exist between self-reported ancestry groups: European-Americans (EA; n = 1387) have a significantly higher systolic response to phenylephrine than African-Americans (AA; n = 1217) and Hispanic/Latinos (HA; n = 1713) (31.3% increase, p value < 6e-08 and 22.9% increase, p value < 5e-05 respectively), after adjusting for genetic ancestry, demographics, and relevant clinical covariates. We performed a genome-wide association study to investigate genetic factors underlying individual differences in this derived phenotype. We discovered genome-wide significant association signals in loci and genes previously associated with BP measured in ambulatory settings, and a general enrichment of association in these genes. Finally, we discovered two low frequency variants, present at ~1% in EAs and AAs, respectively, where patients carrying one copy of these variants show no phenylephrine response. This work demonstrates our ability to derive a quantitative phenotype suited for comparative statistics and genome-wide association studies from dense clinical and physiological measures captured for managing patients during surgery. We identify genetic variants underlying non response to phenylephrine, with implications for preemptive pharmacogenomic screening to improve safety during surgery.

1,082 African American individuals, 1,112 European ancestry individuals, 1,505 Hispanic individuals

Chapter III

Study Statistics

Key metrics and study information

3699
Total Participants
GWAS
Study Type
No
Replicated
Hispanic or Latin American, European, African American or Afro-Caribbean
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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