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March 22, 2026Pharmacogenetics and Genomics0 citations

The potential effect and pathway of valsartan: genome-wide and phenome-wide association study from UK Biobank data

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SZShengyin ZengYLYaxin LiYZYucong Zhang

Key Result

Valsartan use is genetically associated with lower LDL cholesterol (β = -0.56), reduced risk of transient cerebral ischemic attack, and an increased risk of cough (OR = 1.67).

Key Points

  • To identify genetic variants associated with valsartan use and explore its effects on various phenotypes.
  • Selected participants of European ancestry prescribed valsartan
  • Conducted a genome-wide association study (GWAS) for genetic variants
  • Performed a phenome-wide association study (PheWAS) using identified variants
  • Used mendelian randomization to assess causal relationships
  • Identified 19 suggestive single nucleotide polymorphisms associated with valsartan use
  • PheWAS revealed associations with 14 phenotypes, including lowered levels of total cholesterol and LDL-C
  • Mendelian randomization indicated valsartan may causally lower LDL-C and reduce ischemic attack risk

Structured PICO

Does valsartan use have pleiotropic effects and adverse events across a wide range of phenotypes in participants of European ancestry?

P
Population
Participants of European ancestry from the UK Biobank
I
Intervention
Valsartan use (assessed via genetic variants as instruments)
C
Comparator
Controls not prescribed any angiotensin II receptor blockers (ARBs)
O
Outcome
Genetic variants associated with valsartan use and associated phenotypic traits

A genome-wide and phenome-wide association study suggests valsartan may have pleiotropic benefits, including lowering LDL-C and reducing the risk of transient cerebral ischemic attacks.

Abstract

Purpose Valsartan, an angiotensin II receptor blocker, is widely used for hypertension and heart failure. While its cardiovascular benefits are established, its broader pharmacological effects remain incompletely characterized. This study aimed to identify genetic variants associated with valsartan use and to systematically explore its potential effects and adverse events across a wide range of phenotypes. Methods Using UK Biobank data, we selected participants of European ancestry prescribed valsartan as cases, compared with controls not prescribed any ARBs. A genome-wide association study (GWAS) was conducted to identify suggestive genetic variants associated with valsartan use. These variants were then used as instruments in a phenome-wide association study (PheWAS) to screen for associated traits. Mendelian randomization analyses, including inverse-variance weighted and pleiotropy-robust methods, were employed to assess potential causal relationships. Results The GWAS identified 19 suggestive single nucleotide polymorphisms ( P < 1 × 10 −5 ) near genes, including PREP , GCLC , and ZNF133 . The PheWAS analysis revealed associations with 14 phenotypes, including lower levels of total cholesterol ( β = −0.59) and low-density lipoprotein cholesterol (LDL-C) ( β = −0.56), and increased risk of cough (odds ratio = 1.67). Mendelian randomization provided genetic evidence consistent with potential causal effects of valsartan in lowering LDL-C ( β = −2.34 × 10 −3 ) and reducing the risk of transient cerebral ischemic attack. Conclusion Our genetic-based study suggests valsartan use may be associated with lowered LDL-C and reduced risks of certain ischemic cardiovascular events. These findings generate novel hypotheses regarding the drug’s pleiotropic effects and potential applications beyond hypertension management, which warrant further clinical investigation.

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Cite This Study

Zeng et al. (2026) studied this question. Valsartan use is genetically associated with lower LDL cholesterol (β = -0.56), reduced risk of transient cerebral ischemic attack, and an increased risk of cough (OR = 1.67).

synapsesocial.com/papers/69bf898bf665edcd009e93dehttps://doi.org/10.1097/fpc.0000000000000597
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