Phosphodiesterase‐5 Inhibition and Alzheimer's Disease Risk: A Mendelian Randomisation Study

While preclinical studies suggest that Phosphodiesterase 5 (PDE5) inhibition may reduce cognitive impairment, findings from observational studies on whether PDE5 inhibitors reduce Alzheimer's disease (AD) risk have been inconsistent. We performed a two-sample cis-Mendelian Randomisation (MR) analysis to estimate the causal effect of PDE5 inhibition on AD risk. The analysis was performed across four different genome-wide association studies (GWAS) of AD to enhance reliability through triangulation. Additionally, a sex-stratified MR analysis using data from UK Biobank was performed to assess potential sex-specific effects. No evidence of a causal association between PDE5 inhibition and AD risk was found in the main analyses. Similar findings were obtained in the sex-stratified analysis. Our study uses genetic data to triangulate the evidence and suggests that PDE5 inhibitors are unlikely to decrease the risk of AD. Further research is needed to thoroughly understand the impact of PDE5 inhibitors on the risk of Alzheimer's disease.

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Publication Details

Journal
Aging Cell
Published
2025-10-13
DOI
https://doi.org/10.1111/acel.70265
Primary Topic
Phosphodiesterase function and regulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Phosphodiesterase‐5 Inhibition and Alzheimer's Disease Risk: A Mendelian Randomisation Study

Junqing Xie, Danielle Newby, James Yarmolinsky, Laura Winchester et al.
Aging Cell
Phosphodiesterase function and regulation
article

Phosphodiesterase‐5 Inhibition and Alzheimer's Disease Risk: A Mendelian Randomisation Study

Junqing Xie, Danielle Newby, James Yarmolinsky, Laura Winchester, Marta Alcalde-Herraiz, Benjamin Woolf, Daniel Prieto‐Alhambra, Dipender Gill, Emma L. Anderson, Ioanna Tzoulaki
article en

Abstract

While preclinical studies suggest that Phosphodiesterase 5 (PDE5) inhibition may reduce cognitive impairment, findings from observational studies on whether PDE5 inhibitors reduce Alzheimer's disease (AD) risk have been inconsistent. We performed a two-sample cis-Mendelian Randomisation (MR) analysis to estimate the causal effect of PDE5 inhibition on AD risk. The analysis was performed across four different genome-wide association studies (GWAS) of AD to enhance reliability through triangulation. Additionally, a sex-stratified MR analysis using data from UK Biobank was performed to assess potential sex-specific effects. No evidence of a causal association between PDE5 inhibition and AD risk was found in the main analyses. Similar findings were obtained in the sex-stratified analysis. Our study uses genetic data to triangulate the evidence and suggests that PDE5 inhibitors are unlikely to decrease the risk of AD. Further research is needed to thoroughly understand the impact of PDE5 inhibitors on the risk of Alzheimer's disease.

Aging CellVol. 24(12)
University of Ioannina (GR), University of Cambridge (GB), Erasmus MC (NL), Warneford Hospital (GB), Public Health England (GB), University of Bristol (GB), MRC Biostatistics Unit (GB), Oxford BioMedica (United Kingdom) (GB), University College London (GB), Imperial College London (GB), Erasmus University Rotterdam (NL)
National Institute for Health and Care Research
Openalex Percentile: Top 74%
Phosphodiesterase function and regulation
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