Key result
A two-sample cis-Mendelian Randomisation analysis found no evidence of a causal association between genetically proxied PDE5 inhibition and the risk of Alzheimer's disease.
Why the study?
Preclinical studies suggest PDE5 inhibition may reduce cognitive impairment, but findings from observational studies evaluating whether PDE5 inhibitors reduce Alzheimer disease risk have been inconsistent.
Does genetic proxy for PDE5 inhibition reduce the risk of Alzheimer's disease?
Observational
Does genetic proxy for PDE5 inhibition reduce the risk of Alzheimer's disease?
Mendelian randomisation analysis suggests that PDE5 inhibitors are unlikely to decrease the risk of Alzheimer's disease, challenging some preclinical hypotheses.
No support for PDE5 inhibitors in Alzheimer's prevention; challenges preclinical hypotheses but leaves causal effects open to trials.
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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Alcalde‐Herraiz et al. (2025) conducted an observational in Alzheimer's disease. Phosphodiesterase 5 (PDE5) inhibition was evaluated on Alzheimer's disease risk. A two-sample cis-Mendelian Randomisation analysis found no evidence of a causal association between genetically proxied PDE5 inhibition and the risk of Alzheimer's disease.
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