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A drug target for erectile dysfunction to help improve fertility, sexual activity, and wellbeing: mendelian randomisation study.

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Peer-reviewed

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Abstract

OBJECTIVE: To investigate the association of genetically proxied (using a surrogate biomarker) inhibition of phosphodiesterase 5 (PDE5), an established drug target for erectile dysfunction, with fertility, sexual behaviour, and subjective wellbeing. DESIGN: Two sample cis-mendelian randomisation study. SETTING: Summary data on genetic associations obtained from the International Consortium for Blood Pressure and UK Biobank. PARTICIPANTS: Individuals of European ancestry from the International Consortium for Blood Pressure (n=757 601) for estimating PDE5 inhibition (using the surrogate biomarker of diastolic blood pressure reduction), and UK Biobank (n=211 840) for estimating the fertility, sexual behaviour, and subjective wellbeing outcomes in male participants. INTERVENTION: Genetically proxied PDE5 inhibition. MAIN OUTCOME MEASURES: Number of children fathered, number of sexual partners, probability of never having had sexual intercourse, and subjective wellbeing. RESULTS: Genetically proxied PDE5 inhibition was associated with male participants having 0.28 (95% confidence interval 0.16 to 0.39) more children (false discovery rate corrected P<0.001). This association was not identified in female participants. No evidence was found of an association between genetically proxied PDE5 inhibition and number of sexual partners, probability of never having had sexual intercourse, or self-reported wellbeing in male participants. CONCLUSIONS: The findings of this study provide genetic support for PDE5 inhibition potentially increasing the number of children fathered by male individuals. Absence of this association in female participants supports increased propensity for sustained and robust penile erections as a potential underlying mechanism. Further studies are required to confirm this, however, and these findings should not promote indiscriminate use of PDE5 inhibitors, which can also have harmful adverse effects.

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Peer reviewed: True


Acknowledgements: This project was conducted using UK Biobank application No 15825. UK Biobank was established by the Wellcome Trust medical charity, Medical Research Council, Department of Health, Scottish government, and the Northwest Regional Development Agency. It has also had funding from the Welsh government, British Heart Foundation, Cancer Research UK, and Diabetes UK. UK Biobank is supported by the NHS. UK Biobank is open to bona fide researchers anywhere in the world.


Funder: Imperial College London; FundRef: http://dx.doi.org/10.13039/501100000761

Journal Title

BMJ

Conference Name

Journal ISSN

0959-8146
1756-1833

Volume Title

383

Publisher

BMJ

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Medical Research Council (MC_UU_00002/7)
Wellcome Trust (100114/Z/12/Z)
Wellcome Trust (225790/Z/22/Z)