Evidence map›Paper›PMID 38086555›Full record

ArticleBMJ (Clinical research ed.)2023

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

Benjamin Woolf, Skanda Rajasundaram, Héléne T Cronjé, James Yarmolinsky, Stephen Burgess, Dipender Gill

Open access · hybridAbstract read
In one paragraph

Article in BMJ (Clinical research ed.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
8.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Sexual distress in patients after radical cystectomy for bladder cancer: a qualitative study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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  16. Genetic factors associated with erectile dysfunction- mendelian randomisation analysis.American journal of clinical and experimental urology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 2 countries.

Benjamin WoolfSchool of Psychological Science, University of Bristol, Bristol, BS8 1TU, UK benjamin.woolf@bristol.ac.uk.ORCID 0000-0002-1505-2570
Skanda RajasundaramCentre for Evidence-Based Medicine, University of Oxford, Oxford, UK.
Héléne T CronjéDepartment of Public Health, Section of Epidemiology, University of Copenhagen, Copenhagen, Denmark.
James YarmolinskyMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Stephen BurgessMedical Research Council Biostatistics Unit, University of Cambridge, Cambridge, UK.
Dipender GillDepartment of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
University of Cambridge · GBImperial College London · GBUniversity of Bristol · GBUniversity of Copenhagen · DKUniversity of Oxford · GB

Funding

Medical Research Council MC_UU_00002/7Medical Research Council MC_UU_00011/7Wellcome Trust 100114
6 · The paper itself

Abstract

objectiveTo 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.

designTwo sample cis-mendelian randomisation study.

settingSummary data on genetic associations obtained from the International Consortium for Blood Pressure and UK Biobank.

participantsIndividuals 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.

interventionGenetically proxied PDE5 inhibition.

main outcome measuresNumber of children fathered, number of sexual partners, probability of never having had sexual intercourse, and subjective wellbeing.

resultsGenetically 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.

conclusionsThe 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.

Indexed as

Erectile DysfunctionBiomarkersChildFemaleFertilityHumansMalePenile ErectionSexual BehaviorBiomarkers

Identifiers

PMID38086555
PMCPMC10716676
OpenAlexW4389627394

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.