Evidence map›Paper›PMID 41267859›Full record

ArticleFrontiers in medicine2025

Non-alcoholic fatty liver disease is associated with a higher risk of erectile dysfunction than alcoholic fatty liver disease.

Hoi-Bor Chan, Sheng-You Su, Chun Lee, Chao-Yu Hsu

Abstract read
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Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

4 authors.

Hoi-Bor ChanDepartment of Surgery, Ditmanson Medical Foundation, Chia-Yi Christian Hospital, Chia-Yi, Taiwan.
Sheng-You SuClinical Medicine Research Center, Ditmanson Medical Foundation, Chia-Yi Christian Hospital, Chia-Yi, Taiwan.
Chun LeeClinical Data Center, Ditmanson Medical Foundation, Chia-Yi Christian Hospital, Chia-Yi, Taiwan.
Chao-Yu HsuDepartment of Medical Education, Ditmanson Medical Foundation, Chia-Yi Christian Hospital, Chia-Yi, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: In this study, we examine the prevalence and risk of erectile dysfunction (ED) by conducting a comparative analysis between cohorts with alcoholic fatty liver disease (AFLD) and non-alcoholic fatty liver disease (NAFLD). Methods: This retrospective cohort study used the TriNetX database, including anonymized electronic health records from about 190 million patients globally. The study enrolled men aged ≥20 years diagnosed with AFLD or NAFLD between 2011 and 2019. Patients with liver cirrhosis or malignancy were excluded. Propensity score matching controlled for demographics and comorbidities. The primary outcome, incidence of ED, was analyzed at 1, 3 and 5 years using risk ratios (RR), odds ratios (OR) and hazard ratio (HR), ensuring balanced comparisons. Results: There were 9,066 AFLD and 431,064 NAFLD patients were enrolled before propensity score matching. Finally, following matching, 9,066 patients from each group were included for analysis. Within 1 year, NAFLD patients showed higher ED risk (2.394%) compared to AFLD patients (1.836%), with RR of 1.284 (1.052, 1.567), OR of 1.291 (1.054, 1.582) and HR of 1.263 (1.033, 1.544). At 3 years, NAFLD outcomes remained higher (5.228 vs. 4.169%), RR of 1.254 (1.099, 1.431), OR of 1.268 (1.104, 1.456) and HR of 1.221 (1.066, 1.397). By 5 years, NAFLD continued exhibiting greater risks (6.806 vs. 5.824%), RR of 1.169 (1.044, 1.308), OR of 1.181 (1.047, 1.331) and HR of 1.125 (1.002, 1.264). These findings demonstrate consistently elevated clinical risk in NAFLD patients vs. AFLD, highlighting the necessity of careful NAFLD monitoring. Conclusion: NAFLD demonstrates a significantly greater association with ED than AFLD. Clinicians should maintain heightened vigilance for ED when managing patients with NAFLD, particularly during the initial year following diagnosis.

Indexed as

alcoholic fatty liver diseaseerectile dysfunctionfatty livernon-alcoholic fatty liver diseaseTriNetX

Identifiers

PMID41267859
PMCPMC12627059

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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.