Evidence mapPaperPMID 39315306Full record

ArticleSexual medicine2024

Bayesian-based analysis of the causality between 731 immune cells and erectile dysfunction: a two-sample, bidirectional, and multivariable Mendelian randomization study.

Junhao Chen, Yidao Liu, Peiqin Zhan, Tianci Gao, Jieming Zuo, Xiangyun Li, Fangfei Zhang, Haifeng Wang, Shi Fu

Abstract read
In one paragraph

Article in Sexual medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
field-weighted citation impact
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

6 citing papers in PubMed.

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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

9 authors.

Junhao ChenDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, Wuhua District, Kunming, 650032, Yunnan, China.ORCID https://orcid.org/0009-0006-4850-6790
Yidao LiuDepartment of Urology, Dehong People's Hospital, Mangshi City, Dehong, Yunnan Province, 678499, China.
Peiqin ZhanDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, Wuhua District, Kunming, 650032, Yunnan, China.
Tianci GaoThe Second Hospital of Jilin University, Nanguan District, Changchun City, Jilin Province, China.
Jieming ZuoDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, Wuhua District, Kunming, 650032, Yunnan, China.
Xiangyun LiDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, Wuhua District, Kunming, 650032, Yunnan, China.
Fangfei ZhangDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226United States.
Haifeng WangDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, Wuhua District, Kunming, 650032, Yunnan, China.
Shi FuDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, Wuhua District, Kunming, 650032, Yunnan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The causal relationship between certain immune cells and erectile dysfunction (ED) is still uncertain. Aim: The study sought to investigate the causal effect of 731 types of immune cells on ED through Mendelian randomization (MR) using genome-wide association studies (GWAS). Methods: Genetic instruments for 731 immune cells were identified through GWAS, and ED data were obtained from the FinnGen database. Univariable and multivariable bidirectional MR studies were conducted to explore potential causal relationships between these immune cells and ED. The inverse-variance weighted method was primarily used, with Cochran's Q test and MR-Egger intercept test assessing pleiotropy and heterogeneity. Bayesian weighted Mendelian randomization (BWMR) was also employed. Outcomes: Six immune cells were identified as related to ED. CD45 on Natural Killer (NK) cells, CD33dim HLA DR+ CD11b + Absolute Count, CD19 on IgD- CD38dim B cells, and CD3 on CD39+ resting CD4 regulatory T cells were identified as risk factors, whereas CD20 on IgD+ CD38dim B cells and Activated & resting CD4 regulatory T cell %CD4+ T cells were protective factors. Further multivariable MR analysis confirmed that 5 of these immune cells independently impacted ED, except for CD45 on NK cells. Reverse MR analysis indicated that ED occurrence decreases certain immune cell counts, but BWMR found no causal relationship for CD20 on IgD+ CD38dim B cells. Results: Our MR analysis confirmed a potential bidirectional causal relationship between immune cells and ED, providing new insights into potential mechanisms and therapeutic strategies. Clinical Translation: This study provides evidence for the impact of certain immune cells on the development of ED and suggests potential therapeutic targets. Strengths and Limitations: We performed both univariable and multivariable MR to strengthen the causal relationship between exposures and outcomes. However, the population in this study was limited to European ancestry. Conclusion: Our MR analysis confirmed a potential bidirectional causal relationship between immune cells and ED. This provides new insights into potential mechanisms of pathogenesis and subsequent therapeutic strategies.

Indexed as

erectile dysfunctionimmune cellsMendelian randomization

Identifiers

PMID39315306
PMCPMC11416910

What Socratic holds

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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 Socratic graph.