# Assessing the genetic relationship between phimosis and 26 urogenital diseases: a Mendelian randomization study

**Authors:** Wei Li, Ying Yu, Hu Li, Xingliang Yang, Tao Li

PMC · DOI: 10.3389/fendo.2024.1308270 · Frontiers in Endocrinology · 2024-06-10

## TL;DR

This study uses genetic data to explore how phimosis may influence the risk of various urogenital diseases, finding several significant genetic links.

## Contribution

The study is the first to use Mendelian randomization to assess the genetic relationship between phimosis and multiple urogenital diseases.

## Key findings

- Phimosis has a genetic causal relationship with glomerulonephritis and IgA glomerulonephritis.
- Phimosis is genetically linked to kidney stones, urethral strictures, and benign prostatic hyperplasia.
- The study found suggestive evidence linking phimosis to chronic and acute nephritis syndrome and impotence.

## Abstract

This study aims to investigate the impacts of phimosis on the health of the genitourinary system through Mendelian random analysis.

A dual-sample Mendelian randomization (MR) analysis was conducted using the publicly available genome-wide association study (GWAS) data. The inverse variance weighted based on the random effects model (Re-IVW) method was used as the main statistical analysis. Complementary methods, including weighted median, MR-Egger regression, and MR pleiotropy residual sum and outlier (MR-PRESSO), were applied to detect or correct the impact of horizontal pleiotropy.

Re-IVW showed a genetic predictive causal relationship of phimosis on glomerulonephritis (odds ratio [OR]: 1.37 [1.13–1.65], p = 0.00149) and IgA glomerulonephritis (OR: 1.57 [1.18–2.09), p = 0.00187). Suggestive evidence indicated that phimosis was associated with chronic nephritis syndrome (OR: 1.23 (1.00–1.51), p = 0.0481], acute nephritis syndrome (OR: 1.50 [1.13–2.01], p = 0.0058), and impotence (OR: 1.39 [1.11–1.73], p = 0.0035). Kidney and ureteral stone (OR: 1.14 [1.04–1.26], p = 0.0069), urethral strictures (OR: 1.26 [1.07–1.48], p = 0.0050), benign prostatic hyperplasia (OR: 1.07 [1.01–1.13], p = 0.0242), and decreased testicular function (OR: 0.72 [0.56–0.94], p = 0.0141) have genetically predictive causal relationships.

In summary, we employed a series of reliable analytical methods to investigate the association between phimosis and 26 urogenital diseases. We have reported several strong associations, but more research is needed to evaluate whether this discovery is replicated in other environments and to gain a better understanding of potential mechanisms.

## Linked entities

- **Diseases:** glomerulonephritis (MONDO:0002462), IgA glomerulonephritis (MONDO:0005342), impotence (MONDO:0005362), benign prostatic hyperplasia (MONDO:0010811)

## Full-text entities

- **Diseases:** benign prostatic hyperplasia (MESH:D011470), glomerulonephritis (MESH:D005921), decreased testicular function (MESH:D013733), impotence (MESH:D007172), chronic nephritis syndrome (MESH:D009393), Kidney and ureteral stone (MESH:D007669), phimosis (MESH:D010688), urethral strictures (MESH:D014525), IgA glomerulonephritis (MESH:D017098), urogenital diseases (MESH:D000091642), acute nephritis syndrome (MESH:C564356)

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC11194306/full.md

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Source: https://tomesphere.com/paper/PMC11194306