The Firmicutes/Bacteroidetes ratio of the human gut microbiota is associated with prostate enlargement

Prostate. 2021 Dec;81(16):1287-1293. doi: 10.1002/pros.24223. Epub 2021 Sep 13.

Abstract

Background: The pathophysiology of the prostate enlargement underlying lower urinary tract symptoms is unknown. Meanwhile, the gut microbiota can contribute to various host conditions. We hypothesized that the gut microbiota plays a role in prostate enlargement.

Methods: We included 128 patients who underwent prostate biopsies at our hospitals between December 2018 and March 2020, excluding those who had used antibiotics within the past 6 months and those who were diagnosed with prostate cancer of cT3 or higher. Patients with prostate volumes ≥30 ml were defined as the prostate-enlargement (PE) group; those with prostate volumes <30 ml were defined as the non-PE group. Their gut microbiotas were analyzed via 16S rRNA metagenomic analyses of rectal swab samples and were compared between the groups.

Results: The PE group included 66 patients; the non-PE group included 62 patients. Age, body mass index, and prostate-specific antigen levels did not significantly differ between the groups. Linear discriminant analysis effect size analysis indicated a higher proportion of Firmicutes and Actinobacteria in the PE group and a higher proportion of Bacteroidetes in the non-PE group. The Firmicutes/Bacteroidetes (F/B) ratio was significantly higher in the PE group than in the non-PE group (2.21 ± 0.39 vs. 1.61 ± 0.40, p = 0.015).

Conclusion: The F/B ratio of the gut microbiota was associated with prostate enlargement. Although the detailed mechanisms are unclear, the gut microbiota might affect prostate enlargement.

Keywords: bacteria; benign prostatic hyperplasia; microbiome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteroidetes / isolation & purification*
  • Biopsy / methods
  • Biopsy / statistics & numerical data
  • Firmicutes / isolation & purification*
  • Gastrointestinal Microbiome / physiology*
  • Humans
  • Male
  • Metagenomics / methods
  • Middle Aged
  • Neoplasm Staging
  • Organ Size
  • Prostate / pathology*
  • Prostatic Hyperplasia* / diagnosis
  • Prostatic Hyperplasia* / microbiology
  • Prostatic Neoplasms* / microbiology
  • Prostatic Neoplasms* / pathology
  • Prostatic Neoplasms* / physiopathology
  • RNA, Ribosomal, 16S / isolation & purification
  • Risk Factors

Substances

  • RNA, Ribosomal, 16S