Examining potential mechanisms of testicular fibrosis in Klinefelter Syndrome: A review of current understanding

• Published in: Andrology (Oxford) 2023-03, Vol.11 (3), p.435-443
• Main Authors: Bradshaw, Aaron W., Deebel, Nicholas A., Xu, Mark C., Kogan, Stanley, Atala, Anthony, Sadri‐Ardekani, Hooman
• Format: Article
• Language: English
• Subjects: Adult; Fibrosis; Gene expression; Humans; Infertility; Klinefelter; Klinefelter Syndrome - complications; Male; Mens health; Pathophysiology; Seminiferous Tubules - metabolism; Sertoli Cells - metabolism; Testes; testis; Testis - metabolism
• ISSN: 2047-2919; 2047-2927
• DOI: 10.1111/andr.13327

Background Men with Klinefelter Syndrome develop some degree of seminiferous tubule degeneration, hyalinization, and fibrosis by adulthood. However, the pathophysiology surrounding testicular fibrosis in Klinefelter Syndrome patients remains incompletely understood. Objectives To perform a systematic review of literature studying the mechanisms of fibrosis initiation or propagation in Klinefelter Syndrome testes. Materials/methods PubMed was searched systematically for articles specific to Klinefelter Syndrome and the process of fibrosis. Articles that did not contain original data or specifically addressed the target material were excluded. Additional references were extracted when pertinent from the reference lists of included studies. Results Primary search yielded 139 articles for review, which was narrowed to 16 for full‐text review. Following full‐text review, eight contained original data and met topic criteria, with one paper added from reference review for a total of nine papers. Discussion The date range for included papers was 1992–2022. The proposed mechanisms of fibrosis mainly were centered around the impact of altered Sertoli cells on germ cells, the hormonal impact on Leydig cells, the inflammation mediated by mast cells, or the fibrous extracellular matrix deposition by peritubular myoid cells. Additionally, discussions of the role of the altered microvasculature and the specific proteins involved in the blood‐testis barrier or the seminiferous tubule architecture are reviewed. Recent papers have incorporated advanced sequencing and offer future directions for targeted gene expression analysis. Still, much of the published data consists solely of immunohistological assessment by age range, creating difficulties in extrapolating causality. Conclusion The specific initiating factors of fibrosis of the seminiferous tubules and the propagation mechanisms unique to Klinefelter Syndrome remain incompletely understood with a relative paucity of data. Nonetheless, academic interest is increasing in this field as it may further elucidate the pathophysiology behind Klinefelter syndrome.