Peyronie's disease response to intralesional collagenase clostridium histolyticum therapy is independent of baseline testosterone.

Peyronie's disease hypogonadism intralesional collagenase clostridium histolyticum testosterone

Journal

Andrology
ISSN: 2047-2927
Titre abrégé: Andrology
Pays: England
ID NLM: 101585129

Informations de publication

Date de publication:
27 Sep 2023
Historique:
revised: 05 08 2023
received: 21 01 2023
accepted: 06 09 2023
pubmed: 27 9 2023
medline: 27 9 2023
entrez: 27 9 2023
Statut: aheadofprint

Résumé

Testosterone plays an important role in collagen metabolism, transforming growth factor-β1 expression, and wound healing, which are all critical factors in pathogenesis of Peyronie's disease. Some clinical studies have suggested an association between Peyronie's disease and hypogonadism. We sought to investigate whether baseline total testosterone levels influence response to intralesional collagenase clostridium histolyticum in Peyronie's disease. A retrospective review of patients receiving collagenase clostridium histolyticum injections with available total testosterone levels within 1 year of initial injection was conducted at a single institution. Baseline demographics, hypogonadal status, total testosterone, number of collagenase clostridium histolyticum cycles, and pre- and post-treatment degrees of curvature were collected. Hypogonadism was defined as total testosterone <300 ng/dL. Thirty-six men were included with mean age of 58.2 years (SD 10.4) and mean body mass index 26.8 (SD 3.2). The mean total testosterone was 459.2 ng/dL (SD 144.0), and four (11.1%) were hypogonadal. Mean pre-treatment curvature was 47.6°, and mean post-treatment curvature was 27.8°, with mean improvement of 19.9° (40.1%). Hypogonadal status was not significantly associated with more severe curvature, 46.4° among hypogonadal men as to 57.5° among eugonadal men (p = 0.32). On linear regression analysis, total testosterone did not significantly predict improvement in degrees (β = -0.02; R Neither total testosterone nor hypogonadism is associated with a degree of improvement after collagenase clostridium histolyticum treatment.

Sections du résumé

BACKGROUND BACKGROUND
Testosterone plays an important role in collagen metabolism, transforming growth factor-β1 expression, and wound healing, which are all critical factors in pathogenesis of Peyronie's disease. Some clinical studies have suggested an association between Peyronie's disease and hypogonadism.
OBJECTIVE OBJECTIVE
We sought to investigate whether baseline total testosterone levels influence response to intralesional collagenase clostridium histolyticum in Peyronie's disease.
METHODS METHODS
A retrospective review of patients receiving collagenase clostridium histolyticum injections with available total testosterone levels within 1 year of initial injection was conducted at a single institution. Baseline demographics, hypogonadal status, total testosterone, number of collagenase clostridium histolyticum cycles, and pre- and post-treatment degrees of curvature were collected. Hypogonadism was defined as total testosterone <300 ng/dL.
RESULTS AND DISCUSSION CONCLUSIONS
Thirty-six men were included with mean age of 58.2 years (SD 10.4) and mean body mass index 26.8 (SD 3.2). The mean total testosterone was 459.2 ng/dL (SD 144.0), and four (11.1%) were hypogonadal. Mean pre-treatment curvature was 47.6°, and mean post-treatment curvature was 27.8°, with mean improvement of 19.9° (40.1%). Hypogonadal status was not significantly associated with more severe curvature, 46.4° among hypogonadal men as to 57.5° among eugonadal men (p = 0.32). On linear regression analysis, total testosterone did not significantly predict improvement in degrees (β = -0.02; R
CONCLUSION CONCLUSIONS
Neither total testosterone nor hypogonadism is associated with a degree of improvement after collagenase clostridium histolyticum treatment.

Identifiants

pubmed: 37753943
doi: 10.1111/andr.13532
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 American Society of Andrology and European Academy of Andrology.

Références

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Auteurs

Douglas Schneider (D)

Irvine Department of Urology, University of California, Irvine, California, USA.

Mitchell O'Leary (M)

Irvine Department of Urology, University of California, Irvine, California, USA.

Eliad Amini (E)

Irvine Department of Urology, University of California, Irvine, California, USA.

Jake Miller (J)

Irvine Department of Urology, University of California, Irvine, California, USA.

Nick Hassas (N)

Irvine Department of Urology, University of California, Irvine, California, USA.

Jeanie Nguyen (J)

Irvine Department of Urology, University of California, Irvine, California, USA.

Muhammed A Moukhtar Hammad (MAM)

Irvine Department of Urology, University of California, Irvine, California, USA.

David Barham (D)

Irvine Department of Urology, University of California, Irvine, California, USA.

Faysal A Yafi (FA)

Irvine Department of Urology, University of California, Irvine, California, USA.

Classifications MeSH