Proteomic biomarkers in seminal plasma as predictors of reproductive potential in azoospermic men.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2024
Historique:
received: 25 10 2023
accepted: 20 03 2024
medline: 24 4 2024
pubmed: 24 4 2024
entrez: 24 4 2024
Statut: epublish

Résumé

Azoospermia, characterized by an absence of sperm in the ejaculate, represents the most severe form of male infertility. While surgical sperm retrieval in obstructive azoospermia (OA) is successful in the majority of cases, patients with non-obstructive azoospermia (NOA) show retrieval rates of only about 50% and thus frequently have unnecessary surgery. Surgical intervention could be avoided if patients without preserved spermatogenesis are identified preoperatively. This prospective study aimed to discover biomarkers in seminal plasma that could be employed for a non-invasive differential diagnosis of OA/NOA in order to rationalize surgery recommendations and improve success rates. All patients signed written informed consent, underwent comprehensive andrological evaluation, received human genetics to exclude relevant pathologies, and patients with azoospermia underwent surgical sperm retrieval. Using label-free LC-MS/MS, we compared the proteomes of seminal plasma samples from fertile men (healthy controls (HC), n=8) and infertile men diagnosed with 1) OA (n=7), 2) NOA with successful sperm retrieval (mixed testicular atrophy (MTA), n=8), and 3) NOA without sperm retrieval (Sertoli cell-only phenotype (SCO), n=7). Relative abundance changes of two candidate markers of sperm retrieval, HSPA2 and LDHC, were confirmed by Western Blot. We found the protein expression levels of 42 proteins to be significantly down-regulated (p ≤ 0.05) in seminal plasma from SCO NOA patients relative to HC whereas only one protein was down-regulated in seminal plasma from MTA patients. Analysis of tissue and cell expression suggested that the testis-specific proteins LDHC, PGK2, DPEP3, and germ-cell enriched heat-shock proteins HSPA2 and HSPA4L are promising biomarkers of spermatogenic function. Western blotting revealed a significantly lower abundance of LDHC and HSPA2 in the seminal plasma of men with NOA (SCO and MTA) compared to controls. The results indicate that certain testis-specific proteins when measured in seminal plasma, could serve as indicators of the presence of sperm in the testis and predict the success of sperm retrieval. Used in conjunction with conventional clinical assessments, these proteomic biomarkers may assist in the non-invasive diagnosis of idiopathic male infertility.

Identifiants

pubmed: 38654926
doi: 10.3389/fendo.2024.1327800
pmc: PMC11035875
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1327800

Informations de copyright

Copyright © 2024 Fietz, Sgaier, O’Donnell, Stanton, Dagley, Webb, Schuppe, Diemer and Pilatz.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Daniela Fietz (D)

Department of Veterinary Anatomy, Histology and Embryology, Justus Liebig University Giessen, Giessen, Germany.

Raouda Sgaier (R)

Department of Veterinary Anatomy, Histology and Embryology, Justus Liebig University Giessen, Giessen, Germany.
Centre for Reproductive Health, Hudson Institute of Medical Research, Clayton, VIC, Australia.
Department of Urology, Pediatric Urology and Andrology, Justus Liebig University Giessen, Giessen, Germany.

Liza O'Donnell (L)

Centre for Reproductive Health, Hudson Institute of Medical Research, Clayton, VIC, Australia.
Department of Molecular and Translational Sciences, Monash University, Clayton, VIC, Australia.

Peter G Stanton (PG)

Centre for Reproductive Health, Hudson Institute of Medical Research, Clayton, VIC, Australia.
Department of Molecular and Translational Sciences, Monash University, Clayton, VIC, Australia.

Laura F Dagley (LF)

Advanced Technology and Biology Division, Walter and Eliza Hall Institute, Parkville, VIC, Australia.
Department of Molecular and Translational Sciences, School of Clinical Sciences, Monash University, Clayton, VIC, Australia.

Andrew I Webb (AI)

Advanced Technology and Biology Division, Walter and Eliza Hall Institute, Parkville, VIC, Australia.
Department of Molecular and Translational Sciences, School of Clinical Sciences, Monash University, Clayton, VIC, Australia.

Hans-Christian Schuppe (HC)

Department of Urology, Pediatric Urology and Andrology, Justus Liebig University Giessen, Giessen, Germany.

Thorsten Diemer (T)

Department of Urology, Pediatric Urology and Andrology, Justus Liebig University Giessen, Giessen, Germany.

Adrian Pilatz (A)

Department of Urology, Pediatric Urology and Andrology, Justus Liebig University Giessen, Giessen, Germany.

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