Evidence map›Paper›PMID 41422278›Full record

ArticleScientific reports2025

A comparison of sperm parameters DNA fragmentation and telomere length in testicular versus ejaculated spermatozoa.

Malihe Afsari, Haniyeh Nikkhah, Mohsen Ahrari, Ali Nabi, Ehsan Farashahi-Yazd, Azam Agha-Rahimi

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Malihe AfsariResearch and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Haniyeh NikkhahStem Cell Biology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Mohsen AhrariAndrology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Ali NabiResearch and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Ehsan Farashahi-YazdStem Cell Biology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. ehsanfarashahi@gmail.com.
Azam Agha-RahimiResearch and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. 63rahimi@gmail.com.ORCID http://orcid.org/0000-0002-7579-6192

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While previous studies reported conflicting findings on DNA fragmentation in testicular versus ejaculated spermatozoa, this study aimed to perform a detailed analysis of testicular spermatozoa, evaluating sperm parameters and detailed morphology, DNA fragmentation, and relative telomere length across testicular and ejaculated spermatozoa. The study included 60 men in four groups: normozoospermic men (control), men with oligoasthenoteratozoospermia (OAT), men with a history of sperm presence in the semen who were candidates for conventional testicular sperm extraction (TESE), and non-obstructive azoospermia (NOA) patients undergoing microdissection testicular sperm extraction (M-TESE). Spermatozoa were evaluated for vitality (eosin staining), teratozoospermia Index (TZI) and detailed morphology (Diff-Quik staining), DNA fragmentation (sperm chromatin dispersion assay), and relative telomere length (q-PCR). The results demonstrated that sperm vitality was significantly lower in the OAT group. The control group showed markedly higher rate of normal morphology and lower TZI compared to the OAT, TESE, and M-TESE groups. The TESE and M-TESE groups showed higher rates of head-midpiece abnormalities and residual bodies compared to the control group (P < 0.0001, P < 0.0001, respectively). Sperm DNA fragmentation in the control group showed a significant decrease relative to all experimental groups (P < 0.0001). The control group demonstrated a significantly higher proportion of sperm with intact acrosomes than all experimental groups (P < 0.0001). Moreover, the relative sperm telomere length was markedly lower in the M-TESE group compared to the control (P = 0.0006), OAT, and TESE groups (P < 0.0001). Our results demonstrated that testicular sperm have significantly elevated DNA damage levels. Moreover, these spermatozoa exhibit increased frequencies of morphological abnormalities in the head and midpiece regions, reacted acrosomes, and residual bodies.

Indexed as

DNA FragmentationSpermatozoaTelomereTelomere HomeostasisTestisAdultAzoospermiaEjaculationHumansMaleSemen AnalysisSperm RetrievalDNA fragmentationMorphologySperm telomere lengthTesticular spermatozoa

Identifiers

PMID41422278
PMCPMC12847935

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