Is sperm telomere length altered in teratozoospermia specimens? A case-control study.

Male infertility. Sperm Teratozoospermia Telomere

Journal

International journal of reproductive biomedicine
ISSN: 2476-4108
Titre abrégé: Int J Reprod Biomed
Pays: Iran
ID NLM: 101679102

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 08 03 2022
revised: 19 07 2022
accepted: 02 02 2023
medline: 1 5 2023
pubmed: 1 5 2023
entrez: 1 5 2023
Statut: epublish

Résumé

Male factor infertility is a multifactorial defect, and many of its etiologies are unknown. Teratozoospermia is determined by the existence of over 85% morphologically abnormal spermatozoa in semen which are almost incompetent in fertilization function. One of the most novel issues in genetic alterations studies is the variation of sperm telomere lengths (STL) and its collaboration with male infertility. The present study has been focused on STL alterations in teratozoospermia. Investigation of differences in telomere length of teratozoospermia specimens and sperms with normal parameters. In this case-control study, 60 men referred to Arak Fertility Clinic, Markazi province, Iran from November 2017 to February 2018 were categorized into teratozoospermia and normozoospermic groups. Sperm genomic DNA extraction was conducted, and STL were evaluated using quantitative polymerase chain reaction. Statistical evaluation of relative telomere length was calculated by the ratio of telomere to single-copy gene for teratozoospermia and normal specimens. Results significantly demonstrated that relative telomere length in teratozoospermia samples is nearly 3 times shorter than in normal samples (p Our results represent the reduction of telomeres length in teratozoospermia and suggest that this alteration might be one of the factors contributing to the sperm fertility potential of this kind of specimen. However, defining relevant molecular processes requires further detailed investigations.

Sections du résumé

Background UNASSIGNED
Male factor infertility is a multifactorial defect, and many of its etiologies are unknown. Teratozoospermia is determined by the existence of over 85% morphologically abnormal spermatozoa in semen which are almost incompetent in fertilization function. One of the most novel issues in genetic alterations studies is the variation of sperm telomere lengths (STL) and its collaboration with male infertility. The present study has been focused on STL alterations in teratozoospermia.
Objective UNASSIGNED
Investigation of differences in telomere length of teratozoospermia specimens and sperms with normal parameters.
Materials and Methods UNASSIGNED
In this case-control study, 60 men referred to Arak Fertility Clinic, Markazi province, Iran from November 2017 to February 2018 were categorized into teratozoospermia and normozoospermic groups. Sperm genomic DNA extraction was conducted, and STL were evaluated using quantitative polymerase chain reaction.
Results UNASSIGNED
Statistical evaluation of relative telomere length was calculated by the ratio of telomere to single-copy gene for teratozoospermia and normal specimens. Results significantly demonstrated that relative telomere length in teratozoospermia samples is nearly 3 times shorter than in normal samples (p
Conclusion UNASSIGNED
Our results represent the reduction of telomeres length in teratozoospermia and suggest that this alteration might be one of the factors contributing to the sperm fertility potential of this kind of specimen. However, defining relevant molecular processes requires further detailed investigations.

Identifiants

pubmed: 37122888
doi: 10.18502/ijrm.v21i3.13198
pmc: PMC10133734
doi:

Types de publication

Journal Article

Langues

eng

Pagination

229-236

Informations de copyright

Copyright © 2023 Fattahi et al.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interest.

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Auteurs

Maryam Fattahi (M)

Department of Medical Genetics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

Mohadese Maghsudlu (M)

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Mohammad Hasan Sheikhha (M)

Abortion Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

Classifications MeSH