Association between genetic variants in hsa-miR-27a and hsa-miR-146a genes and male infertility

Background: miRNAs have enormous potential to be used as diagnostic and prognostic markers as well as therapeutic targets in male infertility and diseases of the reproductive system. This study aimed to investigate the association between the two functional genetic variants in the hsa-miR27a (rs2910...

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Main Authors: Rajovski Srećko, Matijašević-Joković Suzana, Milanović Nikoleta, Radovanović Nemanja, Brkušanin Miloš, Savić-Pavićević Dušanka, Dobrijević Zorana, Brajušković Goran
Format: Article
Language:English
Published: Society of Medical Biochemists of Serbia, Belgrade 2024-01-01
Series:Journal of Medical Biochemistry
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Online Access:https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2024/1452-82582406936R.pdf
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author Rajovski Srećko
Matijašević-Joković Suzana
Milanović Nikoleta
Radovanović Nemanja
Brkušanin Miloš
Savić-Pavićević Dušanka
Dobrijević Zorana
Brajušković Goran
author_facet Rajovski Srećko
Matijašević-Joković Suzana
Milanović Nikoleta
Radovanović Nemanja
Brkušanin Miloš
Savić-Pavićević Dušanka
Dobrijević Zorana
Brajušković Goran
author_sort Rajovski Srećko
collection DOAJ
description Background: miRNAs have enormous potential to be used as diagnostic and prognostic markers as well as therapeutic targets in male infertility and diseases of the reproductive system. This study aimed to investigate the association between the two functional genetic variants in the hsa-miR27a (rs2910164) and hsa-miR-146a gene (rs895819) and male infertility in North Macedonian population, as well as to test their association with the values of major seminal parameters. Methods: The case group included in this study comprised 158 men initially diagnosed with idiopathic male infertility. The control group included 126 age-matched healthy male volunteers who fathered at least one child. Results: We report the association of rs2910164 minor allele C for the first time with the increased susceptibility to asthenoteratozoospermia. Additionally, our results indicating the association of allele C with low sperm vitality are a novel finding. We did not demonstrate the association between genetic variant rs895819 and the risk of different types of male infertility. Still, the number of participants with CC genotype in subjects diagnosed with asthenoteratozoospermia was null, while in controls, it reached 7.2%. We further detected the rs895819 genotype-dependent difference in rapid progressive sperm motility. Conclusions: The association of rs2910164 and rs895819 with idiopathic male infertility in general is unlikely. However, both of these variants show an association with certain types of male infertility and with sperm abnormalities, which need to be confirmed in later studies in different ethnic groups.
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spelling doaj-art-d180dead37ce46fca29f1187d9f812fe2025-08-20T02:51:00ZengSociety of Medical Biochemists of Serbia, BelgradeJournal of Medical Biochemistry1452-82581452-82662024-01-0143693694510.5937/jomb0-508761452-82582406936RAssociation between genetic variants in hsa-miR-27a and hsa-miR-146a genes and male infertilityRajovski Srećko0Matijašević-Joković Suzana1Milanović Nikoleta2Radovanović Nemanja3Brkušanin Miloš4https://orcid.org/0000-0002-4316-9231Savić-Pavićević Dušanka5https://orcid.org/0000-0002-2079-4077Dobrijević Zorana6Brajušković Goran7https://orcid.org/0000-0002-3935-6755Private Healthcare Institution Clinical Hospital "Acibadem Sistina", Skopje, North Macedoniauniversity of belgrade, faculty of biology, centre for human molecular genetic, Serbiauniversity of belgrade, faculty of biology, centre for human molecular genetic, Serbiauniversity of belgrade, faculty of biology, centre for human molecular genetic, Serbiauniversity of belgrade, faculty of biology, centre for human molecular genetic, Serbiauniversity of belgrade, faculty of biology, centre for human molecular genetic, SerbiaUniversity of Belgrade, Institute for the Application of Nuclear Energy - INEP, Department for Metabolism, Belgrade, Serbiauniversity of belgrade, faculty of biology, centre for human molecular genetic, SerbiaBackground: miRNAs have enormous potential to be used as diagnostic and prognostic markers as well as therapeutic targets in male infertility and diseases of the reproductive system. This study aimed to investigate the association between the two functional genetic variants in the hsa-miR27a (rs2910164) and hsa-miR-146a gene (rs895819) and male infertility in North Macedonian population, as well as to test their association with the values of major seminal parameters. Methods: The case group included in this study comprised 158 men initially diagnosed with idiopathic male infertility. The control group included 126 age-matched healthy male volunteers who fathered at least one child. Results: We report the association of rs2910164 minor allele C for the first time with the increased susceptibility to asthenoteratozoospermia. Additionally, our results indicating the association of allele C with low sperm vitality are a novel finding. We did not demonstrate the association between genetic variant rs895819 and the risk of different types of male infertility. Still, the number of participants with CC genotype in subjects diagnosed with asthenoteratozoospermia was null, while in controls, it reached 7.2%. We further detected the rs895819 genotype-dependent difference in rapid progressive sperm motility. Conclusions: The association of rs2910164 and rs895819 with idiopathic male infertility in general is unlikely. However, both of these variants show an association with certain types of male infertility and with sperm abnormalities, which need to be confirmed in later studies in different ethnic groups.https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2024/1452-82582406936R.pdfmale infertilityrs2910164rs895819polymorphismmir-27amir-146a
spellingShingle Rajovski Srećko
Matijašević-Joković Suzana
Milanović Nikoleta
Radovanović Nemanja
Brkušanin Miloš
Savić-Pavićević Dušanka
Dobrijević Zorana
Brajušković Goran
Association between genetic variants in hsa-miR-27a and hsa-miR-146a genes and male infertility
Journal of Medical Biochemistry
male infertility
rs2910164
rs895819
polymorphism
mir-27a
mir-146a
title Association between genetic variants in hsa-miR-27a and hsa-miR-146a genes and male infertility
title_full Association between genetic variants in hsa-miR-27a and hsa-miR-146a genes and male infertility
title_fullStr Association between genetic variants in hsa-miR-27a and hsa-miR-146a genes and male infertility
title_full_unstemmed Association between genetic variants in hsa-miR-27a and hsa-miR-146a genes and male infertility
title_short Association between genetic variants in hsa-miR-27a and hsa-miR-146a genes and male infertility
title_sort association between genetic variants in hsa mir 27a and hsa mir 146a genes and male infertility
topic male infertility
rs2910164
rs895819
polymorphism
mir-27a
mir-146a
url https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2024/1452-82582406936R.pdf
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