
<ns0:uwmetadata xmlns:ns0="http://phaidra.univie.ac.at/XML/metadata/V1.0" xmlns:ns1="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0" xmlns:ns10="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0" xmlns:ns11="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0/entity" xmlns:ns12="http://phaidra.univie.ac.at/XML/metadata/digitalbook/V1.0" xmlns:ns13="http://phaidra.univie.ac.at/XML/metadata/etheses/V1.0" xmlns:ns2="http://phaidra.univie.ac.at/XML/metadata/extended/V1.0" xmlns:ns3="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/entity" xmlns:ns4="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/requirement" xmlns:ns5="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/educational" xmlns:ns6="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/annotation" xmlns:ns7="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/classification" xmlns:ns8="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/organization" xmlns:ns9="http://phaidra.univie.ac.at/XML/metadata/histkult/V1.0">
  <ns1:general>
    <ns1:identifier>o:35217</ns1:identifier>
    <ns1:title language="en">Association between genetic variants in HSA-MIR-27A and HSA-MIR-146A genes and male infertility</ns1:title>
    <ns2:alt_title language="sr">Asocijacija varijanti u genima HSA-MIR-27A i HSA-MIR-146A sa muškim sterilitetom</ns2:alt_title>
    <ns1:language>en</ns1:language>
    <ns1:description language="en">ABSTRACT
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. </ns1:description>
    <ns1:keyword language="en">male infertility, rs2910164, rs895819, polymorphism, miR-27a, miR-146a</ns1:keyword>
    <ns2:identifiers>
      <ns2:resource>1552099</ns2:resource>
      <ns2:identifier>10.5937/jomb0-50876</ns2:identifier>
    </ns2:identifiers>
    <ns2:identifiers>
      <ns2:resource>1552101</ns2:resource>
      <ns2:identifier>1452-8258</ns2:identifier>
    </ns2:identifiers>
  </ns1:general>
  <ns1:lifecycle>
    <ns1:upload_date>2024-11-25T09:33:55.102Z</ns1:upload_date>
    <ns1:status>44</ns1:status>
    <ns2:peer_reviewed>yes</ns2:peer_reviewed>
    <ns1:contribute seq="0">
      <ns1:role>46</ns1:role>
      <ns1:entity seq="0">
        <ns3:firstname>Srećko </ns3:firstname>
        <ns3:lastname>Rajovski</ns3:lastname>
        <ns3:institution>Private Healthcare Institution Clinical Hospital &quot;Acibadem Sistina&quot;, Skopje, North Macedonia</ns3:institution>
      </ns1:entity>
      <ns1:entity seq="1">
        <ns3:firstname>Nikoleta</ns3:firstname>
        <ns3:lastname>Milanović</ns3:lastname>
        <ns3:institution>University of Belgrade, Faculty of Biology, Centre for Human Molecular Genetics, Belgrade, Serbia</ns3:institution>
        <ns3:type>person</ns3:type>
      </ns1:entity>
      <ns1:entity seq="2">
        <ns3:firstname>Nemanja</ns3:firstname>
        <ns3:lastname>Radovanović</ns3:lastname>
        <ns3:institution>University of Belgrade, Faculty of Biology, Centre for Human Molecular Genetics, Belgrade, Serbia</ns3:institution>
        <ns3:type>person</ns3:type>
      </ns1:entity>
      <ns1:entity seq="3">
        <ns3:firstname>Miloš</ns3:firstname>
        <ns3:lastname>Brkušanin</ns3:lastname>
        <ns3:institution>University of Belgrade, Faculty of Biology, Centre for Human Molecular Genetics, Belgrade, Serbia</ns3:institution>
        <ns3:type>person</ns3:type>
      </ns1:entity>
      <ns1:entity seq="4">
        <ns3:firstname>Dušanka</ns3:firstname>
        <ns3:lastname>Savić-Pavićević</ns3:lastname>
        <ns3:institution>University of Belgrade, Faculty of Biology, Centre for Human Molecular Genetics, Belgrade, Serbia</ns3:institution>
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      </ns1:entity>
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        <ns3:firstname>Zorana</ns3:firstname>
        <ns3:lastname>Dobrijević</ns3:lastname>
        <ns3:institution>University of Belgrade, Institute for the Application of Nuclear Energy INEP, Serbia</ns3:institution>
        <ns3:title1>doktor bioloških nauka</ns3:title1>
        <ns3:type>person</ns3:type>
        <ns3:orcid>0000-0002-4652-7719</ns3:orcid>
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        <ns3:firstname>Goran</ns3:firstname>
        <ns3:lastname>Brajušković</ns3:lastname>
        <ns3:institution>University of Belgrade, Faculty of Biology, Centre for Human Molecular Genetics, Belgrade, Serbia</ns3:institution>
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        <ns3:firstname>Suzana</ns3:firstname>
        <ns3:lastname>Matijašević Joković</ns3:lastname>
        <ns3:institution>University of Belgrade, Faculty of Biology, Centre for Human Molecular Genetics, Belgrade, Serbia</ns3:institution>
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    <ns1:location>https://phaidrabg.bg.ac.rs/o:35217</ns1:location>
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    <ns1:cost>no</ns1:cost>
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  <ns12:digitalbook>
    <ns12:name_magazine language="en">Journal of Medical Biochemistry</ns12:name_magazine>
    <ns12:volume>43</ns12:volume>
    <ns12:booklet>6</ns12:booklet>
    <ns12:from_page>936</ns12:from_page>
    <ns12:to_page>945</ns12:to_page>
    <ns12:releaseyear>2024</ns12:releaseyear>
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