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<article article-type="research-article" dtd-version="1.2" xml:lang="ru" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2658-6533</journal-id><journal-title-group><journal-title>Research Results in Biomedicine</journal-title></journal-title-group><issn pub-type="epub">2658-6533</issn></journal-meta><article-meta><article-id pub-id-type="doi">10.18413/2658-6533-2024-10-1-0-3</article-id><article-id pub-id-type="publisher-id">3334</article-id><article-categories><subj-group subj-group-type="heading"><subject>Genetics</subject></subj-group></article-categories><title-group><article-title>&lt;strong&gt;Sex-specific features of interlocus interactions determining susceptibility to hypertension&lt;/strong&gt;&lt;br /&gt;
&amp;nbsp;</article-title><trans-title-group xml:lang="en"><trans-title>&lt;strong&gt;Sex-specific features of interlocus interactions determining susceptibility to hypertension&lt;/strong&gt;&lt;br /&gt;
&amp;nbsp;</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Ivanova</surname><given-names>Tatyana A.</given-names></name><name xml:lang="en"><surname>Ivanova</surname><given-names>Tatyana A.</given-names></name></name-alternatives><email>ivanova_ta@bsu.edu.ru</email></contrib></contrib-group><pub-date pub-type="epub"><year>2024</year></pub-date><volume>10</volume><issue>1</issue><fpage>0</fpage><lpage>0</lpage><self-uri content-type="pdf" xlink:href="/media/medicine/2024/1/Биомед_исслед-54-69.pdf" /><abstract xml:lang="ru"><p>Background: Hypertension (HT) belongs to a group of widespread diseases in both men and women, but at the same time the disease is more often registered (&amp;asymp;20%) in men than in women. Genetic factors determining the sex characteristics of the prevalence of HT are largely unknown. The aim of the study:&amp;nbsp;To establish sex-specific features of intergenic interactions of GWAS-significant loci determining susceptibility to HT. Materials and methods: The sample of men included 564 patients with HT and 257 controls (total sample size n=821), women &amp;ndash; 375 patients with HT and 209 controls (total sample size n=584). Genotyping of 10 polymorphisms that showed associations with HT (blood pressure (BP)) in previously conducted genome-wide studies (GWAS) was performed. The intergenic interactions determining the susceptibility to HT in men and women were evaluated by the MB-MDR method. Results: In men, susceptibility to HT is determined by the interlocus interaction rs932764-PLCE1 &amp;times; rs7302981-CERS5 &amp;times; rs1799945-HFE &amp;times; rs8068318-TBX2 (Wald St. = 32.12 pperm =0.001) with the most pronounced effect of two-locus interaction rs1799945-HFE &amp;times; rs8068318-TBX2 (determines 0.76% of entropy). Among women, the most significant in relation to HT is the four-locus model, which includes polymorphic loci rs932764-PLCE1 &amp;times; rs8068318-TBX2 &amp;times; rs1173771-AC026703.1 &amp;times; rs167479-RGL3 (Wald St. = 33.53 pperm &amp;lt;0.001) with the maximum contribution to the entropy of the disease (2.26%) of the pair interaction rs8068318-TBX2 &amp;times; rs167479-RGL3. Polymorphisms rs932764-PLCE1 and rs8068318-TBX2 are very significant in both men and women.&amp;nbsp;Conclusion: The intergenic interactions of HT-significant GWAS loci are sex-specific.</p></abstract><trans-abstract xml:lang="en"><p>Background: Hypertension (HT) belongs to a group of widespread diseases in both men and women, but at the same time the disease is more often registered (&amp;asymp;20%) in men than in women. Genetic factors determining the sex characteristics of the prevalence of HT are largely unknown. The aim of the study:&amp;nbsp;To establish sex-specific features of intergenic interactions of GWAS-significant loci determining susceptibility to HT. Materials and methods: The sample of men included 564 patients with HT and 257 controls (total sample size n=821), women &amp;ndash; 375 patients with HT and 209 controls (total sample size n=584). Genotyping of 10 polymorphisms that showed associations with HT (blood pressure (BP)) in previously conducted genome-wide studies (GWAS) was performed. The intergenic interactions determining the susceptibility to HT in men and women were evaluated by the MB-MDR method. Results: In men, susceptibility to HT is determined by the interlocus interaction rs932764-PLCE1 &amp;times; rs7302981-CERS5 &amp;times; rs1799945-HFE &amp;times; rs8068318-TBX2 (Wald St. = 32.12 pperm =0.001) with the most pronounced effect of two-locus interaction rs1799945-HFE &amp;times; rs8068318-TBX2 (determines 0.76% of entropy). Among women, the most significant in relation to HT is the four-locus model, which includes polymorphic loci rs932764-PLCE1 &amp;times; rs8068318-TBX2 &amp;times; rs1173771-AC026703.1 &amp;times; rs167479-RGL3 (Wald St. = 33.53 pperm &amp;lt;0.001) with the maximum contribution to the entropy of the disease (2.26%) of the pair interaction rs8068318-TBX2 &amp;times; rs167479-RGL3. Polymorphisms rs932764-PLCE1 and rs8068318-TBX2 are very significant in both men and women.&amp;nbsp;Conclusion: The intergenic interactions of HT-significant GWAS loci are sex-specific.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>hypertension</kwd><kwd>men</kwd><kwd>women</kwd><kwd>polymorphism</kwd><kwd>associations</kwd><kwd>intergenic interactions</kwd><kwd>GWAS</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hypertension</kwd><kwd>men</kwd><kwd>women</kwd><kwd>polymorphism</kwd><kwd>associations</kwd><kwd>intergenic interactions</kwd><kwd>GWAS</kwd></kwd-group></article-meta></front><back><ref-list><title>Список литературы</title><ref id="B1"><mixed-citation>Williams B, Mancia G, Spiering W, et al. 2018 ESC/ESH Guidelines for the management of arterial hypertension. European Heart Journal. 2018;39(33):3021-3104. DOI: https://doi.org/10.1093/eurheartj/ehy339</mixed-citation></ref><ref id="B2"><mixed-citation>Kobalava ZD, Konradi AO, Nedogoda SV, et al. 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