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        <datestamp>2026-10-01T05:29:38Z</datestamp>
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          <dc:title>Data Sheet 1_A pilot genome-wide association study of ischemic heart disease with co-occurring arterial hypertension in a Kazakh cohort.docx</dc:title>
          <dc:creator>Liliya Skvortsova (11917508)</dc:creator>
          <dc:creator>Kanagat Yergali (21992102)</dc:creator>
          <dc:creator>Assel Zhaxylykova (21992096)</dc:creator>
          <dc:creator>Mamura Begmanova (11917529)</dc:creator>
          <dc:creator>Almagul Mansharipova (25152546)</dc:creator>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>arterial hypertension</dc:subject>
          <dc:subject>Central Asia</dc:subject>
          <dc:subject>genome-wide association study</dc:subject>
          <dc:subject>ischemic heart disease</dc:subject>
          <dc:subject>Kazakh population</dc:subject>
          <dc:subject>ZFHX3</dc:subject>
          <dc:description>Background&lt;p&gt;Genome-wide association studies (GWAS) of ischemic heart disease (IHD) remain underrepresented in Central Asian populations. We conducted a pilot GWAS of ischemic heart disease with co-occurring arterial hypertension (IHD-HTN) in an ethnic Kazakh cohort to identify candidate loci for future replication.&lt;/p&gt;Methods&lt;p&gt;This study included 470 Kazakh individuals, comprising of 240 cases and 230 controls genotyped using the Illumina Infinium Global Screening Array-24 v 3.0. Association testing was performed using logistic regression under an additive genetic model adjusted for age, sex, and the first 10 principal components. Post-imputation GWAS was performed using high-quality imputed variants. Secondary analyses included MAGMA and KGWAS prioritization.&lt;/p&gt;Results&lt;p&gt;In the array-based GWAS, no variant reached the Bonferroni-corrected significance threshold (P &lt; 1.53 × 10&lt;sup&gt;−7&lt;/sup&gt;). The strongest SNP association was observed for rs1511924 at chromosome 16 mapped to the ZFHX3 gene (OR = 0.49, 95% CI = 0.37–0.66; P = 1.00 × 10&lt;sup&gt;−6&lt;/sup&gt;). Post-imputation GWAS supported the same locus with rs12598508 (P = 4.93 × 10&lt;sup&gt;−7&lt;/sup&gt;) and rs1511924 (P = 5.15 × 10&lt;sup&gt;−7&lt;/sup&gt;) among the strongest signals, although neither reached the genome-wide significance. Secondary MAGMA and KGWAS analyses did not provide stable evidence for additional loci.&lt;/p&gt;Conclusion&lt;p&gt;To our knowledge, this is the first pilot GWAS focused on IHD with co-occurring arterial hypertension in a Kazakh cohort. Although no Bonferroni-significant SNP associations were identified, the ZFHX3 region emerged as the strongest suggestive candidate locus and requires independent replication. Larger Central Asian cohorts and population-specific reference resources are required to validate these findings.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T05:29:38Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fgene.2026.1927147.s002</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_A_pilot_genome-wide_association_study_of_ischemic_heart_disease_with_co-occurring_arterial_hypertension_in_a_Kazakh_cohort_docx/34039164</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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