<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li G</submitter><funding>National Key Program of Clinical Science</funding><funding>Beijing Science &amp;amp; Technology Star Program</funding><funding>Beijing Municipal Science &amp;amp;Technology Commission</funding><funding>Graduate innovation fund of Peking Union Medical College</funding><funding>National Key Research program of China</funding><funding>Union Diabetes Research Talent Fund</funding><funding>Development Program of Beijing Chaoyang Hospital</funding><funding>Beijing Natural Science Foundation</funding><pagination>164-171</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6020797</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32</volume><pubmed_abstract>Left ventricular mass index (LVMI) provides a metric for cardiovascular disease risk. We aimed to assess the association of adiponectin-related genetic variants resulting from GWAS in East Asians (loci in/near CDH13, ADIPOQ, WDR11FGF, CMIP and PEPD) with LVMI, and to examine whether sleep duration modified these genetic associations in youth. The 559 subjects aged 15-28 years were recruited from the Beijing Child and Adolescent Metabolic Syndrome study. Among the six loci, CDH13 rs4783244 was significantly correlated with adiponectin levels (p = 8.07 × 10&lt;sup>-7&lt;/sup>). The adiponectin-rising allele in rs4783244 locus was significantly associated with decreased LVMI (p = 6.99 × 10&lt;sup>-4&lt;/sup>) after adjusting for classical cardiovascular risk factors, and further for adiponectin levels, w</pubmed_abstract><journal>EBioMedicine</journal><pubmed_title>Loss of Cardio-Protective Effects at the CDH13 Locus Due to Gene-Sleep Interaction: The BCAMS Study.</pubmed_title><pmcid>PMC6020797</pmcid><funding_grant_id>(#WBYZ 2011–873</funding_grant_id><funding_grant_id>#D111100000611002</funding_grant_id><funding_grant_id>JXPY201606</funding_grant_id><funding_grant_id>(#2017–1002–1-15</funding_grant_id><funding_grant_id>#2004A027</funding_grant_id><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Han L</pubmed_authors><pubmed_authors>Fu J</pubmed_authors><pubmed_authors>Feng D</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Grant SFA</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Gao S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Loss of Cardio-Protective Effects at the CDH13 Locus Due to Gene-Sleep Interaction: The BCAMS Study.</name><description>Left ventricular mass index (LVMI) provides a metric for cardiovascular disease risk. We aimed to assess the association of adiponectin-related genetic variants resulting from GWAS in East Asians (loci in/near CDH13, ADIPOQ, WDR11FGF, CMIP and PEPD) with LVMI, and to examine whether sleep duration modified these genetic associations in youth. The 559 subjects aged 15-28 years were recruited from the Beijing Child and Adolescent Metabolic Syndrome study. Among the six loci, CDH13 rs4783244 was significantly correlated with adiponectin levels (p = 8.07 × 10&lt;sup>-7&lt;/sup>). The adiponectin-rising allele in rs4783244 locus was significantly associated with decreased LVMI (p = 6.99 × 10&lt;sup>-4&lt;/sup>) after adjusting for classical cardiovascular risk factors, and further for adiponectin levels, w</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2025-04-05T13:14:16.079Z</modification><creation>2019-03-26T23:44:27Z</creation></dates><accession>S-EPMC6020797</accession><cross_references><pubmed>29903569</pubmed><doi>10.1016/j.ebiom.2018.05.033</doi></cross_references></HashMap>