<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Harmon QE</submitter><funding>NICHD NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIEHS NIH HHS</funding><pagination>472-84</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4040534</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>71(5)</volume><pubmed_abstract>&lt;h4>Problem&lt;/h4>Inflammatory biomarkers are associated with preeclampsia (PE) and poor fetal growth; however, genetic epidemiologic studies have been limited by reduced gene coverage and the exclusion of African American mothers.&lt;h4>Method of study&lt;/h4>Cases and controls (N = 1646) from a pregnancy cohort were genotyped for 503 tagSNPs in 40 genes related to inflammation. Gene-set analyses were stratified by race and were followed by a single SNP analysis within significant gene sets.&lt;h4>Results&lt;/h4>Gene-level associations were found for IL6 and KLRD1 for term small for gestational age (SGA) among African Americans. LTA/TNF and TBX21 were associated with PE among European Americans. The strongest association was for PE among European Americans for an upstream regulator of TNF with RR = 1.8</pubmed_abstract><journal>American journal of reproductive immunology (New York, N.Y. : 1989)</journal><pubmed_title>Polymorphisms in inflammatory genes are associated with term small for gestational age and preeclampsia.</pubmed_title><pmcid>PMC4040534</pmcid><funding_grant_id>HD37584</funding_grant_id><funding_grant_id>T32 ES007018</funding_grant_id><funding_grant_id>P30 ES010126</funding_grant_id><funding_grant_id>HD28684A</funding_grant_id><funding_grant_id>P2C HD050924</funding_grant_id><funding_grant_id>R01 HD039373</funding_grant_id><funding_grant_id>2-T32-ES07018</funding_grant_id><funding_grant_id>R01 HD037584</funding_grant_id><funding_grant_id>RR00046</funding_grant_id><funding_grant_id>HD28684</funding_grant_id><funding_grant_id>P30ES010126</funding_grant_id><funding_grant_id>R21 HD060207</funding_grant_id><funding_grant_id>M01 RR000046</funding_grant_id><funding_grant_id>HD39373</funding_grant_id><pubmed_authors>Avery CL</pubmed_authors><pubmed_authors>Luo J</pubmed_authors><pubmed_authors>Stuebe AM</pubmed_authors><pubmed_authors>Harmon QE</pubmed_authors><pubmed_authors>Engel SM</pubmed_authors><pubmed_authors>Wu MC</pubmed_authors><pubmed_authors>Moran TM</pubmed_authors><pubmed_authors>Olshan AF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Polymorphisms in inflammatory genes are associated with term small for gestational age and preeclampsia.</name><description>&lt;h4>Problem&lt;/h4>Inflammatory biomarkers are associated with preeclampsia (PE) and poor fetal growth; however, genetic epidemiologic studies have been limited by reduced gene coverage and the exclusion of African American mothers.&lt;h4>Method of study&lt;/h4>Cases and controls (N = 1646) from a pregnancy cohort were genotyped for 503 tagSNPs in 40 genes related to inflammation. Gene-set analyses were stratified by race and were followed by a single SNP analysis within significant gene sets.&lt;h4>Results&lt;/h4>Gene-level associations were found for IL6 and KLRD1 for term small for gestational age (SGA) among African Americans. LTA/TNF and TBX21 were associated with PE among European Americans. The strongest association was for PE among European Americans for an upstream regulator of TNF with RR = 1.8</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 May</publication><modification>2026-05-02T05:33:37.866Z</modification><creation>2019-03-27T01:29:13Z</creation></dates><accession>S-EPMC4040534</accession><cross_references><pubmed>24702779</pubmed><doi>10.1111/aji.12241</doi></cross_references></HashMap>