<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(58)</volume><submitter>Cheng Q</submitter><pubmed_abstract>&lt;h4>Aims&lt;/h4>To investigate the association of several single nucleotide polymorphisms (SNPs) within &lt;i>ACYP2&lt;/i> gene and additional gene- environment interaction with ischemic stroke (IS) risk in a Chinese population.&lt;h4>Results&lt;/h4>IS risk was significantly higher in carriers with the G allele of rs11896604 than those with CC genotype (CG or GG versus CC), adjusted OR (95%CI) =1.60 (1.18-2.20), and higher in carriers with the A allele of rs12615793 than those with GG genotype (GA or AA versus GG), adjusted OR (95%CI) = 1.66 (1.24-2.15). GMDR model shown a significant two-locus model (&lt;i>p&lt;/i> = 0.0010) involving rs11896604 and alcohol drinking, and a significant two-locus model (&lt;i>p&lt;/i> = 0.0010) involving rs12615793 and smoking. Current smokers with rs12615793- GA or AA genotype have the highest IS risk, compared to never- smokers with rs12615793-GG genotype, OR (95%CI) = 2.72 (1.64-3.86); current drinkers with rs11896604-CG or GG genotype have the highest IS risk, compared to never- drinkers with rs11896604-CC genotype, OR (95%CI) = 2.51 (1.70-3.40).&lt;h4>Materials and methods&lt;/h4>A total of 1202 participants (660 males, 542 females) were selected, including 600 IS patients and 602 control participants. The mean age of all participants was 68.2 ± 15.8 years. Generalized multifactor dimensionality reduction (GMDR) was used to screen the best interaction combination. Logistic regression was performed to investigate the impact of 4 SNPs within &lt;i>ACYP2&lt;/i> gene, additional gene-smoking or drinking interaction on IS risk.&lt;h4>Conclusions&lt;/h4>We found that the G allele of rs11896604 and the A allele of rs12615793 within &lt;i>ACYP2&lt;/i> gene, rs12615793- smoking interaction, and rs11896604-alcohol drinking interaction were all associated with increased IS risk.</pubmed_abstract><journal>Oncotarget</journal><pagination>97913-97919</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5716701</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Interactions between &lt;i>ACYP2&lt;/i> genetic polymorphisms and environment factors with susceptibility to ischemic stroke in a Han Chinese Population.</pubmed_title><pmcid>PMC5716701</pmcid><pubmed_authors>Lin Q</pubmed_authors><pubmed_authors>Cheng Q</pubmed_authors><pubmed_authors>Li YK</pubmed_authors><pubmed_authors>Lu F</pubmed_authors><pubmed_authors>Wei W</pubmed_authors><pubmed_authors>Yin L</pubmed_authors><pubmed_authors>Wang YZ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interactions between &lt;i>ACYP2&lt;/i> genetic polymorphisms and environment factors with susceptibility to ischemic stroke in a Han Chinese Population.</name><description>&lt;h4>Aims&lt;/h4>To investigate the association of several single nucleotide polymorphisms (SNPs) within &lt;i>ACYP2&lt;/i> gene and additional gene- environment interaction with ischemic stroke (IS) risk in a Chinese population.&lt;h4>Results&lt;/h4>IS risk was significantly higher in carriers with the G allele of rs11896604 than those with CC genotype (CG or GG versus CC), adjusted OR (95%CI) =1.60 (1.18-2.20), and higher in carriers with the A allele of rs12615793 than those with GG genotype (GA or AA versus GG), adjusted OR (95%CI) = 1.66 (1.24-2.15). GMDR model shown a significant two-locus model (&lt;i>p&lt;/i> = 0.0010) involving rs11896604 and alcohol drinking, and a significant two-locus model (&lt;i>p&lt;/i> = 0.0010) involving rs12615793 and smoking. Current smokers with rs12615793- GA or AA genotype have the highest IS risk, compared to never- smokers with rs12615793-GG genotype, OR (95%CI) = 2.72 (1.64-3.86); current drinkers with rs11896604-CG or GG genotype have the highest IS risk, compared to never- drinkers with rs11896604-CC genotype, OR (95%CI) = 2.51 (1.70-3.40).&lt;h4>Materials and methods&lt;/h4>A total of 1202 participants (660 males, 542 females) were selected, including 600 IS patients and 602 control participants. The mean age of all participants was 68.2 ± 15.8 years. Generalized multifactor dimensionality reduction (GMDR) was used to screen the best interaction combination. Logistic regression was performed to investigate the impact of 4 SNPs within &lt;i>ACYP2&lt;/i> gene, additional gene-smoking or drinking interaction on IS risk.&lt;h4>Conclusions&lt;/h4>We found that the G allele of rs11896604 and the A allele of rs12615793 within &lt;i>ACYP2&lt;/i> gene, rs12615793- smoking interaction, and rs11896604-alcohol drinking interaction were all associated with increased IS risk.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Nov</publication><modification>2024-11-20T10:00:41.918Z</modification><creation>2019-03-27T03:03:56Z</creation></dates><accession>S-EPMC5716701</accession><cross_references><pubmed>29228661</pubmed><doi>10.18632/oncotarget.18430</doi></cross_references></HashMap>