<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14</volume><submitter>Cao M</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Dyslipidemia is an independent predictor of ischemic stroke (IS). Genetic variations in lipid-metabolism related genes may increase the risk of IS. Fatty acid-binding protein 1 (FABP1) and fatty acid-binding protein 2 (FABP2) are lipid chaperones responsible for lipid transport and metabolism. The present study aimed to determine the association between &lt;i>FABP1&lt;/i> or &lt;i>FABP2&lt;/i> and ischemic stroke. &lt;b>Methods:&lt;/b> A total of 251 participants were recruited composed of 138 patients with ischemic stroke and 113 healthy subjects. DNA was extracted from peripheral blood samples. The rs2241883 polymorphism in &lt;i>FABP1&lt;/i> and rs1799883 polymorphism in &lt;i>FABP2&lt;/i> were genotyped using polymerase chain reaction-restriction fragment length polymorphism. Generalized multifactor dimensionality reduction (GMDR) was used to find out the interaction combinations between two SNPs and environmental factors. &lt;b>Results:&lt;/b> The GA genotype of FABP2 rs1799883 increased susceptibility to ischemic stroke under overdominant inheritance model (&lt;i>p&lt;/i> = 0.042). After adjusting for the risk factors of IS, it was associated with a significantly higher risk of IS in the codominant inheritance model (adjust OR = 3.431, 95%CI = 1.060-11.103, &lt;i>p&lt;/i> = 0.04). The interactions of &lt;i>FABP1&lt;/i> rs2241883 and &lt;i>FABP2&lt;/i> rs1799883 were not associated with IS risk (&lt;i>p&lt;/i> = 0.172). Moreover, interaction analysis of two genes (rs1799883 and rs2241883) and two environmental factors (smoking and alcohol consumption) was associated with an increased risk of IS (&lt;i>p&lt;/i> = 0.011). &lt;b>Conclusion:&lt;/b> The GA genotype of FABP2 rs1799883, interactions between rs1799883, rs2241883 and smoking and alcohol consumption were associated with IS risk in Chinese Han populations.</pubmed_abstract><journal>Frontiers in genetics</journal><pagination>1056186</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10117902</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Polymorphism in genes encoding two fatty acid binding proteins increases risk of ischemic stroke in a Chinese Han population.</pubmed_title><pmcid>PMC10117902</pmcid><pubmed_authors>Gong F</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Cao M</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Zhou C</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Liu B</pubmed_authors><pubmed_authors>Zhong J</pubmed_authors><pubmed_authors>Fang L</pubmed_authors><pubmed_authors>Chen D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Polymorphism in genes encoding two fatty acid binding proteins increases risk of ischemic stroke in a Chinese Han population.</name><description>&lt;b>Background:&lt;/b> Dyslipidemia is an independent predictor of ischemic stroke (IS). Genetic variations in lipid-metabolism related genes may increase the risk of IS. Fatty acid-binding protein 1 (FABP1) and fatty acid-binding protein 2 (FABP2) are lipid chaperones responsible for lipid transport and metabolism. The present study aimed to determine the association between &lt;i>FABP1&lt;/i> or &lt;i>FABP2&lt;/i> and ischemic stroke. &lt;b>Methods:&lt;/b> A total of 251 participants were recruited composed of 138 patients with ischemic stroke and 113 healthy subjects. DNA was extracted from peripheral blood samples. The rs2241883 polymorphism in &lt;i>FABP1&lt;/i> and rs1799883 polymorphism in &lt;i>FABP2&lt;/i> were genotyped using polymerase chain reaction-restriction fragment length polymorphism. Generalized multifactor dimensionality reduction (GMDR) was used to find out the interaction combinations between two SNPs and environmental factors. &lt;b>Results:&lt;/b> The GA genotype of FABP2 rs1799883 increased susceptibility to ischemic stroke under overdominant inheritance model (&lt;i>p&lt;/i> = 0.042). After adjusting for the risk factors of IS, it was associated with a significantly higher risk of IS in the codominant inheritance model (adjust OR = 3.431, 95%CI = 1.060-11.103, &lt;i>p&lt;/i> = 0.04). The interactions of &lt;i>FABP1&lt;/i> rs2241883 and &lt;i>FABP2&lt;/i> rs1799883 were not associated with IS risk (&lt;i>p&lt;/i> = 0.172). Moreover, interaction analysis of two genes (rs1799883 and rs2241883) and two environmental factors (smoking and alcohol consumption) was associated with an increased risk of IS (&lt;i>p&lt;/i> = 0.011). &lt;b>Conclusion:&lt;/b> The GA genotype of FABP2 rs1799883, interactions between rs1799883, rs2241883 and smoking and alcohol consumption were associated with IS risk in Chinese Han populations.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-25T20:16:45.963Z</modification><creation>2025-04-06T08:17:18.678Z</creation></dates><accession>S-EPMC10117902</accession><cross_references><pubmed>37091779</pubmed><doi>10.3389/fgene.2023.1056186</doi></cross_references></HashMap>