<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Zou D</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> There is a growing body of evidence indicating a possible association between genetic variations and attention-deficit hyperactivity disorder (ADHD), although the results have been inconsistent. The objective of this study was to evaluate the correlation between the GRIN2A, GRIN2B and GRM7 gene polymorphisms and ADHD. &lt;b>Methods:&lt;/b> A comprehensive meta-analysis and subgroup evaluation was conducted using a fixed-effects model to analyze the association between ADHD and GRIN2B (rs2284411), GRIN2A (rs2229193), and GRM7 (rs3792452) in six genetic models (dominant, recessive, overdominant, homozygous, heterozygous, and allele models). &lt;b>Results:&lt;/b> The meta-analysis comprised 8 studies. The overall analysis showed that the GRIN2B rs2284411 T allele and T carries were significantly associated with a decreased risk of ADHD (dominant model:TT + CT vs. CC: OR = 0.783; 95% CI: 0.627-0.980; &lt;i>p&lt;/i> = 0.032, allele model:T vs. C: OR = 0.795; 95% CI: 0.656-0.964; &lt;i>p&lt;/i> = 0.019), especially in the Korean subgroup (dominant model:TT + CT vs. CC: OR = 0.640; 95% CI: 0.442-0.928; &lt;i>p&lt;/i> = 0.019, overdominant model: CT vs. TT + CC: OR = 0.641; 95% CI: 0.438-0.938; &lt;i>p&lt;/i> = 0.022, allele model:T vs. C: OR = 0.712; 95% CI: 0.521-0.974; &lt;i>p&lt;/i> = 0.034 and heterozygous model: CT vs. CC: OR = 0.630; 95% CI: 0.429-0.925; &lt;i>p&lt;/i> = 0.018). However, no meaningful associations were found for rs2229193 and rs3792452. &lt;b>Conclusion:&lt;/b> The results of the meta-analysis provide strong evidence that the rs2284411 T allele is significantly associated with reduced susceptibility to ADHD, particularly in the Korean population.</pubmed_abstract><journal>Frontiers in genetics</journal><pagination>1348387</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10965694</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Association of glutamate receptor gene polymorphisms with attention-deficit hyperactivity disorder susceptibility: a systematic review and meta-analysis.</pubmed_title><pmcid>PMC10965694</pmcid><pubmed_authors>Zeng Q</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>He RR</pubmed_authors><pubmed_authors>Liu P</pubmed_authors><pubmed_authors>Zou D</pubmed_authors><pubmed_authors>Guo R</pubmed_authors><pubmed_authors>Wei Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of glutamate receptor gene polymorphisms with attention-deficit hyperactivity disorder susceptibility: a systematic review and meta-analysis.</name><description>&lt;b>Background:&lt;/b> There is a growing body of evidence indicating a possible association between genetic variations and attention-deficit hyperactivity disorder (ADHD), although the results have been inconsistent. The objective of this study was to evaluate the correlation between the GRIN2A, GRIN2B and GRM7 gene polymorphisms and ADHD. &lt;b>Methods:&lt;/b> A comprehensive meta-analysis and subgroup evaluation was conducted using a fixed-effects model to analyze the association between ADHD and GRIN2B (rs2284411), GRIN2A (rs2229193), and GRM7 (rs3792452) in six genetic models (dominant, recessive, overdominant, homozygous, heterozygous, and allele models). &lt;b>Results:&lt;/b> The meta-analysis comprised 8 studies. The overall analysis showed that the GRIN2B rs2284411 T allele and T carries were significantly associated with a decreased risk of ADHD (dominant model:TT + CT vs. CC: OR = 0.783; 95% CI: 0.627-0.980; &lt;i>p&lt;/i> = 0.032, allele model:T vs. C: OR = 0.795; 95% CI: 0.656-0.964; &lt;i>p&lt;/i> = 0.019), especially in the Korean subgroup (dominant model:TT + CT vs. CC: OR = 0.640; 95% CI: 0.442-0.928; &lt;i>p&lt;/i> = 0.019, overdominant model: CT vs. TT + CC: OR = 0.641; 95% CI: 0.438-0.938; &lt;i>p&lt;/i> = 0.022, allele model:T vs. C: OR = 0.712; 95% CI: 0.521-0.974; &lt;i>p&lt;/i> = 0.034 and heterozygous model: CT vs. CC: OR = 0.630; 95% CI: 0.429-0.925; &lt;i>p&lt;/i> = 0.018). However, no meaningful associations were found for rs2229193 and rs3792452. &lt;b>Conclusion:&lt;/b> The results of the meta-analysis provide strong evidence that the rs2284411 T allele is significantly associated with reduced susceptibility to ADHD, particularly in the Korean population.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-21T21:29:54.191Z</modification><creation>2025-04-05T18:22:46.665Z</creation></dates><accession>S-EPMC10965694</accession><cross_references><pubmed>38544802</pubmed><doi>10.3389/fgene.2024.1348387</doi></cross_references></HashMap>