<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Doherty C</submitter><funding>NCATS NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>131-136</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8299517</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>94</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>The objective of this study was to determine whether three common genetic polymorphisms [apolipoprotein (APOE) ε4 (rs42938 and rs7412), brain derived neurotrophic factor (BDNF) Met (rs6265), and catechol-O-methyltransferase (COMT) Val (rs4680)] are associated with increased psychiatric symptomatology in individuals with pharmacoresistant epilepsy.&lt;h4>Methods&lt;/h4>One hundred forty-eight adults (M&lt;sub>age&lt;/sub> = 38 years; 53% female) with refractory epilepsy completed self-report measures of mood, anxiety, and/or personality/psychopathology. Mann-Whitney U, t-tests, and Fisher's exact tests were used to determine if APOE4, BDNF Val66Met, or COMT Val158Met are associated with increased psychiatric symptomatology in people with epilepsy.&lt;h4>Results&lt;/h4>As a group, BDNF Met carriers reported greater symptoms of depression on the Personality Assessment Inventory (PAI) than those without a Met allele (p = 0.004); COMT Val carriers reported greater symptoms on the PAI Schizophrenia (p = 0.007), Antisocial Features (p = 0.04), and Alcohol Problems (p = 0.03) scales than noncarriers. On the individual level, a significantly greater proportion of BDNF Met carriers demonstrated elevated PAI Depression scores compared to those without a Met allele (p = 0.046). There was also a larger proportion of COMT Val carriers with elevated PAI Anxiety scores as compared to those without a Val allele (p = 0.036).&lt;h4>Significance&lt;/h4>This retrospective cross-sectional study provides preliminary evidence for a genetic basis of psychiatric comorbidities in epilepsy and suggests that BDNF and COMT may play an important role in the pathophysiology of mental health problems in this vulnerable population.</pubmed_abstract><journal>Epilepsy &amp; behavior : E&amp;B</journal><pubmed_title>BDNF and COMT, but not APOE, alleles are associated with psychiatric symptoms in refractory epilepsy.</pubmed_title><pmcid>PMC8299517</pmcid><funding_grant_id>KL2 TR000440</funding_grant_id><funding_grant_id>UL1 TR000439</funding_grant_id><funding_grant_id>K23 NS091344</funding_grant_id><pubmed_authors>Busch RM</pubmed_authors><pubmed_authors>Altemus JB</pubmed_authors><pubmed_authors>Hogue O</pubmed_authors><pubmed_authors>Floden DP</pubmed_authors><pubmed_authors>Doherty C</pubmed_authors><pubmed_authors>Najm IM</pubmed_authors><pubmed_authors>Eng C</pubmed_authors></additional><is_claimable>false</is_claimable><name>BDNF and COMT, but not APOE, alleles are associated with psychiatric symptoms in refractory epilepsy.</name><description>&lt;h4>Objective&lt;/h4>The objective of this study was to determine whether three common genetic polymorphisms [apolipoprotein (APOE) ε4 (rs42938 and rs7412), brain derived neurotrophic factor (BDNF) Met (rs6265), and catechol-O-methyltransferase (COMT) Val (rs4680)] are associated with increased psychiatric symptomatology in individuals with pharmacoresistant epilepsy.&lt;h4>Methods&lt;/h4>One hundred forty-eight adults (M&lt;sub>age&lt;/sub> = 38 years; 53% female) with refractory epilepsy completed self-report measures of mood, anxiety, and/or personality/psychopathology. Mann-Whitney U, t-tests, and Fisher's exact tests were used to determine if APOE4, BDNF Val66Met, or COMT Val158Met are associated with increased psychiatric symptomatology in people with epilepsy.&lt;h4>Results&lt;/h4>As a group, BDNF Met carriers reported greater symptoms of depression on the Personality Assessment Inventory (PAI) than those without a Met allele (p = 0.004); COMT Val carriers reported greater symptoms on the PAI Schizophrenia (p = 0.007), Antisocial Features (p = 0.04), and Alcohol Problems (p = 0.03) scales than noncarriers. On the individual level, a significantly greater proportion of BDNF Met carriers demonstrated elevated PAI Depression scores compared to those without a Met allele (p = 0.046). There was also a larger proportion of COMT Val carriers with elevated PAI Anxiety scores as compared to those without a Val allele (p = 0.036).&lt;h4>Significance&lt;/h4>This retrospective cross-sectional study provides preliminary evidence for a genetic basis of psychiatric comorbidities in epilepsy and suggests that BDNF and COMT may play an important role in the pathophysiology of mental health problems in this vulnerable population.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 May</publication><modification>2022-02-10T22:42:36.374Z</modification><creation>2022-02-10T22:42:36.374Z</creation></dates><accession>S-EPMC8299517</accession><cross_references><pubmed>30909076</pubmed><doi>10.1016/j.yebeh.2019.02.032</doi></cross_references></HashMap>