<HashMap><database>biostudies-literature</database><scores/><additional><submitter>McFarquhar M</submitter><funding>Department of Health</funding><funding>Medical Research Council</funding><pagination>1743-53</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4023148</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>39(7)</volume><pubmed_abstract>Evidence suggests that depression is a risk factor for dementia; however, the relationship between the two conditions is not fully understood. A novel gene (TOMM40) has been consistently associated with Alzheimer's disease (AD), but has received no attention in depression. We conducted a three-level cross-sectional study to investigate the association of the TOMM40 rs2075650 SNP with depression. We recruited a community sample of 1220 participants (571 controls, 649 lifetime depression) to complete a psychiatric background questionnaire, the Brief Symptom Inventory, and Big Five Inventory at Level-1, 243 (102 controls, 97 remitted, 44 currently depressed) to complete a face-to-face clinical interview and neuropsychological testing at Level-2 and 58 (33 controls, 25 remitted) to complete an emotional face-processing task during fMRI at Level-3. Our results indicated that the TOMM40 rs2075650 G allele was a significant risk factor for lifetime depression (p = 0.00006) and, in depressed subjects, was a significant predictor of low extraversion (p = 0.009). Currently depressed risk allele carriers showed subtle executive dysfunction (p = 0.004) and decreased positive memory bias (p = 0.021) together with reduced activity in the posterior (p(FWE) = 0.045) and anterior (p(FWE) = 0.041) cingulate during sad face emotion processing. Our results suggest that TOMM40 rs2075650 may be a risk factor for the development of depression characterized by reduced extraversion, impaired executive function, and decreased positive emotional recall, and reduced top-down cortical control during sad emotion processing.</pubmed_abstract><journal>Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology</journal><pubmed_title>TOMM40 rs2075650 may represent a new candidate gene for vulnerability to major depressive disorder.</pubmed_title><pmcid>PMC4023148</pmcid><funding_grant_id>973638</funding_grant_id><funding_grant_id>NF-SI-0509-10229</funding_grant_id><pubmed_authors>Anderson IM</pubmed_authors><pubmed_authors>Mekli K</pubmed_authors><pubmed_authors>McKie S</pubmed_authors><pubmed_authors>McFarquhar M</pubmed_authors><pubmed_authors>Juhasz G</pubmed_authors><pubmed_authors>Downey D</pubmed_authors><pubmed_authors>Toth ZG</pubmed_authors><pubmed_authors>Thomas E</pubmed_authors><pubmed_authors>Elliott R</pubmed_authors><pubmed_authors>Deakin JF</pubmed_authors></additional><is_claimable>false</is_claimable><name>TOMM40 rs2075650 may represent a new candidate gene for vulnerability to major depressive disorder.</name><description>Evidence suggests that depression is a risk factor for dementia; however, the relationship between the two conditions is not fully understood. A novel gene (TOMM40) has been consistently associated with Alzheimer's disease (AD), but has received no attention in depression. We conducted a three-level cross-sectional study to investigate the association of the TOMM40 rs2075650 SNP with depression. We recruited a community sample of 1220 participants (571 controls, 649 lifetime depression) to complete a psychiatric background questionnaire, the Brief Symptom Inventory, and Big Five Inventory at Level-1, 243 (102 controls, 97 remitted, 44 currently depressed) to complete a face-to-face clinical interview and neuropsychological testing at Level-2 and 58 (33 controls, 25 remitted) to complete an emotional face-processing task during fMRI at Level-3. Our results indicated that the TOMM40 rs2075650 G allele was a significant risk factor for lifetime depression (p = 0.00006) and, in depressed subjects, was a significant predictor of low extraversion (p = 0.009). Currently depressed risk allele carriers showed subtle executive dysfunction (p = 0.004) and decreased positive memory bias (p = 0.021) together with reduced activity in the posterior (p(FWE) = 0.045) and anterior (p(FWE) = 0.041) cingulate during sad face emotion processing. Our results suggest that TOMM40 rs2075650 may be a risk factor for the development of depression characterized by reduced extraversion, impaired executive function, and decreased positive emotional recall, and reduced top-down cortical control during sad emotion processing.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jun</publication><modification>2021-02-20T01:29:47Z</modification><creation>2019-03-27T01:28:20Z</creation></dates><accession>S-EPMC4023148</accession><cross_references><pubmed>24549102</pubmed><doi>10.1038/npp.2014.22</doi></cross_references></HashMap>