{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T05:41:09Z","timestamp":1790401269179,"version":"4.1.0"},"reference-count":60,"publisher":"Cambridge University Press (CUP)","issue":"6","license":[{"start":{"date-parts":[[2015,5,20]],"date-time":"2015-05-20T00:00:00Z","timestamp":1432080000000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/www.cambridge.org\/core\/terms"}],"content-domain":{"domain":["www.cambridge.org"],"crossmark-restriction":true},"short-container-title":["Acta Neuropsychiatr."],"published-print":{"date-parts":[[2015,12]]},"abstract":"<jats:sec id=\"S0924270815000253_abs1\" sec-type=\"general\"><jats:title>Objective<\/jats:title><jats:p>In major depressive disorder (MDD), single nucleotide polymorphisms (SNPs) in monoaminergic genes may impact disease susceptibility, treatment response, and brain volume. The objective of this study was to examine the effect of such polymorphisms on hippocampal volume in patients with treatment-resistant MDD and healthy controls. Candidate gene risk alleles were hypothesised to be associated with reductions in hippocampal volume.<\/jats:p><\/jats:sec><jats:sec id=\"S0924270815000253_abs2\" sec-type=\"methods\"><jats:title>Methods<\/jats:title><jats:p>A total of 26 outpatients with treatment-resistant MDD and 27 matched healthy controls underwent magnetic resonance imaging and genotyping for six SNPs in monoaminergic genes [serotonin transporter (<jats:italic>SLC6A4<\/jats:italic>), norepinephrine transporter (<jats:italic>SLC6A2<\/jats:italic>), serotonin 1A and 2A receptors (<jats:italic>HTR1A<\/jats:italic> and <jats:italic>HTR2A<\/jats:italic>), catechol-O-methyltransferase (<jats:italic>COMT<\/jats:italic>), and brain-derived neurotrophic factor (<jats:italic>BDNF<\/jats:italic>)]. Hippocampal volume was estimated using an automated segmentation algorithm (FreeSurfer).<\/jats:p><\/jats:sec><jats:sec id=\"S0924270815000253_abs3\" sec-type=\"results\"><jats:title>Results<\/jats:title><jats:p>Hippocampal volume did not differ between patients and controls. Within the entire study sample irrespective of diagnosis, C allele-carriers for both the NET\u2212182 T\/C [rs2242446] and 5-HT<jats:sub>1A<\/jats:sub>\u22121019C\/G [rs6295] polymorphisms had smaller hippocampal volumes relative to other genotypes. For the 5-HTTLPR (rs25531) polymorphism, there was a significant diagnosis by genotype interaction effect on hippocampal volume. Among patients only, homozygosity for the 5-HTTLPR short (S) allele was associated with smaller hippocampal volume. There was no association between the 5-HT<jats:sub>2A<\/jats:sub>, <jats:italic>COMT<\/jats:italic>, and <jats:italic>BDNF<\/jats:italic> SNPs and hippocampal volume.<\/jats:p><\/jats:sec><jats:sec id=\"S0924270815000253_abs4\" sec-type=\"conclusion\"><jats:title>Conclusion<\/jats:title><jats:p>The results indicate that the volume of the hippocampus may be influenced by serotonin- and norepinephrine-related gene polymorphisms. The NET and 5-HT<jats:sub>1A<\/jats:sub> polymorphisms appear to have similar effects on hippocampal volume in patients and controls while the 5-HTTLPR polymorphism differentially affects hippocampal volume in the presence of depression.<\/jats:p><\/jats:sec>","DOI":"10.1017\/neu.2015.25","type":"journal-article","created":{"date-parts":[[2015,5,20]],"date-time":"2015-05-20T06:09:15Z","timestamp":1432102155000},"page":"353-361","update-policy":"https:\/\/doi.org\/10.1017\/policypage","source":"Crossref","is-referenced-by-count":24,"title":["Impact of monoamine-related gene polymorphisms on hippocampal volume in treatment-resistant depression"],"prefix":"10.1017","volume":"27","author":[{"given":"Jennifer Lynne","family":"Phillips","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lisa 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