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0 reviewsINTRODUCTION: Major depressive disorder (MDD) is a leading cause of suicide and disability. Better understanding changes toserotonin2A receptors (5-HT2ARs) in MDD and suicide may help to improve treatments. We systematically reviewed and metaanalysed positron emission tomography (PET), single photon emission computed tomography (SPECT) and post-mortemradioligand binding studies of cortical 5-HT2ARs in MDD and suicide.1234567890();,:METHODS: Databases were searched from inception to August/September 2024. Binding data were extracted and pooled beforerandom-effects meta-analyses of mean difference (Hedges’ g) and variance were undertaken. Simple linear regression wasperformed to investigate the relationship between receptor binding and depression severity at baseline in PET and SPECT studies.We also assessed study quality and tested for evidence of publication bias.RESULTS: Data on 556 MDD patients or suicide victims and 526 controls from 31 studies were included. Cortical 5-HT2AR bindingwas significantly lower in living MDD patients, who had not taken antidepressants for between one week and forever, than controlsin frontal, prefrontal, cingulate, anterior cingulate and, upon sensitivity analysis, temporal cortex (Hedges’ g = –0.40 to –0.57). Infrontal and cingulate regions, binding effect size correlated with depression severity at baseline. There was study-level evidence oflower regional binding in never-medicated MDD patients than controls which, upon exploratory meta-analysis, reached significancein anterior cingulate cortex. Most PET or SPECT studies were of good or fair quality. The results of most post-mortem analyses werenegative and included studies were of variable quality. There was limited evidence of publication bias.CONCLUSION: In vivo 5-HT2AR binding is reduced in MDD in frontal, cingulate and temporal cortex. This finding is based mainly onstudies that used antagonist or inverse agonist radiotracers