Genetic contributions to brain serotonin transporter levels in healthy adults

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作者
Silvia Elisabetta Portis Bruzzone
Arafat Nasser
Sagar Sanjay Aripaka
Marie Spies
Brice Ozenne
Peter Steen Jensen
Gitte Moos Knudsen
Vibe Gedsoe Frokjaer
Patrick MacDonald Fisher
机构
[1] Copenhagen University Hospital Rigshospitalet,Neurobiology Research Unit
[2] University of Copenhagen,Faculty of Health and Medical Sciences
[3] Medical University of Vienna,Department of Psychiatry and Psychotherapy
[4] University of Copenhagen,Department of Public Health, Section of Biostatistics
[5] Psychiatric Centre Copenhagen,Department of Drug Design and Pharmacology
[6] University of Copenhagen,undefined
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Scientific Reports | / 13卷
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摘要
The serotonin transporter (5-HTT) critically shapes serotonin neurotransmission by regulating extracellular brain serotonin levels; it remains unclear to what extent 5-HTT levels in the human brain are genetically determined. Here we applied [11C]DASB positron emission tomography to image brain 5-HTT levels and evaluated associations with five common serotonin-related genetic variants that might indirectly regulate 5-HTT levels (BDNF rs6265, SLC6A4 5-HTTLPR, HTR1A rs6295, HTR2A rs7333412, and MAOA rs1137070) in 140 healthy volunteers. In addition, we explored whether these variants could predict in vivo 5-HTT levels using a five-fold cross-validation random forest framework. MAOA rs1137070 T-carriers showed significantly higher brain 5-HTT levels compared to C-homozygotes (2–11% across caudate, putamen, midbrain, thalamus, hippocampus, amygdala and neocortex). We did not observe significant associations for the HTR1A rs6295 and HTR2A rs7333412 genotypes. Our previously observed lower subcortical 5-HTT availability for rs6265 met-carriers remained in the presence of these additional variants. Despite this significant association, our prediction models showed that genotype moderately improved prediction of 5-HTT in caudate, but effects were not statistically significant after adjustment for multiple comparisons. Our observations provide additional evidence that serotonin-related genetic variants modulate adult human brain serotonin neurotransmission.
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