TY - JOUR
T1 - An integrative analysis of 5HTT-mediated mechanism of hyperactivity to non-threatening voices
AU - Chen, Chenyi
AU - Martínez, Róger M.
AU - Liao, Tsai Tsen
AU - Chen, Chin Yau
AU - Yang, Chih Yung
AU - Cheng, Yawei
N1 - Funding Information:
We thank Chenyi Su and Yu Huang for assisting with the data collection. The study was funded by the Ministry of Science and Technology (MOST 108-2410-H-010-005-MY3; 108-2636-H-038-001-; 109-2636-H-038-001-; 108-2636-B-038-001-; 109-2636-B-038-001-), National Yang-Ming University Hospital (RD2019-003; RD2020-003), Taipei Medical University (DP2-108-21121-01-N-03-03; TMU108-AE1-B25), and the Brain Research Center, National Yang-Ming University from The Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education (MOE) in Taiwan (108BRC-B501).
PY - 2020/3/10
Y1 - 2020/3/10
N2 - The tonic model delineating the serotonin transporter polymorphism’s (5-HTTLPR) modulatory effect on anxiety points towards a universal underlying mechanism involving a hyper-or-elevated baseline level of arousal even to non-threatening stimuli. However, to our knowledge, this mechanism has never been observed in non-clinical cohorts exhibiting high anxiety. Moreover, empirical support regarding said association is mixed, potentially because of publication bias with a relatively small sample size. Hence, how the 5-HTTLPR modulates neural correlates remains controversial. Here we show that 5-HTTLPR short-allele carriers had significantly increased baseline ERPs and reduced fearful MMN, phenomena which can nevertheless be reversed by acute anxiolytic treatment. This provides evidence that the 5-HTT affects the automatic processing of threatening and non-threatening voices, impacts broadly on social cognition, and conclusively asserts the heightened baseline arousal level as the universal underlying neural mechanism for anxiety-related susceptibilities, functioning as a spectrum-like distribution from high trait anxiety non-patients to anxiety patients.
AB - The tonic model delineating the serotonin transporter polymorphism’s (5-HTTLPR) modulatory effect on anxiety points towards a universal underlying mechanism involving a hyper-or-elevated baseline level of arousal even to non-threatening stimuli. However, to our knowledge, this mechanism has never been observed in non-clinical cohorts exhibiting high anxiety. Moreover, empirical support regarding said association is mixed, potentially because of publication bias with a relatively small sample size. Hence, how the 5-HTTLPR modulates neural correlates remains controversial. Here we show that 5-HTTLPR short-allele carriers had significantly increased baseline ERPs and reduced fearful MMN, phenomena which can nevertheless be reversed by acute anxiolytic treatment. This provides evidence that the 5-HTT affects the automatic processing of threatening and non-threatening voices, impacts broadly on social cognition, and conclusively asserts the heightened baseline arousal level as the universal underlying neural mechanism for anxiety-related susceptibilities, functioning as a spectrum-like distribution from high trait anxiety non-patients to anxiety patients.
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U2 - 10.1038/s42003-020-0850-3
DO - 10.1038/s42003-020-0850-3
M3 - Article
C2 - 32157156
AN - SCOPUS:85081575403
SN - 2399-3642
VL - 3
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 113
ER -