Is serotonin transporter brain binding associated with the cortisol awakening response? An independent non-replication

PLoS One. 2023 Aug 31;18(8):e0290663. doi: 10.1371/journal.pone.0290663. eCollection 2023.

Abstract

Background: Serotonergic brain signaling is considered critical for an appropriate and dynamic adaptation to stress, seemingly through modulating limbic system functions, such as the hypothalamic-pituitary-adrenal (HPA)-axis. This interplay is of great interest since it holds promise as a target for preventing stress-related brain disorders, e.g., major depression. Our group has previously observed that prefrontal serotonin transporter (5-HTT) binding, imaged with positron emission tomography (PET), is positively associated with the cortisol awakening response (CAR), an index of HPA axis stress hormone dynamics. The aim of this cross-sectional study was to replicate the previous finding in a larger independent group of healthy individuals.

Methods: Molecular imaging and cortisol data were available for 90 healthy individuals. Prefrontal 5-HTT binding was imaged with [11C]DASB brain PET. Non-displaceable 5-HTT binding potential (BPND) was quantified using the Multilinear Reference Tissue Model 2 (MRTM2) with cerebellum as the reference region. CAR was based on five serial salivary cortisol samples within the first hour upon awakening. The association between CAR and prefrontal 5-HTT BPND was evaluated using a multiple linear regression model adjusted for age and sex. Further, we tested for sex differences in the association. Finally, an exploratory analysis of the association, was performed in 8 additional brain regions.

Results: We observed no statistically significant association between 5-HTT binding and CAR corrected for age and sex in the prefrontal cortex (β = -0.28, p = 0.26). We saw no interaction with sex on the association (p = 0.99).

Conclusion: We could not confirm a positive association between CAR and prefrontal 5-HTT BPND in this independent dataset. Also, sex differences in the association were not apparent. Our data do not exclude that the serotonin transporter system is involved in the regulation of stress responses in at-risk or manifest depressed states.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain / diagnostic imaging
  • Cross-Sectional Studies
  • Depressive Disorder, Major*
  • Female
  • Humans
  • Hydrocortisone
  • Hypothalamo-Hypophyseal System
  • Male
  • Pituitary-Adrenal System
  • Serotonin Plasma Membrane Transport Proteins*

Substances

  • Serotonin Plasma Membrane Transport Proteins
  • Hydrocortisone

Grants and funding

The financial support for this study's database infrastructure was provided by The Research Council of Rigshospitalet (https://www.rigshospitalet.dk/research) in the form of a grant (A6594) awarded to VF, JC, JS, and SL. Additional financial support for this study's database infrastructure was provided by The Lundbeck Foundation (https://lundbeckfonden.com/en) in the form of grants (279-2018-1145 and R90-A7722) awarded to VF, JC, JS, and SVL. This study was also financially supported by "Ivan Nielsens fond for personer med specielle sindslidelser" (https://www.legatbogen.dk/ivan-nielsens-fond-for-personer-med-specielle-sindslidelser) in the form of a grant (R162-A7167) awarded to JC. This study was also financially supported by Independent Research Fund Denmark (https://dff.dk/en) in the form of a grant (7025-00111B) awarded to JC, and grants (0134-00278B and 7025-00111B) awarded to SVL. This study was also financially supported by Capital Region's Research Foundation for Health Research (https://research.regionh.dk/en/) in the form of a grant (R162-A7167) awarded to JS. This study was also financially supported by The Swedish Brain Foundation in the form of a grant awarded to JS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.