Association between brain serotonin 4 receptor binding and reactivity to emotional faces in depressed and healthy individuals

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Association between brain serotonin 4 receptor binding and reactivity to emotional faces in depressed and healthy individuals. / Sankar, Anjali; Ozenne, Brice; Dam, Vibeke H.; Svarer, Claus; Jorgensen, Martin B.; Miskowiak, Kamilla W.; Frokjaer, Vibe G.; Knudsen, Gitte M.; Fisher, Patrick M.

In: Translational Psychiatry, Vol. 13, No. 1, 165, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Sankar, A, Ozenne, B, Dam, VH, Svarer, C, Jorgensen, MB, Miskowiak, KW, Frokjaer, VG, Knudsen, GM & Fisher, PM 2023, 'Association between brain serotonin 4 receptor binding and reactivity to emotional faces in depressed and healthy individuals', Translational Psychiatry, vol. 13, no. 1, 165. https://doi.org/10.1038/s41398-023-02440-3

APA

Sankar, A., Ozenne, B., Dam, V. H., Svarer, C., Jorgensen, M. B., Miskowiak, K. W., Frokjaer, V. G., Knudsen, G. M., & Fisher, P. M. (2023). Association between brain serotonin 4 receptor binding and reactivity to emotional faces in depressed and healthy individuals. Translational Psychiatry, 13(1), [165]. https://doi.org/10.1038/s41398-023-02440-3

Vancouver

Sankar A, Ozenne B, Dam VH, Svarer C, Jorgensen MB, Miskowiak KW et al. Association between brain serotonin 4 receptor binding and reactivity to emotional faces in depressed and healthy individuals. Translational Psychiatry. 2023;13(1). 165. https://doi.org/10.1038/s41398-023-02440-3

Author

Sankar, Anjali ; Ozenne, Brice ; Dam, Vibeke H. ; Svarer, Claus ; Jorgensen, Martin B. ; Miskowiak, Kamilla W. ; Frokjaer, Vibe G. ; Knudsen, Gitte M. ; Fisher, Patrick M. / Association between brain serotonin 4 receptor binding and reactivity to emotional faces in depressed and healthy individuals. In: Translational Psychiatry. 2023 ; Vol. 13, No. 1.

Bibtex

@article{0a07c3a816a14f0d854f66a9beaa9882,
title = "Association between brain serotonin 4 receptor binding and reactivity to emotional faces in depressed and healthy individuals",
abstract = "Brain serotonergic (5-HT) signaling is posited to modulate neural responses to emotional stimuli. Dysfunction in 5-HT signaling is implicated in major depressive disorder (MDD), a disorder associated with significant disturbances in emotion processing. In MDD, recent evidence points to altered 5-HT4 receptor (5-HT4R) levels, a promising target for antidepressant treatment. However, how these alterations influence neural processing of emotions in MDD remains poorly understood. This is the first study to examine the association between 5-HT4R binding and neural responses to emotions in patients with MDD and healthy controls. The study included one hundred and thirty-eight participants, comprising 88 outpatients with MDD from the NeuroPharm clinical trial (ClinicalTrials.gov identifier: NCT02869035) and 50 healthy controls. Participants underwent an [C-11]SB207145 positron emission tomography (PET) scan to quantify 5-HT4R binding (BPND) and a functional magnetic resonance imaging (fMRI) scan during which they performed an emotional face matching task. We examined the association between regional 5-HT4R binding and corticolimbic responses to emotional faces using a linear latent variable model, including whether this association was moderated by depression status. We observed a positive correlation between 5-HT4R BPND and the corticolimbic response to emotional faces across participants (r = 0.20, p = 0.03). This association did not differ between groups (parameter estimate difference = 0.002, 95% CI = -0.008: 0.013, p = 0.72). Thus, in the largest PET/fMRI study of associations between serotonergic signaling and brain function, we found a positive association between 5-HT4R binding and neural responses to emotions that appear unaltered in MDD. Future clinical trials with novel pharmacological agents targeting 5-HT4R are needed to confirm whether they ameliorate emotion processing biases in MDD.",
keywords = "POSITRON-EMISSION-TOMOGRAPHY, TRANSPORTER BINDING, ANTIDEPRESSANT TREATMENT, AMYGDALA REACTIVITY, MAJOR DEPRESSION, 1A BINDING, PET, METAANALYSIS, DISORDER, ACTIVATION",
author = "Anjali Sankar and Brice Ozenne and Dam, {Vibeke H.} and Claus Svarer and Jorgensen, {Martin B.} and Miskowiak, {Kamilla W.} and Frokjaer, {Vibe G.} and Knudsen, {Gitte M.} and Fisher, {Patrick M.}",
year = "2023",
doi = "10.1038/s41398-023-02440-3",
language = "English",
volume = "13",
journal = "Translational Psychiatry",
issn = "2158-3188",
publisher = "nature publishing group",
number = "1",

}

RIS

TY - JOUR

T1 - Association between brain serotonin 4 receptor binding and reactivity to emotional faces in depressed and healthy individuals

AU - Sankar, Anjali

AU - Ozenne, Brice

AU - Dam, Vibeke H.

AU - Svarer, Claus

AU - Jorgensen, Martin B.

AU - Miskowiak, Kamilla W.

AU - Frokjaer, Vibe G.

AU - Knudsen, Gitte M.

AU - Fisher, Patrick M.

PY - 2023

Y1 - 2023

N2 - Brain serotonergic (5-HT) signaling is posited to modulate neural responses to emotional stimuli. Dysfunction in 5-HT signaling is implicated in major depressive disorder (MDD), a disorder associated with significant disturbances in emotion processing. In MDD, recent evidence points to altered 5-HT4 receptor (5-HT4R) levels, a promising target for antidepressant treatment. However, how these alterations influence neural processing of emotions in MDD remains poorly understood. This is the first study to examine the association between 5-HT4R binding and neural responses to emotions in patients with MDD and healthy controls. The study included one hundred and thirty-eight participants, comprising 88 outpatients with MDD from the NeuroPharm clinical trial (ClinicalTrials.gov identifier: NCT02869035) and 50 healthy controls. Participants underwent an [C-11]SB207145 positron emission tomography (PET) scan to quantify 5-HT4R binding (BPND) and a functional magnetic resonance imaging (fMRI) scan during which they performed an emotional face matching task. We examined the association between regional 5-HT4R binding and corticolimbic responses to emotional faces using a linear latent variable model, including whether this association was moderated by depression status. We observed a positive correlation between 5-HT4R BPND and the corticolimbic response to emotional faces across participants (r = 0.20, p = 0.03). This association did not differ between groups (parameter estimate difference = 0.002, 95% CI = -0.008: 0.013, p = 0.72). Thus, in the largest PET/fMRI study of associations between serotonergic signaling and brain function, we found a positive association between 5-HT4R binding and neural responses to emotions that appear unaltered in MDD. Future clinical trials with novel pharmacological agents targeting 5-HT4R are needed to confirm whether they ameliorate emotion processing biases in MDD.

AB - Brain serotonergic (5-HT) signaling is posited to modulate neural responses to emotional stimuli. Dysfunction in 5-HT signaling is implicated in major depressive disorder (MDD), a disorder associated with significant disturbances in emotion processing. In MDD, recent evidence points to altered 5-HT4 receptor (5-HT4R) levels, a promising target for antidepressant treatment. However, how these alterations influence neural processing of emotions in MDD remains poorly understood. This is the first study to examine the association between 5-HT4R binding and neural responses to emotions in patients with MDD and healthy controls. The study included one hundred and thirty-eight participants, comprising 88 outpatients with MDD from the NeuroPharm clinical trial (ClinicalTrials.gov identifier: NCT02869035) and 50 healthy controls. Participants underwent an [C-11]SB207145 positron emission tomography (PET) scan to quantify 5-HT4R binding (BPND) and a functional magnetic resonance imaging (fMRI) scan during which they performed an emotional face matching task. We examined the association between regional 5-HT4R binding and corticolimbic responses to emotional faces using a linear latent variable model, including whether this association was moderated by depression status. We observed a positive correlation between 5-HT4R BPND and the corticolimbic response to emotional faces across participants (r = 0.20, p = 0.03). This association did not differ between groups (parameter estimate difference = 0.002, 95% CI = -0.008: 0.013, p = 0.72). Thus, in the largest PET/fMRI study of associations between serotonergic signaling and brain function, we found a positive association between 5-HT4R binding and neural responses to emotions that appear unaltered in MDD. Future clinical trials with novel pharmacological agents targeting 5-HT4R are needed to confirm whether they ameliorate emotion processing biases in MDD.

KW - POSITRON-EMISSION-TOMOGRAPHY

KW - TRANSPORTER BINDING

KW - ANTIDEPRESSANT TREATMENT

KW - AMYGDALA REACTIVITY

KW - MAJOR DEPRESSION

KW - 1A BINDING

KW - PET

KW - METAANALYSIS

KW - DISORDER

KW - ACTIVATION

U2 - 10.1038/s41398-023-02440-3

DO - 10.1038/s41398-023-02440-3

M3 - Journal article

C2 - 37169780

VL - 13

JO - Translational Psychiatry

JF - Translational Psychiatry

SN - 2158-3188

IS - 1

M1 - 165

ER -

ID: 347001150