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Candidate Biological Markers for Social Anxiety Disorder: A Systematic Review

Social anxiety disorder (SAD) is a common psychiatric condition associated with a high risk of psychiatric comorbidity and impaired social/occupational functioning when not promptly treated. The identification of biological markers may facilitate the diagnostic process, leading to an early and prope...

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Autores principales: Caldiroli, Alice, Capuzzi, Enrico, Affaticati, Letizia M., Surace, Teresa, Di Forti, Carla L., Dakanalis, Antonios, Clerici, Massimo, Buoli, Massimiliano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821596/
https://www.ncbi.nlm.nih.gov/pubmed/36614278
http://dx.doi.org/10.3390/ijms24010835
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author Caldiroli, Alice
Capuzzi, Enrico
Affaticati, Letizia M.
Surace, Teresa
Di Forti, Carla L.
Dakanalis, Antonios
Clerici, Massimo
Buoli, Massimiliano
author_facet Caldiroli, Alice
Capuzzi, Enrico
Affaticati, Letizia M.
Surace, Teresa
Di Forti, Carla L.
Dakanalis, Antonios
Clerici, Massimo
Buoli, Massimiliano
author_sort Caldiroli, Alice
collection PubMed
description Social anxiety disorder (SAD) is a common psychiatric condition associated with a high risk of psychiatric comorbidity and impaired social/occupational functioning when not promptly treated. The identification of biological markers may facilitate the diagnostic process, leading to an early and proper treatment. Our aim was to systematically review the available literature about potential biomarkers for SAD. A search in the main online repositories (PubMed, ISI Web of Knowledge, PsychInfo, etc.) was performed. Of the 662 records screened, 61 were included. Results concerning cortisol, neuropeptides and inflammatory/immunological/neurotrophic markers remain inconsistent. Preliminary evidence emerged about the role of chromosome 16 and the endomannosidase gene, as well as of epigenetic factors, in increasing vulnerability to SAD. Neuroimaging findings revealed an altered connectivity of different cerebral areas in SAD patients and amygdala activation under social threat. Some parameters such as salivary alpha amylase levels, changes in antioxidant defenses, increased gaze avoidance and QT dispersion seem to be associated with SAD and may represent promising biomarkers of this condition. However, the preliminary positive correlations have been poorly replicated. Further studies on larger samples and investigating the same biomarkers are needed to identify more specific biological markers for SAD.
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spelling pubmed-98215962023-01-07 Candidate Biological Markers for Social Anxiety Disorder: A Systematic Review Caldiroli, Alice Capuzzi, Enrico Affaticati, Letizia M. Surace, Teresa Di Forti, Carla L. Dakanalis, Antonios Clerici, Massimo Buoli, Massimiliano Int J Mol Sci Review Social anxiety disorder (SAD) is a common psychiatric condition associated with a high risk of psychiatric comorbidity and impaired social/occupational functioning when not promptly treated. The identification of biological markers may facilitate the diagnostic process, leading to an early and proper treatment. Our aim was to systematically review the available literature about potential biomarkers for SAD. A search in the main online repositories (PubMed, ISI Web of Knowledge, PsychInfo, etc.) was performed. Of the 662 records screened, 61 were included. Results concerning cortisol, neuropeptides and inflammatory/immunological/neurotrophic markers remain inconsistent. Preliminary evidence emerged about the role of chromosome 16 and the endomannosidase gene, as well as of epigenetic factors, in increasing vulnerability to SAD. Neuroimaging findings revealed an altered connectivity of different cerebral areas in SAD patients and amygdala activation under social threat. Some parameters such as salivary alpha amylase levels, changes in antioxidant defenses, increased gaze avoidance and QT dispersion seem to be associated with SAD and may represent promising biomarkers of this condition. However, the preliminary positive correlations have been poorly replicated. Further studies on larger samples and investigating the same biomarkers are needed to identify more specific biological markers for SAD. MDPI 2023-01-03 /pmc/articles/PMC9821596/ /pubmed/36614278 http://dx.doi.org/10.3390/ijms24010835 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Caldiroli, Alice
Capuzzi, Enrico
Affaticati, Letizia M.
Surace, Teresa
Di Forti, Carla L.
Dakanalis, Antonios
Clerici, Massimo
Buoli, Massimiliano
Candidate Biological Markers for Social Anxiety Disorder: A Systematic Review
title Candidate Biological Markers for Social Anxiety Disorder: A Systematic Review
title_full Candidate Biological Markers for Social Anxiety Disorder: A Systematic Review
title_fullStr Candidate Biological Markers for Social Anxiety Disorder: A Systematic Review
title_full_unstemmed Candidate Biological Markers for Social Anxiety Disorder: A Systematic Review
title_short Candidate Biological Markers for Social Anxiety Disorder: A Systematic Review
title_sort candidate biological markers for social anxiety disorder: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821596/
https://www.ncbi.nlm.nih.gov/pubmed/36614278
http://dx.doi.org/10.3390/ijms24010835
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