Telomere Shortening and Psychiatric Disorders: A Systematic Review

Telomeres are aging biomarkers, as they shorten while cells undergo mitosis. The aim of this study was to evaluate whether psychiatric disorders marked by psychological distress lead to alterations to telomere length (TL), corroborating the hypothesis that mental disorders might have a deeper impact...

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Main Authors: Pedro A. Pousa, Raquel M. Souza, Paulo Henrique M. Melo, Bernardo H. M. Correa, Tamires S. C. Mendonça, Ana Cristina Simões-e-Silva, Débora M. Miranda
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/6/1423
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author Pedro A. Pousa
Raquel M. Souza
Paulo Henrique M. Melo
Bernardo H. M. Correa
Tamires S. C. Mendonça
Ana Cristina Simões-e-Silva
Débora M. Miranda
author_facet Pedro A. Pousa
Raquel M. Souza
Paulo Henrique M. Melo
Bernardo H. M. Correa
Tamires S. C. Mendonça
Ana Cristina Simões-e-Silva
Débora M. Miranda
author_sort Pedro A. Pousa
collection DOAJ
description Telomeres are aging biomarkers, as they shorten while cells undergo mitosis. The aim of this study was to evaluate whether psychiatric disorders marked by psychological distress lead to alterations to telomere length (TL), corroborating the hypothesis that mental disorders might have a deeper impact on our physiology and aging than it was previously thought. A systematic search of the literature using MeSH descriptors of psychological distress (“Traumatic Stress Disorder” or “Anxiety Disorder” or “depression”) and telomere length (“cellular senescence”, “oxidative stress” and “telomere”) was conducted on PubMed, Cochrane Library and ScienceDirect databases. A total of 56 studies (113,699 patients) measured the TL from individuals diagnosed with anxiety, depression and posttraumatic disorders and compared them with those from healthy subjects. Overall, TL negatively associates with distress-related mental disorders. The possible underlying molecular mechanisms that underly psychiatric diseases to telomere shortening include oxidative stress, inflammation and mitochondrial dysfunction linking. It is still unclear whether psychological distress is either a cause or a consequence of telomere shortening.
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spelling doaj.art-82fd2b8c8b014a44847e93147b00c4f52023-11-21T23:10:33ZengMDPI AGCells2073-44092021-06-01106142310.3390/cells10061423Telomere Shortening and Psychiatric Disorders: A Systematic ReviewPedro A. Pousa0Raquel M. Souza1Paulo Henrique M. Melo2Bernardo H. M. Correa3Tamires S. C. Mendonça4Ana Cristina Simões-e-Silva5Débora M. Miranda6Interdisciplinary Laboratory of Medical Investigation, Faculty of Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 30130-100, BrazilInterdisciplinary Laboratory of Medical Investigation, Faculty of Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 30130-100, BrazilInterdisciplinary Laboratory of Medical Investigation, Faculty of Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 30130-100, BrazilInterdisciplinary Laboratory of Medical Investigation, Faculty of Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 30130-100, BrazilInterdisciplinary Laboratory of Medical Investigation, Faculty of Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 30130-100, BrazilInterdisciplinary Laboratory of Medical Investigation, Faculty of Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 30130-100, BrazilDepartment of Pediatrics, Laboratory of Molecular Medicine, UFMG, Belo Horizonte, Minas Gerais 30130-100, BrazilTelomeres are aging biomarkers, as they shorten while cells undergo mitosis. The aim of this study was to evaluate whether psychiatric disorders marked by psychological distress lead to alterations to telomere length (TL), corroborating the hypothesis that mental disorders might have a deeper impact on our physiology and aging than it was previously thought. A systematic search of the literature using MeSH descriptors of psychological distress (“Traumatic Stress Disorder” or “Anxiety Disorder” or “depression”) and telomere length (“cellular senescence”, “oxidative stress” and “telomere”) was conducted on PubMed, Cochrane Library and ScienceDirect databases. A total of 56 studies (113,699 patients) measured the TL from individuals diagnosed with anxiety, depression and posttraumatic disorders and compared them with those from healthy subjects. Overall, TL negatively associates with distress-related mental disorders. The possible underlying molecular mechanisms that underly psychiatric diseases to telomere shortening include oxidative stress, inflammation and mitochondrial dysfunction linking. It is still unclear whether psychological distress is either a cause or a consequence of telomere shortening.https://www.mdpi.com/2073-4409/10/6/1423psychological distresstelomeretraumatic stress disorderdepressionanxiety
spellingShingle Pedro A. Pousa
Raquel M. Souza
Paulo Henrique M. Melo
Bernardo H. M. Correa
Tamires S. C. Mendonça
Ana Cristina Simões-e-Silva
Débora M. Miranda
Telomere Shortening and Psychiatric Disorders: A Systematic Review
Cells
psychological distress
telomere
traumatic stress disorder
depression
anxiety
title Telomere Shortening and Psychiatric Disorders: A Systematic Review
title_full Telomere Shortening and Psychiatric Disorders: A Systematic Review
title_fullStr Telomere Shortening and Psychiatric Disorders: A Systematic Review
title_full_unstemmed Telomere Shortening and Psychiatric Disorders: A Systematic Review
title_short Telomere Shortening and Psychiatric Disorders: A Systematic Review
title_sort telomere shortening and psychiatric disorders a systematic review
topic psychological distress
telomere
traumatic stress disorder
depression
anxiety
url https://www.mdpi.com/2073-4409/10/6/1423
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