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Psychiatric risk and resilience: Plasticity genes and positive mental health

OBJECTIVE: The at‐risk mental state (ARMS) for psychosis has long played a key role in diathesis‐stress models of schizophrenia. More recent studies, however, have called for extending the boundaries of the ARMS construct beyond attenuated psychosis in nonhelp‐seeking samples to include not only oth...

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Autores principales: Nestor, Paul G., Choate Hasler, Victoria, O'Donovan, Keira, Lapp, Hannah E., Boodai, Sara B., Hunter, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213923/
https://www.ncbi.nlm.nih.gov/pubmed/33932264
http://dx.doi.org/10.1002/brb3.2137
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author Nestor, Paul G.
Choate Hasler, Victoria
O'Donovan, Keira
Lapp, Hannah E.
Boodai, Sara B.
Hunter, Richard
author_facet Nestor, Paul G.
Choate Hasler, Victoria
O'Donovan, Keira
Lapp, Hannah E.
Boodai, Sara B.
Hunter, Richard
author_sort Nestor, Paul G.
collection PubMed
description OBJECTIVE: The at‐risk mental state (ARMS) for psychosis has long played a key role in diathesis‐stress models of schizophrenia. More recent studies, however, have called for extending the boundaries of the ARMS construct beyond attenuated psychosis in nonhelp‐seeking samples to include not only other vulnerability indicators but also protective factors related to genotype, mental health, personality, and cognition. METHOD: Accordingly, we assessed in a sample of 100 college students, the ARMS construct with the Brief Prodromal Questionnaire (PQ‐B) for psychosis, in conjunction with measures of positive mental health, childhood adversity, psychiatric symptoms, personality traits, social cognition, and genetic variables derived from assays of the serotonin transporter (5‐HTTLPR) and the brain‐derived neurotrophic factor (BDNF). RESULTS: Higher PQ‐B scores correlated positively with vulnerability indicators of childhood adversity and heightened levels of a wide variety of psychiatric symptoms but correlated negatively with protective factors of better overall mental health, social cognition as well as with a distinct NEO profile marked by reduced neuroticism and elevated agreeableness and conscientiousness. Multivariate analyses indicated that a composite ARMS measure comprised of PQ‐B scores plus anxiety and depression symptoms revealed significant genotype differences, with lowest risk and highest resilience for allelic carriers of 5‐HTTLPR‐short and BDNF Met polymorphisms. CONCLUSIONS: Results provided support for extending the ARMS construct, pointing to important contributions of personality, social cognition, and genes that support neural plasticity in mitigating vulnerability and enhancing resilience and well‐being.
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spelling pubmed-82139232021-06-28 Psychiatric risk and resilience: Plasticity genes and positive mental health Nestor, Paul G. Choate Hasler, Victoria O'Donovan, Keira Lapp, Hannah E. Boodai, Sara B. Hunter, Richard Brain Behav Original Research OBJECTIVE: The at‐risk mental state (ARMS) for psychosis has long played a key role in diathesis‐stress models of schizophrenia. More recent studies, however, have called for extending the boundaries of the ARMS construct beyond attenuated psychosis in nonhelp‐seeking samples to include not only other vulnerability indicators but also protective factors related to genotype, mental health, personality, and cognition. METHOD: Accordingly, we assessed in a sample of 100 college students, the ARMS construct with the Brief Prodromal Questionnaire (PQ‐B) for psychosis, in conjunction with measures of positive mental health, childhood adversity, psychiatric symptoms, personality traits, social cognition, and genetic variables derived from assays of the serotonin transporter (5‐HTTLPR) and the brain‐derived neurotrophic factor (BDNF). RESULTS: Higher PQ‐B scores correlated positively with vulnerability indicators of childhood adversity and heightened levels of a wide variety of psychiatric symptoms but correlated negatively with protective factors of better overall mental health, social cognition as well as with a distinct NEO profile marked by reduced neuroticism and elevated agreeableness and conscientiousness. Multivariate analyses indicated that a composite ARMS measure comprised of PQ‐B scores plus anxiety and depression symptoms revealed significant genotype differences, with lowest risk and highest resilience for allelic carriers of 5‐HTTLPR‐short and BDNF Met polymorphisms. CONCLUSIONS: Results provided support for extending the ARMS construct, pointing to important contributions of personality, social cognition, and genes that support neural plasticity in mitigating vulnerability and enhancing resilience and well‐being. John Wiley and Sons Inc. 2021-05-01 /pmc/articles/PMC8213923/ /pubmed/33932264 http://dx.doi.org/10.1002/brb3.2137 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Nestor, Paul G.
Choate Hasler, Victoria
O'Donovan, Keira
Lapp, Hannah E.
Boodai, Sara B.
Hunter, Richard
Psychiatric risk and resilience: Plasticity genes and positive mental health
title Psychiatric risk and resilience: Plasticity genes and positive mental health
title_full Psychiatric risk and resilience: Plasticity genes and positive mental health
title_fullStr Psychiatric risk and resilience: Plasticity genes and positive mental health
title_full_unstemmed Psychiatric risk and resilience: Plasticity genes and positive mental health
title_short Psychiatric risk and resilience: Plasticity genes and positive mental health
title_sort psychiatric risk and resilience: plasticity genes and positive mental health
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213923/
https://www.ncbi.nlm.nih.gov/pubmed/33932264
http://dx.doi.org/10.1002/brb3.2137
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