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Preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound

OBJECTIVE: Early‐onset psychosis (EOP) and bipolar disorder (EOBP) (at <18 years of age), are associated with an increased future risk of cardiovascular disease (CVD) and premature death. Yet it is unknown whether the arteries show visible signs of atherosclerosis in EOP and EOBP. This study inve...

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Autores principales: Bohman, Hannes, Agartz, Ingrid, Mansouri, Shiva, Naessen, Tord, Lundberg, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749529/
https://www.ncbi.nlm.nih.gov/pubmed/32997440
http://dx.doi.org/10.1002/brb3.1862
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author Bohman, Hannes
Agartz, Ingrid
Mansouri, Shiva
Naessen, Tord
Lundberg, Mathias
author_facet Bohman, Hannes
Agartz, Ingrid
Mansouri, Shiva
Naessen, Tord
Lundberg, Mathias
author_sort Bohman, Hannes
collection PubMed
description OBJECTIVE: Early‐onset psychosis (EOP) and bipolar disorder (EOBP) (at <18 years of age), are associated with an increased future risk of cardiovascular disease (CVD) and premature death. Yet it is unknown whether the arteries show visible signs of atherosclerosis in EOP and EOBP. This study investigated whether having EOP or EOBP was associated with detectable signs of preclinical atherosclerosis. METHOD: By using 22 MHz high‐frequency ultrasound, different layers of the arterial wall of the left common carotid artery (LCCA) were assessed in 77 individuals with EOP (n = 25), EOBP (n = 22), and in age‐matched healthy controls (n = 30). Conventional CVD confounders were included in the analyses. RESULTS: Adolescents with EOP and EOBP, compared to controls, had a significantly thicker LCCA intima thickness (0.132 vs. 0.095 mm, p < .001) and intima/media ratio (0.24 vs. 0.17 p < .001). There was a nonsignificant intima difference between EOP and EOBP. Conventional CVD risk factors did not explain the association between EOP/EOBP and intima thickness. In the group of EOP/EOBP, there was a significant correlation between the dose of current antipsychotic medication and intima thickness; however, the correlation was attenuated to a nonsignificant level when adjusted for global function. CONCLUSIONS: Adolescents with EOP or EOBP had an increased LCCA intima thickness, interpreted as a sign of preclinical atherosclerosis. Global function of the disorders was the strongest determinant of intima thickness. The findings, if replicated, might have implications for long‐term treatment of EOP and EOBP in order to reduce a future risk of CVD.
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spelling pubmed-77495292020-12-23 Preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound Bohman, Hannes Agartz, Ingrid Mansouri, Shiva Naessen, Tord Lundberg, Mathias Brain Behav Original Research OBJECTIVE: Early‐onset psychosis (EOP) and bipolar disorder (EOBP) (at <18 years of age), are associated with an increased future risk of cardiovascular disease (CVD) and premature death. Yet it is unknown whether the arteries show visible signs of atherosclerosis in EOP and EOBP. This study investigated whether having EOP or EOBP was associated with detectable signs of preclinical atherosclerosis. METHOD: By using 22 MHz high‐frequency ultrasound, different layers of the arterial wall of the left common carotid artery (LCCA) were assessed in 77 individuals with EOP (n = 25), EOBP (n = 22), and in age‐matched healthy controls (n = 30). Conventional CVD confounders were included in the analyses. RESULTS: Adolescents with EOP and EOBP, compared to controls, had a significantly thicker LCCA intima thickness (0.132 vs. 0.095 mm, p < .001) and intima/media ratio (0.24 vs. 0.17 p < .001). There was a nonsignificant intima difference between EOP and EOBP. Conventional CVD risk factors did not explain the association between EOP/EOBP and intima thickness. In the group of EOP/EOBP, there was a significant correlation between the dose of current antipsychotic medication and intima thickness; however, the correlation was attenuated to a nonsignificant level when adjusted for global function. CONCLUSIONS: Adolescents with EOP or EOBP had an increased LCCA intima thickness, interpreted as a sign of preclinical atherosclerosis. Global function of the disorders was the strongest determinant of intima thickness. The findings, if replicated, might have implications for long‐term treatment of EOP and EOBP in order to reduce a future risk of CVD. John Wiley and Sons Inc. 2020-09-30 /pmc/articles/PMC7749529/ /pubmed/32997440 http://dx.doi.org/10.1002/brb3.1862 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC. This is an open access article under the terms of the http://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
Bohman, Hannes
Agartz, Ingrid
Mansouri, Shiva
Naessen, Tord
Lundberg, Mathias
Preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound
title Preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound
title_full Preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound
title_fullStr Preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound
title_full_unstemmed Preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound
title_short Preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound
title_sort preclinical atherosclerosis in adolescents with psychotic or bipolar disorders investigated with carotid high‐frequency ultrasound
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749529/
https://www.ncbi.nlm.nih.gov/pubmed/32997440
http://dx.doi.org/10.1002/brb3.1862
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