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Arterial Stiffness in Patients with Bipolar Disorder
OBJECTIVE: Bipolar disorder (BD) is an inflammatory and metabolic disease. The disease and the drugs used to treat it may affect cardiovascular disease (CVD) risk. The aim of this study is to investigate arterial stiffness in patients with BD and compare them with healthy controls. METHODS: Thirty-n...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean College of Neuropsychopharmacology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10335908/ https://www.ncbi.nlm.nih.gov/pubmed/37424419 http://dx.doi.org/10.9758/cpn.22.1009 |
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author | Kılıçaslan, Aslı Kazgan Emir, Burcu Sırlıer Yıldız, Sevler Kılıçaslan, Gülhan Kurt, Osman |
author_facet | Kılıçaslan, Aslı Kazgan Emir, Burcu Sırlıer Yıldız, Sevler Kılıçaslan, Gülhan Kurt, Osman |
author_sort | Kılıçaslan, Aslı Kazgan |
collection | PubMed |
description | OBJECTIVE: Bipolar disorder (BD) is an inflammatory and metabolic disease. The disease and the drugs used to treat it may affect cardiovascular disease (CVD) risk. The aim of this study is to investigate arterial stiffness in patients with BD and compare them with healthy controls. METHODS: Thirty-nine patients with BD type I in remission and 39 healthy control subjects were included in the study. Carotid and femoral artery intima-media thickness (IMT) and arterial thickness parameters were measured by Doppler ultrasonography. RESULTS: The elastic modulus value of the carotid artery was significantly higher in the patients than in the control group (p = 0.015). Although the IMT of both carotid and femoral artery was thicker in patients than in healthy control subjects, this difference was not statistically significant (p = 0.105; p = 0.391). There was a significant positive correlation between chlorpromazine equivalent dose and femoral elastic modulus value (p = 0.021, r = 0.539). There was a positive correlation between lithium equivalent dose and carotid compliance; a significant negative correlation between lithium equivalent dose and carotid elastic modulus was also determined (both p = 0.007, r = 0.466; p = 0.027, r = −0.391, respect-ively). No predictor was observed between drug dose and arterial stiffness parameters. CONCLUSION: Arterial stiffness might be investigated for its potential to reduce CVD risk in patients with BD. Given the established CVD complications in this patient population, further studies are needed to determine whether the results are specific to antipsychotic treatment or BD and to clarify the potential arterial protective effects of mood stabilizers. |
format | Online Article Text |
id | pubmed-10335908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Korean College of Neuropsychopharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-103359082023-08-31 Arterial Stiffness in Patients with Bipolar Disorder Kılıçaslan, Aslı Kazgan Emir, Burcu Sırlıer Yıldız, Sevler Kılıçaslan, Gülhan Kurt, Osman Clin Psychopharmacol Neurosci Original Article OBJECTIVE: Bipolar disorder (BD) is an inflammatory and metabolic disease. The disease and the drugs used to treat it may affect cardiovascular disease (CVD) risk. The aim of this study is to investigate arterial stiffness in patients with BD and compare them with healthy controls. METHODS: Thirty-nine patients with BD type I in remission and 39 healthy control subjects were included in the study. Carotid and femoral artery intima-media thickness (IMT) and arterial thickness parameters were measured by Doppler ultrasonography. RESULTS: The elastic modulus value of the carotid artery was significantly higher in the patients than in the control group (p = 0.015). Although the IMT of both carotid and femoral artery was thicker in patients than in healthy control subjects, this difference was not statistically significant (p = 0.105; p = 0.391). There was a significant positive correlation between chlorpromazine equivalent dose and femoral elastic modulus value (p = 0.021, r = 0.539). There was a positive correlation between lithium equivalent dose and carotid compliance; a significant negative correlation between lithium equivalent dose and carotid elastic modulus was also determined (both p = 0.007, r = 0.466; p = 0.027, r = −0.391, respect-ively). No predictor was observed between drug dose and arterial stiffness parameters. CONCLUSION: Arterial stiffness might be investigated for its potential to reduce CVD risk in patients with BD. Given the established CVD complications in this patient population, further studies are needed to determine whether the results are specific to antipsychotic treatment or BD and to clarify the potential arterial protective effects of mood stabilizers. Korean College of Neuropsychopharmacology 2023-08-31 2023-08-31 /pmc/articles/PMC10335908/ /pubmed/37424419 http://dx.doi.org/10.9758/cpn.22.1009 Text en Copyright© 2023, Korean College of Neuropsychopharmacology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kılıçaslan, Aslı Kazgan Emir, Burcu Sırlıer Yıldız, Sevler Kılıçaslan, Gülhan Kurt, Osman Arterial Stiffness in Patients with Bipolar Disorder |
title | Arterial Stiffness in Patients with Bipolar Disorder |
title_full | Arterial Stiffness in Patients with Bipolar Disorder |
title_fullStr | Arterial Stiffness in Patients with Bipolar Disorder |
title_full_unstemmed | Arterial Stiffness in Patients with Bipolar Disorder |
title_short | Arterial Stiffness in Patients with Bipolar Disorder |
title_sort | arterial stiffness in patients with bipolar disorder |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10335908/ https://www.ncbi.nlm.nih.gov/pubmed/37424419 http://dx.doi.org/10.9758/cpn.22.1009 |
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