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Coronary heart disease risk in patients with schizophrenia: a Lebanese cross-sectional study
BACKGROUND: Coronary heart disease (CHD) is a leading cause of premature death in patients with schizophrenia. CHD risk in Lebanese patients with schizophrenia remains unknown. OBJECTIVES: To (i) evaluate CHD risk of patients with schizophrenia in Lebanon; and (ii) detect the modifiable and non-modi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Swiss Medical Press GmbH
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556440/ https://www.ncbi.nlm.nih.gov/pubmed/29090191 http://dx.doi.org/10.15256/joc.2017.7.107 |
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author | Haddad, Chadia Hallit, Souheil Salameh, Pascale Bou-Assi, Tarek Zoghbi, Marouan |
author_facet | Haddad, Chadia Hallit, Souheil Salameh, Pascale Bou-Assi, Tarek Zoghbi, Marouan |
author_sort | Haddad, Chadia |
collection | PubMed |
description | BACKGROUND: Coronary heart disease (CHD) is a leading cause of premature death in patients with schizophrenia. CHD risk in Lebanese patients with schizophrenia remains unknown. OBJECTIVES: To (i) evaluate CHD risk of patients with schizophrenia in Lebanon; and (ii) detect the modifiable and non-modifiable factors affecting this risk. METHODS: Cross-sectional study of 329 patients with schizophrenia aged 20–75 years. Ten-year hard CHD risk was calculated using the Framingham risk score. A logistic regression was conducted taking the dichotomous hard CHD (<10% and ≥10%) as the dependent variable. RESULTS: Ten-year hard CHD risk was low (<10%) in 60.8% of patients, intermediate (10–20%) in 31.6%, and high (>20%) in 7.6%. Multivariate analysis showed that the mean 10-year hard CHD risk was 8.76±6.92 (10.82±6.83 in men and 3.18±2.90 in women). Ten-year hard CHD risk was higher in patients with the metabolic syndrome (odds ratio [OR] 2.67, confidence interval [CI] 1.54–4.64), a longer duration of schizophrenia (OR 1.03, CI 1.01–1.05), a history of other medical illnesses (OR 2.02, CI 1.18–3.47), and in those participating in art therapy (OR 2.13, CI 1.25–3.64) or therapeutic education (OR 1.93, CI 0.93–4.01). Ten-year hard CHD risk was lower in patients receiving risperidone (OR 0.23, CI 0.08–0.68), any anti-epileptic (OR 0.41, CI 0.24–0.73), or any benzodiazepine (OR 0.33, CI 0.17–0.66) medication. CONCLUSION: CHD is prevalent in patients with schizophrenia in Lebanon. Physicians are recommended to monitor the components of the metabolic syndrome to identify patients with increased risk of cardiovascular diseases. |
format | Online Article Text |
id | pubmed-5556440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Swiss Medical Press GmbH |
record_format | MEDLINE/PubMed |
spelling | pubmed-55564402017-10-31 Coronary heart disease risk in patients with schizophrenia: a Lebanese cross-sectional study Haddad, Chadia Hallit, Souheil Salameh, Pascale Bou-Assi, Tarek Zoghbi, Marouan J Comorb Original Article BACKGROUND: Coronary heart disease (CHD) is a leading cause of premature death in patients with schizophrenia. CHD risk in Lebanese patients with schizophrenia remains unknown. OBJECTIVES: To (i) evaluate CHD risk of patients with schizophrenia in Lebanon; and (ii) detect the modifiable and non-modifiable factors affecting this risk. METHODS: Cross-sectional study of 329 patients with schizophrenia aged 20–75 years. Ten-year hard CHD risk was calculated using the Framingham risk score. A logistic regression was conducted taking the dichotomous hard CHD (<10% and ≥10%) as the dependent variable. RESULTS: Ten-year hard CHD risk was low (<10%) in 60.8% of patients, intermediate (10–20%) in 31.6%, and high (>20%) in 7.6%. Multivariate analysis showed that the mean 10-year hard CHD risk was 8.76±6.92 (10.82±6.83 in men and 3.18±2.90 in women). Ten-year hard CHD risk was higher in patients with the metabolic syndrome (odds ratio [OR] 2.67, confidence interval [CI] 1.54–4.64), a longer duration of schizophrenia (OR 1.03, CI 1.01–1.05), a history of other medical illnesses (OR 2.02, CI 1.18–3.47), and in those participating in art therapy (OR 2.13, CI 1.25–3.64) or therapeutic education (OR 1.93, CI 0.93–4.01). Ten-year hard CHD risk was lower in patients receiving risperidone (OR 0.23, CI 0.08–0.68), any anti-epileptic (OR 0.41, CI 0.24–0.73), or any benzodiazepine (OR 0.33, CI 0.17–0.66) medication. CONCLUSION: CHD is prevalent in patients with schizophrenia in Lebanon. Physicians are recommended to monitor the components of the metabolic syndrome to identify patients with increased risk of cardiovascular diseases. Swiss Medical Press GmbH 2017-07-13 /pmc/articles/PMC5556440/ /pubmed/29090191 http://dx.doi.org/10.15256/joc.2017.7.107 Text en Copyright: © 2017 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the Creative Commons Attribution-NonCommercial License, which permits all noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Original Article Haddad, Chadia Hallit, Souheil Salameh, Pascale Bou-Assi, Tarek Zoghbi, Marouan Coronary heart disease risk in patients with schizophrenia: a Lebanese cross-sectional study |
title | Coronary heart disease risk in patients with schizophrenia: a Lebanese cross-sectional study |
title_full | Coronary heart disease risk in patients with schizophrenia: a Lebanese cross-sectional study |
title_fullStr | Coronary heart disease risk in patients with schizophrenia: a Lebanese cross-sectional study |
title_full_unstemmed | Coronary heart disease risk in patients with schizophrenia: a Lebanese cross-sectional study |
title_short | Coronary heart disease risk in patients with schizophrenia: a Lebanese cross-sectional study |
title_sort | coronary heart disease risk in patients with schizophrenia: a lebanese cross-sectional study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556440/ https://www.ncbi.nlm.nih.gov/pubmed/29090191 http://dx.doi.org/10.15256/joc.2017.7.107 |
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