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Dyslipidemia in Muscular Dystrophy: A Systematic Review and Meta-Analysis

BACKGROUND: Muscular dystrophies (MDs) are characterized by chronic muscle wasting but also poorly understood metabolic co-morbidities. We have recently shown that Duchenne MD (DMD) patients, dogs and asymptomatic carriers are affected by a new form of dyslipidemia that may exacerbate muscle damage....

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Autores principales: Sun, Zeren, Wang, Xindi, White, Zoe, Dormuth, Colin, Morales, Fernando, Bernatchez, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357159/
https://www.ncbi.nlm.nih.gov/pubmed/37182897
http://dx.doi.org/10.3233/JND-230064
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author Sun, Zeren
Wang, Xindi
White, Zoe
Dormuth, Colin
Morales, Fernando
Bernatchez, Pascal
author_facet Sun, Zeren
Wang, Xindi
White, Zoe
Dormuth, Colin
Morales, Fernando
Bernatchez, Pascal
author_sort Sun, Zeren
collection PubMed
description BACKGROUND: Muscular dystrophies (MDs) are characterized by chronic muscle wasting but also poorly understood metabolic co-morbidities. We have recently shown that Duchenne MD (DMD) patients, dogs and asymptomatic carriers are affected by a new form of dyslipidemia that may exacerbate muscle damage. OBJECTIVE: We aimed to perform a systematic review and meta-analysis for evidence that other types of MDs are associated with dyslipidemia compared to healthy controls. METHODS: Search was conducted using MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials for reports that compare plasma/serum lipids from MD patients and controls, and meta-analysis of cross-sectional studies quantifying total cholesterol, high-density lipoprotein, low density lipoprotein and triglycerides was performed. RESULTS: Out of 749 studies, 17 met our inclusion criteria for meta-analysis. 14 of the 17 studies (82%) included investigated myotonic dystrophy (DM); other studies were on pseudohypertrophic MD (PMD) or DMD. As a whole, MD individuals had significantly higher levels of circulating total cholesterol (Hedges’ g with 95% confidence interval [CI], 0.80 [0.03 – 1.56]; p = 0.04) and triglycerides (Hedges’ g with 95% confidence interval [CI], 2.28[0.63 – 3.92]; p = 0.01) compared to controls. Meta-regression analysis showed the percentage of male gender was significantly associated with the difference in total cholesterol (beta = 0.05; 95% CI, – 0.02 to 0.11; p = 0.043) and high-density lipoprotein (beta = – 9.38; 95% CI, – 16.26 to – 2.50; p = 0.028). CONCLUSIONS: MD is associated with significantly higher circulating levels of total cholesterol and triglycerides. However, caution on the interpretation of these findings is warranted and future longitudinal research is required to better understand this relationship.
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spelling pubmed-103571592023-07-21 Dyslipidemia in Muscular Dystrophy: A Systematic Review and Meta-Analysis Sun, Zeren Wang, Xindi White, Zoe Dormuth, Colin Morales, Fernando Bernatchez, Pascal J Neuromuscul Dis Systematic Review BACKGROUND: Muscular dystrophies (MDs) are characterized by chronic muscle wasting but also poorly understood metabolic co-morbidities. We have recently shown that Duchenne MD (DMD) patients, dogs and asymptomatic carriers are affected by a new form of dyslipidemia that may exacerbate muscle damage. OBJECTIVE: We aimed to perform a systematic review and meta-analysis for evidence that other types of MDs are associated with dyslipidemia compared to healthy controls. METHODS: Search was conducted using MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials for reports that compare plasma/serum lipids from MD patients and controls, and meta-analysis of cross-sectional studies quantifying total cholesterol, high-density lipoprotein, low density lipoprotein and triglycerides was performed. RESULTS: Out of 749 studies, 17 met our inclusion criteria for meta-analysis. 14 of the 17 studies (82%) included investigated myotonic dystrophy (DM); other studies were on pseudohypertrophic MD (PMD) or DMD. As a whole, MD individuals had significantly higher levels of circulating total cholesterol (Hedges’ g with 95% confidence interval [CI], 0.80 [0.03 – 1.56]; p = 0.04) and triglycerides (Hedges’ g with 95% confidence interval [CI], 2.28[0.63 – 3.92]; p = 0.01) compared to controls. Meta-regression analysis showed the percentage of male gender was significantly associated with the difference in total cholesterol (beta = 0.05; 95% CI, – 0.02 to 0.11; p = 0.043) and high-density lipoprotein (beta = – 9.38; 95% CI, – 16.26 to – 2.50; p = 0.028). CONCLUSIONS: MD is associated with significantly higher circulating levels of total cholesterol and triglycerides. However, caution on the interpretation of these findings is warranted and future longitudinal research is required to better understand this relationship. IOS Press 2023-07-04 /pmc/articles/PMC10357159/ /pubmed/37182897 http://dx.doi.org/10.3233/JND-230064 Text en © 2023 – The authors. Published by IOS Press 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 (CC BY-NC 4.0) License (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 Systematic Review
Sun, Zeren
Wang, Xindi
White, Zoe
Dormuth, Colin
Morales, Fernando
Bernatchez, Pascal
Dyslipidemia in Muscular Dystrophy: A Systematic Review and Meta-Analysis
title Dyslipidemia in Muscular Dystrophy: A Systematic Review and Meta-Analysis
title_full Dyslipidemia in Muscular Dystrophy: A Systematic Review and Meta-Analysis
title_fullStr Dyslipidemia in Muscular Dystrophy: A Systematic Review and Meta-Analysis
title_full_unstemmed Dyslipidemia in Muscular Dystrophy: A Systematic Review and Meta-Analysis
title_short Dyslipidemia in Muscular Dystrophy: A Systematic Review and Meta-Analysis
title_sort dyslipidemia in muscular dystrophy: a systematic review and meta-analysis
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357159/
https://www.ncbi.nlm.nih.gov/pubmed/37182897
http://dx.doi.org/10.3233/JND-230064
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