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Diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis

There is no consensus on the prevalence of sarcopenia or its impact on mortality in end‐stage renal disease patients undergoing dialysis. This review aimed to summarize the diagnostic criteria of sarcopenia and its prevalence and impact on the mortality of end‐stage renal disease patients undergoing...

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Autores principales: Shu, Xiaoyu, Lin, Taiping, Wang, Hui, Zhao, Yanli, Jiang, Tingting, Peng, Xuchao, Yue, Jirong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818609/
https://www.ncbi.nlm.nih.gov/pubmed/34989172
http://dx.doi.org/10.1002/jcsm.12890
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author Shu, Xiaoyu
Lin, Taiping
Wang, Hui
Zhao, Yanli
Jiang, Tingting
Peng, Xuchao
Yue, Jirong
author_facet Shu, Xiaoyu
Lin, Taiping
Wang, Hui
Zhao, Yanli
Jiang, Tingting
Peng, Xuchao
Yue, Jirong
author_sort Shu, Xiaoyu
collection PubMed
description There is no consensus on the prevalence of sarcopenia or its impact on mortality in end‐stage renal disease patients undergoing dialysis. This review aimed to summarize the diagnostic criteria of sarcopenia and its prevalence and impact on the mortality of end‐stage renal disease patients undergoing dialysis. Embase, MEDLINE, PubMed, and Cochrane Library were searched from inception to 8 May 2021 to retrieve eligible studies that assessed muscle mass by commonly used instruments, such as dual‐energy X‐ray absorptiometry, bioelectrical impedance analysis, magnetic resonance imaging, and body composition monitor. Two assessment tools matched to study designs were employed to evaluate study quality. Pooled sarcopenia prevalence was calculated with 95% confidence interval (CI), and heterogeneity was estimated using the I (2) test. Associations of sarcopenia with mortality were expressed as hazard ratio (HR) and 95% CI. The search identified 3272 studies, and 30 studies (6162 participants, mean age from 47.5 to 77.5 years) were analysed in this review. The risk of bias in the included studies was low to moderate. Twenty‐two studies defined sarcopenia based on low muscle mass (LMM) plus low muscle strength and/or low physical performance, while eight studies used LMM alone. Muscle mass was assessed by different instruments, and a wide range of cut‐off points were used to define LMM. Overall, sarcopenia prevalence was 28.5% (95% CI 22.9–34.1%) and varied from 25.9% (I (2) = 94.9%, 95% CI 20.4–31.3%; combined criteria) to 34.6% (I (2) = 98.1%, 95% CI 20.9–48.2%; LMM alone) (P = 0.247 between subgroups). The statistically significant differences were not found in the subgroups of diagnostic criteria (P > 0.05) and dialysis modality (P > 0.05). Additionally, the sarcopenia prevalence could not be affected by average age [regression coefficient 0.004 (95% CI: −0.005 to 0.012), P = 0.406] and dialysis duration [regression coefficient 0.002 (95% CI −0.002 to 0.005), P = 0.327] in the meta‐regression. The pooled analyses showed that combined criteria of sarcopenia were related to a higher mortality risk [HR 1.82 (I (2) = 26.3%, 95% CI 1.38–2.39)], as was LMM [HR 1.61 (I (2) = 26.0%, 95% CI 1.31–1.99)] and low muscle strength [HR 2.04 (I (2) = 80.4%, 95% CI 1.19–3.5)]. Although there are substantial differences in diagnostic criteria, sarcopenia is highly prevalent in dialysis patients and is linked to increased mortality. The standardization of sarcopenia diagnostic criteria would be beneficial, and future longitudinal studies are needed to investigate the prevalence and prognostic value of sarcopenia in dialysis patients.
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spelling pubmed-88186092022-02-09 Diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis Shu, Xiaoyu Lin, Taiping Wang, Hui Zhao, Yanli Jiang, Tingting Peng, Xuchao Yue, Jirong J Cachexia Sarcopenia Muscle Reviews There is no consensus on the prevalence of sarcopenia or its impact on mortality in end‐stage renal disease patients undergoing dialysis. This review aimed to summarize the diagnostic criteria of sarcopenia and its prevalence and impact on the mortality of end‐stage renal disease patients undergoing dialysis. Embase, MEDLINE, PubMed, and Cochrane Library were searched from inception to 8 May 2021 to retrieve eligible studies that assessed muscle mass by commonly used instruments, such as dual‐energy X‐ray absorptiometry, bioelectrical impedance analysis, magnetic resonance imaging, and body composition monitor. Two assessment tools matched to study designs were employed to evaluate study quality. Pooled sarcopenia prevalence was calculated with 95% confidence interval (CI), and heterogeneity was estimated using the I (2) test. Associations of sarcopenia with mortality were expressed as hazard ratio (HR) and 95% CI. The search identified 3272 studies, and 30 studies (6162 participants, mean age from 47.5 to 77.5 years) were analysed in this review. The risk of bias in the included studies was low to moderate. Twenty‐two studies defined sarcopenia based on low muscle mass (LMM) plus low muscle strength and/or low physical performance, while eight studies used LMM alone. Muscle mass was assessed by different instruments, and a wide range of cut‐off points were used to define LMM. Overall, sarcopenia prevalence was 28.5% (95% CI 22.9–34.1%) and varied from 25.9% (I (2) = 94.9%, 95% CI 20.4–31.3%; combined criteria) to 34.6% (I (2) = 98.1%, 95% CI 20.9–48.2%; LMM alone) (P = 0.247 between subgroups). The statistically significant differences were not found in the subgroups of diagnostic criteria (P > 0.05) and dialysis modality (P > 0.05). Additionally, the sarcopenia prevalence could not be affected by average age [regression coefficient 0.004 (95% CI: −0.005 to 0.012), P = 0.406] and dialysis duration [regression coefficient 0.002 (95% CI −0.002 to 0.005), P = 0.327] in the meta‐regression. The pooled analyses showed that combined criteria of sarcopenia were related to a higher mortality risk [HR 1.82 (I (2) = 26.3%, 95% CI 1.38–2.39)], as was LMM [HR 1.61 (I (2) = 26.0%, 95% CI 1.31–1.99)] and low muscle strength [HR 2.04 (I (2) = 80.4%, 95% CI 1.19–3.5)]. Although there are substantial differences in diagnostic criteria, sarcopenia is highly prevalent in dialysis patients and is linked to increased mortality. The standardization of sarcopenia diagnostic criteria would be beneficial, and future longitudinal studies are needed to investigate the prevalence and prognostic value of sarcopenia in dialysis patients. John Wiley and Sons Inc. 2022-01-05 2022-02 /pmc/articles/PMC8818609/ /pubmed/34989172 http://dx.doi.org/10.1002/jcsm.12890 Text en © 2022 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. 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 Reviews
Shu, Xiaoyu
Lin, Taiping
Wang, Hui
Zhao, Yanli
Jiang, Tingting
Peng, Xuchao
Yue, Jirong
Diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis
title Diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis
title_full Diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis
title_fullStr Diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis
title_full_unstemmed Diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis
title_short Diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis
title_sort diagnosis, prevalence, and mortality of sarcopenia in dialysis patients: a systematic review and meta‐analysis
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818609/
https://www.ncbi.nlm.nih.gov/pubmed/34989172
http://dx.doi.org/10.1002/jcsm.12890
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