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Diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: A systematic review and meta‐analysis

The prevalence of sarcopenia and its clinical predictors and clinical impact vary among kidney transplant recipients (KTRs), in part because of different diagnostic criteria. This study aimed to assess the reported diagnosis criteria of sarcopenia and compare them in terms of prevalence, clinical pr...

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Autores principales: Zhang, Jin‐Zhi, Shi, Wei, Zou, Min, Zeng, Qi‐Shan, Feng, Yue, Luo, Zhen‐Yi, Gan, Hua‐Tian
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/PMC9891953/
https://www.ncbi.nlm.nih.gov/pubmed/36403578
http://dx.doi.org/10.1002/jcsm.13130
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author Zhang, Jin‐Zhi
Shi, Wei
Zou, Min
Zeng, Qi‐Shan
Feng, Yue
Luo, Zhen‐Yi
Gan, Hua‐Tian
author_facet Zhang, Jin‐Zhi
Shi, Wei
Zou, Min
Zeng, Qi‐Shan
Feng, Yue
Luo, Zhen‐Yi
Gan, Hua‐Tian
author_sort Zhang, Jin‐Zhi
collection PubMed
description The prevalence of sarcopenia and its clinical predictors and clinical impact vary among kidney transplant recipients (KTRs), in part because of different diagnostic criteria. This study aimed to assess the reported diagnosis criteria of sarcopenia and compare them in terms of prevalence, clinical predictors, and impact of sarcopenia. The Medline, Embase, and Cochrane Library were searched for the full‐length reports published until 28 January 2022. The subgroup analysis, meta‐regression, and sensitivity analysis were performed and heterogeneity was assessed using the I (2). A total of 681 studies were retrieved, among which only 23 studies (including 2535 subjects, 59.7% men, mean age 49.8 years) were eventually included in the final analysis. The pooled prevalence in these included studies was 26% [95% confidence interval (95% CI): 20–34%, I (2) = 93.45%], including 22% (95% CI: 14–32%, I (2) = 88.76%) in men and 27% (95% CI: 14–41%, I (2) = 90.56%) in women (P = 0.554 between subgroups). The prevalence of sarcopenia diagnosed using low muscle mass was 34% (95% CI: 21–48%, I (2) = 95.28%), and the prevalence of using low muscle mass in combination with low muscle strength and/or low physical performance was 21% (95% CI: 15–28%, I (2) = 90.37%) (P = 0.08 between subgroups). In meta‐regression analyses, the mean age (regression coefficient: 1.001, 95% CI: 0.991–1.011) and percentage male (regression coefficient: 0.846, 95% CI: 0.367–1.950) could not predict the effect size. Lower body mass index (odds ratio (OR): 0.57, 95% CI: 0.39–0.84, I (2) = 61.5%), female sex (OR: 0.31, 95% CI: 0.16–0.61, I (2) = 0.0%), and higher age (OR: 1.08, 95% CI: 1.05–1.10, I (2) = 10.1%) were significantly associated with a higher risk for sarcopenia in KTRs, but phase angle (OR: 0.81, 95% CI: 0.16–4.26, I (2) = 84.5%) was not associated with sarcopenia in KTRs. Sarcopenia was not associated with rejections (risk ratio (RR): 0.67, 95% CI: 0.23–1.92, I (2) = 12.1%), infections (RR: 1.03, 95% CI: 0.34–3.12, I (2) = 87.4%), delayed graft functions (RR: 0.81, 95% CI: 0.46–1.43, I (2) = 0.0%), and death (RR: 0.95, 95% CI: 0.32–2.82, I (2) = 0.0%) in KRTs. Sarcopenia was found to be very common in KRTs. However, we have not found that sarcopenia had a negative impact on clinical health after kidney transplantation. Large study cohorts and multicentre longitudinal studies in the future are urgently needed to explore the prevalence and prognosis of sarcopenia in kidney transplant patients.
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spelling pubmed-98919532023-02-02 Diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: A systematic review and meta‐analysis Zhang, Jin‐Zhi Shi, Wei Zou, Min Zeng, Qi‐Shan Feng, Yue Luo, Zhen‐Yi Gan, Hua‐Tian J Cachexia Sarcopenia Muscle Reviews The prevalence of sarcopenia and its clinical predictors and clinical impact vary among kidney transplant recipients (KTRs), in part because of different diagnostic criteria. This study aimed to assess the reported diagnosis criteria of sarcopenia and compare them in terms of prevalence, clinical predictors, and impact of sarcopenia. The Medline, Embase, and Cochrane Library were searched for the full‐length reports published until 28 January 2022. The subgroup analysis, meta‐regression, and sensitivity analysis were performed and heterogeneity was assessed using the I (2). A total of 681 studies were retrieved, among which only 23 studies (including 2535 subjects, 59.7% men, mean age 49.8 years) were eventually included in the final analysis. The pooled prevalence in these included studies was 26% [95% confidence interval (95% CI): 20–34%, I (2) = 93.45%], including 22% (95% CI: 14–32%, I (2) = 88.76%) in men and 27% (95% CI: 14–41%, I (2) = 90.56%) in women (P = 0.554 between subgroups). The prevalence of sarcopenia diagnosed using low muscle mass was 34% (95% CI: 21–48%, I (2) = 95.28%), and the prevalence of using low muscle mass in combination with low muscle strength and/or low physical performance was 21% (95% CI: 15–28%, I (2) = 90.37%) (P = 0.08 between subgroups). In meta‐regression analyses, the mean age (regression coefficient: 1.001, 95% CI: 0.991–1.011) and percentage male (regression coefficient: 0.846, 95% CI: 0.367–1.950) could not predict the effect size. Lower body mass index (odds ratio (OR): 0.57, 95% CI: 0.39–0.84, I (2) = 61.5%), female sex (OR: 0.31, 95% CI: 0.16–0.61, I (2) = 0.0%), and higher age (OR: 1.08, 95% CI: 1.05–1.10, I (2) = 10.1%) were significantly associated with a higher risk for sarcopenia in KTRs, but phase angle (OR: 0.81, 95% CI: 0.16–4.26, I (2) = 84.5%) was not associated with sarcopenia in KTRs. Sarcopenia was not associated with rejections (risk ratio (RR): 0.67, 95% CI: 0.23–1.92, I (2) = 12.1%), infections (RR: 1.03, 95% CI: 0.34–3.12, I (2) = 87.4%), delayed graft functions (RR: 0.81, 95% CI: 0.46–1.43, I (2) = 0.0%), and death (RR: 0.95, 95% CI: 0.32–2.82, I (2) = 0.0%) in KRTs. Sarcopenia was found to be very common in KRTs. However, we have not found that sarcopenia had a negative impact on clinical health after kidney transplantation. Large study cohorts and multicentre longitudinal studies in the future are urgently needed to explore the prevalence and prognosis of sarcopenia in kidney transplant patients. John Wiley and Sons Inc. 2022-11-20 /pmc/articles/PMC9891953/ /pubmed/36403578 http://dx.doi.org/10.1002/jcsm.13130 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-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Zhang, Jin‐Zhi
Shi, Wei
Zou, Min
Zeng, Qi‐Shan
Feng, Yue
Luo, Zhen‐Yi
Gan, Hua‐Tian
Diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: A systematic review and meta‐analysis
title Diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: A systematic review and meta‐analysis
title_full Diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: A systematic review and meta‐analysis
title_fullStr Diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: A systematic review and meta‐analysis
title_full_unstemmed Diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: A systematic review and meta‐analysis
title_short Diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: A systematic review and meta‐analysis
title_sort diagnosis, prevalence, and outcomes of sarcopenia in kidney transplantation recipients: a systematic review and meta‐analysis
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891953/
https://www.ncbi.nlm.nih.gov/pubmed/36403578
http://dx.doi.org/10.1002/jcsm.13130
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