Associations between skeletal muscle strength and chronic kidney disease in patients with MASLD

Background A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is uncertain. This study examined the associations between S...

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Published inCommunications medicine Vol. 5; no. 1; pp. 118 - 9
Main Authors Zhang, Xin-Lei, Gu, Yeqing, Zhao, Jing, Zhu, Pei-Wu, Chen, Wen-Ying, Li, Gang, Liu, Wen-Yue, Zheng, Wen, Zhang, Ni, Chen, Li-Li, Targher, Giovanni, Byrne, Christopher D., Niu, Kaijun, Sun, Dan-Qin, Zheng, Ming-Hua
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Published London Nature Publishing Group UK 16.04.2025
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Abstract Background A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is uncertain. This study examined the associations between SMS and the risk of CKD in MASLD population. Method We performed a large-scale study with four cohorts: PERSONS and NHANES 2011–2014 cohorts for the cross-sectional investigation, and TCLSIH and UK Biobank cohorts for the longitudinal investigation. A handgrip dynamometer measured handgrip strength as a proxy for overall SMS. Participants were stratified according to CKD status [non-CKD vs. CKD (stages 1–5) groups]. Results In the PERSONS cohort, the CKD group has a lower handgrip strength than the non-CKD group (27.14 ± 9.19 vs. 33.59 ± 11.92 kg, P < 0.001). Higher handgrip strength is associated with lower odds of abnormal albuminuria or CKD (OR: 0.96, 95%CI:0.92-0.99 and OR:0.95, 95%CI: 0.91-0.99 respectively). The highest handgrip strength tertile is associated with the lowest risk of having abnormal albuminuria or CKD (compared with the lowest or middle tertile). Results are similar in NHANES cohort. Furthermore, the highest handgrip strength is independently associated with the lowest risk of incident CKD in MASLD (HR: 0.95, 95%CI: 0.92-0.99 and HR:0.99, 95%CI: 0.98-0.99 in TCLSIH and UK Biobank cohorts). In Kaplan-Meier curve analysis, the cumulative incidence of CKD is lowest in the highest handgrip strength tertile compared to the lowest or the middle tertile. Conclusions Higher handgrip/muscle strength is independently associated with a lower risk of CKD and abnormal albuminuria in MASLD population. Plain language summary Metabolic dysfunction-associated steatotic liver disease (MASLD) occurs when there is too much fat in the liver. People with MASLD have an increased risk of developing chronic kidney disease (CKD). Skeletal muscles are responsible for voluntary movements and are crucial for movement and health. We investigated whether skeletal muscle strength (SMS), assessed using handgrip strength, was associated with the risk of CKD in individuals with MASLD. Based on data from over 14,000 participants we found that higher SMS was associated with a lower risk of CKD. These findings suggest that preserving skeletal muscle strength may help prevent people with MASLD developing kidney disease. Zhang and Gu used four cohorts to examine associations between skeletal muscle strength (SMS) and chronic kidney disease (CKD) in people with metabolic dysfunction-associated steatotic liver disease (MASLD). Higher handgrip/muscle strength is closely associated with a lower prevalence and incidence of CKD in people with MASLD.
AbstractList BackgroundA skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is uncertain. This study examined the associations between SMS and the risk of CKD in MASLD population.MethodWe performed a large-scale study with four cohorts: PERSONS and NHANES 2011–2014 cohorts for the cross-sectional investigation, and TCLSIH and UK Biobank cohorts for the longitudinal investigation. A handgrip dynamometer measured handgrip strength as a proxy for overall SMS. Participants were stratified according to CKD status [non-CKD vs. CKD (stages 1–5) groups].ResultsIn the PERSONS cohort, the CKD group has a lower handgrip strength than the non-CKD group (27.14 ± 9.19 vs. 33.59 ± 11.92 kg, P < 0.001). Higher handgrip strength is associated with lower odds of abnormal albuminuria or CKD (OR: 0.96, 95%CI:0.92-0.99 and OR:0.95, 95%CI: 0.91-0.99 respectively). The highest handgrip strength tertile is associated with the lowest risk of having abnormal albuminuria or CKD (compared with the lowest or middle tertile). Results are similar in NHANES cohort. Furthermore, the highest handgrip strength is independently associated with the lowest risk of incident CKD in MASLD (HR: 0.95, 95%CI: 0.92-0.99 and HR:0.99, 95%CI: 0.98-0.99 in TCLSIH and UK Biobank cohorts). In Kaplan-Meier curve analysis, the cumulative incidence of CKD is lowest in the highest handgrip strength tertile compared to the lowest or the middle tertile.ConclusionsHigher handgrip/muscle strength is independently associated with a lower risk of CKD and abnormal albuminuria in MASLD population.Plain language summaryMetabolic dysfunction-associated steatotic liver disease (MASLD) occurs when there is too much fat in the liver. People with MASLD have an increased risk of developing chronic kidney disease (CKD). Skeletal muscles are responsible for voluntary movements and are crucial for movement and health. We investigated whether skeletal muscle strength (SMS), assessed using handgrip strength, was associated with the risk of CKD in individuals with MASLD. Based on data from over 14,000 participants we found that higher SMS was associated with a lower risk of CKD. These findings suggest that preserving skeletal muscle strength may help prevent people with MASLD developing kidney disease.
Background A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is uncertain. This study examined the associations between SMS and the risk of CKD in MASLD population. Method We performed a large-scale study with four cohorts: PERSONS and NHANES 2011–2014 cohorts for the cross-sectional investigation, and TCLSIH and UK Biobank cohorts for the longitudinal investigation. A handgrip dynamometer measured handgrip strength as a proxy for overall SMS. Participants were stratified according to CKD status [non-CKD vs. CKD (stages 1–5) groups]. Results In the PERSONS cohort, the CKD group has a lower handgrip strength than the non-CKD group (27.14 ± 9.19 vs. 33.59 ± 11.92 kg, P < 0.001). Higher handgrip strength is associated with lower odds of abnormal albuminuria or CKD (OR: 0.96, 95%CI:0.92-0.99 and OR:0.95, 95%CI: 0.91-0.99 respectively). The highest handgrip strength tertile is associated with the lowest risk of having abnormal albuminuria or CKD (compared with the lowest or middle tertile). Results are similar in NHANES cohort. Furthermore, the highest handgrip strength is independently associated with the lowest risk of incident CKD in MASLD (HR: 0.95, 95%CI: 0.92-0.99 and HR:0.99, 95%CI: 0.98-0.99 in TCLSIH and UK Biobank cohorts). In Kaplan-Meier curve analysis, the cumulative incidence of CKD is lowest in the highest handgrip strength tertile compared to the lowest or the middle tertile. Conclusions Higher handgrip/muscle strength is independently associated with a lower risk of CKD and abnormal albuminuria in MASLD population. Plain language summary Metabolic dysfunction-associated steatotic liver disease (MASLD) occurs when there is too much fat in the liver. People with MASLD have an increased risk of developing chronic kidney disease (CKD). Skeletal muscles are responsible for voluntary movements and are crucial for movement and health. We investigated whether skeletal muscle strength (SMS), assessed using handgrip strength, was associated with the risk of CKD in individuals with MASLD. Based on data from over 14,000 participants we found that higher SMS was associated with a lower risk of CKD. These findings suggest that preserving skeletal muscle strength may help prevent people with MASLD developing kidney disease. Zhang and Gu used four cohorts to examine associations between skeletal muscle strength (SMS) and chronic kidney disease (CKD) in people with metabolic dysfunction-associated steatotic liver disease (MASLD). Higher handgrip/muscle strength is closely associated with a lower prevalence and incidence of CKD in people with MASLD.
Metabolic dysfunction-associated steatotic liver disease (MASLD) occurs when there is too much fat in the liver. People with MASLD have an increased risk of developing chronic kidney disease (CKD). Skeletal muscles are responsible for voluntary movements and are crucial for movement and health. We investigated whether skeletal muscle strength (SMS), assessed using handgrip strength, was associated with the risk of CKD in individuals with MASLD. Based on data from over 14,000 participants we found that higher SMS was associated with a lower risk of CKD. These findings suggest that preserving skeletal muscle strength may help prevent people with MASLD developing kidney disease. Zhang and Gu used four cohorts to examine associations between skeletal muscle strength (SMS) and chronic kidney disease (CKD) in people with metabolic dysfunction-associated steatotic liver disease (MASLD). Higher handgrip/muscle strength is closely associated with a lower prevalence and incidence of CKD in people with MASLD.
A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is uncertain. This study examined the associations between SMS and the risk of CKD in MASLD population.BACKGROUNDA skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is uncertain. This study examined the associations between SMS and the risk of CKD in MASLD population.We performed a large-scale study with four cohorts: PERSONS and NHANES 2011-2014 cohorts for the cross-sectional investigation, and TCLSIH and UK Biobank cohorts for the longitudinal investigation. A handgrip dynamometer measured handgrip strength as a proxy for overall SMS. Participants were stratified according to CKD status [non-CKD vs. CKD (stages 1-5) groups].METHODWe performed a large-scale study with four cohorts: PERSONS and NHANES 2011-2014 cohorts for the cross-sectional investigation, and TCLSIH and UK Biobank cohorts for the longitudinal investigation. A handgrip dynamometer measured handgrip strength as a proxy for overall SMS. Participants were stratified according to CKD status [non-CKD vs. CKD (stages 1-5) groups].In the PERSONS cohort, the CKD group has a lower handgrip strength than the non-CKD group (27.14 ± 9.19 vs. 33.59 ± 11.92 kg, P < 0.001). Higher handgrip strength is associated with lower odds of abnormal albuminuria or CKD (OR: 0.96, 95%CI:0.92-0.99 and OR:0.95, 95%CI: 0.91-0.99 respectively). The highest handgrip strength tertile is associated with the lowest risk of having abnormal albuminuria or CKD (compared with the lowest or middle tertile). Results are similar in NHANES cohort. Furthermore, the highest handgrip strength is independently associated with the lowest risk of incident CKD in MASLD (HR: 0.95, 95%CI: 0.92-0.99 and HR:0.99, 95%CI: 0.98-0.99 in TCLSIH and UK Biobank cohorts). In Kaplan-Meier curve analysis, the cumulative incidence of CKD is lowest in the highest handgrip strength tertile compared to the lowest or the middle tertile.RESULTSIn the PERSONS cohort, the CKD group has a lower handgrip strength than the non-CKD group (27.14 ± 9.19 vs. 33.59 ± 11.92 kg, P < 0.001). Higher handgrip strength is associated with lower odds of abnormal albuminuria or CKD (OR: 0.96, 95%CI:0.92-0.99 and OR:0.95, 95%CI: 0.91-0.99 respectively). The highest handgrip strength tertile is associated with the lowest risk of having abnormal albuminuria or CKD (compared with the lowest or middle tertile). Results are similar in NHANES cohort. Furthermore, the highest handgrip strength is independently associated with the lowest risk of incident CKD in MASLD (HR: 0.95, 95%CI: 0.92-0.99 and HR:0.99, 95%CI: 0.98-0.99 in TCLSIH and UK Biobank cohorts). In Kaplan-Meier curve analysis, the cumulative incidence of CKD is lowest in the highest handgrip strength tertile compared to the lowest or the middle tertile.Higher handgrip/muscle strength is independently associated with a lower risk of CKD and abnormal albuminuria in MASLD population.CONCLUSIONSHigher handgrip/muscle strength is independently associated with a lower risk of CKD and abnormal albuminuria in MASLD population.
A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is uncertain. This study examined the associations between SMS and the risk of CKD in MASLD population. We performed a large-scale study with four cohorts: PERSONS and NHANES 2011-2014 cohorts for the cross-sectional investigation, and TCLSIH and UK Biobank cohorts for the longitudinal investigation. A handgrip dynamometer measured handgrip strength as a proxy for overall SMS. Participants were stratified according to CKD status [non-CKD vs. CKD (stages 1-5) groups]. In the PERSONS cohort, the CKD group has a lower handgrip strength than the non-CKD group (27.14 ± 9.19 vs. 33.59 ± 11.92 kg, P < 0.001). Higher handgrip strength is associated with lower odds of abnormal albuminuria or CKD (OR: 0.96, 95%CI:0.92-0.99 and OR:0.95, 95%CI: 0.91-0.99 respectively). The highest handgrip strength tertile is associated with the lowest risk of having abnormal albuminuria or CKD (compared with the lowest or middle tertile). Results are similar in NHANES cohort. Furthermore, the highest handgrip strength is independently associated with the lowest risk of incident CKD in MASLD (HR: 0.95, 95%CI: 0.92-0.99 and HR:0.99, 95%CI: 0.98-0.99 in TCLSIH and UK Biobank cohorts). In Kaplan-Meier curve analysis, the cumulative incidence of CKD is lowest in the highest handgrip strength tertile compared to the lowest or the middle tertile. Higher handgrip/muscle strength is independently associated with a lower risk of CKD and abnormal albuminuria in MASLD population.
Abstract Background A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is uncertain. This study examined the associations between SMS and the risk of CKD in MASLD population. Method We performed a large-scale study with four cohorts: PERSONS and NHANES 2011–2014 cohorts for the cross-sectional investigation, and TCLSIH and UK Biobank cohorts for the longitudinal investigation. A handgrip dynamometer measured handgrip strength as a proxy for overall SMS. Participants were stratified according to CKD status [non-CKD vs. CKD (stages 1–5) groups]. Results In the PERSONS cohort, the CKD group has a lower handgrip strength than the non-CKD group (27.14 ± 9.19 vs. 33.59 ± 11.92 kg, P < 0.001). Higher handgrip strength is associated with lower odds of abnormal albuminuria or CKD (OR: 0.96, 95%CI:0.92-0.99 and OR:0.95, 95%CI: 0.91-0.99 respectively). The highest handgrip strength tertile is associated with the lowest risk of having abnormal albuminuria or CKD (compared with the lowest or middle tertile). Results are similar in NHANES cohort. Furthermore, the highest handgrip strength is independently associated with the lowest risk of incident CKD in MASLD (HR: 0.95, 95%CI: 0.92-0.99 and HR:0.99, 95%CI: 0.98-0.99 in TCLSIH and UK Biobank cohorts). In Kaplan-Meier curve analysis, the cumulative incidence of CKD is lowest in the highest handgrip strength tertile compared to the lowest or the middle tertile. Conclusions Higher handgrip/muscle strength is independently associated with a lower risk of CKD and abnormal albuminuria in MASLD population.
ArticleNumber 118
Author Zhang, Ni
Li, Gang
Niu, Kaijun
Liu, Wen-Yue
Zhu, Pei-Wu
Zhang, Xin-Lei
Zheng, Ming-Hua
Chen, Li-Li
Zhao, Jing
Targher, Giovanni
Chen, Wen-Ying
Gu, Yeqing
Sun, Dan-Qin
Zheng, Wen
Byrne, Christopher D.
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  organization: MAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University
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  surname: Byrne
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  surname: Niu
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  organization: School of Public Health of Tianjin University of Traditional Chinese Medicine, School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Nutritional Epidemiology Institute and School of Public Health, Tianjin Medical University
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  givenname: Dan-Qin
  surname: Sun
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  email: zhengmh@wmu.edu.cn
  organization: MAFLD Research Center, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Key Laboratory of Diagnosis and Treatment for The Development of Chronic Liver Disease in Zhejiang Province
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Cites_doi 10.1007/s11914-015-0261-4
10.1053/j.ajkd.2014.03.020
10.1038/s41581-021-00498-0
10.3390/jcm11144151
10.1016/j.pulmoe.2022.09.007
10.1681/ASN.0000000000000240
10.4093/dmj.2022.0048
10.1186/s12933-021-01256-z
10.3390/ijms232113320
10.1371/journal.pmed.1001680
10.1038/s41581-021-00519-y
10.7326/0003-4819-150-9-200905050-00006
10.1007/s12072-022-10420-w
10.1136/gutjnl-2024-332398
10.1136/egastro-2023-100005
10.1053/j.ajkd.2021.04.016
10.1038/nrgastro.2017.109
10.7326/M22-3228
10.1038/s41575-023-00846-4
10.2337/dc09-S302
10.1097/HEP.0000000000000696
10.1002/hep.20701
10.1002/jcsm.13001
10.1002/jcsm.12791
10.1007/s12072-023-10543-8
10.21037/hbsn-22-421
10.1002/jcsm.12598
10.1111/acel.13923
10.1093/ageing/afz068
10.1016/S0140-6736(19)31138-9
10.1016/j.metabol.2020.154433
10.1002/oby.23512
10.1002/hep.29910
10.1002/jcsm.13180
10.1186/s12877-024-04917-2
10.20517/mtod.2024.06
10.1016/j.jhep.2023.08.025
10.1101/cshperspect.a029785
10.1002/hep.28132
10.1080/1354750X.2020.1819418
10.1111/apt.17308
10.1016/j.jhep.2022.01.010
10.1016/j.jhep.2014.12.012
10.1007/s40279-021-01605-8
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References MM Cusick (821_CR43) 2023; 176
821_CR20
P Charatcharoenwitthaya (821_CR21) 2022; 13
H Perazzo (821_CR18) 2024; 80
G Musso (821_CR35) 2014; 11
A Hara (821_CR31) 2020; 25
H Noor (821_CR39) 2021; 12
DE Kleiner (821_CR19) 2005; 41
J Zhou (821_CR34) 2023; 1
821_CR27
JJ Fyfe (821_CR44) 2022; 52
821_CR3
S Ha (821_CR17) 2024; 74
CD Byrne (821_CR4) 2024; 4
DQ Sun (821_CR8) 2023; 12
821_CR1
DQ Sun (821_CR9) 2021; 115
F Petermann-Rocha (821_CR15) 2022; 76
AS Levey (821_CR24) 2009; 150
AJ Cruz-Jentoft (821_CR11) 2019; 393
XH Wang (821_CR30) 2022; 18
A Berzigotti (821_CR37) 2016; 63
FKW Ho (821_CR22) 2019; 48
KG Avin (821_CR28) 2015; 13
821_CR10
821_CR32
XD Zhou (821_CR7) 2023; 17
821_CR36
RA DeFronzo (821_CR33) 2009; 32
DH Seo (821_CR12) 2022; 30
T Li (821_CR42) 2024; 24
TC Peng (821_CR26) 2018; 68
TY Wang (821_CR6) 2022; 18
P He (821_CR29) 2023; 14
S Heiwe (821_CR40) 2014; 64
LJ Tang (821_CR16) 2023; 17
XL Zhang (821_CR41) 2022; 46
C Delgado (821_CR25) 2024; 35
JP Lopez-Lopez (821_CR13) 2021; 20
S Kang (821_CR14) 2020; 11
A Henry (821_CR38) 2023; 57
LA Inker (821_CR23) 2021; 78
Z Younossi (821_CR2) 2018; 15
CD Byrne (821_CR5) 2015; 62
References_xml – volume: 13
  start-page: 173
  year: 2015
  ident: 821_CR28
  publication-title: Curr. Osteoporos. Rep.
  doi: 10.1007/s11914-015-0261-4
– volume: 64
  start-page: 383
  year: 2014
  ident: 821_CR40
  publication-title: Am. J. Kidney Dis.
  doi: 10.1053/j.ajkd.2014.03.020
– volume: 18
  start-page: 138
  year: 2022
  ident: 821_CR30
  publication-title: Nat. Rev. Nephrol.
  doi: 10.1038/s41581-021-00498-0
– ident: 821_CR27
  doi: 10.3390/jcm11144151
– ident: 821_CR20
  doi: 10.1016/j.pulmoe.2022.09.007
– volume: 35
  start-page: 66
  year: 2024
  ident: 821_CR25
  publication-title: J. Am. Soc. Nephrol.
  doi: 10.1681/ASN.0000000000000240
– volume: 46
  start-page: 391
  year: 2022
  ident: 821_CR41
  publication-title: Diab. Metab. J.
  doi: 10.4093/dmj.2022.0048
– volume: 20
  start-page: 68
  year: 2021
  ident: 821_CR13
  publication-title: Cardiovasc. Diabetol.
  doi: 10.1186/s12933-021-01256-z
– ident: 821_CR10
  doi: 10.3390/ijms232113320
– volume: 11
  start-page: e1001680
  year: 2014
  ident: 821_CR35
  publication-title: PLoS Med.
  doi: 10.1371/journal.pmed.1001680
– volume: 18
  start-page: 259
  year: 2022
  ident: 821_CR6
  publication-title: Nat. Rev. Nephrol.
  doi: 10.1038/s41581-021-00519-y
– volume: 150
  start-page: 604
  year: 2009
  ident: 821_CR24
  publication-title: Ann. Intern. Med.
  doi: 10.7326/0003-4819-150-9-200905050-00006
– volume: 17
  start-page: 190
  year: 2023
  ident: 821_CR16
  publication-title: Hepatol. Int.
  doi: 10.1007/s12072-022-10420-w
– volume: 74
  start-page: 141
  year: 2024
  ident: 821_CR17
  publication-title: Gut
  doi: 10.1136/gutjnl-2024-332398
– volume: 1
  start-page: e100005
  year: 2023
  ident: 821_CR34
  publication-title: eGastroenterology
  doi: 10.1136/egastro-2023-100005
– volume: 78
  start-page: 736
  year: 2021
  ident: 821_CR23
  publication-title: Am. J. Kidney Dis.
  doi: 10.1053/j.ajkd.2021.04.016
– volume: 15
  start-page: 11
  year: 2018
  ident: 821_CR2
  publication-title: Nat. Rev. Gastroenterol. Hepatol.
  doi: 10.1038/nrgastro.2017.109
– volume: 176
  start-page: 788
  year: 2023
  ident: 821_CR43
  publication-title: Ann. Intern. Med.
  doi: 10.7326/M22-3228
– ident: 821_CR1
  doi: 10.1038/s41575-023-00846-4
– volume: 32
  start-page: S157
  year: 2009
  ident: 821_CR33
  publication-title: Diab. Care
  doi: 10.2337/dc09-S302
– ident: 821_CR3
  doi: 10.1097/HEP.0000000000000696
– volume: 41
  start-page: 1313
  year: 2005
  ident: 821_CR19
  publication-title: Hepatology
  doi: 10.1002/hep.20701
– volume: 13
  start-page: 2393
  year: 2022
  ident: 821_CR21
  publication-title: J. Cachexia Sarcopenia Muscle
  doi: 10.1002/jcsm.13001
– volume: 12
  start-page: 1621
  year: 2021
  ident: 821_CR39
  publication-title: J. Cachexia Sarcopenia Muscle
  doi: 10.1002/jcsm.12791
– volume: 17
  start-page: 773
  year: 2023
  ident: 821_CR7
  publication-title: Hepatol. Int.
  doi: 10.1007/s12072-023-10543-8
– volume: 12
  start-page: 386
  year: 2023
  ident: 821_CR8
  publication-title: Hepatobiliary Surg. Nutr.
  doi: 10.21037/hbsn-22-421
– volume: 11
  start-page: 1232
  year: 2020
  ident: 821_CR14
  publication-title: J. Cachexia Sarcopenia Muscle
  doi: 10.1002/jcsm.12598
– ident: 821_CR32
  doi: 10.1111/acel.13923
– volume: 48
  start-page: 684
  year: 2019
  ident: 821_CR22
  publication-title: Age Ageing
  doi: 10.1093/ageing/afz068
– volume: 393
  start-page: 2636
  year: 2019
  ident: 821_CR11
  publication-title: Lancet
  doi: 10.1016/S0140-6736(19)31138-9
– volume: 115
  year: 2021
  ident: 821_CR9
  publication-title: Metabolism
  doi: 10.1016/j.metabol.2020.154433
– volume: 30
  start-page: 2034
  year: 2022
  ident: 821_CR12
  publication-title: Obesity (Silver Spring)
  doi: 10.1002/oby.23512
– volume: 68
  start-page: 788
  year: 2018
  ident: 821_CR26
  publication-title: Hepatology
  doi: 10.1002/hep.29910
– volume: 14
  start-page: 805
  year: 2023
  ident: 821_CR29
  publication-title: J. Cachexia Sarcopenia Muscle
  doi: 10.1002/jcsm.13180
– volume: 24
  start-page: 351
  year: 2024
  ident: 821_CR42
  publication-title: BMC Geriatr.
  doi: 10.1186/s12877-024-04917-2
– volume: 4
  start-page: 10
  year: 2024
  ident: 821_CR4
  publication-title: Metab. Target Organ Damage
  doi: 10.20517/mtod.2024.06
– volume: 80
  start-page: e72
  year: 2024
  ident: 821_CR18
  publication-title: J. Hepatol.
  doi: 10.1016/j.jhep.2023.08.025
– ident: 821_CR36
  doi: 10.1101/cshperspect.a029785
– volume: 63
  start-page: 1026
  year: 2016
  ident: 821_CR37
  publication-title: Hepatology
  doi: 10.1002/hep.28132
– volume: 25
  start-page: 587
  year: 2020
  ident: 821_CR31
  publication-title: Biomarkers
  doi: 10.1080/1354750X.2020.1819418
– volume: 57
  start-page: 709
  year: 2023
  ident: 821_CR38
  publication-title: Aliment Pharm. Ther.
  doi: 10.1111/apt.17308
– volume: 76
  start-page: 1021
  year: 2022
  ident: 821_CR15
  publication-title: J. Hepatol.
  doi: 10.1016/j.jhep.2022.01.010
– volume: 62
  start-page: S47
  year: 2015
  ident: 821_CR5
  publication-title: J. Hepatol.
  doi: 10.1016/j.jhep.2014.12.012
– volume: 52
  start-page: 463
  year: 2022
  ident: 821_CR44
  publication-title: Sports Med.
  doi: 10.1007/s40279-021-01605-8
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Snippet Background A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in...
A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in individuals...
BackgroundA skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease (CKD) in...
Metabolic dysfunction-associated steatotic liver disease (MASLD) occurs when there is too much fat in the liver. People with MASLD have an increased risk of...
Abstract Background A skeletal muscle strength (SMS) decline is associated with metabolic diseases, but whether SMS also declines with chronic kidney disease...
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692/4022/1585/104
Adults
Biobanks
Biopsy
Body mass index
Creatinine
Epidemiology
Ethics
Hepatitis
Histology
Hypertension
Kidney diseases
Liver diseases
Medicine
Medicine & Public Health
Metabolism
Missing data
Muscle strength
Musculoskeletal system
Population
Regression analysis
Review boards
Ultrasonic imaging
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Title Associations between skeletal muscle strength and chronic kidney disease in patients with MASLD
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