» Articles » PMID: 28508131

Muscle Wasting in Chronic Kidney Disease

Overview
Journal Pediatr Nephrol
Specialties Nephrology
Pediatrics
Date 2017 May 17
PMID 28508131
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Loss of lean body mass is a relevant component of the cachexia, or protein energy wasting (PEW), syndrome. Reduced muscle mass seems to be the most solid criterion for the presence of cachexia/PEW in patients with chronic kidney disease (CKD), and those with greater muscle mass loss have a higher risk of death. Children with CKD have many risk factors for lean mass and muscle wasting, including poor appetite, inflammation, growth hormone resistance, and metabolic acidosis. Mortality risks in patients with CKD increases as body mass index (BMI) and weight decreases. However, data regarding cachexia/PEW and muscle wasting in children with CKD is scarce due to lack of consensus in diagnostic criteria and an appropriate investigative methodology. Further research is urgently needed to address this important complication in the pediatric CKD setting, which may have fundamental impact on clinical outcomes.

Citing Articles

Protein energy wasting in children with chronic kidney disease: is lean body mass by DEXA a key diagnostic biomarker?.

Mak R Pediatr Nephrol. 2024; 39(5):1323-1326.

PMID: 38177413 DOI: 10.1007/s00467-023-06261-w.


Editorial: Immunology of cachexia.

Kumar V, Stewart 4th J Front Immunol. 2023; 14:1339263.

PMID: 38116001 PMC: 10728869. DOI: 10.3389/fimmu.2023.1339263.


Automated temporalis muscle quantification and growth charts for children through adulthood.

Zapaishchykova A, Liu K, Saraf A, Ye Z, Catalano P, Benitez V Nat Commun. 2023; 14(1):6863.

PMID: 37945573 PMC: 10636102. DOI: 10.1038/s41467-023-42501-1.


Malnutrition and protein energy wasting are associated with severity and progression of pediatric chronic kidney disease.

Shen C, Liebstein D, Fernandez H Pediatr Nephrol. 2023; 39(1):243-250.

PMID: 37464056 DOI: 10.1007/s00467-023-06078-7.


Malnutrition Patterns in Children with Chronic Kidney Disease.

Karava V, Dotis J, Kondou A, Printza N Life (Basel). 2023; 13(3).

PMID: 36983870 PMC: 10053690. DOI: 10.3390/life13030713.


References
1.
Wetzsteon R, Kalkwarf H, Shults J, Zemel B, Foster B, Griffin L . Volumetric bone mineral density and bone structure in childhood chronic kidney disease. J Bone Miner Res. 2011; 26(9):2235-44. PMC: 3304436. DOI: 10.1002/jbmr.427. View

2.
Foley R, Wang C, Ishani A, Collins A, Murray A . Kidney function and sarcopenia in the United States general population: NHANES III. Am J Nephrol. 2007; 27(3):279-86. DOI: 10.1159/000101827. View

3.
Kanazawa Y, Nakao T, Murai S, Okada T, Matsumoto H . Diagnosis and prevalence of protein-energy wasting and its association with mortality in Japanese haemodialysis patients. Nephrology (Carlton). 2016; 22(7):541-547. DOI: 10.1111/nep.12814. View

4.
Kalantar-Zadeh K, Streja E, Molnar M, Lukowsky L, Krishnan M, Kovesdy C . Mortality prediction by surrogates of body composition: an examination of the obesity paradox in hemodialysis patients using composite ranking score analysis. Am J Epidemiol. 2012; 175(8):793-803. PMC: 3390012. DOI: 10.1093/aje/kwr384. View

5.
Kopple J, Greene T, Chumlea W, Hollinger D, Maroni B, Merrill D . Relationship between nutritional status and the glomerular filtration rate: results from the MDRD study. Kidney Int. 2000; 57(4):1688-703. DOI: 10.1046/j.1523-1755.2000.00014.x. View