Evidence map›Paper›PMID 29202452›Full record

ArticleJCI insight2017

Systemic inflammation is associated with exaggerated skeletal muscle protein catabolism in maintenance hemodialysis patients.

Serpil M Deger, Adriana M Hung, Jorge L Gamboa, Edward D Siew, Charles D Ellis, Cindy Booker, Feng Sha, Haiming Li, Aihua Bian, Thomas G Stewart and 4 more

Abstract read
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Dialysis in the Elderly: A Practical Guide for the Clinician.International journal of nephrology · 2025
    Review
  16. Article
  17. Review
  18. Review
  19. Sarcopenia in chronic kidney disease: from bench to bedside.The Korean journal of internal medicine · 2023
    Review
  20. The impact of senescence on muscle wasting in chronic kidney disease.Journal of cachexia, sarcopenia and muscle · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Serpil M DegerDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.
Adriana M HungDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.
Jorge L GamboaDivision of Clinical Pharmacology, and.
Edward D SiewDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.
Charles D EllisDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.
Cindy BookerDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.
Feng ShaDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.
Haiming LiDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.
Aihua BianDepartment of Biostatistics, VUMC, Nashville, Tennessee, USA.
Thomas G StewartDepartment of Biostatistics, VUMC, Nashville, Tennessee, USA.
Roy ZentDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.
William E MitchSelzman Institute for Kidney Health, Baylor College of Medicine, Department of Medicine, Houston, Texas, USA.
Naji N AbumradDepartment of Surgery, VUMC, Nashville, Tennessee, USA.
T Alp IkizlerDivision of Nephrology, Vanderbilt University Medical Center (VUMC), Nashville, Tennessee, USA.

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
The Laminin Receptors in Kidney FibrosisR01DK069921 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ROY ZENT · 2005 to 2026
$9.5M
Nutrition and Metabolism in Dialysis PatientsK24DK062849 · NIDDK · VANDERBILT UNIVERSITY · PI IKIZLER, TALAT ALP · 2003 to 2012
$1.6M
MALNUTRITION IN DIALYSIS PATIENTSR01DK045604 · NIDDK · VANDERBILT UNIVERSITY · PI IKIZLER, TALAT ALP · 1992 to 2006
$1.2M
Mitochondrial Dysfunction in Chronic Kidney DiseaseK23DK100533 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GAMBOA, JORGE LUIS · 2013 to 2017
$763k
Nutrition, Inflammation and Insulin Resistance in End-Stage Renal DiseaseI01CX000414 · VA · VETERANS HEALTH ADMINISTRATION · PI IKIZLER, TALAT ALP · 2012 to 2015
–
CSRD VA I01 CX000414NCATS NIH HHS UL1 TR000445NIDDK NIH HHS K23 DK100533NIDDK NIH HHS K24 DK062849NIDDK NIH HHS R01 DK045604NIDDK NIH HHS R01 DK069921
6 · The paper itself

Abstract

backgroundSystemic inflammation and muscle wasting are highly prevalent and coexist in patients on maintenance hemodialysis (MHD). We aimed to determine the effects of systemic inflammation on skeletal muscle protein metabolism in MHD patients.

methodsWhole body and skeletal muscle protein turnover were assessed by stable isotope kinetic studies. We incorporated expressions of E1, E214K, E3αI, E3αII, MuRF-1, and atrogin-1 in skeletal muscle tissue from integrin β1 gene KO CKD mice models.

resultsAmong 129 patients with mean (± SD) age 47 ± 12 years, 74% were African American, 73% were male, and 22% had diabetes mellitus. Median high-sensitivity C-reactive protein (hs-CRP) concentration was 13 (interquartile range 0.8, 33) mg/l. There were statistically significant associations between hs-CRP and forearm skeletal muscle protein synthesis, degradation, and net forearm skeletal muscle protein balance (P < 0.001 for all). The associations remained statistically significant after adjustment for clinical and demographic confounders, as well as in sensitivity analysis, excluding patients with diabetes mellitus. In attempting to identify potential mechanisms involved in this correlation, we show increased expressions of E1, E214K, E3αI, E3αII, MuRF-1, and atrogin-1 in skeletal muscle tissue obtained from an animal model of chronic kidney disease.

conclusionThese data suggest that systemic inflammation is a strong and independent determinant of skeletal muscle protein homeostasis in MHD patients, providing rationale for further studies using anticytokine therapies in patients with underlying systemic inflammation.

fundingThis study was in part supported by NIH grants R01 DK45604 and 1K24 DK62849, the Clinical Translational Science Award UL1-TR000445 from the National Center for Advancing Translational Sciences, the Veterans Administration Merit Award I01 CX000414, the SatelliteHealth Normon Coplon Extramural Grant Program, and the FDA grant 000943.

Indexed as

InflammationRenal DialysisAdultAnimalsBiomarkersC-Reactive ProteinCytokinesDisease Models, AnimalFemaleHomeostasisHumansIntegrin beta1KineticsMaleMiceMice, KnockoutBiomarkersC-Reactive ProteinCytokinesFBXO32 protein, humanFbxo32 protein, mouseIntegrin beta1Muscle ProteinsSKP Cullin F-Box Protein LigasesTRIM63 protein, humanTripartite Motif ProteinsUbiquitin-Protein LigasesChronic kidney diseaseMetabolismNephrology

Identifiers

PMID29202452
PMCPMC5752392

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.