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1000 Titel
  • Leucine disposal rate for assessment of amino acid metabolism in maintenance hemodialysis patients
1000 Autor/in
  1. Denny, Gerald B. |
  2. Deger, Serpil M. |
  3. Chen, Guanhua |
  4. Bian, Aihua |
  5. Sha, Feng |
  6. Booker, Cindy |
  7. Kesler, Jaclyn T. |
  8. David, Sthuthi |
  9. Ellis, Charles D. |
  10. Ikizler, T. Alp |
1000 Erscheinungsjahr 2016
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2016-06-03
1000 Erschienen in
1000 Quellenangabe
  • 2:31
1000 Copyrightjahr
  • 2016
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s40795-016-0071-9 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939826/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • BACKGROUND: Protein energy wasting (PEW) is common in patients undergoing maintenance hemodialysis (MHD) and closely associated with poor outcomes. Insulin resistance and associated alterations in amino acid metabolism are potential pathways leading to PEW. We hypothesized that the measurement of leucine disposal during a hyperinsulinemic- euglycemic-euaminoacidemic clamp (HEAC) procedure would accurately measure the sensitivity to insulin for its actions on concomitant carbohydrate and protein metabolism in MHD patients. METHODS: We examined 35 MHD patients and 17 control subjects with normal kidney function by hyperinsulinemic-euglycemic clamp (HEGC) followed by HEAC clamp procedure to obtain leucine disposal rate (LDR) along with isotope tracer methodology to assess whole body protein turnover. RESULTS: The glucose disposal rate (GDR) by HEGC was 5.1 ± 2.1 mg/kg/min for the MHD patients compared to 6.3 ± 3.9 mg/kg/min for the controls (p = 0.38). The LDR during HEAC was 0.09 ± 0.03 mg/kg/min for the MHD patients compared to 0.11 ± 0.05 mg/kg/min for the controls (p = 0.009). The LDR level was correlated with whole body protein synthesis (r = 0.25; p = 0.08), with whole body protein breakdown (r = −0.38 p = 0.01) and net protein balance (r = 0.85; p < 0.001) in the overall study population. Correlations remained significant in subgroup analysis. The GDR derived by HEGC and LDR correlated well in the controls (r = 0.79, p < 0.001), but less so in the MHD patients (r = 0.58, p < 0.001). CONCLUSIONS: Leucine disposal rate reliably measures amino acid utilization in MHD patients and controls in response to high dose insulin.
1000 Sacherschließung
lokal Leucine disposal rate
lokal Maintenance hemodialysis
lokal Insulin resistance
lokal Protein energy wasting
lokal Glucose disposal rate
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/creator/RGVubnksIEdlcmFsZCBCLg==|https://frl.publisso.de/adhoc/creator/RGVnZXIsIFNlcnBpbCBNLg==|https://frl.publisso.de/adhoc/creator/Q2hlbiwgR3Vhbmh1YQ==|https://frl.publisso.de/adhoc/creator/QmlhbiwgQWlodWE=|https://frl.publisso.de/adhoc/creator/U2hhLCBGZW5n|https://frl.publisso.de/adhoc/creator/Qm9va2VyLCBDaW5keQ==|https://frl.publisso.de/adhoc/creator/S2VzbGVyLCBKYWNseW4gVC4=|https://frl.publisso.de/adhoc/creator/RGF2aWQsIFN0aHV0aGk=|https://frl.publisso.de/adhoc/creator/RWxsaXMsIENoYXJsZXMgRC4=|https://frl.publisso.de/adhoc/creator/SWtpemxlciwgVC4gQWxw
1000 Label
1000 Förderer
  1. U.S. Department of Veterans Affairs |
  2. National Center for Advancing Translational Sciences |
  3. Vanderbilt Diabetes Research and Training Center |
  4. National Institute of Diabetes and Digestive and Kidney Diseases |
  5. National Institute of Environmental Health Sciences |
  6. American Heart Association |
1000 Fördernummer
  1. 1I01CX000414
  2. UL1TR000445
  3. P30 DK020593
  4. P30 DK079341; T32 DK007569; K24 DK62849
  5. P30 ES000267
  6. -
1000 Förderprogramm
  1. -
  2. Clinical Translational Science Award
  3. -
  4. Vanderbilt O’Brien Mouse Kidney Center
  5. Vanderbilt Center in Molecular Toxicology
  6. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer U.S. Department of Veterans Affairs |
    1000 Förderprogramm -
    1000 Fördernummer 1I01CX000414
  2. 1000 joinedFunding-child
    1000 Förderer National Center for Advancing Translational Sciences |
    1000 Förderprogramm Clinical Translational Science Award
    1000 Fördernummer UL1TR000445
  3. 1000 joinedFunding-child
    1000 Förderer Vanderbilt Diabetes Research and Training Center |
    1000 Förderprogramm -
    1000 Fördernummer P30 DK020593
  4. 1000 joinedFunding-child
    1000 Förderer National Institute of Diabetes and Digestive and Kidney Diseases |
    1000 Förderprogramm Vanderbilt O’Brien Mouse Kidney Center
    1000 Fördernummer P30 DK079341; T32 DK007569; K24 DK62849
  5. 1000 joinedFunding-child
    1000 Förderer National Institute of Environmental Health Sciences |
    1000 Förderprogramm Vanderbilt Center in Molecular Toxicology
    1000 Fördernummer P30 ES000267
  6. 1000 joinedFunding-child
    1000 Förderer American Heart Association |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6411342.rdf
1000 Erstellt am 2018-11-22T12:30:04.597+0100
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1000 Zuletzt bearbeitet Fri Oct 08 17:07:17 CEST 2021
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1000 Vgl. frl:6411342
1000 Oai Id
  1. oai:frl.publisso.de:frl:6411342 |
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