BACKGROUND: Glucagon-like peptide 1 (GLP-1) is an incretin hormone, which stimulates glucosedependent insulin secretion from the pancreas and holds immune-regulatory properties. A marked increase of GLP-1 has been found in critically ill patients. This study was performed to elucidate the underlying mechanism and evaluate its prognostic value. METHODS: GLP-1 plasma levels were determined in 3 different patient cohorts: 1) critically ill patients admitted to our intensive care unit (n = 215); 2) patients with chronic kidney disease on hemodialysis (n = 173); and 3) a control group (no kidney disease, no acute inflammation, n = 105). In vitro experiments were performed to evaluate GLP-1 secretion in response to human serum samples from the above-described cohorts. RESULTS: Critically ill patients presented with 6.35-fold higher GLP-1 plasma level in comparison with the control group. There was a significant correlation of GLP-1 levels with markers for the severity of inflammation, but also kidney function. Patients with end-stage renal disease displayed 4.46-fold higher GLP-1 concentrations in comparison with the control group. In vitro experiments revealed a strong GLP-1inducing potential of serum from critically ill patients, while serum from hemodialysis patients only modestly increased GLP-1 secretion. GLP-1 levels independently predicted mortality in critically ill patients and patients with end-stage renal disease. CONCLUSIONS: Chronic and acute inflammatory processes like sepsis or chronic kidney disease increase circulating GLP-1 levels. This most likely reflects a sum effect of increased GLP-1 secretion and decreased GLP-1 clearance. GLP-1 plasma levels independently predict the outcome of critically ill and end-stage renal disease patients. (C) 2017 Elsevier Inc. All rights reserved.
机构:
Wayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
Pinelli, Nicole R.
Jones, Mathew C.
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Johns Hopkins Univ Hosp, Dept Pharm, Baltimore, MD 21287 USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
Jones, Mathew C.
Monday, Lea M.
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Harper Univ Hosp, Dept Pharm, Detroit, MI USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
Monday, Lea M.
Smith, Zachary
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Henry Ford Hosp, Dept Pharm Serv, Detroit, MI 48202 USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
Smith, Zachary
Rhoney, Denise H.
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Wayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
机构:
Wayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
Pinelli, Nicole R.
Jones, Mathew C.
论文数: 0引用数: 0
h-index: 0
机构:
Johns Hopkins Univ Hosp, Dept Pharm, Baltimore, MD 21287 USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
Jones, Mathew C.
Monday, Lea M.
论文数: 0引用数: 0
h-index: 0
机构:
Harper Univ Hosp, Dept Pharm, Detroit, MI USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
Monday, Lea M.
Smith, Zachary
论文数: 0引用数: 0
h-index: 0
机构:
Henry Ford Hosp, Dept Pharm Serv, Detroit, MI 48202 USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
Smith, Zachary
Rhoney, Denise H.
论文数: 0引用数: 0
h-index: 0
机构:
Wayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USAWayne State Univ, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA