Circulating retinol binding protein 4 in critically ill patients before specific treatment: prognostic impact and correlation with organ function, metabolism and inflammation

被引:34
作者
Koch, Alexander [1 ]
Weiskirchen, Ralf [2 ]
Sanson, Edouard [1 ]
Zimmermann, Henning W. [1 ]
Voigt, Sebastian [1 ]
Dueckers, Hanna [1 ]
Trautwein, Christian [1 ]
Tacke, Frank [1 ]
机构
[1] RWTH Univ Hosp Aachen, Dept Med 3, D-52074 Aachen, Germany
[2] RWTH Univ Hosp Aachen, Inst Clin Chem & Pathobiochem, D-52074 Aachen, Germany
来源
CRITICAL CARE | 2010年 / 14卷 / 05期
关键词
INTENSIVE INSULIN THERAPY; CHRONIC LIVER-DISEASE; HOSPITAL MORTALITY; GLUCOSE CONTROL; SERUM-LEVELS; VITAMIN-A; RESISTANCE; PLASMA; RETINOL-BINDING-PROTEIN-4; SEPSIS;
D O I
10.1186/cc9285
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Introduction: Hyperglycemia and insulin resistance are well-known features of critical illness and impact the mortality rate, especially in sepsis. Retinol binding protein 4 (RBP4) promotes insulin resistance in mice and is systemically elevated in patients with obesity and type 2 diabetes. We investigated the potential role of RBP4 in critically ill patients. Methods: We conducted a prospective single-center study of serum RBP4 concentrations in critically ill patients. One hundred twenty-three patients (85 with sepsis, 38 without sepsis) were studied at admission to a medical intensive care unit (ICU) before initiation of specific intensive care treatment measures and compared to 42 healthy nondiabetic controls. Clinical data, various laboratory parameters and metabolic and endocrine functions were assessed. Patients were followed for approximately 3 years. Results: Serum RBP4 was significantly reduced in ICU patients, independently of sepsis, as compared to healthy controls (P < 0.001). Patients with liver cirrhosis as the primary underlying diagnosis for ICU admission had significantly lower RBP4 levels as compared with other ICU patients. Accordingly, in all ICU patients, serum RBP4 closely correlated with liver function and increased with renal failure. No significant differences of serum RBP4 concentrations in septic patients with pulmonary or other origins of sepsis or nonseptic patients could be revealed. Acute phase proteins were inversely correlated with RBP4 in sepsis patients. RBP4 did not differ between patients with or without obesity or preexisting diabetes. However, serum RBP4 levels correlated with endogenous insulin secretion (C-peptide) and insulin resistance (HOMA index). Low serum RBP4 upon admission was an adverse predictor of short-term survival in the ICU, but was not associated with overall survival during long-term follow-up. Conclusions: Serum RBP4 concentrations are significantly reduced in critically ill patients. The strong associations with hepatic and renal function, insulin resistance and acute mortality collectively suggest a role of RBP4 in the pathogenesis of critical illness, possibly as a negative acute phase reactant, and allow a proposition as a potential novel biomarker for ICU patients.
引用
收藏
页数:11
相关论文
共 34 条
[1]   The adipocyte as an active participant in energy balance and metabolism [J].
Badman, Michael K. ;
Flier, Jeffrey S. .
GASTROENTEROLOGY, 2007, 132 (06) :2103-2115
[2]   Decreased hepatic RBP4 secretion is correlated with reduced hepatic glucose production but is not associated with insulin resistance in patients with liver cirrhosis [J].
Bahr, Matthias J. ;
Boeker, Klaus H. W. ;
Manns, Michael P. ;
Tietge, Uwe J. F. .
CLINICAL ENDOCRINOLOGY, 2009, 70 (01) :60-65
[3]   Insulin resistance in critically ill patients with acute renal failure [J].
Basi, S ;
Pupim, LB ;
Simmons, EM ;
Sezer, MT ;
Shyr, Y ;
Freedman, S ;
Chertow, GM ;
Mehta, RL ;
Paganini, E ;
Himmelfarb, J ;
Ikizler, TA .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2005, 289 (02) :F259-F264
[4]   Intensive insulin therapy and pentastarch resuscitation in severe sepsis [J].
Brunkhorst, Frank M. ;
Engel, Christoph ;
Bloos, Frank ;
Meier-Hellmann, Andreas ;
Ragaller, Max ;
Weiler, Norbert ;
Moerer, Onnen ;
Gruendling, Matthias ;
Oppert, Michael ;
Grond, Stefan ;
Olthoff, Derk ;
Jaschinski, Ulrich ;
John, Stefan ;
Rossaint, Rolf ;
Welte, Tobias ;
Schaefer, Martin ;
Kern, Peter ;
Kuhnt, Evelyn ;
Kiehntopf, Michael ;
Hartog, Christiane ;
Natanson, Charles ;
Loeffler, Markus ;
Reinhart, Konrad .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (02) :125-139
[5]   Plasma retinol-binding protein-4 concentrations are elevated in human subjects with impaired glucose tolerance and type 2 diabetes [J].
Cho, Young Min ;
Youn, Byung-Soo ;
Lee, Hyewon ;
Lee, Namseok ;
Min, Sung-Shik ;
Kwak, Soo Heon ;
Lee, Hong Kyu ;
Park, Kyong Soo .
DIABETES CARE, 2006, 29 (11) :2457-2461
[6]   Intensive blood glucose control in acute and prolonged critical illness: endogenous secretion contributes more to plasma insulin than exogenous insulin infusion [J].
Duska, Frantisek ;
Andel, Michal .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2008, 57 (05) :669-671
[7]   Glucose control and mortality in critically ill patients [J].
Finney, SJ ;
Zekveld, C ;
Elia, A ;
Evans, TW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (15) :2041-2047
[8]   Retinol-binding protein 4 and insulin resistance in lean, obese, and diabetic subjects [J].
Graham, Timothy E. ;
Yang, Qin ;
Blueher, Matthias ;
Hammarstedt, Ann ;
Ciaraldi, Theodore P. ;
Henry, Robert R. ;
Wason, Christopher J. ;
Oberbach, Andreas ;
Jansson, Per-Anders ;
Smith, Ulf ;
Kahn, Barbara B. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (24) :2552-2563
[9]   High C5a levels are associated with increased mortality in sepsis patients - No enhancing effect by actin-free Gc-globulin [J].
Gressner, Olav A. ;
Koch, Alexander ;
Sanson, Edouard ;
Trautwein, Christian ;
Tacke, Frank .
CLINICAL BIOCHEMISTRY, 2008, 41 (12) :974-980
[10]   Evidence That Kidney Function but Not Type 2 Diabetes Determines Retinol-Binding Protein 4 Serum Levels [J].
Henze, Andrea ;
Frey, Simone K. ;
Raila, Jens ;
Tepel, Martin ;
Scholze, Alexandra ;
Pfeiffer, Andreas F. H. ;
Weickert, Martin O. ;
Spranger, Joachim ;
Schweigert, Florian J. .
DIABETES, 2008, 57 (12) :3323-3326