PMID- 17825714 OWN - NLM STAT- MEDLINE DCOM- 20070928 LR - 20220330 IS - 1558-3597 (Electronic) IS - 0735-1097 (Linking) VI - 50 IP - 11 DP - 2007 Sep 11 TI - Prognostic utility of growth differentiation factor-15 in patients with chronic heart failure. PG - 1054-60 AB - OBJECTIVES: We explored the prognostic utility of growth differentiation factor (GDF)-15 in patients with chronic heart failure (CHF). BACKGROUND: Growth differentiation factor-15 is a stress-responsive member of the transforming growth factor-beta cytokine superfamily. It has recently been observed that patients with CHF have increased circulating levels of GDF-15. The relations of GDF-15 to other biomarkers and to mortality in CHF have never been studied. METHODS: Circulating levels of GDF-15 were determined by immunoradiometric assay in 455 patients with CHF with a median left ventricular ejection fraction (LVEF) of 32% (interquartile range 25% to 39%). RESULTS: The median GDF-15 level was 1,949 ng/l (interquartile range 1,194 to 3,577); 74.9% of the patients presented with GDF-15 levels >1,200 ng/l, the upper limit of normal in healthy elderly individuals. The GDF-15 levels were closely related to New York Heart Association (NYHA) functional class and to amino-terminal pro-B-type natriuretic peptide (NT-proBNP). The risk of death during follow-up increased with increasing quartiles of GDF-15. Mortality rates at 48 months were 10.0%, 9.4%, 33.4%, and 56.2% in the respective quartiles (p < 0.001). After adjustment for clinical variables and established biomarkers of adverse prognosis, including NT-proBNP, renal dysfunction, anemia, and hyperuricemia, GDF-15 remained an independent predictor of mortality (adjusted hazard ratio for 1 U in the Ln scale 2.26; 95% confidence interval 1.52 to 3.37; p < 0.001). Growth differentiation factor 15 provided prognostic information in clinically relevant patient subgroups (defined according to age, body mass index, heart failure etiology, concomitant medical therapy, renal function, and the levels of hemoglobin and uric acid) and added prognostic information to NYHA functional class, LVEF, and NT-proBNP. CONCLUSIONS: Growth differentiation factor 15 is a new biomarker of the risk of death in patients with CHF that provides prognostic information beyond established clinical and biochemical markers. FAU - Kempf, Tibor AU - Kempf T AD - Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany. FAU - von Haehling, Stephan AU - von Haehling S FAU - Peter, Timo AU - Peter T FAU - Allhoff, Tim AU - Allhoff T FAU - Cicoira, Mariantonietta AU - Cicoira M FAU - Doehner, Wolfram AU - Doehner W FAU - Ponikowski, Piotr AU - Ponikowski P FAU - Filippatos, Gerasimos S AU - Filippatos GS FAU - Rozentryt, Piotr AU - Rozentryt P FAU - Drexler, Helmut AU - Drexler H FAU - Anker, Stefan D AU - Anker SD FAU - Wollert, Kai C AU - Wollert KC LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20070824 PL - United States TA - J Am Coll Cardiol JT - Journal of the American College of Cardiology JID - 8301365 RN - 0 (Biomarkers) RN - 0 (Bone Morphogenetic Proteins) RN - 0 (GDF15 protein, human) RN - 0 (Growth Differentiation Factor 15) SB - IM CIN - J Am Coll Cardiol. 2007 Sep 11;50(11):1061-3. PMID: 17825715 MH - Aged MH - Biomarkers/blood MH - Bone Morphogenetic Proteins/*blood MH - Cohort Studies MH - Female MH - Growth Differentiation Factor 15 MH - Heart Failure/*blood/diagnosis/*mortality MH - Humans MH - Male MH - Middle Aged MH - Predictive Value of Tests MH - Prognosis MH - Risk Factors MH - Survival Rate EDAT- 2007/09/11 09:00 MHDA- 2007/09/29 09:00 CRDT- 2007/09/11 09:00 PHST- 2007/01/09 00:00 [received] PHST- 2007/03/02 00:00 [revised] PHST- 2007/04/01 00:00 [accepted] PHST- 2007/09/11 09:00 [pubmed] PHST- 2007/09/29 09:00 [medline] PHST- 2007/09/11 09:00 [entrez] AID - S0735-1097(07)02005-0 [pii] AID - 10.1016/j.jacc.2007.04.091 [doi] PST - ppublish SO - J Am Coll Cardiol. 2007 Sep 11;50(11):1054-60. doi: 10.1016/j.jacc.2007.04.091. Epub 2007 Aug 24.