PMID- 22886030 OWN - NLM STAT- MEDLINE DCOM- 20130726 LR - 20220318 IS - 1861-0692 (Electronic) IS - 1861-0684 (Linking) VI - 102 IP - 2 DP - 2013 Feb TI - Galectin-3 is an independent marker for ventricular remodeling and mortality in patients with chronic heart failure. PG - 103-10 LID - 10.1007/s00392-012-0500-y [doi] AB - BACKGROUND: Galectin-3 (Gal-3) is a recently discovered marker for myocardial fibrosis and elevated levels are associated with an impaired outcome after short-term follow-up in heart failure (HF) patients. However, whether Gal-3 is related to cardiac remodeling and outcome after long-term follow-up is unknown. Therefore, we determined the utility of Gal-3 as a novel biomarker for left ventricular remodeling and long-term outcome in patients with severe chronic HF. METHODS AND RESULTS: A total of 240 HF patients with New York Heart Association (NYHA) Class III and IV were included. Patients were followed for 8.7 +/- 1 years, had a mean age of 71 +/- 0.6 years and 73 % of the study population was male. Circulating levels of NT-proBNP and Gal-3 were measured. Serial echocardiography was performed at baseline and at 3 months. At baseline median left ventricular end-diastolic volume (LVEDV) was 267 mL [interquartile range 232-322]. Patients were divided into three groups according to the change in LVEDV. Patients in whom the LVEDV decreased over time had significant lower levels of Gal-3 at entry compared to patients in whom the LVEDV was stable or increased (14.7 vs. 17.9 vs. 19.0 ng/mL; p = 0.004 for trend), whereas no significant differences were seen in levels of NT-proBNP (p = 0.33). Multivariate linear regression analyses revealed that Gal-3 levels were positively correlated to change in LVEDV (p = 0.007). In addition, Gal-3 was a significant predictor of mortality after long-term follow-up (p = 0.001). CONCLUSION: Gal-3 is associated with left ventricular remodeling determined by serial echocardiography and predicts long-term mortality in patients with severe chronic HF. FAU - Lok, Dirk J AU - Lok DJ AD - Deventer Hospital, Nico Bolkesteinlaan 75, 7415 CM, Deventer, The Netherlands. lokd@dz.nl FAU - Lok, Sjoukje I AU - Lok SI FAU - Bruggink-Andre de la Porte, Pieta W AU - Bruggink-Andre de la Porte PW FAU - Badings, Erik AU - Badings E FAU - Lipsic, Eric AU - Lipsic E FAU - van Wijngaarden, Jan AU - van Wijngaarden J FAU - de Boer, Rudolf A AU - de Boer RA FAU - van Veldhuisen, Dirk J AU - van Veldhuisen DJ FAU - van der Meer, Peter AU - van der Meer P LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20120812 PL - Germany TA - Clin Res Cardiol JT - Clinical research in cardiology : official journal of the German Cardiac Society JID - 101264123 RN - 0 (Biomarkers) RN - 0 (Galectin 3) RN - 0 (Peptide Fragments) RN - 0 (pro-brain natriuretic peptide (1-76)) RN - 114471-18-0 (Natriuretic Peptide, Brain) SB - IM MH - Aged MH - Biomarkers/blood MH - Chronic Disease MH - Female MH - Galectin 3/*blood MH - Heart Failure/*blood/diagnostic imaging/*mortality/physiopathology MH - Humans MH - Kaplan-Meier Estimate MH - Linear Models MH - Male MH - Multivariate Analysis MH - Natriuretic Peptide, Brain/blood MH - Peptide Fragments/blood MH - Predictive Value of Tests MH - Prognosis MH - Proportional Hazards Models MH - Risk Assessment MH - Risk Factors MH - Severity of Illness Index MH - Stroke Volume MH - Time Factors MH - Ultrasonography MH - *Ventricular Function, Left MH - *Ventricular Remodeling EDAT- 2012/08/14 06:00 MHDA- 2013/07/28 06:00 CRDT- 2012/08/14 06:00 PHST- 2012/04/27 00:00 [received] PHST- 2012/07/24 00:00 [accepted] PHST- 2012/08/14 06:00 [entrez] PHST- 2012/08/14 06:00 [pubmed] PHST- 2013/07/28 06:00 [medline] AID - 10.1007/s00392-012-0500-y [doi] PST - ppublish SO - Clin Res Cardiol. 2013 Feb;102(2):103-10. doi: 10.1007/s00392-012-0500-y. Epub 2012 Aug 12.