Galectin-3 and Risk of Heart Failure and Death in Blacks and Whites.

Pubmed ID: 27178204

Pubmed Central ID: PMC4889181

Journal: Journal of the American Heart Association

Publication Date: May 13, 2016

Affiliation: Department of Epidemiology and the Welch Center for Prevention, Epidemiology and Clinical Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD eselvin@jhu.edu.

MeSH Terms: Humans, Male, Female, Aged, Cohort Studies, Middle Aged, Proportional Hazards Models, Heart Failure, Cause of Death, Prognosis, Incidence, Mortality, Blood Proteins, Galectin 3, White People, Black or African American, Galectins

Grants: K24 DK106414

Authors: Ballantyne CM, Selvin E, McEvoy JW, Blumenthal RS, Chen Y, Halushka MK, Christenson E, Christenson RH

Cite As: McEvoy JW, Chen Y, Halushka MK, Christenson E, Ballantyne CM, Blumenthal RS, Christenson RH, Selvin E. Galectin-3 and Risk of Heart Failure and Death in Blacks and Whites. J Am Heart Assoc 2016 May 13;5. (5).

Studies:

Abstract

BACKGROUND: The association between galectin-3 and heart failure (HF) or death is well established for white, but not for black, adults. METHODS AND RESULTS: Galectin-3 was measured in 1809 participants (1375 white, 434 black), enrolled in a substudy of the Atherosclerosis Risk in Communities (ARIC) observational cohort during 2004-2005. We used Cox proportional hazard models to estimate the adjusted association between galectin-3 and outcomes. Analyses were conducted overall and by race category. Median (interquartile range) galectin-3 levels were 13.4 (11.2-16.4) and 14.8 (12-17.6) ng/mL, in white and black participants, respectively. In the sample overall, galectin-3 was not independently associated with HF or death over a maximum of 7.9 years. However, in race-stratified analyses, galectin-3 was independently associated with a composite of HF or death among whites (eg, hazard ratio 2.2, 95% CI 1.2-3.9, comparing Q4 versus Q1); but not among blacks (hazard ratio of 0.8 [0.4-1.8] for Q4 versus Q1, race interaction P=0.03). Associations between galectin-3 and both outcomes analyzed individually also demonstrated similar racial differences. Furthermore, results were qualitatively similar with galectin-3 modeled as a continuous exposure. In addition, galectin-3 improved discrimination for the composite of HF or death among whites (increase in Harrell's C statistic from 0.729 to 0.735 [difference of +0.006], P=0.049), but not among blacks (0.696 to 0.695 [difference of -0.001], P=0.814). CONCLUSIONS: In contrast to whites, galectin-3 may have limited prognostic utility for predicting HF and death in blacks. While our results require replication, they could reflect racial differences in the processes by which galectin-3 mediates disease.