e58
Correspondence
Dr Januzzi raises several interesting points regarding galectin-3 lev-
els after acute myocardial infarction. We found that galectin-3 increased
modestly but significantly (by ≈12%) between baseline (≈day 2) and 24
weeks.
1
Serial measurement of galectin-3 in healthy volunteers suggests
a reference change value of the order of 61% for galectin-3.
2
A recent
analysis of serial galectin-3 levels in 2 chronic heart failure trials sug-
gests, however, that a rise in galectin-3 of only ≥15% for 3 to 6 months
confers an increased risk of adverse outcomes.
3
It is perhaps possible
that smaller fluctuations of galectin-3 in the setting of profibrotic disease
states (such as acute myocardial infarction and chronic heart failure) are
pathophysiologically relevant. It is also feasible that plasma galectin-3
concentrations may not correlate directly with tissue levels; myocardial
galectin-3 content may be significantly in excess of circulating galectin-3.
We found that galectin-3 concentrations increased significantly (by
≈14%) in patients treated with eplerenone in our study. Further analy-
sis, as requested by Dr Januzzi, revealed no effect of eplerenone on
remodeling, whether baseline galectin-3 levels were low (<median)
or high (≥median). We agree that the rise in galectin-3 in eplerenone-
treated patients is at odds with conventional wisdom, which would
predict a decrease in galectin-3 with the use of a mineralocorticoid
receptor antagonist. Although this may simply relate to our trial
design—it was powered for cardiac MRI end points—a rise in galec-
tin-3 in those receiving mineralocorticoid receptor antagonists was also
seen in patients enrolled in the Controlled Rosuvastatin Multinational
Trial in Heart Failure (CORONA). Whether the antifibrotic effects of
mineralocorticoid receptor antagonists trigger feedback upregulation
of galectin-3 (and if so, by what mechanism), whether galectin-3 rises
in response to mineralocorticoid receptor antagonist–induced renal
dysfunction, or whether there is any relationship at all between galec-
tin-3 and the aldosterone pathway remains unclear and is the focus
of ongoing study. Galectin-3 is undoubtedly a risk marker in patients
with heart failure; whether it represents a modifiable therapeutic target
to improve outcome and reduce remodeling in both acute myocardial
infarction and chronic heart failure remains unknown.
Disclosures
None.
Robin A.P. Weir, MD
Cardiology Department
Hairmyres Hospital
Lanarkshire, Scotland, UK
Colin J. Petrie, MBChB
C. Aengus Murphy, MD
Cardiology Department
Monklands Hospital
Lanarkshire, Scotland, UK
Suzanne Clements, BSc
Cardiology Department
Hairmyres Hospital
Lanarkshire, Scotland, UK
Tracey Steedman, BSc
Cardiology Department
Western Infirmary
Glasgow, Scotland, UK
Ashley M. Miller, PhD
Iain B. McInnes, PhD
Division of Immunology, Infection, and Inflammation
Glasgow Biomedical Research Centre
University of Glasgow
Scotland, UK
Iain B. Squire, MD
Leong L. Ng, MD
Department of Cardiovascular Sciences
Leicester Royal Infirmary
Leicester, UK and
Leicester National Institute for Health Research Cardiovascular
Biomedical Research Unit
Leicester, UK
Henry J. Dargie, MBChB
Cardiology Department
Western Infirmary
Glasgow, Scotland, UK
John J.V. McMurray, MD
BHF Cardiovascular Research Centre
University of Glasgow
Scotland, UK
References
1. Weir RA, Petrie CJ, Murphy CA, Clements S, Steedman T, Miller AM,
McInnes IB, Squire IB, Ng LL, Dargie HJ, McMurray JJ. Galectin-3 and
cardiac function in survivors of acute myocardial infarction. Circ Heart
Fail. 2013;6:492–498.
2. Wu AH, Wians F, Jaffe A. Biological variation of galectin-3 and soluble
ST2 for chronic heart failure: Implications on interpretation of test results.
Am Heart J. 2013; 165: 995–999.
3. van der Velde AR, Gullestad L, Ueland T, Aukrust P, Guo Y, Adourian A,
Muntendam P, van Veldhuisen DJ, de Boer RA. Prognostic value of changes
in galectin-3 levels over time in patients with heart failure. Circ Heart Fail.
2013;6:219–226.
(Circ Heart Fail. 2013;6:e58.)
© 2013 American Heart Association, Inc.
Circ Heart Fail is available at http://circheartfailure.ahajournals.org DOI: 10.1161/CIRCHEARTFAILURE.113.000382
Response to Letter Regarding Article, “Galectin-3
and Cardiac Function in Survivors of Acute
Myocardial Infarction”
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