Haptoglobin Polymorphism Predicts 30-Day Mortality and Heart Failure in Patients With Diabetes and Acute Myocardial Infarction
- Mahmoud Suleiman1,
- Doron Aronson1,
- Rabea Asleh2,
- Michael R. Kapeliovich1,
- Ariel Roguin1,
- Simcha R. Meisel1,
- Michael Shochat1,
- Abeer Sulieman2,
- Shimon A. Reisner1,
- Walter Markiewicz1,
- Haim Hammerman1,
- Rachel Lotan2,
- Nina S. Levy2 and
- Andrew P. Levy2
- 1Department of Cardiology, Rambam Medical Center, Haifa, Israel
- 2Technion Faculty of Medicine, Haifa, Israel
- Address correspondence and reprint requests to Andrew P. Levy MD, PhD, FACC, Technion Faculty of Medicine, Rappaport Building, Bat Galim, Haifa, 31096, Israel. E-mail: alevy{at}tx.technion.ac.il
Abstract
Patients with diabetes presenting with acute myocardial infarction (AMI) have an increased rate of death and heart failure. Patients with diabetes homozygous for the haptoglobin (Hp) 1 allele (Hp 1-1) develop fewer vascular complications. We tested the hypothesis that Hp type is related to the outcome of patients with diabetes presenting with AMI. We prospectively assessed the relationship between Hp type and 30-day mortality and heart failure in 1,437 patients with AMI (506 with diabetes). Multivariate logistic regression identified a significant interaction between Hp type and diabetes status on these outcome measures. Hp type was not related to outcome among patients without diabetes. In contrast, Hp 1-1 was associated with a strong protective effect with regard to the primary end point of death (OR 0.14, P = 0.015) and for death and heart failure (OR 0.35; 95% CI 0.15–0.86, P = 0.018) among patients with diabetes. Finally, among patients with diabetes, Hp 1-1 was associated with smaller infarct size. This study demonstrates that in patients with diabetes and AMI, the Hp type is an important determinant of clinical outcome and infarct size.
Footnotes
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M.S. and D.A. contributed equally to this study.
A.P.L. has served on the advisory board of, holds stock in, and has received honoraria from Haptoguard.
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- Accepted May 23, 2005.
- Received February 20, 2005.
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