Usefulness of Myeloperoxidase Levels in Healthy Elderly Subjects to Predict Risk of Developing Heart Failure
Increased systemic myeloperoxidase (MPO) has been associated with both the presence and severity of heart failure (HF). This study tested the hypothesis that increased systemic MPO in apparently healthy elderly subjects may predict increased risk of developing HF. Systemic MPO was measured in all available samples from the 1992 to 1993 visit of the Cardiovascular Health Study (CHS). After excluding subjects without available blood samples or with a history of prevalent HF, myocardial infarction (MI), or stroke, 3,733 subjects were included. A total of 569 subjects developed incident HF during 7.2 ± 2.3 years of follow-up. Patients in the highest MPO quartile (>432 pmol/L) showed higher risk of developing incident HF after adjusting for MI, age, gender, systolic blood pressure, smoking, low-density lipoprotein cholesterol, diabetes mellitus, and any subclinical cardiovascular disease (hazard ratio 1.34, 95% confidence interval 1.06 to 1.72, p = 0.013). However, the relation was more apparent after censoring subjects with incident MI before incident HF, even when adjusted for C-reactive protein and cystatin C (hazard ratio 1.46, 95% confidence interval 1.08 to 1.97, p = 0.02). Interestingly, stratified analyses showed that the relation between increased MPO and HF risk was stronger in subjects without traditional cardiovascular risk factors (≤75 years old, systolic blood pressure ≤136 mm Hg, no subclinical cardiovascular disease, and no diabetes mellitus). In conclusion, an independent association between increased MPO and the development of HF in apparently healthy elderly subjects was observed, particularly beyond MI and traditional cardiac risk factors.
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This work was supported by Grants No. P01 HL076491-055328, HL077107-050004, and P01 HL087018-020001 from the National Institutes of Health, Bethesda, Maryland, and contracts previously supporting development of the Cardiovascular Health Study, including N01-HC-85079 through N01-HC-85086, N01-HC-35129, N01 HC-15103, N01 HC-55222, and U01 HL080295 from the National Heart, Lung, and Blood Institute, Bethesda, Maryland, with additional contribution from the National Institute of Neurological Disorders and Stroke, Bethesda, Maryland. Drs. Hazen and Tang were supported by Grant No. 1UL1RR024989 from the National Institutes of Health. Dr. Tang reports having received research grant support and honorarium from Abbott Laboratories. Dr. Hazen is named as co-inventor on pending and issued patents filed by the Cleveland Clinic that relate to the use of biomarkers in inflammatory and cardiovascular disease; reports he is the scientific founder of PrognostiX Inc.; has received speaking honoraria from Pfizer, AstraZeneca, Merck, Merck Schering Plough, BioSite, Lilly, Wyeth, and Abbott; has received research grant support from Abbott Diagnostics, Pfizer, Merck, PrognostiX Inc., Hawaii Biotech, ArgiNOx, Sanofi, and Takeda; and has received consulting fees from Abbott Laboratories, Pfizer, PrognostiX Inc., Wyeth, BioPhysical, and AstraZeneca.
PII: S0002-9149(09)00120-9
doi:10.1016/j.amjcard.2009.01.026
© 2009 Elsevier Inc. All rights reserved.
