Title | Association of monocyte myeloperoxidase with incident cardiovascular disease: The Atherosclerosis Risk in Communities Study. |
Publication Type | Journal Article |
Year of Publication | 2018 |
Authors | Oyenuga AO, Couper DJ, Matsushita K, Boerwinkle E |
Secondary Authors | Folsom AR |
Journal | PLoS One |
Volume | 13 |
Issue | 10 |
Pagination | e0205310 |
Date Published | 2018 |
ISSN | 1932-6203 |
Keywords | Aged, Atherosclerosis, Coronary Disease, Female, Flow Cytometry, Heart Failure, Humans, Male, Middle Aged, Monocytes, Peroxidase, Risk Factors |
Abstract | Myeloperoxidase (MPO) is a heme-containing peroxidase found in azurophilic granules of neutrophils and monocytes. Epidemiological studies have reported greater plasma MPO concentration to be associated with increased incidence of several cardiovascular diseases (CVD), but the association of intracellular monocyte MPO (mMPO) with CVD is unclear. The prospective population-based Atherosclerosis Risk in Communities (ARIC) cohort study measured mMPO using flow cytometry in 1,465 participants. The association of mMPO with incident cardiovascular disease (CVD, comprising incident coronary heart disease (CHD), heart failure, stroke, peripheral artery disease, and cardiovascular mortality) was examined over a median 9.6 years of follow-up (n = 290 CVD events). There was no statistically significant association between mMPO and all incident CVD events in either age, sex, and race-adjusted proportional hazards models (HR (95% CI) across tertiles of mMPO: 1, 1.09 (0.76, 1.57), and 0.78 (0.52, 1.15), P-trend = 0.21) or adjusted for other major CVD risk factors (HR (95% CI): 1, 1.17 (0.81, 1.69), and 0.87 (0.58, 1.29), P-trend = 0.50). There also was no association between mMPO tertiles and incident CHD, heart failure, or all-cause mortality, examined separately. In conclusion, intracellular monocyte myeloperoxidase was not associated with incident cardiovascular disease in this prospective population-based study. |
DOI | 10.1371/journal.pone.0205310 |
Alternate Journal | PLoS One |
PubMed ID | 30300402 |
PubMed Central ID | PMC6177167 |
Grant List | HHSN268201700001I / HL / NHLBI NIH HHS / United States HHSN268201700002I / HL / NHLBI NIH HHS / United States HHSN268201700003I / HL / NHLBI NIH HHS / United States HHSN268201700004I / HL / NHLBI NIH HHS / United States HHSN268201700005I / HL / NHLBI NIH HHS / United States U01 HL075572 / HL / NHLBI NIH HHS / United States |