Each year more than 1,400,000 men and women in the United States (U.S.) experience an acute coronary event. Most of these coronary events, including coronary death, result from plaque rupture and thrombosis on non-critical coronary stenoses. However, mechanisms responsible for conversion of chronic coronary atherosclerosis to acute coronary events are not well understood. Lower extremity peripheral arterial disease (PAD) affects 8 million men and women in the U.S. Compared to those without PAD, men and women with PAD have an increased rate of coronary events. Our preliminary data from annually measured biomarkers in persons with PAD demonstrate that elevated levels of annually measured C-reactive protein (CRP), serum amyloid A (SAA), and D-dimer are more closely associated with near-term cardiovascular or all-cause mortality than later-term (remote) cardiovascular or all- cause mortality. Our preliminary data also demonstrate that greater annual increases in these biomarkers are associated with higher rates of cardiovascular mortality during the year after the increase. Based on our preliminary data, we hypothesize that among persons with PAD, biomarker levels are higher during time periods immediately preceding an acute coronary event compared to time periods not immediately preceding a coronary event. While our preliminary data from annually measured biomarkers in persons with PAD support this hypothesis, this phenomenon has not been definitively demonstrated.
Our aims will be tested in a cohort of 650 participants with PAD, followed prospectively for two years. Biomarkers we will study are CRP, SAA, and D-dimer. Biomarkers will be measured at baseline and every two months during follow-up. The primary aims of this study are as follows.
Specific Aim #1. Among participants with PAD who experience an acute coronary event during follow-up, we will determine whether biomarker levels measured immediately prior to the coronary event are higher than levels that do not immediately precede coronary events.
Specific Aim #2, Part 1. We will determine whether participants who experience a coronary event (cases) have higher biomarker levels at the visit immediately prior to the event than participants who have not experienced a coronary event (controls) at the time of the case event.
Specific Aim #2, Part 2. We will determine whether participants who experience a coronary event (cases) have a greater increase in biomarkers during the time period leading up to the event compared to participants who have not experienced a coronary event (controls). Results of this study are expected to provide important information about the pathophysiology of acute coronary events. This information is expected to lead to improved therapies, in subsequent studies, for prevention and treatment of acute coronary events.

Public Health Relevance

In the United States, more than 1,400,000 men and women suffer a heart attack or other similar coronary event each year. Mechanisms responsible for converting chronic, stable coronary atherosclerosis to an acute coronary event are not well understood. The purpose of this study is to determine whether levels of specific circulating biomarkers rapidly increase during the weeks immediately preceding coronary events in persons who are at high risk for coronary events. Findings may help clinicians identify patients who are at particularly high-risk for an impending heart attack. Results are also expected to elucidate specific triggers of acute coronary events.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL089619-03
Application #
8072699
Study Section
Cardiovascular and Sleep Epidemiology (CASE)
Program Officer
Fleg, Jerome
Project Start
2009-06-15
Project End
2013-05-31
Budget Start
2011-06-01
Budget End
2012-05-31
Support Year
3
Fiscal Year
2011
Total Cost
$709,640
Indirect Cost
Name
Northwestern University at Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Green, David; Tian, Lu; Greenland, Philip et al. (2017) Association of the von Willebrand Factor-ADAMTS13 Ratio With Incident Cardiovascular Events in Patients With Peripheral Arterial Disease. Clin Appl Thromb Hemost 23:807-813
McDermott, Mary M; Polonsky, Tamar S; Kibbe, Melina R et al. (2017) Racial differences in functional decline in peripheral artery disease and associations with socioeconomic status and education. J Vasc Surg 66:826-834
McDermott, Mary McGrae; Tian, Lu; Wunderink, Richard G et al. (2017) Pulmonary hospitalizations and ischemic heart disease events in patients with peripheral artery disease. Vasc Med 22:218-224
McDermott, Mary M; Guralnik, Jack M; Ferrucci, Luigi et al. (2016) Community walking speed, sedentary or lying down time, and mortality in peripheral artery disease. Vasc Med 21:120-9
McDermott, Mary McGrae; Liu, Kiang; Green, David et al. (2016) Changes in D-dimer and inflammatory biomarkers before ischemic events in patients with peripheral artery disease: The BRAVO Study. Vasc Med 21:12-20
White, Sarah H; McDermott, Mary M; Sufit, Robert L et al. (2016) Walking performance is positively correlated to calf muscle fiber size in peripheral artery disease subjects, but fibers show aberrant mitophagy: an observational study. J Transl Med 14:284
McDermott, Mary M; Greenland, Philip; Tian, Lu et al. (2015) Association of 6-Minute Walk Performance and Physical Activity With Incident Ischemic Heart Disease Events and Stroke in Peripheral Artery Disease. J Am Heart Assoc 4:
McDermott, Mary M; Greenland, Philip; Liu, Kiang et al. (2014) Vulnerable blood in high risk vascular patients: study design and methods. Contemp Clin Trials 38:121-9
Huang, Chiang-Ching; McDermott, Mary M; Liu, Kiang et al. (2013) Plasma metabolomic profiles predict near-term death among individuals with lower extremity peripheral arterial disease. J Vasc Surg 58:989-96.e1