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Submitted on June 17, 2008
From the UT Southwestern Medical Center, Department of Medicine (J.D.B.), Dallas, Tex; Northwestern University, Departments of Preventive Medicine (K.L., D.M.L.-J., C.C.) and Medicine (K.L., D.M.L.-J.), Chicago, Ill; University of Minnesota, Division of Epidemiology and Community Health, Minneapolis (A.R.F.); University of Alabama at Birmingham, Department of Preventive Medicine (C.E.L.); Wake Forest University School of Medicine, Division of Public Health Sciences and Department of Internal Medicine, Section of Cardiology, Winston-Salem, NC (J.J.C.); Tufts University School of Medicine, Department of Radiology, Boston, Mass (J.F.P., D.H.O.); Departments of Medicine and Epidemiology, Columbia University, New York, NY (S. Shea); and Kaiser Permanente Northern California, Oakland (S. Sidney). * To whom correspondence should be addressed. E-mail: jarett.berry{at}utsouthwestern.edu.
Background—We hypothesized that individuals with low 10-year but high lifetime cardiovascular disease risk would have a greater burden of subclinical atherosclerosis than those with low 10-year but low lifetime risk. Methods and Results—We included 2988 individuals Conclusions—Individuals with low 10-year but high lifetime risk have a greater subclinical disease burden and greater incidence of atherosclerotic progression compared with individuals with low 10-year and low lifetime risk, even at younger ages.
Accepted on October 14, 2008
Prevalence and Progression of Subclinical Atherosclerosis in Younger Adults With Low Short-Term but High Lifetime Estimated Risk For Cardiovascular Disease. The Coronary Artery Risk Development in Young Adults Study and Multi-Ethnic Study of Atherosclerosis
Jarett D. Berry MD, MS*,
50 years of age at examination year 15 from the Coronary Artery Risk Development in Young Adults (CARDIA) study and 1076 individuals
50 of age at study entry from the Multi-Ethnic Study of Atherosclerosis (MESA). The 10-year risk and lifetime risk for cardiovascular disease were estimated for each participant, permitting stratification into 3 groups: low 10-year (<10%)/low lifetime (<39%) risk, low 10-year (<10%)/high lifetime risk (
39%), and high 10-year risk (
10%) or diagnosed diabetes mellitus. Baseline levels and change in levels of subclinical atherosclerosis (coronary artery calcium or carotid intima-media thickness) were compared across risk strata. Among participants with low 10-year risk (91% of all participants) in CARDIA, those with a high lifetime risk compared with low lifetime risk had significantly greater common (0.83 versus 0.80 mm in men; 0.79 versus 0.75 mm in women) and internal (0.85 versus 0.80 mm in men; 0.80 versus 0.76 mm in women) carotid intima-media thickness, higher coronary artery calcium prevalence (16.6% versus 9.8% in men; 7.1% versus 2.3% in women), and significantly greater incidence of coronary artery calcium progression (22.3% versus 15.4% in men; 8.7% versus 5.3% in women). Similar results were observed in MESA.
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