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Development and validation of a coronary risk prediction model for older U.S. and European persons in the Cardiovascular Health Study and the Rotterdam Study.

TitleDevelopment and validation of a coronary risk prediction model for older U.S. and European persons in the Cardiovascular Health Study and the Rotterdam Study.
Publication TypeJournal Article
Year of Publication2012
AuthorsKoller, MT, Leening, MJG, Wolbers, M, Steyerberg, EW, Hunink, MGMyriam, Schoop, R, Hofman, A, Bucher, HC, Psaty, BM, Lloyd-Jones, DM, Witteman, JCM
JournalAnn Intern Med
Volume157
Issue6
Pagination389-97
Date Published2012 Sep 18
ISSN1539-3704
KeywordsAged, Aged, 80 and over, Algorithms, Cause of Death, Coronary Disease, European Continental Ancestry Group, Female, Humans, Incidence, Male, Models, Statistical, Multivariate Analysis, Netherlands, Prospective Studies, Risk Assessment, Risk Factors, United States
Abstract<p><b>BACKGROUND: </b>Risk scores for prediction of coronary heart disease (CHD) in older adults are needed.</p><p><b>OBJECTIVE: </b>To develop a sex-specific CHD risk prediction model for older adults that accounts for competing risks for death.</p><p><b>DESIGN: </b>2 observational cohort studies, using data from 4946 participants in the Cardiovascular Health Study (CHS) and 4303 participants in the Rotterdam Study (RS).</p><p><b>SETTING: </b>Community settings in the United States (CHS) and Rotterdam, the Netherlands (RS).</p><p><b>PARTICIPANTS: </b>Persons aged 65 years or older who were free of cardiovascular disease.</p><p><b>MEASUREMENTS: </b>A composite of nonfatal myocardial infarction and coronary death.</p><p><b>RESULTS: </b>During a median follow-up of 16.5 and 14.9 years, 1166 CHS and 698 RS participants had CHD events, respectively. Deaths from noncoronary causes largely exceeded the number of CHD events, complicating accurate CHD risk predictions. The prediction model had moderate ability to discriminate between events and nonevents (c-statistic, 0.63 in both U.S. and European men and 0.67 and 0.68 in U.S. and European women). The model was well-calibrated; predicted risks were in good agreement with observed risks. Compared with the Framingham point scores, the prediction model classified elderly U.S. persons into higher risk categories but elderly European persons into lower risk categories. Differences in classification accuracy were not consistent and depended on cohort and sex. Adding newer cardiovascular risk markers to the model did not substantially improve performance.</p><p><b>LIMITATION: </b>The model may be less applicable in nonwhite populations, and the comparison Framingham model was not designed for adults older than 79 years.</p><p><b>CONCLUSION: </b>A CHD risk prediction model that accounts for deaths from noncoronary causes among older adults provided well-calibrated risk estimates but was not substantially more accurate than Framingham point scores. Moreover, adding newer risk markers did not improve accuracy. These findings emphasize the difficulties of predicting CHD risk in elderly persons and the need to improve these predictions.</p><p><b>PRIMARY FUNDING SOURCE: </b>National Heart, Lung, and Blood Institute; National Institute of Neurological Disorders and Stroke; The Netherlands Organisation for Scientific Research; and the Netherlands Organisation for Health Research and Development.</p>
DOI10.7326/0003-4819-157-6-201209180-00002
Alternate JournalAnn. Intern. Med.
PubMed ID22986376
PubMed Central IDPMC3644640
Grant ListN01-HC-80007 / HC / NHLBI NIH HHS / United States
U01 HL080295 / HL / NHLBI NIH HHS / United States
N01 HC015103 / HC / NHLBI NIH HHS / United States
N01HC55222 / HL / NHLBI NIH HHS / United States
N01-HC-85086 / HC / NHLBI NIH HHS / United States
N01HC85086 / HL / NHLBI NIH HHS / United States
N01 HC-55222 / HC / NHLBI NIH HHS / United States
N01-HC-75150 / HC / NHLBI NIH HHS / United States
R01 HL080295 / HL / NHLBI NIH HHS / United States
N01HC75150 / HL / NHLBI NIH HHS / United States
N01-HC-85079 / HC / NHLBI NIH HHS / United States
N01HC85079 / HL / NHLBI NIH HHS / United States
N01 HC045133 / HC / NHLBI NIH HHS / United States
/ / Wellcome Trust / United Kingdom
N01 HC035129 / HC / NHLBI NIH HHS / United States