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. 2008 Mar 15;371(9616):923-31.
doi: 10.1016/S0140-6736(08)60418-3.

Laboratory-based versus non-laboratory-based method for assessment of cardiovascular disease risk: the NHANES I Follow-up Study cohort

Affiliations

Laboratory-based versus non-laboratory-based method for assessment of cardiovascular disease risk: the NHANES I Follow-up Study cohort

Thomas A Gaziano et al. Lancet. .

Abstract

Background: Around 80% of all cardiovascular deaths occur in developing countries. Assessment of those patients at high risk is an important strategy for prevention. Since developing countries have limited resources for prevention strategies that require laboratory testing, we assessed if a risk prediction method that did not require any laboratory tests could be as accurate as one requiring laboratory information.

Methods: The National Health and Nutrition Examination Survey (NHANES) was a prospective cohort study of 14 407 US participants aged between 25-74 years at the time they were first examined (between 1971 and 1975). Our follow-up study population included participants with complete information on these surveys who did not report a history of cardiovascular disease (myocardial infarction, heart failure, stroke, angina) or cancer, yielding an analysis dataset N=6186. We compared how well either method could predict first-time fatal and non-fatal cardiovascular disease events in this cohort. For the laboratory-based model, which required blood testing, we used standard risk factors to assess risk of cardiovascular disease: age, systolic blood pressure, smoking status, total cholesterol, reported diabetes status, and current treatment for hypertension. For the non-laboratory-based model, we substituted body-mass index for cholesterol.

Findings: In the cohort of 6186, there were 1529 first-time cardiovascular events and 578 (38%) deaths due to cardiovascular disease over 21 years. In women, the laboratory-based model was useful for predicting events, with a c statistic of 0.829. The c statistic of the non-laboratory-based model was 0.831. In men, the results were similar (0.784 for the laboratory-based model and 0.783 for the non-laboratory-based model). Results were similar between the laboratory-based and non-laboratory-based models in both men and women when restricted to fatal events only.

Interpretation: A method that uses non-laboratory-based risk factors predicted cardiovascular events as accurately as one that relied on laboratory-based values. This approach could simplify risk assessment in situations where laboratory testing is inconvenient or unavailable.

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Conflict of interest statement

Conflict of interest statement

We declare that we have no conflict of interest.

Figures

Figure 1
Figure 1
ROC curves for laboratory-based and non-laboratory-based methods for prediction of cardiovascular disease
Figure 2
Figure 2
Actual and predicted cardiovascular disease events by deciles of risk for the non-laboratory-based model
Figure 3
Figure 3
Patients correctly classified as high or low risk at various cutoff levels of 5-year risk
Figure 4
Figure 4
Risk prediction chart for cardiovascular disease using non-laboratory-based measures (women)
Figure 5
Figure 5
Risk prediction chart for cardiovascular disease using non-laboratory-based measures (men)

Comment in

References

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