Longitudinal analysis of the dynamics and risk of coronary heart disease in the Framingham Study.

Journal Article (Journal Article)

Statistical methods designed specifically for the analysis of chronic disease incidence and progression in longitudinal studies are presented. These method model the risk of acute phases of chronic disease separately from the temporal change in risk variables. This could be accomplished because, under a specific biological model of the disease mechanism, the problems of estimating the risk of an acute event and of predicting the change in risk variables are independent. Specifically, a quadratic equation relating risk variable values to chronic disease risk and a system of linear equations predicting future risk variable values from present values may beestimated separately. Taken together, they utilize the full information available in a longitudinal study on the temporal dimension of chronic disease progression. In addition, the model is found to possess a number of attractive statistical and theoretical properties. These methods are applied to longitudinal data from the Framingham Study on coronary heart disease (CHD) in males. A quadratic function relating the risk of a CHD event to selected risk variables (age, and the natural logarithms of serum cholesterol, uric acid, diastolic blood pressure and pulse pressure) was estimated from measurements made at four points equally spaced in time (two years) with a further morbidity follow-up at a fifth point. The risk function was found to predict CHD risk accurately. It showed that, apart from the linear effects of the risk variables, cohort effects, quadratic effects and interaction effects were important predictors of CHD risk. The linear regression equations used to predict future risk variable values showed that there was an intricate network of cross-temporal associations. Study of the two types of equations jointly show that putative risk variables could affect the risk of CHD incidence both directly, by being associated with higher levels of risk, and indirectly, by causing other risk variable values to change with time. The results led us to identify several different roles that risk variables might play in CHD incidence.

Full Text

Duke Authors

Cited Authors

  • Woodbury, MA; Manton, KG; Stallard, E

Published Date

  • September 1, 1979

Published In

Volume / Issue

  • 35 / 3

Start / End Page

  • 575 - 585

PubMed ID

  • 497343

Electronic International Standard Serial Number (EISSN)

  • 1541-0420

International Standard Serial Number (ISSN)

  • 0006-341X

Digital Object Identifier (DOI)

  • 10.2307/2530248


  • eng