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Analysis of Longitudinal Cardiopulmonary Data - Article


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Heart Diseases

Cardiac Arrest; Cardiac Diseases; Endocarditis; Heart Disease; Heart Disease and the Mind-Body Constitution; Heart Disease, Congenital; Heart Diseases (General); Heart Diseases--Prevention; Heart Infection, Endocarditis


Clinical Trial: Analysis of Longitudinal Cardiopulmonary Data

This study is no longer recruiting patients.

Sponsored by: National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)

Purpose

To perform a comparative study of statistical models on datasets from nine large epidemiological studies in the cardiopulmonary field in order to develop tools for identifying appropriate classes of statistical models for use in analyzing longitudinal data.

Condition
Cardiovascular Diseases
Heart Diseases
Lung Diseases

MedlinePlus related topics:  Heart Diseases;   Heart Diseases--Prevention;   Respiratory Diseases;   Vascular Diseases

Study Type: Observational
Study Design: Natural History

Further Study Details: 

Study start: April 1988;  Study completion: December 2003

BACKGROUND: Longitudinal designs are frequently encountered in epidemiologic research, particularly in the cardiopulmonary field. Many different statistical models have been proposed for the analysis of longitudinal data in the statistical literature. These include the general linear model, autoregressive models, random effects models, and simple models based on an analysis of slopes over time. Complex models are not widely used in the epidemiologic literature, due mainly to a lack of understanding of their underlying utility and the types of questions that could be answered with complex models that cannot be addressed using simple models. An additional problem is a lack of software available for fitting complex models. The study has important public health implications, since longitudinal data continue to accumulate rapidly and no guidelines are available as to the appropriate methods of analysis for specific research questions. Furthermore, it is often only through the modelling of longitudinal data that processes pertaining to change can be understood.

DESIGN NARRATIVE: The nine datasets used included: for pulmonary data, the Childhood Respiratory Disease Study, the Netherlands data from Vlagtwedde and Vlaardingen, the Boston Police Study, the Fletcher Study data from England; for cardiopulmonary data, the Veterans Administration Normative Aging Study; for blood pressure data, the Wales Study, the Zinner/Kass Study, the Lee/Zinner Study, and the East Boston Childhood Blood Pressure Study. For each of the nine datasets the following models were fitted and compared for adults, children, and for adults and children combined: autoregressive models both serial-correlation and state-dependence; random-effects models; regression models with intraclass correlation structure; general linear models; models based on fitting slopes to individual persons. New methods for analyzing longitudinal data were developed and included fitting of higher-order autoregressive models with unequally spaced data, nonparametric methods, familial and other clustering effects in the analysis of longitudinal pulmonary function data, robust methods, empirical Bayes methods for estimation of slopes, and hierarchial models based on old and new methods.

The study was renewed in 1996 to perform a comparative study of complex models on datasets from four large epidemiologic studies in the cardiopulmonary field. The models were compared as regards goodness of fit, ease of implementation, and interpretability. In addition, new statistical methods were developed to model phenomena which seemed poorly-fitted by existing models, including adult longitudinal bp and pulmonary function data. The overall goal was to develop tools for identifying appropriate classes of longitudinal statistical models. This has important public health implications, since longitudinal data continue to accumulate rapidly and no guidelines exist as to appropriate methods of analysis. Furthermore, it is often only through modelling of longitudinal data rather than through cross-sectional or separate two time-point analyses that underlying processes pertaining to change can be understood.

The study was renewed in February 2000 to extend and enhance several techniques in the analyses of longitudinal data frequently encountered in epidemiological studies. The techniques include: methods for control for time-dependent confounding in epidemiological studies; developing an incidence model for benign breast disease using the Nurses' Health Study; analysis of incomplete longitudinal data from the Normative Aging Study; extending the penalized likelihood procedures for quantile regression to the repeated measures setting; and development of methods to estimate correlated ROC curves to measure the predictive accuracy of GEE regression models for longitudinal data.

Eligibility

Genders Eligible for Study:  Male

Criteria

No eligibility criteria

Location Information

Study chairs or principal investigators

Bernard Rosner,  Brigham and Women's Hospital   

More Information

Publications

Rosner B. Multivariate methods for binary longitudinal data with heterogeneous correlation over time. Stat Med. 1992 Oct-Nov;11(14-15):1915-28.

Munoz A, Carey V, Schouten JP, Segal M, Rosner B. A parametric family of correlation structures for the analysis of longitudinal data. Biometrics. 1992 Sep;48(3):733-42.

Rosner B. Multivariate methods for clustered binary data with multiple subclasses, with application to binary longitudinal data. Biometrics. 1992 Sep;48(3):721-31.

Beckett LA, Rosner B, Roche AF, Guo S. Serial changes in blood pressure from adolescence into adulthood. Am J Epidemiol. 1992 May 15;135(10):1166-77.

Rosner B, Langford HG. Judging the effectiveness of antihypertensive therapy in an individual patient. J Clin Epidemiol. 1991;44(8):831-8.

Smith L, Rosner B. Estimation of variance components for censored data with applications to blood pressure variability. Stat Med. 1991 Sep;10(9):1441-52.

D'Agostino RB Jr, Sparrow D, Weiss S, Rosner B. Longitudinal models for analysis of respiratory function. Stat Med. 1995 Oct 30;14(20):2205-16.

Cook NR, Rosner BA. An optimal rule for screening subjects for clinical trials in the presence of within-person variability. Control Clin Trials. 1994 Jun;15(3):173-86.

Schmid CH, Rosner B. A Bayesian approach to logistic regression models having measurement error following a mixture distribution. Stat Med. 1993 Jun 30;12(12):1141-53.

Cook NR, Gillman MW, Rosner BA, Taylor JO, Hennekens CH. Prediction of young adult blood pressure from childhood blood pressure, height, and weight. J Clin Epidemiol. 1997 May;50(5):571-9.

Rockhill B, Colditz GA, Rosner B. Bias in breast cancer analyses due to error in age at menopause. Am J Epidemiol. 2000 Feb 15;151(4):404-8.

Cook NR, Gillman MW, Rosner BA, Taylor JO, Hennekens CH. Combining annual blood pressure measurements in childhood to improve prediction of young adult blood pressure. Stat Med. 2000 Oct 15;19(19):2625-40.

Tishler PV, Carey VJ, Reed T, Fabsitz RR. The role of genotype in determining the effects of cigarette smoking on pulmonary function. Genet Epidemiol. 2002 Mar;22(3):272-82.

Carey VJ, Rosner BA. Analysis of longitudinally observed irregularly timed multivariate outcomes: regression with focus on cross-component correlation. Stat Med. 2001 Jan 15;20(1):21-31.

Rosner B, Grove D. Use of the Mann-Whitney U-test for clustered data. Stat Med. 1999 Jun 15;18(11):1387-400.

Lee ML, Rosner BA, Weiss ST. Relationship of blood pressure to cardiovascular death: the effects of pulse pressure in the elderly. Ann Epidemiol. 1999 Feb;9(2):101-7.

Carey VJ. Using hypertext and the Internet for structure and management of observational studies. Stat Med. 1997 Aug 15;16(15):1667-82.

Cook NR, Rosner BA, Chen W, Srinivasan SR, Berenson GS. Using the area under the curve to reduce measurement error in predicting young adult blood pressure from childhood measures. Stat Med. 2004 Nov 30;23(22):3421-35.

Study ID Numbers:  1100
Record last reviewed:  December 2004
Last Updated:  January 10, 2005
Record first received:  May 25, 2000
ClinicalTrials.gov Identifier:  NCT00005221
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 8, 2005


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