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The Framingham Study: Examining DNA Markers and Links to Diseases
This study has been completed.
Study NCT00062777   Information provided by National Institutes of Health Clinical Center (CC)
First Received: June 13, 2003   Last Updated: August 24, 2009   History of Changes

June 13, 2003
August 24, 2009
June 2003
June 2007   (final data collection date for primary outcome measure)
 
To evaluate the toxicity and efficacy of transfusing selectively depleted donor lymphocytes as part of a nonmyeloablative peripheral blood stem cell transplant in a population of older adults with hematologic malignancies.
Complete list of historical versions of study NCT00062777 on ClinicalTrials.gov Archive Site
 
To define the incidence and severity of acute and chronic GVHD with this approach.
 
The Framingham Study: Examining DNA Markers and Links to Diseases
A Genome-Wide Scan for Quantitative Trait Loci of Hematocrit - A Framingham Study

Since 1948, residents of Framingham, Massachusetts, have participated in a program that collects blood samples and clinical data to provide a rare and valuable database for scientific research.

The purpose of this study is to support this national resource by aiding in its research capacity. Specifically, researchers in this study will (1) investigate heart, lung, and blood diseases; stroke; memory loss; joint disease; bone loss; deafness; cancer; blood vessel diseases and other health conditions, and (2) examine DNA and its relationship to risk of developing these disease and health conditions.

Approximately 330 families have participated in the Framingham Study. Participants will be required to undergo a four-hour exam and to take that exam every two years thereafter. During the exam, the Framingham investigators will (1) interview participants about medical status, health issues, and lifestyles; (2) perform a regular physical exam; (3) obtain blood and urine samples and administer a glucose-tolerance test; (4) supervise a brisk six-minute treadmill walk; (5) administer an ultrasound procedure; and (6) review and obtain copies of medical and hospital records. Participants will also be asked to complete a questionnaire at home regarding dietary and health habits.

Many studies have shown that hematocrit (HCT) levels are associated with cerebrovascular disease, cardiovascular disease (CVD), peripheral vascular disease, as well as all-cause mortality. Twin studies have shown that HCT variation is largely determined by genetic factors with heritability estimated as 40% - 65%. So far, no linkage analysis in humans between HCT and DNA markers have been reported. The purpose of this protocol is to identify chromosome regions that contain quantitative trait loci (QTL) involved in controlling HCT levels. In the Framingham Study, a 10cM genome scan (about 400 markers) has been conducted in 330 families. HCT was measured in the original cohort and Framingham offspring. These data provide us the opportunity to undertake linkage analyses using variance component method to map quantitative trait loci (QTL) of HCT.

 
Observational
 
Vascular Diseases
 
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
330
 
June 2007   (final data collection date for primary outcome measure)
  • INCLUSION /EXCLUSION CRITERIA

The study population will include the members of the 330 Framingham Study families with genome scan.

Both
 
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00062777
 
030219, 03-H-0219
National Heart, Lung, and Blood Institute (NHLBI)
 
 
National Institutes of Health Clinical Center (CC)
May 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP