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Am J Epidemiol 2002; 156:311-318.
Copyright © 2002 by the Johns Hopkins Bloomberg School of Public Health


HUMAN GENOME EPIDEMIOLOGY

Genetic Test Evaluation: Information Needs of Clinicians, Policy Makers, and the Public

Wylie Burke1, David Atkins2, Marta Gwinn3, Alan Guttmacher4, James Haddow5, Joseph Lau6, Glenn Palomaki5, Nancy Press7, C. Sue Richards8, Louise Wideroff9 and Georgia L. Wiesner10

1 University of Washington, Seattle, WA.
2 Agency for Healthcare Research and Quality, Bethesda, MD.
3 Centers for Disease Control and Prevention, Atlanta, GA.
4 National Human Genome Research Institute, Bethesda, MD.
5 Foundation for Blood Research, Scarborough, ME.
6 New England Medical Center, Boston, MA.
7 Oregon Health Sciences University, Portland, OR.
8 Baylor College of Medicine, Houston, TX.
9 National Cancer Institute, Bethesda, MD.
10 Case Western Reserve University, Cleveland, OH.

Growing knowledge about gene-disease associations will lead to new opportunities for genetic testing. Many experts predict that genetic testing will become increasingly important as a guide to prevention, clinical management, and drug treatment based on genetic susceptibilities. As part of a Human Genetic Epidemiology workshop convened by the Centers for Disease Control and Prevention, a group of experts evaluated the evidence needed when considering the appropriate use of new genetic tests. Because new tests are likely to vary in their predictive value, their potential to direct prevention or treatment efforts, and their personal and social consequences, the task of determining appropriate use will require careful consideration of a variety of factors, including the analytic validity, clinical validity, clinical utility, and ethical, legal, and social implications of the test. Standardized formats are needed to summarize what is known and not known about new genetic tests with respect to each of these features. Following criteria for the objective assessment of test properties, reports should be structured to enable policy makers, clinicians, and the public to identify the available evidence, so that uncertainties can be taken into account when considering test use and planning future research.

factor V; genetic markers; genetic predisposition to disease; genetic screening; genetics; phenylketonurias

Abbreviations: Abbreviations: HNPCC, hereditary nonpolyposis colorectal cancer; HuGE, Human Genome Epidemiology.


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