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  Vol. 294 No. 6, August 10, 2005 TABLE OF CONTENTS
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Racial Differences in BRCA Testing

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

To the Editor: We are concerned about aspects of the study design in the article on racial differences in BRCA1/2 testing by Dr Armstrong and colleagues, and believe that the results should be interpreted with caution.1 In a case-control study, controls should be sampled from the population that gave rise to the cases.2-3 However, the description of this study leaves questions about whether appropriate sampling has occurred.

First, more detail is needed regarding the selection of controls, including the number of women mailed a survey, the proportion of eligible patients obtained from this group, and the characteristics (particularly race) of nonresponders. Second, the predicted risk of a BRCA1/2 mutation is significantly different between the controls (4.62) and the cases (8.40), and almost 60% of the controls (vs 13% of the cases) reported having only a second-degree relative affected. The lower risk in the control group could justify genetic counseling not . . . [Full Text of this Article]

Sharon Hensley Alford, MPH
salford1@hfhs.org
Josephine Ford Cancer Center
Henry Ford Health System
Detroit, Mich

Judy Mouchawar, MD
Medical Genetics
Kaiser Permanente Colorado
Denver


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