CDC - Blogs - Genomics and Health Impact Blog – Emerging Evidence for the Benefits of Systematic Collection of Family History in Primary Care: - Enviado mediante la barra Google
February 23rd, 2012 1:05 pm
ET -
Muin J Khoury, Director, Office of Public Health
Genomics, Centers for Disease Control and Prevention

When it comes to the use of genomic tests and technologies in practice,
Dr Al Berg is a skeptic
. Dr Berg is the founding chair of the CDC-sponsored Evaluation of Genomic Applications in Practice and Prevention
(EGAPP) Working Group
that has been evaluating genomic tests for more than 5 years. He also chaired the
National Institutes of Health State-of-the-Science Conference on family history
. The EGAPP group has
recommended only one genomic test for use in clinical practice among a handful of tests they have assessed so far
.
The NIH conference found “insufficient evidence” for supporting
systematic collection of family history in primary care. Since then,
Dr Berg has repeatedly
urged caution regarding claims that genetic tests and family history can improve health outcomes
.
Dr Berg is the first to admit “how nice it is to be shown that I
might be wrong on both counts by a single study”. In the current issue
of the Annals of Internal Medicine,
Qureshi and collaborators
report on the value of adding systematic collection of family history
to assessment of heart disease risk. The authors found an increase in
the number of persons identified as having high risk when family history
was systematically collected. The results suggest that in a clinical
practice of an adult population of
5,000
people, we would find an additional 200 to 250 patients who were at
high risk, many of whom might benefit from risk-lowering interventions
.
Although this one study did not evaluate health outcomes, it “strongly
suggests that a well-conducted evaluation would have a good chance of
demonstrating clinical benefit
if fully implemented and followed for a sufficient time
.”
Dr Berg further states
:
“The complex design and analysis were meticulously planned and
rigorously executed… That this study was done at all speaks to the
better support for high-quality research in primary care in the United
Kingdom; finding support for a study like this would be extraordinarily
difficult in the United States … I look forward to further research and
quality improvement evaluations documenting clinical results, and I hope
that more work in this clinical domain can be done in the United
States.“
Indeed, the
CDC Office of Public Health Genomics
has taken this task very seriously for the past few years. Promoting
the rigorous study of family history in clinical practice, the office
designed
a unique randomized clinical trial
to evaluate the impact of collecting family history for 6 common
chronic diseases on health behaviors, screening and clinical practice.
This study has led to
a number of recent publications, and more are to come.
Although we are the first to admit that family history
is not a perfect tool , it is simple and when available can be very informative. We agree with
Dr Berg’s statement
“It is time to take systematic family history collection more seriously”
We welcome our readers’ thoughts and suggestions.
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