(Circulation. 2000;101:e207.)
© 2000 American Heart Association, Inc.
Circulation Electronic Pages |
Institute of Cardiology and Division of Hematology, Catholic University, 00168 Rome, Italy, felicita.andreotti@iol.it
Department of Vascular Medicine and Pharmacology Consorzio Mario Negri Sud, 66030 S. Maria Imbaro, Italy
| Introduction |
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We would like to offer our interpretation of the recent article by Ridker et al,1 which was derived from the Physicians Health Study (PHS). To our knowledge, this is the only report that does not confirm the association between the G20210A prothrombin mutation and deep vein thrombosis. In this report, the mutation was also unrelated to myocardial infarction and stroke.1
The G20210A allele is associated with increased prothrombin
levels in blood and, since 1996, it has been reported concordantly as a
moderate and significant risk factor for deep vein thrombosis by
12
different case-control studies (published in extenso) involving 2657
patients and 4070 healthy controls (for partial review see Reference
2).
The PHS was conceived as a randomized trial to investigate the
effects of aspirin versus placebo on cardiovascular
mortality during a 5- to 10-year follow-up period.1 3
Enrolled subjects constituted a special group: American male
physicians, 41 to 84 years of age, who were selected according to the
absence of previous thrombotic events (ie, with a low
cardiovascular risk profile, which was reduced even
further by the intake of aspirin).1 3 The extremely low
risk of the PHS population is supported by the participants initial
healthy conditions, despite a mean age at enrollment of 60 years, and
by the authors own statement at follow-up, that
"cardiovascular death rates in this trial were
exceptionally low... only 15% of that expected for a general
population of white men with the same age distribution over a similar
period."3 Thus, the PHS
Brigham and Womens Hospital, Boston, Mass
Washington University St. Louis, Mo
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