J Med Screen 2009;16:212-214
doi:10.1258/jms.2009.009087
© 2009 Medical Screening Society
The value of C-reactive protein in screening for future coronary heart disease events
David S Wald
,
Senior Lecturer and Consultant Cardiologist, Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, Charterhouse Square, London EC1M 6BQ, UK
Anuradhani Kasturiratne
,
Visiting Research Fellow, Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, Charterhouse Square, London EC1M 6BQ, UK
Jonathan P Bestwick
,
Academic Fellow in Medical Statistics, Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, Charterhouse Square, London EC1M 6BQ, UK
Correspondence to: David S Wald, Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, Charterhouse Square, London EC1M 6BQ, UK; d.s.wald{at}qmul.ac.uk
Measurement of C-reactive protein (CRP), an inflammatory marker
associated with coronary heart disease (CHD) events, has been
proposed as a means of screening for future CHD. In prospective
studies about a three-fold increase in risk of CHD observed
between the top fifth and bottom fifth of the CRP distribution
has been taken to support the use of CRP as a screening test.
This however gives an over-optimistic impression of its value,
because people in the middle of the distribution, where most
CHD events occur, are excluded from the analysis. A different
analysis is needed to assess whether screening is worthwhile.
Examination of the relative frequency distributions of CRP in
individuals from 22 prospective studies of individuals without
previous cardiovascular disease who subsequently did and did
not have a CHD event shows that the detection rate (or sensitivity)
was 18% for a false-positive rate of 10% (CRP cut-off 6.65 mg/L);
a poor screening test. Whatever CRP cut-off is used, the overlap
in CRP values between affected and unaffected individuals is
too great for CRP to usefully discriminate between those who
will and will not have a CHD event.

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