Published in Volume
112, Issue 2 (July 15, 2003)
J Clin Invest. 2003;112(2):299–299.
doi:10.1172/JCI18921C1.
Copyright ©
2003, The American Society for
Clinical Investigation.
Corrigendum
C-reactive protein: a critical update
Mark B. Pepys and Gideon M. Hirschfield
Published July 15, 2003
Original citation: J. Clin. Invest.
111:1805–1812 (2003). doi:10.1172/JCI18921.
Citation for this corrigendum: J. Clin. Invest.
112:299 (2003). doi:10.1172/JCI18921C1.
The authors wish to correct an error that appeared in the text. The corrected paragraph
appears below.
However, it is critically important to recognize that the CRP response is nonspecific and
is triggered by many disorders unrelated to cardiovascular disease (Table 2). In using
CRP for assessment of cardiovascular risk, it is therefore essential to clearly
establish true base-line CRP values that are not distorted by either trivial or serious
intercurrent pathologies. If the initial CRP result is in the low-risk range, less than
1 mg/l, a single measurement is sufficient, but if it is in the higher-risk range,
greater than about 2.5 mg/l, two or more serial samples taken at intervals of 1 week or
more should be retested until a stable base-line value is seen. If the CRP value
persistently remains above 10 mg/l, indicating the presence of a significant acute-phase
response, a full history and physical examination of the patient is indicated, ideally
together with relevant investigations, to determine the cause and alleviate it if
possible. Interestingly, chronic inflammatory conditions, such as rheumatoid arthritis
and hemodialysis for end-stage renal failure, that are characterized by persistently
elevated CRP concentrations in some individuals, are associated with premature
cardiovascular disease.