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High-sensitivity C-reactive protein elevation in patients with prior myocardial infarction in the United States - 30/10/18

Doi : 10.1016/j.ahj.2018.07.014 
Neha J. Pagidipati, MD, MPH a, , Anne S. Hellkamp, MS a, Puza P. Sharma, MBBS, MPH, PhD b, Tracy Y. Wang, MD, MHS, MSc a, Gregg C. Fonarow, MD c, Michael Pencina, PhD a
a Duke Clinical Research Institute, Duke University, Durham, NC 
b Novartis Pharmaceutical Corporation, East Hanover, NJ 
c David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 

Reprint requests: Neha J. Pagidipati, MD, MPH, Duke Clinical Research Institute, Duke University School of Medicine, PO Box 17969, Durham, NC 27715.Duke Clinical Research Institute, Duke University School of MedicinePO Box 17969DurhamNC27715

Abstract

Importance

The extent to which levels of high-sensitivity C-reactive protein (hs-CRP), a known marker of increased cardiovascular risk, are elevated and are associated with standard cardiovascular risk factors in patients with a history of myocardial infarction (MI) is unknown.

Objectives

To determine the pattern and determinants of the distribution of hs-CRP in those with a prior MI in the United States using a nationally representative sample.

Design and Participants

Adults with hs-CRP data in the National Health and Nutrition Examination Surveys from 1999–2010.

Results

Among 1296 individuals in our cohort, the median age was 65 years and the median hs-CRP level was 2.69 mg/L, measured an average of 7.1 years after the MI. Among these patients, 22% had hs-CRP levels of <1 mg/L, 61% had ≥2 mg/L, and 48% had ≥3 mg/L. Increasing hs-CRP was associated in a multivariable model with increasing body mass index (partial R2 [pR2] 0.113, P < .001), increasing non-high-density lipoprotein [HDL] (pR2 0.030, P < .001), increasing age (pR2 0.008, P = .017), and decreasing HDL (pR2 0.005, P = .046). Adjusted mean hs-CRP was also higher in women (3.6 vs 2.7 mg/L; P < .001), in people with hypertension (3.5 vs. 2.8, P = .030), and among smokers (4.2 vs 2.3 mg/L; P < .001), and lower in people with hyperlipidemia (2.8 vs. 3.5, P = .007). Standard cardiovascular risk factors accounted for only 22% of the variability in hs-CRP levels.

Conclusions and Relevance

Among patients with prior MI, elevated hs-CRP is prevalent several years after the MI, and standard cardiovascular risk factors explain only a small proportion of hs-CRP variability. In light of emerging evidence on the importance of inflammation in the pathogenesis of cardiovascular disease, the high prevalence of elevated hs-CRP in patients with prior MI in the United States may have public health implications.

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 Disclosures:
NJP: Ownership: Freedom Health, Inc; Physician Partners, LLC; RXAdvance, LLC; Florida Medical Associates, LLC.
ASH: None.
PPS: Employed by Novartis Pharmaceutical Corp.
TYW: Research grants to the Duke Clinical Research Institute from AstraZeneca, Boston Scientific, Bristol-Myers Squibb, Daiichi Sankyo, Eli Lilly, Gilead Sciences, Novartis, Pfizer, and Regeneron, as well as consulting or honoraria from Merck, Gilead, and Pfizer, Inc.
GCF: Consulting: Amgen, Janssen, Novartis.
MP: Grant from Novartis to Duke.
 Funding: Novartis Pharmaceutical Corporation.


© 2018  Elsevier Inc. Tutti i diritti riservati.
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Vol 204

P. 151-155 - ottobre 2018 Ritorno al numero
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