C-reactive protein, fibrinogen, and cardiovascular disease prediction.

dc.contributor.author

Emerging Risk Factors Collaboration

dc.contributor.author

Kaptoge, Stephen

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Di Angelantonio, Emanuele

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Pennells, Lisa

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Wood, Angela M

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White, Ian R

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Gao, Pei

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Walker, Matthew

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Thompson, Alexander

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Sarwar, Nadeem

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Caslake, Muriel

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Butterworth, Adam S

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Amouyel, Philippe

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Assmann, Gerd

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Bakker, Stephan JL

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Barr, Elizabeth LM

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Barrett-Connor, Elizabeth

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Benjamin, Emelia J

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Björkelund, Cecilia

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Brenner, Hermann

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Brunner, Eric

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Clarke, Robert

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Cooper, Jackie A

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Cremer, Peter

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Cushman, Mary

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Dagenais, Gilles R

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D'Agostino, Ralph B

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Dankner, Rachel

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Davey-Smith, George

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Deeg, Dorly

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Dekker, Jacqueline M

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Engström, Gunnar

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Folsom, Aaron R

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Fowkes, F Gerry R

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Gallacher, John

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Gaziano, J Michael

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Giampaoli, Simona

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Gillum, Richard F

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Hofman, Albert

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Howard, Barbara V

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Ingelsson, Erik

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Iso, Hiroyasu

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Jørgensen, Torben

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Kiechl, Stefan

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Kitamura, Akihiko

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Kiyohara, Yutaka

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Koenig, Wolfgang

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Kromhout, Daan

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Kuller, Lewis H

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Lawlor, Debbie A

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Meade, Tom W

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Nissinen, Aulikki

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Nordestgaard, Børge G

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Onat, Altan

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Panagiotakos, Demosthenes B

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Psaty, Bruce M

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Rodriguez, Beatriz

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Rosengren, Annika

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Salomaa, Veikko

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Kauhanen, Jussi

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Salonen, Jukka T

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Shaffer, Jonathan A

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Shea, Steven

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Ford, Ian

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Stehouwer, Coen DA

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Strandberg, Timo E

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Tipping, Robert W

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Tosetto, Alberto

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Wassertheil-Smoller, Sylvia

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Wennberg, Patrik

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Westendorp, Rudi G

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Whincup, Peter H

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Wilhelmsen, Lars

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Woodward, Mark

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Lowe, Gordon DO

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Wareham, Nicholas J

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Khaw, Kay-Tee

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Sattar, Naveed

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Packard, Chris J

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Gudnason, Vilmundur

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Ridker, Paul M

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Pepys, Mark B

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Thompson, Simon G

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Danesh, John

dc.date.accessioned

2019-06-18T14:04:01Z

dc.date.available

2019-06-18T14:04:01Z

dc.date.issued

2012-10

dc.date.updated

2019-06-18T14:04:00Z

dc.description.abstract

There is debate about the value of assessing levels of C-reactive protein (CRP) and other biomarkers of inflammation for the prediction of first cardiovascular events.We analyzed data from 52 prospective studies that included 246,669 participants without a history of cardiovascular disease to investigate the value of adding CRP or fibrinogen levels to conventional risk factors for the prediction of cardiovascular risk. We calculated measures of discrimination and reclassification during follow-up and modeled the clinical implications of initiation of statin therapy after the assessment of CRP or fibrinogen.The addition of information on high-density lipoprotein cholesterol to a prognostic model for cardiovascular disease that included age, sex, smoking status, blood pressure, history of diabetes, and total cholesterol level increased the C-index, a measure of risk discrimination, by 0.0050. The further addition to this model of information on CRP or fibrinogen increased the C-index by 0.0039 and 0.0027, respectively (P<0.001), and yielded a net reclassification improvement of 1.52% and 0.83%, respectively, for the predicted 10-year risk categories of "low" (<10%), "intermediate" (10% to <20%), and "high" (≥20%) (P<0.02 for both comparisons). We estimated that among 100,000 adults 40 years of age or older, 15,025 persons would initially be classified as being at intermediate risk for a cardiovascular event if conventional risk factors alone were used to calculate risk. Assuming that statin therapy would be initiated in accordance with Adult Treatment Panel III guidelines (i.e., for persons with a predicted risk of ≥20% and for those with certain other risk factors, such as diabetes, irrespective of their 10-year predicted risk), additional targeted assessment of CRP or fibrinogen levels in the 13,199 remaining participants at intermediate risk could help prevent approximately 30 additional cardiovascular events over the course of 10 years.In a study of people without known cardiovascular disease, we estimated that under current treatment guidelines, assessment of the CRP or fibrinogen level in people at intermediate risk for a cardiovascular event could help prevent one additional event over a period of 10 years for every 400 to 500 people screened. (Funded by the British Heart Foundation and others.).

dc.identifier.issn

0028-4793

dc.identifier.issn

1533-4406

dc.identifier.uri

https://hdl.handle.net/10161/18957

dc.language

eng

dc.publisher

Massachusetts Medical Society

dc.relation.ispartof

The New England journal of medicine

dc.relation.isversionof

10.1056/NEJMoa1107477

dc.subject

Emerging Risk Factors Collaboration

dc.subject

Humans

dc.subject

Cardiovascular Diseases

dc.subject

Lipids

dc.subject

C-Reactive Protein

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Fibrinogen

dc.subject

Mass Screening

dc.subject

Prognosis

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Proportional Hazards Models

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Risk Factors

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Cohort Studies

dc.subject

Adult

dc.subject

Middle Aged

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Female

dc.subject

Male

dc.subject

Practice Guidelines as Topic

dc.subject

Biomarkers

dc.title

C-reactive protein, fibrinogen, and cardiovascular disease prediction.

dc.type

Journal article

pubs.begin-page

1310

pubs.end-page

1320

pubs.issue

14

pubs.organisational-group

School of Medicine

pubs.organisational-group

Duke

pubs.organisational-group

Duke Clinical Research Institute

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Biostatistics & Bioinformatics

pubs.organisational-group

Basic Science Departments

pubs.publication-status

Published

pubs.volume

367

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