Inflammatory markers and extent and progression of early atherosclerosis: Meta-analysis of individual-participant-data from 20 prospective studies of the PROG-IMT collaboration.

dc.contributor.author

Willeit, Peter

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Thompson, Simon G

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Agewall, Stefan

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Bergström, Göran

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Bickel, Horst

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Catapano, Alberico L

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Chien, Kuo-Liong

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de Groot, Eric

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Empana, Jean-Philippe

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Etgen, Thorleif

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Franco, Oscar H

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Iglseder, Bernhard

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Johnsen, Stein H

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Kavousi, Maryam

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Lind, Lars

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Liu, Jing

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Mathiesen, Ellisiv B

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Norata, Giuseppe D

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Olsen, Michael H

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Papagianni, Aikaterini

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Poppert, Holger

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Price, Jackie F

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Sacco, Ralph L

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Yanez, David N

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Zhao, Dong

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Schminke, Ulf

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Bülbül, Alpaslan

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Polak, Joseph F

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Sitzer, Matthias

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Hofman, Albert

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Grigore, Liliana

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Dörr, Marcus

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Su, Ta-Chen

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Ducimetière, Pierre

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Xie, Wuxiang

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Ronkainen, Kimmo

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Kiechl, Stefan

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Rundek, Tatjana

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Robertson, Christine

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Fagerberg, Björn

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Bokemark, Lena

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Steinmetz, Helmuth

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Ikram, M Arfan

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Völzke, Henry

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Lin, Hung-Ju

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Plichart, Matthieu

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Tuomainen, Tomi-Pekka

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Desvarieux, Moise

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McLachlan, Stela

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Schmidt, Caroline

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Kauhanen, Jussi

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Willeit, Johann

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Lorenz, Matthias W

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Sander, Dirk

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PROG-IMT study group

dc.date.accessioned

2024-06-11T13:48:30Z

dc.date.available

2024-06-11T13:48:30Z

dc.date.issued

2016-01

dc.description.abstract

Background

Large-scale epidemiological evidence on the role of inflammation in early atherosclerosis, assessed by carotid ultrasound, is lacking. We aimed to quantify cross-sectional and longitudinal associations of inflammatory markers with common-carotid-artery intima-media thickness (CCA-IMT) in the general population.

Methods

Information on high-sensitivity C-reactive protein, fibrinogen, leucocyte count and CCA-IMT was available in 20 prospective cohort studies of the PROG-IMT collaboration involving 49,097 participants free of pre-existing cardiovascular disease. Estimates of associations were calculated within each study and then combined using random-effects meta-analyses.

Results

Mean baseline CCA-IMT amounted to 0.74 mm (SD = 0.18) and mean CCA-IMT progression over a mean of 3.9 years to 0.011 mm/year (SD = 0.039). Cross-sectional analyses showed positive linear associations between inflammatory markers and baseline CCA-IMT. After adjustment for traditional cardiovascular risk factors, mean differences in baseline CCA-IMT per one-SD higher inflammatory marker were: 0.0082 mm for high-sensitivity C-reactive protein (p < 0.001); 0.0072 mm for fibrinogen (p < 0.001); and 0.0025 mm for leucocyte count (p = 0.033). 'Inflammatory load', defined as the number of elevated inflammatory markers (i.e. in upper two quintiles), showed a positive linear association with baseline CCA-IMT (p < 0.001). Longitudinal associations of baseline inflammatory markers and changes therein with CCA-IMT progression were null or at most weak. Participants with the highest 'inflammatory load' had a greater CCA-IMT progression (p = 0.015).

Conclusion

Inflammation was independently associated with CCA-IMT cross-sectionally. The lack of clear associations with CCA-IMT progression may be explained by imprecision in its assessment within a limited time period. Our findings for 'inflammatory load' suggest important combined effects of the three inflammatory markers on early atherosclerosis.
dc.identifier

2047487314560664

dc.identifier.issn

2047-4873

dc.identifier.issn

2047-4881

dc.identifier.uri

https://hdl.handle.net/10161/31169

dc.language

eng

dc.publisher

Oxford University Press (OUP)

dc.relation.ispartof

European journal of preventive cardiology

dc.relation.isversionof

10.1177/2047487314560664

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.subject

PROG-IMT study group

dc.subject

Humans

dc.subject

Disease Progression

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Inflammation

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C-Reactive Protein

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Fibrinogen

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Leukocyte Count

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Atherosclerosis

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Carotid Intima-Media Thickness

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Biomarkers

dc.title

Inflammatory markers and extent and progression of early atherosclerosis: Meta-analysis of individual-participant-data from 20 prospective studies of the PROG-IMT collaboration.

dc.type

Journal article

duke.contributor.orcid

Yanez, David N|0000-0002-2501-5028

pubs.begin-page

194

pubs.end-page

205

pubs.issue

2

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

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Basic Science Departments

pubs.organisational-group

Biostatistics & Bioinformatics

pubs.organisational-group

Biostatistics & Bioinformatics, Division of Biostatistics

pubs.publication-status

Published

pubs.volume

23

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