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Sökning: WFRF:(Lindahl Birgitta) > (2020-2021) > Screening of biomar...

Screening of biomarkers for prediction of multisite artery disease in patients with recent myocardial infarction

Jönelid, Birgitta (författare)
Uppsala universitet,Kardiologi
Christersson, Christina (författare)
Uppsala universitet,Kardiologi
Hedberg, Pär (författare)
Uppsala universitet,Klinisk fysiologi
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Leppert, Jerzy (författare)
Uppsala universitet,Centrum för klinisk forskning, Västerås
Lindahl, Bertil, 1957- (författare)
Uppsala universitet,Kardiologi,Uppsala kliniska forskningscentrum (UCR)
Lindhagen, Lars (författare)
Uppsala universitet,Uppsala kliniska forskningscentrum (UCR)
Oldgren, Jonas, 1964- (författare)
Uppsala universitet,Kardiologi,Uppsala kliniska forskningscentrum (UCR)
Siegbahn, Agneta, 1947- (författare)
Uppsala universitet,Klinisk kemi
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 (creator_code:org_t)
2021-08-04
2021
Engelska.
Ingår i: Scandinavian Journal of Clinical and Laboratory Investigation. - : Taylor & Francis. - 0036-5513 .- 1502-7686. ; 81:5, s. 353-360
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • A few studies have examined biomarkers in patients with myocardial infarction (MI) and peripheral artery disease (PAD), i.e. multisite artery disease (MSAD). The aim of the study was firstly, to associate biomarkers with the occurrence of PAD/MSAD and secondly, if those can, in addition to clinical characteristics, identify MI patients with MSAD.In two prospectively observational studies including unselected patients with recent MI, PAD was defined as an abnormal ankle-brachial index (ABI) score (1.4). The proximity extension assay (PEA) technique was used, simultaneously analyzing 92 biomarkers with association to cardiovascular disease. Biomarkers were tested for univariate associations with PAD. Random forest was used to identify biomarkers with a higher association to PAD. The additional discriminatory accuracy of adding biomarkers to clinical characteristics was analyzed by the c-statistics. Nine biomarkers were identified as significantly associated with MSAD/PAD in the primary patient cohort, analyzed early after the MI. In the prediction analysis, six biomarkers were identified associated with PAD. Three of these; Tumor necrosis factor receptor (TNFR-1), Tumor necrosis factor receptor 2 (TNFR-2) and Growth Differentiation Factor 15 (GDF-15) improved c-statistics when added to clinical characteristics from 0.683 (95% CI 0.610-0.756) to 0.715 (95% CI 0.645-0.784) in the primary patient cohort with a similar result, 0.729 (95% CI 0.687-0.770) to 0.752 (95% CI 0.771-0.792) in the secondary patient cohort. Biomarkers associated with inflammatory pathways are associated with MSAD in MI patients. Three biomarkers of 92; TNFR-1, TNFR-2 and GDF-15, in this exploratory added information in the prediction of MSAD and emphasis the importance of further studies.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Acute coronary disease
peripheral artery disease
multisite artery disease
biomarkers
atherosclerosis

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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