Literature DB >> 25495610

Inflammation markers and their trajectories after deep vein thrombosis in relation to risk of post-thrombotic syndrome.

A Rabinovich1, J M Cohen, M Cushman, P S Wells, M A Rodger, M J Kovacs, D R Anderson, V Tagalakis, A Lazo-Langner, S Solymoss, M J Miron, E Yeo, R Smith, S Schulman, J Kassis, C Kearon, I Chagnon, T Wong, C Demers, R Hanmiah, S Kaatz, R Selby, S Rathbun, S Desmarais, L Opatrny, T L Ortel, J S Ginsberg, S R Kahn.   

Abstract

BACKGROUND: Post-thrombotic syndrome (PTS) is a frequent chronic complication of deep vein thrombosis (DVT).
OBJECTIVE: In the BioSOX study, we investigated whether inflammation markers predict the risk of PTS after DVT.
METHODS: We measured C-reactive protein (CRP), ICAM-1, interleukin (IL)-6, and IL-10, at baseline, and 1 month and 6 months after a first proximal DVT, among 803 participants in the SOX trial. Participants were prospectively followed for 24 months for development of PTS.
RESULTS: Median CRP levels at 1 month, ICAM-1 levels at baseline, 1 month and 6 months, IL-6 levels at 1 month and 6 months and IL-10 levels at 6 months were higher in patients who developed PTS than in those who did not. Multivariable regression with the median as a cutoff showed risk ratios (RRs) for PTS of 1.23 (95% confidence interval [CI] 1.05-1.45) and 1.25 (95% CI 1.05-1.48) for ICAM-1 at 1 month and 6 months, respectively, and 1.27 (95% CI 1.07-1.51) for IL-10 at 6 months. Quartile-based analysis demonstrated a dose-response association between ICAM-1 and PTS. ICAM-1 and IL-10 were also associated with PTS severity. Analysis of biomarker trajectories after DVT demonstrated an association between the highest-trajectory group of ICAM-1 and PTS.
CONCLUSIONS: In this prospective study, ICAM-1 over time was most consistently associated with the risk of PTS. Further study is required to confirm these findings and assess their potential clinical relevance.
© 2014 International Society on Thrombosis and Haemostasis.

Entities:  

Keywords:  biological markers; deep vein thrombosis; inflammation; postthrombotic syndrome; risk factors

Mesh:

Substances:

Year:  2015        PMID: 25495610     DOI: 10.1111/jth.12814

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


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