Inflammation markers and their trajectories after deep vein thrombosis in relation to risk of post‐thrombotic syndrome. (10th February 2015)
- Record Type:
- Journal Article
- Title:
- Inflammation markers and their trajectories after deep vein thrombosis in relation to risk of post‐thrombotic syndrome. (10th February 2015)
- Main Title:
- Inflammation markers and their trajectories after deep vein thrombosis in relation to risk of post‐thrombotic syndrome
- Authors:
- Rabinovich, A.
Cohen, J. M.
Cushman, M.
Wells, P. S.
Rodger, M. A.
Kovacs, M. J.
Anderson, D. R.
Tagalakis, V.
Lazo‐Langner, A.
Solymoss, S.
Miron, M. J.
Yeo, E.
Smith, R.
Schulman, S.
Kassis, J.
Kearon, C.
Chagnon, I.
Wong, T.
Demers, C.
Hanmiah, R.
Kaatz, S.
Selby, R.
Rathbun, S.
Desmarais, S.
Opatrny, L.
Ortel, T. L.
Ginsberg, J. S.
Kahn, S. R. - Abstract:
- <abstract abstract-type="main" id="jth12814-abs-0001"> <title>Summary</title> <sec id="jth12814-sec-0001" sec-type="section"> <title>Background</title> <p>Post‐thrombotic syndrome (PTS) is a frequent chronic complication of deep vein thrombosis (DVT).</p> </sec> <sec id="jth12814-sec-0002" sec-type="section"> <title>Objective</title> <p>In the BioSOX study, we investigated whether inflammation markers predict the risk of PTS after DVT.</p> </sec> <sec id="jth12814-sec-0003" sec-type="section"> <title>Methods</title> <p>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.</p> </sec> <sec id="jth12814-sec-0004" sec-type="section"> <title>Results</title> <p>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.<abstract abstract-type="main" id="jth12814-abs-0001"> <title>Summary</title> <sec id="jth12814-sec-0001" sec-type="section"> <title>Background</title> <p>Post‐thrombotic syndrome (PTS) is a frequent chronic complication of deep vein thrombosis (DVT).</p> </sec> <sec id="jth12814-sec-0002" sec-type="section"> <title>Objective</title> <p>In the BioSOX study, we investigated whether inflammation markers predict the risk of PTS after DVT.</p> </sec> <sec id="jth12814-sec-0003" sec-type="section"> <title>Methods</title> <p>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.</p> </sec> <sec id="jth12814-sec-0004" sec-type="section"> <title>Results</title> <p>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.</p> </sec> <sec id="jth12814-sec-0005" sec-type="section"> <title>Conclusions</title> <p>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.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of thrombosis and haemostasis. Volume 13:Number 3(2015:Mar.)
- Journal:
- Journal of thrombosis and haemostasis
- Issue:
- Volume 13:Number 3(2015:Mar.)
- Issue Display:
- Volume 13, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 13
- Issue:
- 3
- Issue Sort Value:
- 2015-0013-0003-0000
- Page Start:
- 398
- Page End:
- 408
- Publication Date:
- 2015-02-10
- Subjects:
- Thrombosis -- Periodicals
Hemostasis -- Periodicals
Blood coagulation disorders -- Periodicals
616.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1538-7836 ↗
http://www.blackwellpublishing.com/journals/jth ↗
https://www.sciencedirect.com/journal/journal-of-thrombosis-and-haemostasis ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jth.12814 ↗
- Languages:
- English
- ISSNs:
- 1538-7933
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5069.345000
British Library DSC - BLDSS-3PM
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