| Literature DB >> 26403997 |
Stefano de Franciscis1,2, Luca Gallelli3, Bruno Amato1,4, Lucia Butrico2, Alessio Rossi5, Gianluca Buffone2,6, Francesco G Caliò6, Giovanni De Caridi7, Raffaele Grande2, Raffaele Serra1,2.
Abstract
Post-thrombotic syndrome (PTS) is a condition that can develop in about half of the patients with deep vein thrombosis (DVT) of lower limbs. In the present study, we evaluated the expression of inflammatory biomarkers in the early phases of DVT and their correlation with the onset of PTS. Patients were enrolled after the first episode of DVT and were followed up for 1, 4, 8, 12 and 18 months. At each visit, blood sample was collected to evaluate plasma levels of matrix metalloproteinase (MMP)-1,-2,-3,-7,-8 and -9 MMP inhibitors, TIMP-1,-2, neutrophil gelatinase-associated lipocalin (NGAL) and cytokines TNF-α and IL-6. Analysis included 201 patients [86 males (42·79%) and 115 females (57·21%); average age 56 ± 7 years]. Of the 201 patients, 47 (23·38%; 21 males, 26 females) developed PTS during the follow-up period. The control group was made up of 60 individuals without DVT (22 males and 38 females). High plasma levels of MMPs, NGAL and cytokines were recorded during the acute phase after DVT. Moreover, patients with PTS showed higher levels of MMP-1 and MMP-8 with respect to patients without PTS. There is a close relationship between DVT, the individual risk of PTS and specific biomarkers such as MMPs and other related molecules, which may help guide prevention and therapy based on the patient's individual risk profile, and has to be studied in future.Entities:
Keywords: Cytokines; Deep vein thrombosis; Matrix metalloproteinases; Post-thrombotic syndrome; Post-thrombotic ulceration
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Year: 2015 PMID: 26403997 PMCID: PMC7949807 DOI: 10.1111/iwj.12489
Source DB: PubMed Journal: Int Wound J ISSN: 1742-4801 Impact factor: 3.315