Extracellular Matrix Alteration Clinical Trial
Official title:
New Biomarkers in Post Thrombotic Syndrome
This study aims to deepen the investigators knowledge of Post Thrombotic Syndrome and MMPs (and other related molecules such as TIMPS, NGAL and cytokines) to find a predictive molecular system to better classify the risk of patients to develop a PTS after a DVT episode, in order to monitorate more strictly the patients at high risk for developing this complication.
Post-thrombotic syndrome (PTS) is a problem that can develop in nearly half of all patients
who experience a deep vein thrombosis (DVT) of lower limbs. PTS symptoms include chronic leg
pain, swelling, redness, and skin ulcers. PTS lowers patients' quality of life after DVT,
specifically with regards to physical and psychological symptoms and limitations in daily
activities. Secondly, the treatment of PTS adds significantly to the cost of treating DVT.
PTS also causes lost work productivity: patients with severe PTS and venous ulcers lose up
to 2 work days per year Nowadays, there are no effective measures to reduces significatively
PTS onset following a DVT episode.
Biomarkers can be of use in further exploring the etiology as well as in developing risk
stratification tools for PTS. The relationship between PTS and specific biomarkers may help
guide prevention and therapy based on a patient's individual risk profile.
Recent studies showed that MMPs play a significant role in vascular remodeling and
endothelial dysfunction and they may explain a role in aneurysm formation as well as in all
the clinical manifestations of venous disease (both for acute and chronic related events)
but the cellular and molecular mechanisms involved in thrombus resolution and vein wall
fibrosis remain undefined.
The presence of MMPs and TIMPs in acute venous occlusion model suggests that there is an
important early interplay between protease and inhibitor during events that precede the
development of venous disease.
This study aims to deepen the investigators knowledge of PTS and MMPs (and other related
molecules such as NGAL and cytokines) to find a predictive molecular system to better
classify the risk of patients to develop a PTS after a DVT episode, in order to monitorate
more strictly the patients at high risk for developing this complication.
Patients will be recruited at their first episode of DVT and will be followed up according
to standard protocols for DVT at 1,4,8,12,24, 36 months. At each visit blood sample will be
collected from venipuncture in order to evaluate MMPs (and other related molecules) plasma
levels.
These data will be related to clinical findings.
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Observational Model: Cohort, Time Perspective: Prospective
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