Cardiovascular Biomarkers in Peripheral Artery Disease.

NCT ID: NCT05757258

Last Updated: 2023-03-07

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 207 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-10-24
• Study Completion Date: 2023-10-31

Brief Summary

Despite the best medical management, many patients with peripheral artery disease (PAD) who undergo lower extremity endovascular revascularization experience adverse cardiovascular outcomes and postoperative complications that may increase the risk of acute limb ischemia or amputation. There are no clear molecular associations that could explain the differences in outcomes after endovascular therapy in patients with PAD. The variable outcomes following endovascular therapy may depend, at least in part, on the profile of cytokines involved in inflammatory and atherosclerotic processes.

The goal of this observational study is to evaluate the potential use of circulating IL-1, IL-6, TNF-alpha, C reactive protein, HMGB-1, osteoprotegerin, sortilin and omentin-1 levels as biomarkers of major adverse limb events (MALE) and major adverse cardiovascular events (MACE) in diabetic patients with PAD and chronic limb-threatening ischemia (CLTI) requiring a procedure of endovascular revascularization.

The main questions it aims to answer are:

• association between serum levels of IL-1, IL-6, TNF-alpha, C reactive protein, HMGB-1, osteoprotegerin, sortilin and omentin-1 at baseline and major adverse limb events (MALE) after lower extremity revascularization.
• association between serum levels of IL-1, IL-6, TNF-alpha, C reactive protein, HMGB-1, osteoprotegerin, sortilin and omentin-1 at baseline and major adverse cardiovascular events (MACE) after lower extremity revascularization.

Diabetic patients with CLTI requiring lower extremity endovascular revascularization will undergo blood sampling for the dosage of circulating IL-1, IL-6, TNF-alpha, C reactive protein, HMGB-1, osteoprotegerin, sortilin and omentin-1 before the endovascular procedure.

Incidence of MALE and MACE will be collected in a 12-months follow-up and will be associated with IL-1, IL-6, TNF-alpha, C reactive protein, HMGB-1, osteoprotegerin, sortilin and omentin-1 serum levels.

Conditions

Peripheral Artery Disease

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• age of at least 18 years
• diagnosis of T2DM present for a least one year
• Ankle/Brachial Index (ABI) of less than 0.80
• lower limb stenosis greater than 50% documented by Ultrasound Color Doppler (US)
• category 4 or 5 of PAD in accordance with the Rutherford classification
• presence of CLTI requiring endovascular treatment

Exclusion Criteria

• pregnancy
• acute infections at present or in the previous month
• diabetic foot ulcers with sign of infection or osteomyelitis
• previous lower-limb endovascular or surgical revascularization within the past 3 months
• diabetic peripheral neuropathy
• liver disease with a functional status B or C in accord to Child-Pugh classification
• congenital or acquired thrombophilia
• active autoimmune disease
• active cancer
• organ transplantation
• life expectancy < 12 months
• contraindication to antiplatelet therapy
• contraindication to endovascular revascularization

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

OTHER

Sponsor Role: lead

Responsible Party

Flex Andrea

MD, PhD

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Andrea Flex, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Fondazione Policlinico Universitario A. Gemelli, IRCCS

Locations

Fondazione Policlinico Universitario A. Gemelli IRCCS

Rome, , Italy

Countries

Italy

Other Identifiers

2012

Identifier Type: -

Identifier Source: org_study_id