Effects of 5-day Statin Withdrawal on Endothelial Progenitor Cells and Inflammatory Markers in Type 2 Diabetic Patients
NCT ID: NCT01600690
Last Updated: 2013-08-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
34 participants
INTERVENTIONAL
2012-05-31
2013-08-31
Brief Summary
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The effects of a short term statin withdrawal on endothelial progenitor cells (EPC) and monocyte/macrophage polarization is unknown.
In this study, the investigators will explore the effects of a 5-day statin withdrawal on EPC and monocyte/macrophage polarization, together with other inflammatory biomarkers in type 2 diabetic patients. The investigators hypothesize that statin withdrawal determines a reduction in EPC levels and an inflammatory cell polarization.
Patients will be randomized to continue their habitual statin regimen or to withdraw statin. At baseline and 5 days later, blood samples will be collected for experimental measures.
Detailed Description
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Endothelial integrity is accomplished through the contribution of circulating endothelial progenitor cells (EPC) which repair the damaged endothelial layer and contribute to cardiovascular health in general. EPC are stimulated by statins, but there is no data on the effect of statin withdrawal on EPCs.
One important aspect of inflammation is the pro- versus anti-inflammatory polarization of circulating monocyte/macrophage (MM) cells. Schematically, MM can exist in 2 different states of activation: the classically activated pro-inflammatory cells (M1) and the alternatively activated anti-inflammatory cells (M2). The balance between these 2 (M1/M2 ratio) reflects the state of MM polarization. The effects of statin withdrawal on MM polarization is unknown.
In this study, we will explore the effects of a 5-day statin withdrawal on EPC and monocyte/macrophage polarization, together with other inflammatory biomarkers (namely high sensitive C-reactive protein) in type 2 diabetic patients. We hypothesise that statin withdrawal determines a reduction in EPC levels and an inflammatory cell polarization.
Patients will be randomized to continue their habitual statin regimen or to withdraw statin. At baseline and 5 days later, blood samples will be collected for experimental measures (EPC, M1, M2 and hsCRP).
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Continue statin regimen
Patients randomized to this arm will continue their usual statin regimen and dose, without any intervention.
No interventions assigned to this group
Statin withdrawal
Patients randomized to this arm will stop statin treatment for 5 days.
Statin withdrawal
Patients are instructed to stop taking statin pills for the duration of the study. The rest of therapy will remain unchanged.
Interventions
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Statin withdrawal
Patients are instructed to stop taking statin pills for the duration of the study. The rest of therapy will remain unchanged.
Eligibility Criteria
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Inclusion Criteria
* Age 35-80
* Males and Females
* eGFR\>30 ml/min/1.73 mq
* On statin therapy from at least 6 months
* Minimal statin dosage: Simvastatin 10 mg; Pravastatin 40 mg; Fluvastatin 80 mg; Rosuvastatin 5 mg; Atorvastatin 10 mg.
Exclusion Criteria
* Age \<35 or \>80
* Chronic renal failure (eGFR\<30 ml/min/1.73 mq)
* Recent (within 1 month) acute diseases or trauma or surgery
* Chronic inflammatory diseases (e.g. rheumatoid arthritis)
* Active cancer
* LDL cholesterol \> 160 mg/dL
* Carotid atherosclerosis (\>30% stenosis), coronary artery disease, peripheral arterial disease (Leriche stages II-IV)
* On ezetimibe, fibrates, or niacin
* Therapy with EP hormones
* Pregnancy or lactation
* Inability to provide informed consent
35 Years
80 Years
ALL
No
Sponsors
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University of Padova
OTHER
Responsible Party
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Gian Paolo Fadini
Assistant Professor
Principal Investigators
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Gian Paolo Fadini, M.D.
Role: STUDY_CHAIR
University of Padova
Locations
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University Hospital Diabetes Outpatient Clinic
Padua, , Italy
Countries
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Other Identifiers
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2616P
Identifier Type: -
Identifier Source: org_study_id