Characterization of High Density Lipoprotein (HDL) in Type 2 Diabetes (T2D) After Fenofibrate or Niacin Treatment
Information source: Institut Investigacio Sanitaria Pere Virgili
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Type 2 Diabetes Mellitus; Dyslipidemia
Intervention: Fenofibrate (Drug); Niacin plus laropiprant (Drug)
Phase: Phase 4
Status: Completed
Sponsored by: Institut Investigacio Sanitaria Pere Virgili Official(s) and/or principal investigator(s): Luis Masana, Professor, Study Director, Affiliation: Institut Investigacio Sanitaria Pere Virgili
Summary
The structural and functional alterations of high density lipoproteins (HDL) levels in type
2 diabetes (T2D) patients linked to hypertriglyceridemia, hyperglycemia, insulin resistance,
inflammation and oxidation, play a major role in the increased macrovascular risk in these
patients. An impaired function of the adipose tissue (AT) in T2D contributes to low HDL
concentrations.
Objectives: 1) Quantitative and qualitative characterisation of HDL subclasses by
ultracentrifugation, proteomic and metabolomic techniques. 2) To study the relationship
between the HDL subclasses, preβ1 HDL and remnant HDL, and clinical determinants of
arteriosclerosis. 3) Functional in vitro studies of the HDL subclasses determined in
Objective 1. 4) To study the role of AT determining the low HDL levels. 5) To study the
impact of HDL increasing drugs on HDL qualitative changes.
Clinical Details
Official title: Qualitative and Quantitative Characterization of HDL in T2D After Fenofibrate or Niacin Treatment in Spanish Population
Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention
Primary outcome: HDL particles size and number assessed by nuclear magnetic resonance (NMR) and reported as nm and micromol/L
Secondary outcome: Apolipoprotein A1 (Apo A1), apolipoprotein A2 (Apo A2), paraoxonase (PON) HDL concentration (g/l - mg/l)
Detailed description:
Groups of subjects: a) Diabetic patients with low HDL; b) Non-diabetic patients with low
HDL; c) Diabetic patients with normal HDL levels; and d) Non-diabetic patients with normal
HDL levels. The studies will be performed after washing out lipid lowering drugs. Intima
media thickness (IMT) will be performed in all groups. Main biochemical techniques will be
centralised. Isolation and characterisation of HDL subclasses and remnant HDL, as well as a
determination and preβ1 HDL will be performed. HDL studies examining HDL proteomic and
metabolomic profiles will be performed. Functional studies will determine the effects on the
endothelium, inflammation, cholesterol efflux and oxidation according the qualitative
changes. These HDL measurements will be repeated in group (a), after they are treated with
fibrates or Niacin. HDL metabolism in adipocytes will be extensively studied, and the
clinical associations between HDL alterations and plasma AT-derived molecules will be
examined.
Eligibility
Minimum age: 30 Years.
Maximum age: 70 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Type 2 diabetic patients
- Age from 30 years to 70 years
- HDL not exceeding 50 mg/dl in men or 60 mg/dl in women
Exclusion Criteria:
- to be a smoker
- To be diagnosed with diabetes less than three months before
- To have triglyceride levels above 400 mg/dl
- Glycated hemoglobin higher than 9%
- Albuminuria above 300 mg/mg creatinine
- Chronic kidney disease (eFGR <30 ml/min/1. 73 m2)
- Advanced retinopathy
- Neuropathy
- Cardiovascular disease in the last three months
- Chronic liver insufficiency
- Neoplastic disease or any chronic or incapacitating disease
Locations and Contacts
Hospital Universitari Sant Joan, Reus, Tarragona 43204, Spain
Additional Information
Institut Investigacio Sanitaria Pere Virgili- Pere Virgili Health Research institute
Starting date: February 2009
Last updated: June 2, 2014
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