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The Effect of the GLP-1 Receptor Agonists on Blood Levels of Lipoprotein (a) (EGLIPA)

Primary Purpose

Diabetes Mellitus Type 2

Status
Unknown status
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Liraglutide
metformin
Sponsored by
Hospital Universitari Vall d'Hebron Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus Type 2 focused on measuring Lipoprotein (a)

Eligibility Criteria

50 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 2 diabetes
  • age between 50-65 years
  • written informed consent

Exclusion Criteria:

  • active GLP-1R agonist, insulin or DPP-IV treatment.
  • Liver failure (3lsn AST and/or ALT)
  • Kidney failure (FG <30ml/min/1,73m2),
  • HbA1c> 10%
  • LDL-cholesterol> 180 mg/dl
  • Triglycerides> 350 mg/dl

Sites / Locations

  • Hospital Universitari Vall d'HebronRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Group A

Group B

Arm Description

Type 2 diabetic patients whom were prescribed GLP-1R agonists by the endocrinologist, according to usual clinical practice (liraglutide, exenatide, lixisenatide). The intervention is the prescription of an GLP-1R agonist (liraglutide, exenatide, lixisenatide)

Type 2 diabetic patients whom were prescribed metformin and/or sulphonilurea, according to usual clinical practice.

Outcomes

Primary Outcome Measures

Change in blood levels of Lipoprotein (a) (Lp(a))

Secondary Outcome Measures

Full Information

First Posted
July 16, 2015
Last Updated
July 20, 2015
Sponsor
Hospital Universitari Vall d'Hebron Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02501850
Brief Title
The Effect of the GLP-1 Receptor Agonists on Blood Levels of Lipoprotein (a)
Acronym
EGLIPA
Official Title
The Effect of the GLP-1 Receptor Agonists on Blood Levels of Lipoprotein (a)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Unknown status
Study Start Date
October 2014 (undefined)
Primary Completion Date
July 2015 (Anticipated)
Study Completion Date
October 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitari Vall d'Hebron Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Lipoprotein (a) [Lp (a)] is an independent cardiovascular risk (CVR) both in the general population and in patients with type 2 diabetes mellitus (DM-2). Until now no effective treatment is known to decrease the levels of Lp (a) levels and thus achieve a reduction of CVR. Among the new antidiabetic drugs are GLP-1Receptor agonists(GLP-1R). In addition to lowering blood glucose, these drugs have other beneficial effects. In our laboratory we have demonstrated that both native GLP-1 and various GLP-1R agonsits reduce the synthesis of Lp (a) in hepatocytes. The objective of the study is to test in humans the results observed in vitro. We will analyze whether treatment with GLP-1R agonists (Liraglutide, Exenatide or Lixisenatida) will reduce serum levels of Lp (a) in patients with DM-2.
Detailed Description
Background: Lipoprotein (a) [Lp (a)] is an independent cardiovascular risk (CVR) both in the general population and in patients with type 2 diabetes mellitus (DM-2). Until now no effective treatment is known to decrease the levels of Lp (a) levels and thus achieve a reduction of CVR. Among the new antidiabetic drugs are GLP-1Receptor agonists(GLP-1R). In addition to lowering blood glucose, these drugs have other beneficial effects. In our laboratory we have demonstrated that both native GLP-1 and various GLP-1R agonsits reduce the synthesis of Lp (a) in hepatocytes. Hypothesis: Treatment with GLP-1R agonists will lower the levels of Lp (a) in patients with DM-2. Objective: The objective of the study is to confirm in humans the results observed in vitro. We will analyze whether treatment with GLP-1R agonists (Liraglutide, Exenatide or Lixisenatida) will reduce serum levels of Lp (a) in patients with DM-2. Methods: we will evaluate 40 patients with DM-2 treated at the Endocrinology Department of the Vall d'Hebron University Hospital. The patients will be distributed in two groups according to the treatment prescribed by the endocrinologist during the visit of routine monitoring: group A (20 patients who were prescribred treatment with GLP-1R agonists) and group B (20 patients who were not prescribed this treatment). According to the current guidelines for treating DM-2, the GLP-1R agonists are situated as a second line treatment after metformin, and the treatment should be individualized according to the characteristics of each patient. (Inzucchi et al. Management of hyperglycemia in type 2 diabetes: a patient-centered approach: position statement of the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD) Diabetes Care 2012; 35 (6):.. 1364-1379). Following these recommendations, the GLP-1R agonists are usually selected when there is obesity and / or very important to avoid hypoglycaemia. The decision to prescribe a GLP-1R agonist is made by the endocrinologist before and independently of the patient´s participation in the study. Blood levels of Lp(a) will be evaluated at baseline and at 2 months (+/- 15 days). Diabetic patients who are treated with insulin, enzyme inhibitors DPP-4 (IDDP-4) or already treated with receptor agonists GLP-1, presenting with kidney and liver failure, HbA1c> 10%, LDL-cholesterol> 180 mg / dl and / or triglycerides> 350 mg / dl will excluded. Relevance: The results will identify a potential treatment for lowering levels of Lp (a) in patients with DM-2 and thus reducing cardiovascular risk associated with this lipoprotein.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus Type 2
Keywords
Lipoprotein (a)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Experimental
Arm Description
Type 2 diabetic patients whom were prescribed GLP-1R agonists by the endocrinologist, according to usual clinical practice (liraglutide, exenatide, lixisenatide). The intervention is the prescription of an GLP-1R agonist (liraglutide, exenatide, lixisenatide)
Arm Title
Group B
Arm Type
Active Comparator
Arm Description
Type 2 diabetic patients whom were prescribed metformin and/or sulphonilurea, according to usual clinical practice.
Intervention Type
Drug
Intervention Name(s)
Liraglutide
Other Intervention Name(s)
Exenatide, Lixisenatide
Intervention Description
Treatment with liraglutide, exenatide or lixisenatide
Intervention Type
Drug
Intervention Name(s)
metformin
Other Intervention Name(s)
sulphonilurea
Intervention Description
Treatment with metformin and/or sulphonilurea
Primary Outcome Measure Information:
Title
Change in blood levels of Lipoprotein (a) (Lp(a))
Time Frame
Baseline and two months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 2 diabetes age between 50-65 years written informed consent Exclusion Criteria: active GLP-1R agonist, insulin or DPP-IV treatment. Liver failure (3lsn AST and/or ALT) Kidney failure (FG <30ml/min/1,73m2), HbA1c> 10% LDL-cholesterol> 180 mg/dl Triglycerides> 350 mg/dl
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cristina Hernandez, MD, PhD
Phone
+34 934894172
Ext
4172
Email
cristina.hernandez@vhir.org
First Name & Middle Initial & Last Name or Official Title & Degree
Andreea Ciudin, PhD
Phone
+34 932744736
Ext
4736
Email
aciudin@vhebron.net
Facility Information:
Facility Name
Hospital Universitari Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andreea Ciudin, PhD
Phone
+34932744736
Email
aciudin@vhebron.net
First Name & Middle Initial & Last Name & Degree
Cristina Hernandez, MD, PhD
Phone
+34 932746591
Email
cristina.hernandez@vhir.org
First Name & Middle Initial & Last Name & Degree
Cristina Hernandez, MD, PhD
First Name & Middle Initial & Last Name & Degree
Andreea Ciudin, MD
First Name & Middle Initial & Last Name & Degree
Olga Simó-Servat, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
15793200
Citation
Hernandez C, Francisco G, Chacon P, Simo R. Lipoprotein(a) as a risk factor for cardiovascular mortality in type 2 diabetic patients: a 10-year follow-up study. Diabetes Care. 2005 Apr;28(4):931-3. doi: 10.2337/diacare.28.4.931. No abstract available.
Results Reference
background
PubMed Identifier
12964817
Citation
Hernandez C, Francisco G, Chacon P, Mesa J, Simo R. Biological variation of lipoprotein(a) in a diabetic population. Analysis of the causes and clinical implications. Clin Chem Lab Med. 2003 Aug;41(8):1075-80. doi: 10.1515/CCLM.2003.166.
Results Reference
background
PubMed Identifier
21500721
Citation
Genser B, Dias KC, Siekmeier R, Stojakovic T, Grammer T, Maerz W. Lipoprotein (a) and risk of cardiovascular disease--a systematic review and meta analysis of prospective studies. Clin Lab. 2011;57(3-4):143-56.
Results Reference
background

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The Effect of the GLP-1 Receptor Agonists on Blood Levels of Lipoprotein (a)

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