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Clinical Trials/NCT04314167
NCT04314167
Terminated
Not Applicable

Effect of Serum LDL Cholesterol Concentration on Pancreatic Insulin Secretion

University Hospital Tuebingen1 site in 1 country9 target enrollmentJuly 28, 2020

Overview

Phase
Not Applicable
Intervention
Lowering cholesterol concentrations by PCSK-9 inhibitor
Conditions
Hypercholesterolemia
Sponsor
University Hospital Tuebingen
Enrollment
9
Locations
1
Primary Endpoint
Change in insulin secretion.
Status
Terminated
Last Updated
last year

Overview

Brief Summary

Dyslipidemia is characterized by low levels of HDLs, hypertriglyceridemia as well as an increases proportion of small dense LDLs. Changes in lipoprotein particles and its concentrations, especially increased levels of pro-atherogenic LDL particles play an important role in the development of cardiovascular diseases. It is well established that statin/PCSK9-inhibitor treatment is very effective in lowering LDL cholesterol levels and therefore in preventing cardiovascular events. Besides the beneficial effects on cardiovascular system, these therapies are unfortunately linked to increased risk for type 2 diabetes.

However underlying mechanisms for the association between LDL cholesterol levels and the risk for type 2 diabetes remains largely unknown.Type 2 diabetes is especially characterized by insulin resistance and impaired insulin secretion from pancreatic beta-cells. Insulin resistance alone is insufficient to cause type 2 diabetes, as long as the ß-cell is able to compensate for the increased demand for insulin. Once this compensatory mechanism reaches its physiological limits, individuals progress to type 2 diabetes. Accordingly we aimed to investigate the associations between LDL cholesterol concentrations and the key issue in the pathogenesis of type 2 diabetes, insulin secretion before and after lowering cholesterol concentration by treatment with Evolocumab for 12 weeks in patients with medical indication for a treatment with a PCSK9-inhibitor. Therefore, patients will either undergo a hyperglycemic clamp or a oral glucose tolerance test in randomized manner.

Registry
clinicaltrials.gov
Start Date
July 28, 2020
End Date
March 1, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures
  • Medical indication for the treatment with a PCSK9-inhibitor
  • HbA1c \< 6,5%

Exclusion Criteria

  • Diabetes mellitus
  • Pregnant women or breastfeeding
  • Hb \< 11.5 g/dl (males) or Hb \< 10.5 g/dl (females)
  • treatment with any medication that effects on blood glucose concentrations, e.g. antidiabetic drugs or steroids
  • Any pancreatic disease

Arms & Interventions

LDL lowering therapy

Patients will receive the PCSK9-inhibitor Evolocumab as part of routine clinical management within the indication of this drug.

Intervention: Lowering cholesterol concentrations by PCSK-9 inhibitor

Outcomes

Primary Outcomes

Change in insulin secretion.

Time Frame: before and after 12 weeks of treatment with a PCSK9-inhibitor.

Effect of lowering LDL cholesterol levels on insulins secretion.This will be quantified in half of the patients by a hyperglycemic clamp and in the other half by a 75 g oral glucose tolerance test (randomized assignment).

Secondary Outcomes

  • Change in glucose tolerance.(before and after 12 weeks of treatment with a PCSK9-inhibitor.)
  • Change in insulin sensitivity.(before and after 12 weeks of treatment with a PCSK9-inhibitor.)
  • Change in insulin clearance.(before and after 12 weeks of treatment with a PCSK9-inhibitor.)

Study Sites (1)

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