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The Effect of Liraglutide on Bone Turnover, Bone Mass and Bone Cell Function (LIRABONE)

Primary Purpose

Diabetes Complications, Osteoporosis

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Liraglutide
Placebo
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Complications

Eligibility Criteria

30 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Informed consent
  • Diagnosis of type 2 diabetes (HbA1c > 48 mmol/mol)
  • Age older than 30 years

Exclusion Criteria:

  • Type 1 diabetes
  • Treatment with insulin
  • Body weight > 140 kg
  • HbA1c > 75 mmol/mol
  • Treatment with GLP-1 analogues, Dipeptidyl peptidase-4 inhibitors, or glitazones
  • Chronic kidney disease
  • Hepatic disease
  • Pancreatitis
  • Inflammatory bowel disease
  • Osteoporosis
  • Family or personal history of medullary thyroid carcinoma
  • Treatment with glucocorticoids
  • Hormone replacement therapy
  • Diabetic gastroparesis
  • Pregnancy or lactation

Sites / Locations

  • Department of Endocrinology and Internal Medicine, Aarhus University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Liraglutide

Placebo

Arm Description

Liraglutide ("Victoza"), subcutaneous 1,8 mg once daily for 180 days

Saline, subcutaneous once daily for 180 days

Outcomes

Primary Outcome Measures

Change in collagen I cross-linked C-terminal telopeptide measured in serum
Collagen I cross-linked C-terminal telopeptide has been chosen as primary endpoint as the expected mechanism of action is reduction in bone resorption, and as it is the most responsive bone resorption marker.

Secondary Outcome Measures

Change in bone alkaline phosphatase measured in serum
Change in BMD evaluated by DXA
Change in bone structure evaluated by QCT and HRpQCT
Change in HbA1c
Change in osteocalcin measured in serum
Change in procollagen type I N-terminal propeptide measured in serum

Full Information

First Posted
June 8, 2015
Last Updated
September 25, 2018
Sponsor
University of Aarhus
Collaborators
Aarhus University Hospital, Novo Nordisk A/S
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1. Study Identification

Unique Protocol Identification Number
NCT02473809
Brief Title
The Effect of Liraglutide on Bone Turnover, Bone Mass and Bone Cell Function
Acronym
LIRABONE
Official Title
The Effect of Liraglutide on Bone Turnover, Bone Mass and Bone Cell Function
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
August 2015 (undefined)
Primary Completion Date
October 2017 (Actual)
Study Completion Date
October 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
Aarhus University Hospital, Novo Nordisk A/S

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to test whether liraglutide, a drug approved and widely used in the treatment of type 2 diabetes, has an effect on bone mass and bone cell function. Type 2 diabetes may cause multiple complications, and it is well known that patients with type 2 diabetes have a higher risk of fractures. If Liraglutide can be demonstrated to have a positive effect on bone, this may be one among other factors to consider before the decision about specific treatment of type 2 diabetes is made for the individual patient.
Detailed Description
Background: Type 2 diabetes may cause complications such as ischemic heart disease, nephropathy, neuropathy, and retinopathy. Several epidemiologic and animal studies also suggest that fracture risk is increased in diabetes. Bone is remodelled throughout life through bone resorption by the bone resorbing cells, the osteoclasts, and by bone formation by the bone forming cells, the osteoblasts. Bone remodelling can be monitored by biochemical markers of bone turnover and the effect of bone remodelling can be measured by changes in bone mineral density (BMD) by Dual X-ray absorptiometry (DXA) or bone structure by quantitative CT (QCT) or high resolution peripheral QCT (HRpQCT). The remodelling activity and the balance between resorption and formation are influenced by many factors including food consumption. The gut hormone glucagon-like polypeptide 1 (GLP-1) is released in relation to food intake and reduces serum levels of glucagon, increases serum levels of insulin, and reduces blood glucose in diabetes. Liraglutide is a GLP-1 analogue and has been approved for the treatment of type 2 diabetes. Aim: To investigate the effect of the GLP-1 analogue Liraglutide on bone turnover, bone mass, and bone structure in patients with type 2 diabetes. Methods: The clinical study will be conducted as a randomised, double-blinded, placebo-controlled, prospective, clinical trial with comparative treatment regimes with either subcutaneous Liraglutide or subcutaneous placebo injections. Perspectives: The project will bring new knowledge about the possible effects of GLP-1 analogues on bone turnover and structure. This is important given that type 2 diabetes deteriorates bone health and increases risk of fractures. If Liraglutide can be demonstrated to have a positive effect on bone, this may be one among other factors to consider before the decision about specific treatment of type 2 diabetes is made for the individual patient.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Complications, Osteoporosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Liraglutide
Arm Type
Experimental
Arm Description
Liraglutide ("Victoza"), subcutaneous 1,8 mg once daily for 180 days
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Saline, subcutaneous once daily for 180 days
Intervention Type
Drug
Intervention Name(s)
Liraglutide
Other Intervention Name(s)
Victoza
Intervention Description
Once daily
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Saline
Intervention Description
Once daily
Primary Outcome Measure Information:
Title
Change in collagen I cross-linked C-terminal telopeptide measured in serum
Description
Collagen I cross-linked C-terminal telopeptide has been chosen as primary endpoint as the expected mechanism of action is reduction in bone resorption, and as it is the most responsive bone resorption marker.
Time Frame
Days 0, 7, 28, 90, 180
Secondary Outcome Measure Information:
Title
Change in bone alkaline phosphatase measured in serum
Time Frame
Days 0, 7, 28, 90, 180
Title
Change in BMD evaluated by DXA
Time Frame
Days 0, 90, 180
Title
Change in bone structure evaluated by QCT and HRpQCT
Time Frame
Days 0, 90, 180
Title
Change in HbA1c
Time Frame
Days 0, 180
Title
Change in osteocalcin measured in serum
Time Frame
Days 0, 7, 28, 90, 180
Title
Change in procollagen type I N-terminal propeptide measured in serum
Time Frame
Days 0, 7, 28, 90, 180

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed consent Diagnosis of type 2 diabetes (HbA1c > 48 mmol/mol) Age older than 30 years Exclusion Criteria: Type 1 diabetes Treatment with insulin Body weight > 140 kg HbA1c > 75 mmol/mol Treatment with GLP-1 analogues, Dipeptidyl peptidase-4 inhibitors, or glitazones Chronic kidney disease Hepatic disease Pancreatitis Inflammatory bowel disease Osteoporosis Family or personal history of medullary thyroid carcinoma Treatment with glucocorticoids Hormone replacement therapy Diabetic gastroparesis Pregnancy or lactation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bente L Langdahl, MD PhD DMSc
Organizational Affiliation
Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Denmark
Official's Role
Study Director
Facility Information:
Facility Name
Department of Endocrinology and Internal Medicine, Aarhus University Hospital
City
Aarhus
State/Province
Aarhus C
ZIP/Postal Code
8000
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
7479679
Citation
Fehmann HC, Hering BJ, Wolf MJ, Brandhorst H, Brandhorst D, Bretzel RG, Federlin K, Goke B. The effects of glucagon-like peptide-I (GLP-I) on hormone secretion from isolated human pancreatic islets. Pancreas. 1995 Aug;11(2):196-200. doi: 10.1097/00006676-199508000-00014.
Results Reference
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PubMed Identifier
23023946
Citation
Leslie WD, Rubin MR, Schwartz AV, Kanis JA. Type 2 diabetes and bone. J Bone Miner Res. 2012 Nov;27(11):2231-7. doi: 10.1002/jbmr.1759. Epub 2012 Sep 28. Erratum In: J Bone Miner Res. 2017 Nov;32(11):2319.
Results Reference
background
PubMed Identifier
17925191
Citation
Schwartz AV, Sellmeyer DE. Diabetes, fracture, and bone fragility. Curr Osteoporos Rep. 2007 Sep;5(3):105-11. doi: 10.1007/s11914-007-0025-x.
Results Reference
background
PubMed Identifier
17068657
Citation
Vestergaard P. Discrepancies in bone mineral density and fracture risk in patients with type 1 and type 2 diabetes--a meta-analysis. Osteoporos Int. 2007 Apr;18(4):427-44. doi: 10.1007/s00198-006-0253-4. Epub 2006 Oct 27.
Results Reference
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PubMed Identifier
18039776
Citation
Yamada C, Yamada Y, Tsukiyama K, Yamada K, Udagawa N, Takahashi N, Tanaka K, Drucker DJ, Seino Y, Inagaki N. The murine glucagon-like peptide-1 receptor is essential for control of bone resorption. Endocrinology. 2008 Feb;149(2):574-9. doi: 10.1210/en.2007-1292. Epub 2007 Nov 26.
Results Reference
background
PubMed Identifier
21372151
Citation
Nuche-Berenguer B, Lozano D, Gutierrez-Rojas I, Moreno P, Marinoso ML, Esbrit P, Villanueva-Penacarrillo ML. GLP-1 and exendin-4 can reverse hyperlipidic-related osteopenia. J Endocrinol. 2011 May;209(2):203-10. doi: 10.1530/JOE-11-0015. Epub 2011 Mar 3.
Results Reference
background
PubMed Identifier
25074632
Citation
Su B, Sheng H, Zhang M, Bu L, Yang P, Li L, Li F, Sheng C, Han Y, Qu S, Wang J. Risk of bone fractures associated with glucagon-like peptide-1 receptor agonists' treatment: a meta-analysis of randomized controlled trials. Endocrine. 2015 Feb;48(1):107-15. doi: 10.1007/s12020-014-0361-4. Epub 2014 Jul 30.
Results Reference
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The Effect of Liraglutide on Bone Turnover, Bone Mass and Bone Cell Function

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