GH and Cardiovascular Risk Factors
Primary Purpose
Growth Hormone Deficiency, Cardiovascular Diseases, Metabolic Syndrome
Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Change in daily dosage of Growth Hormone
Sponsored by
About this trial
This is an interventional treatment trial for Growth Hormone Deficiency
Eligibility Criteria
Inclusion Criteria:
- Ongoing surveillance at our centre (VUmc)
- Stable substitution therapy for other pituitary hormone deficiencies
Exclusion Criteria:
- Subjects with a craniopharyngioma as cause of their GHD or pituitary deficiencies
- Contraindications for the use of GH treatment
- (Receiving treatment for) malignant disease (in the past)
- Cardiovascular event less than one year prior to inclusion
- Participation in other studies
- Subjects, who in the opinion of the investigator, are unsuitable in any other way to participate in this study
Sites / Locations
- VU University Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Low dose Growth Hormone
High dose Growth Hormone
Arm Description
Halve of the group of men and group of women will receive a decrease of their regular dose of Growth Hormone treatment, with the IGF-I target level of -2 - -1 SD score (low dose=LD).
Halve of the group of men and group of women will receive an increase of their regular dose of Growth Hormone treatment, with the IGF-I target level of 1 - 2 SD score (high dose=HD).
Outcomes
Primary Outcome Measures
Change in cardiovascular risk (body composition and lipid profile)
Secondary Outcome Measures
Change in cardiovascular risk (inflammatory markers, vascular stiffness, endothelial function, presence of the metabolic syndrome)
Change in physical performance (muscle strength, physical activity)
Change in glucose metabolism (fasting and 2hr postprandial glucose, insulin resistance)
Change in neuropsychological functioning (QoL, cognition, mood)
Full Information
NCT ID
NCT01877512
First Posted
June 11, 2013
Last Updated
May 6, 2014
Sponsor
Amsterdam UMC, location VUmc
1. Study Identification
Unique Protocol Identification Number
NCT01877512
Brief Title
GH and Cardiovascular Risk Factors
Official Title
Effect of Growth Hormone Replacement Therapy on Cardiovascular Risk Factors in Adult Patients With Severe Growth Hormone Deficiency: Association With IGF-I Concentration
Study Type
Interventional
2. Study Status
Record Verification Date
May 2014
Overall Recruitment Status
Completed
Study Start Date
May 2013 (undefined)
Primary Completion Date
April 2014 (Actual)
Study Completion Date
April 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Amsterdam UMC, location VUmc
4. Oversight
5. Study Description
Brief Summary
Rationale: Abnormally low and high levels of insulin-like growth factor-I (IGF-I) are both associated with increased metabolic risk. Since (U-shaped) associations of IGF-I, within the normal range, have also been found with cardiovascular risk factors and disease in the general population, it would be interesting to investigate if this association can also be found in growth hormone deficient (GHD) adults treated with Growth Hormone (GH). This could be of interest for endocrinologists prescribing GH in clinical practice because strict dosing may become even more important. Next to that, scientific evidence for clinical practice is wanted.
Objective: Next to cardiovascular risk factors (main objectives: body composition and lipid profile; secondary objectives: remainder) we investigate the effect on glucose metabolism, physical performance, and neuropsychological functioning of different levels of IGF-I in GH treated GHD men and women.
Study design: Open-label randomized trial.
Study population: At least 32 subjects, both childhood as adult onset GHD men and women, receiving GH treatment for at least one year, with an age between 20 and 65 years.
Intervention: At entry subjects are already receiving GH treatment according to general clinical practice, and are expected to demonstrate an IGF-I concentration of 0 - 1 SD score (SDS) (normal dose). The group of men and group of women will be randomized to receive either a decrease of their regular dose of GH treatment (IGF-I target level of -2 - -1 SDS) (low dose), or an increase of their regular dose, (IGF-I target level of 1 - 2 SDS) (high dose) for at least 24 weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Growth Hormone Deficiency, Cardiovascular Diseases, Metabolic Syndrome, Cognition, Physical Activity
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Low dose Growth Hormone
Arm Type
Active Comparator
Arm Description
Halve of the group of men and group of women will receive a decrease of their regular dose of Growth Hormone treatment, with the IGF-I target level of -2 - -1 SD score (low dose=LD).
Arm Title
High dose Growth Hormone
Arm Type
Active Comparator
Arm Description
Halve of the group of men and group of women will receive an increase of their regular dose of Growth Hormone treatment, with the IGF-I target level of 1 - 2 SD score (high dose=HD).
Intervention Type
Drug
Intervention Name(s)
Change in daily dosage of Growth Hormone
Other Intervention Name(s)
Change in daily dosage of Somatropin
Primary Outcome Measure Information:
Title
Change in cardiovascular risk (body composition and lipid profile)
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Change in cardiovascular risk (inflammatory markers, vascular stiffness, endothelial function, presence of the metabolic syndrome)
Time Frame
24 weeks
Title
Change in physical performance (muscle strength, physical activity)
Time Frame
24 weeks
Title
Change in glucose metabolism (fasting and 2hr postprandial glucose, insulin resistance)
Time Frame
24 weeks
Title
Change in neuropsychological functioning (QoL, cognition, mood)
Time Frame
24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Ongoing surveillance at our centre (VUmc)
Stable substitution therapy for other pituitary hormone deficiencies
Exclusion Criteria:
Subjects with a craniopharyngioma as cause of their GHD or pituitary deficiencies
Contraindications for the use of GH treatment
(Receiving treatment for) malignant disease (in the past)
Cardiovascular event less than one year prior to inclusion
Participation in other studies
Subjects, who in the opinion of the investigator, are unsuitable in any other way to participate in this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Madeleine L. Drent, MD PhD
Organizational Affiliation
Amsterdam UMC, location VUmc
Official's Role
Principal Investigator
Facility Information:
Facility Name
VU University Medical Center
City
Amsterdam
State/Province
PO Box 7057
ZIP/Postal Code
1007 MB
Country
Netherlands
12. IPD Sharing Statement
Citations:
PubMed Identifier
33633687
Citation
van Bunderen CC, Meijer RI, Lips P, Kramer MH, Serne EH, Drent ML. Titrating Growth Hormone Dose to High-Normal IGF-1 Levels Has Beneficial Effects on Body Fat Distribution and Microcirculatory Function Despite Causing Insulin Resistance. Front Endocrinol (Lausanne). 2021 Feb 9;11:619173. doi: 10.3389/fendo.2020.619173. eCollection 2020.
Results Reference
derived
PubMed Identifier
29980224
Citation
van Bunderen CC, Deijen JB, Drent ML. Effect of low-normal and high-normal IGF-1 levels on memory and wellbeing during growth hormone replacement therapy: a randomized clinical trial in adult growth hormone deficiency. Health Qual Life Outcomes. 2018 Jul 6;16(1):135. doi: 10.1186/s12955-018-0963-2.
Results Reference
derived
Learn more about this trial
GH and Cardiovascular Risk Factors
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