Abdominal Obesity, Cardiovascular Inflammation, and Effects of Growth Hormone Releasing Hormone Analogue

Abdominal Obesity Clinical Trial

Official title:

Abdominal Obesity, Cardiovascular Inflammation, and Effects of a Growth Hormone Releasing Hormone Analogue to Reduce Inflammation

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01632592
• Other study ID #: 2012p-000917
• Status: Withdrawn
• Phase: N/A
• First received: June 27, 2012
• Last updated: January 23, 2014
• Start date: January 2014
• Est. completion date: January 2014

Study information

• Verified date: January 2014
• Source: Massachusetts General Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Obesity is strongly associated with risk of cardiovascular disease (CVD). Data increasingly suggest that visceral adipose tissue (VAT) accumulation -- or increased abdominal fat -- is particularly deleterious to cardiovascular health, but further study is needed to test this idea. Increased abdominal fat may also be associated with lower secretion of a hormone called growth hormone (GH), which helps the body burn fat. The current study aims to carefully characterize relationships between abdominal fat and CVD. In addition, by using a medication called growth hormone releasing hormone, which is a strategy to reduce abdominal fat, the investigators will test the hypothesis that abdominal fat contributes uniquely to increased arterial inflammation.

In the first part of this study, the investigators will investigate both lean (healthy weight) individuals and individuals with increased abdominal fat. The investigators will study their body composition, cardiovascular risk measures, insulin sensitivity, and growth hormone dynamics, with the hypothesis that abdominal fat, independent of general obesity, will be strongly associated with arterial wall thickening and atherosclerotic inflammation. The investigators will assess arterial wall thickness, plaque morphology, and atherosclerotic inflammation, and the investigators will determine associations between these variables and regional fat accumulation, with particular attention to abdominal fat.

The second, treatment part of the study will be only for individuals with increased abdominal fat who are found to have low growth hormone secretion. In that part of the study, the investigators will test the effects of a growth hormone releasing hormone (GHRH) analogue to reduce abdominal fat and, consequently, reduce arterial inflammation. The investigators hypothesize that abdominal fat reduction, independent of changes in growth hormone, will reduce arterial inflammation and arterial wall thickness.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: January 2014
• Est. primary completion date: January 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 55 Years

Eligibility

Inclusion/Exclusion Criteria:

Inclusion Criteria for Lean Controls:

1. Men and women age 18-55y

2. BMI > 18.5 and < 25 kg/m2

3. Waist circumference < 102 cm in men and <88cm in women

Inclusion criteria for Abdominal Obesity:

1. Men and women age 18-55y

2. BMI = 30kg/m2

3. Abdominal obesity as defined by waist circumference = 102 cm in men and = 88 cm in women

4. Relative GH deficiency as demonstrated by peak GH to arginine/GHRH stimulation test of < 9mcg/L (for treatment portion only)

5. Negative age-appropriate screening for cancer performed by primary care physician (e.g., negative mammogram if F > 50yo) (For treatment portion only)

Exclusion criteria for all subjects:

1. Obesity due to known secondary causes

2. Use of weight-lowering drugs or previous weight loss surgery

3. Use of gonadal steroids, GH, GHRH, glucocorticoids, megesterol acetate, antidiabetic agents, or any other hormonal medication judged by the investigator to be inappropriate within the past 6 months. Use of physiologic testosterone replacement will be allowed.

4. Statin use

5. Known coronary artery disease or peripheral vascular disease, or any history of stroke or significant chest pain

6. Known auto-immune or inflammatory disease

7. Any surgery or significant injury (including fracture or other trauma) within the past 6 months

8. Hemoglobin < 11g/dL, fasting glucose > 126mg/dL, creatinine <1.5mg/dL, or AST > 2.5x upper limit of normal

9. FSH > 20 IU/L (women only)

10. Positive urine pregnancy test, actively seeking pregnancy, or breastfeeding

11. Prior history of pituitary disease, pituitary surgery, or head irradiation, or any other condition known to affect pituitary function

12. Infectious illness in the past 3 months, or chronic infectious illness

13. Allergy to iodine containing contrast media

14. Active illicit drug use

15. For women of childbearing potential, failure to use an acceptable form of non-hormonal birth control

16. Active malignancy: For the treatment part of the study, all active malignancy will be excluded. For the observational part of the study (which involves no intervention) basal cell carcinoma and low grade cervical or anal intraepithelial neoplasms will be allowed.

17. History of colon cancer (treatment part only)

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Abdominal Obesity
• Inflammation
• Obesity
• Obesity, Abdominal

Intervention

Drug:
• Tesamorelin
The Growth Hormone Releasing Hormone analogue tesamorelin, 2mg subcutaneously daily by injection
• Placebo
placebo given by injection 2mg subcutaneously daily

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	aortic "target to background ratio" (Aortic TBR)	aortic target-to-background ratio is a measure of the inflammation in the wall of the aorta that is made by positron emission tomography (PET) scanning in conjunction with computed tomography (CT) scanning.	12 months	No