Abdominal Obesity, Cardiovascular Inflammation, and Effects of Growth Hormone Releasing Hormone Analogue
| Status: | Not yet recruiting |
|---|---|
| Conditions: | Obesity Weight Loss |
| Therapuetic Areas: | Endocrinology |
| Healthy: | No |
| Age Range: | 18 - 55 |
| Updated: | 1/1/2014 |
| Start Date: | January 2014 |
| End Date: | June 2019 |
| Contact: | Steven Grinspoon, MD |
| Email: | sgrinspoon@partners.org |
| Phone: | 617-724-9109 |
Abdominal Obesity, Cardiovascular Inflammation, and Effects of a Growth Hormone Releasing Hormone Analogue to Reduce Inflammation
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.
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.
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)
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