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Sex Steroids, Sleep, and Metabolic Dysfunction in Women (SCOR)

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The Washington University

Status

Completed

Conditions

Obesity
Obstructive Sleep Apnea
Polycystic Ovary Syndrome (PCOS)

Treatments

Other: Control
Device: continuous positive airway pressure
Drug: Progesterone
Drug: Estrogen
Drug: testosterone
Drug: glucocorticoid

Study type

Interventional

Funder types

Other

Identifiers

NCT00805207
07-0692
NIH P50 HD057796

Details and patient eligibility

About

Increased plasma triglyceride concentration is a common feature of the metabolic abnormalities associated with obesity and a major risk factor for cardiovascular disease. Obesity is a major risk factor for two conditions that appear to be increasing in prevalence in women: the polycystic ovary syndrome (PCOS) and sleep disordered breathing. PCOS affects 5-8% of women. Sleep disordered breathing affects up to 10% of women. Obstructive sleep apnea (OSA) is the most common cause for sleep disordered breathing and particularly prevalent in obese women with PCOS (~50%). Both PCOS and OSA augment the increase in plasma triglyceride (TG) concentration associated with obesity, and the effects of PCOS and OSA on plasma TG concentration appear to be additive. The mechanisms responsible for the adverse effects on plasma TG metabolism are not known. The primary goal of this project, therefore, is to determine the mechanisms responsible for the increase in plasma TG concentration in obese women with PCOS and OSA. It is our general hypothesis that alterations in the hormonal milieu that are characteristic of these two conditions are, at least in part, responsible for the increase in plasma TG concentration in obese women with the conditions. Furthermore, we hypothesize that the hormonal aberrations characteristic of the two conditions are particularly harmful to obese, compared with lean, women.

The effects of PCOS on skeletal muscle protein metabolism are also not known. However, sex hormones are thought to be important regulators of muscle protein turnover suggesting that muscle protein metabolism is likely to be affected by PCOS. We will examine this by determining the effect of individual sex hormones on muscle protein metabolism and hypothesize that testosterone administration will stimulate muscle protein metabolism while estrogen and progesterone administration will inhibit muscle protein metabolism.

Enrollment

61 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women aged 18-75 years and men 45-75 years
  • Healthy lean, overweight and obese women (BMI 18-40 kg/m2) and obese men (BMI 30-40 kg/m2)
  • Obese women (BMI 30-40 kg/m2) with OSA or PCOS

Exclusion criteria

  • Pregnant, lactating, peri- or postmenopausal women will be excluded from the study because of potential confounding influences of these factors and potential ethical concerns (pregnant women)
  • Women taking medications known to affect substrate metabolism and those with evidence of significant organ dysfunction (e.g. impaired glucose tolerance, diabetes mellitus, liver disease, hypo- or hyper-thyroidism) other than PCOS and OSA
  • Severe hypertriglyceridemia (fasting plasma TG concentration >400 mg/dl)
  • Subjects with OSA who have an apnea-hypopnea index (AHI) score >30 (the total number of obstructive events divided by the total hours of sleep) will be excluded and instructed to seek medical care

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

61 participants in 9 patient groups

Progesterone - PCOS
Experimental group
Description:
Women with obesity and polycystic ovary syndrome
Treatment:
Drug: Progesterone
Testosterone - premenopausal women
Experimental group
Description:
Healthy premenopausal women.
Treatment:
Drug: testosterone
Continuous positive airway pressure
Experimental group
Description:
Women and men with obesity and obstructive sleep apnea
Treatment:
Device: continuous positive airway pressure
Glucocorticoid
Experimental group
Description:
Lean and obese healthy women, and obese men
Treatment:
Drug: glucocorticoid
Estrogen
Experimental group
Description:
Postmenopausal women
Treatment:
Drug: Estrogen
control
Other group
Description:
Postmenopausal women - tested before and after no treatment. Duration between before and after testing ranged from 31 to 78 days with an average of 46 days between visits
Treatment:
Other: Control
control - baseline testing only
No Intervention group
Description:
Healthy men and women
Progesterone - Postmenopausal women
Experimental group
Description:
Postmenopausal women
Treatment:
Drug: Progesterone
Testosterone - Postmenopausal women
Experimental group
Description:
Postmenopausal women
Treatment:
Drug: testosterone

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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