Obesity Clinical Trial
Official title:
Mediators of Abnormal Reproductive Function in Obesity
The study is seeking to understand how being overweight and obese makes women less fertile.
The studies the investigators have done so far indicate that there is a hormone or other
substance produced by fat that goes into the blood and reduces reproductive hormones in
women who are overweight and obese. The present study will try to find the most promising
substances by studying small numbers of women and trying to remove the substances that are
causing the problem.
Hypothesis: A circulating factor or factors, either hormonal, inflammatory or metabolic,
causes relative pituitary hypofunction and correction of this reproductive deficit will
allow obese women with infertility who have failed to reduce their body weight to normal to
conceive, and may also prevent the horizontal passage of an adverse metabolic phenotype to
the offspring.
Specific Aim 1: To determine whether aromatase activity is measurable in adipose tissue
using the 'compound' (see appendix) as a precursor and whether aromatase is decreased in the
adipose tissue of obese women, and whether this varies by regional fat location. The
investigators will accomplish this by examining precursor/product ratios of hormones infused
through microdialysis using the 'compound' as a substrate.
Hypothesis for specific aim 1: Aromatase activity will be measurable in adipose tissue using
testosterone as a precursor. Estradiol, but not estrone production from androgen precursors
will be decreased in obese women relative to those of normal weight.
Specific Aim 2: To determine whether nonspecific, systemic suppression of inflammation will
lead to improved reproductive hormonal profiles of luteinizing hormone (LH), follicle
stimulating hormone(FSH), Estrone conjugates (E1c) and pregnandiol glucuronide (Pdg) in
obese women who undergo two menstrual cycles of study: one off treatment and one on
treatment. This aim shall be accomplished by performing daily urinary hormone monitoring of
two menstrual cycles, one prior to and one during treatment with low-dose aspirin and
polyunsaturated fatty acids (PUFAs).
Hypothesis for specific aim 2: A nonspecific, systemic inflammatory suppression therapy will
result in improved urinary profiles of LH, FSH, E1c and Pdg.
Specific Aim 3: To determine whether 4 weeks of reduction of circulating insulin will result
in improved reproductive hormonal profiles of LH, FSH, Estrone conjugates (E1c) and
pregnandiol glucuronide (Pdg) in obese women who undergo two menstrual cycles of study: one
off treatment and one on treatment. This aim shall be accomplished by performing daily
urinary hormone monitoring of two menstrual cycles, one prior to and one during treatment
with pioglitazone.
Hypothesis for specific aim 3: Chronic lowering of insulin with pioglitazone treatment of
obese women will result in improved urinary profiles of LH, FSH, E1c and Pdg.
;
Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science
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