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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01927471
Other study ID # IRB #: 1108002383
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2011
Est. completion date July 2019

Study information

Verified date February 2024
Source Cornell University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators would like to determine how aspects of metabolism and age influence ovarian function. The purpose of the study is to understand how nutrition and metabolism relate to follicle development in women with regular cycles, irregular cycles, or polycystic ovary syndrome (PCOS). We also plan to identify lifestyle factors associated with PCOS and understand how diet and activity levels impact features of PCOS.


Description:

In the ovaries, eggs rest in fluid filled sacs called follicles. When follicles grow they form small fluid-filled cysts that can be easily seen when we use ultrasound to view the ovaries. In women with regular menstrual cycles, groups of follicles grow and regress 2 to 3 times during their cycle (usually over a 28- day period). Several of these follicles grow to a stage where they begin to develop the potential to ovulate - but in general only one follicle is chosen to ovulate. Thus, at any given time during the menstrual cycle, numerous fluid-filled follicles can be visualized in a woman's ovaries at various stages of development using transvaginal ultrasonography. In women with absent or infrequent menstrual cycles, very little is known about the growth patterns of their follicles and how factors such as metabolic hormones, might play a role in the failure to ovulate. Being underweight or overweight increases your chances of having irregular or absent menstrual cycles and a history of abnormal reproductive function compounds your risks for chronic diseases such as infertility, diabetes, hypertension, atherosclerosis and certain cancers. This is particularly the case for women with PCOS that have menstrual cycles that appear to worsen or improve depending on their body weight and metabolic status. Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects 6-12% of reproductive-aged women within the general population. The hallmark features of PCOS are menstrual irregularity, increased levels of androgens, and polycystic ovaries. The current diagnostic criteria require 2 out of 3 of these features to be present for the diagnosis, therefore a number of phenotypes of PCOS exist. However, the metabolic and reproductive differences across the phenotypic spectrum of PCOS are not well understood. Women with PCOS characteristically have polycystic ovaries, where up to 10 times more follicles are present in the ovary at any given time. Further, the follicle-size populations and overall distribution throughout the ovary varies in women - follicles may be situated around the periphery of the ovary or may be distributed throughout the ovary. Presumably these small follicles are arrested in development - but emerging data from the Lujan laboratory suggest that this is not the case. Rather, follicles continue to grow in a dynamic pattern during these prolonged periods of anovulation. By comparing follicle populations, reproductive hormones and markers of metabolism in women with regular cycles, women with irregular cycles, and women with a history of PCOS, the researchers plan to identify what factors might explain why fertility potential and long-term health are compromised in some women but not in others. By including women at both early and late stages of their reproductive potential, the researchers will also be able to assess what influence age has on these factors. The ultimate goal of this research is to understand how nutrition and metabolism regulate follicle development in women so we can better develop lifestyle and drug therapies to help women preserve their fertility and long-term health. Since obesity has recently become the leading cause of infertility in North America, these studies are especially important. Current research has failed to thoroughly examine the relationships between dietary intake, energy expenditure and PCOS. The purpose of this proposed study is to identify lifestyle factors associated with PCOS. Through dietary intake and energy expenditure data, the researchers plan to examine potential lifestyle differences between PCOS and healthy women, as well as between BMI classifications within women with PCOS. The Research Team will also be able to evaluate the diet quality according to the USDA Dietary Guidelines for Americans of all women included in the study. The Research Team is also interested in the relationships between biological markers and lifestyle endpoints in women with and without PCOS. Previous literature has shown there are biological marker differences between those with and without PCOS. By examining these relationships, researchers may further understand whether PCOS status is associated with lifestyle parameters. To accomplish these objectives, the investigators plan to recruit 120 women with regular menstrual cycles and 240 women with irregular menstrual cycles, with or without PCOS (sub-grouped into 120 women with irregular menstrual cycles and 120 women with a history of PCOS). Their goal is to recruit an equal number of women in each group such that they are matched for age (18 - 48 years old) and body mass index (BMI; Normal weight = 18 - 24.9 kg/m2; Overweight = 25 - 29.9 kg/m2; Obese ≥ 30kg/m2). Women will be included in the PCOS sub-group if they have a confirmed PCOS diagnosis from their primary care provider. Ultrasound scans of the ovaries will be assessed for the total number, size, and distribution of follicles using both two- and three-dimensional imaging techniques. Participants will have blood samples collected determine serum concentrations of luteinizing hormone (LH), follicle stimulating hormone (FSH), estradiol, progesterone, anti-müllerian hormone (AMH), and inhibin B. The following metabolic parameters will be assessed: (1) 75-gram oral glucose tolerance test to characterize glucose and insulin dynamics at 0, 30, 60, 90, and 120 minutes post-glucose ingestion; (2) dual X-ray absorptiometry (DXA) scan to quantify body fat and lean muscle distribution; (3) vitals and anthropometry assessment to measure waist and hip circumference, height, weight, blood pressure, and heart rate, and (4) fasting blood tests to detect serum concentrations of androgens (i.e., total testosterone, androstenedione, free androgen index) and serum markers of metabolic syndrome (i.e., lipids and hemoglobin A1C). Participants will complete a food frequency questionnaire, a semi-structured dietary interview, and physical activity questionnaire. A researcher may also provide participants with an accelerometer to wear for a week. Participants may also elect to participate in an optional subcutaneous fat biopsy.


Recruitment information / eligibility

Status Completed
Enrollment 129
Est. completion date July 2019
Est. primary completion date July 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 48 Years
Eligibility Inclusion Criteria: - Between 18 and 48 years - BMI = 18 kg/m2 Either: - Regular menstrual cycles (21-35 days); - Irregular menstrual cycles (>36 days); or - Previous diagnosis of PCOS from a primary care provider - If 21 years of age or older, must have had a healthy pelvic exam w/in the past 2 years Exclusion Criteria: - Current use of medication(s) known or suspected to interfere with reproductive function (eg. oral contraceptives) or insulin sensitivity - Pregnant or breastfeeding - Not otherwise healthy - Significant weight changes within the last three months

Study Design


Locations

Country Name City State
United States Human Metabolic Research Unit, Cornell University Ithaca New York
United States CRC at University of Rochester Medical Center Rochester New York
United States Strong Fertility Center Rochester New York

Sponsors (2)

Lead Sponsor Collaborator
Cornell University University of Rochester

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Follicle number per ovary The number and size of all follicles in each ovary will be assess by ultrasonography for each participant with regular menstrual cycles, irregular menstrual cycles and PCOS. 1 day
Primary Insulin sensitivity Insulin sensitivity will be determined by administration of an oral glucose tolerance test and compared across groups. 1 day
Secondary Ovarian Volume The size of each ovary will be determined by ultrasonography for each participant and compared across groups. 1 day
Secondary Anti-Müllerian hormone Circulating AMH levels in the serum will be determined for each participant and compared across groups. 1 day
Secondary LH-FSH ratio The ratio of circulating LH to FSH concentrations in the serum will be determined for each participant and compared across groups. 1 day
Secondary Androgen concentrations Total testosterone, androstenedione and free androgen index concentrations in serum will be determined and compared across groups. 1 day
Secondary Menstrual Cycle Length Average menstrual cycle length as determined by self-reported history will be determined and compared across groups. 1 day
Secondary Hirsutism Degree of hirsutism as judged by the Ferriman-Gallwey scale will be determined and compared across groups. 1 day
Secondary Serum markers of metabolic syndrome Lipids, glucose and HbA1C concentrations will be determined and compared across groups. 1 day
Secondary Blood Pressure Blood pressure will be determined and compared across groups. 1 day
Secondary Body mass index The ratio of weight to height will be determined and compared across groups. 1 day
Secondary Waist-to-hip ratio The ratio of waist circumference to hip circumference will be determined and compared across groups. 1 day
Secondary Body fat distribution Percentage and distribution of fat and lean mass as assessed using DXA technology will be compared across groups. 1 day
Secondary Differences in diet composition between women with and without PCOS A food frequency questionnaire will be administered to assess diet composition for the last three months 1 week
Secondary Differences in energy expenditure between women with and without PCOS Participants will be asked to wear a small accelerometer device to assess physical activity 1 week
Secondary Subcutaneous fat biopsy (optional) Subcutaneous fat biopsies will be conducted to assess differences in fat cell populations (major site of reproductive hormone synthesis) between groups 1 day
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