Meal Timing on Glucose Metabolism and Hyperandrogenism in Lean Women With Polycystic Ovary Syndrome

Insulin Resistance Clinical Trial

— M-PCOS  

Official title:

Influence of Meal Timing on Glucose Metabolism and Hyperandrogenism in Lean Women With Polycystic Ovary Syndrome

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01569425
• Other study ID #: 0048-12-WOMC
• Status: Active, not recruiting
• Phase: N/A
• First received: March 30, 2012
• Last updated: April 7, 2015
• Start date: March 2012
• Est. completion date: June 2015

Study information

• Verified date: April 2015
• Source: Tel Aviv University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Israel: Ethics Commission
• Study type: Interventional

Clinical Trial Summary

In obese women with polycystic ovary syndrome (PCOS), weight loss improves insulin resistance and hyperandrogenism, resulting in improvement of clinical symptoms. Weight loss is not required in lean PCOS patients; nevertheless, the influence of meal timing and composition on glucose metabolism and hyperandrogenism may have clinical value. In this study the investigators investigate the effects of two isocaloric diets with different meal timing distribution on insulin resistance and hyperandrogenism in lean PCOS patients.

Description:

Insulin resistance and hyperinsulinemia plays a pivotal role in the pathogenesis of polycystic ovary syndrome (PCOS). Hyperinsulinemia stimulates ovarian cytochrome P450c17 alpha activity, in obese and nonobese women with PCOS, thereby increasing serum levels of 17-alpha-hydroxyprogesterone, androgens concentrations, decreasing SHBG and promoting the clinical features of hyperandrogenism.

In women with PCOS, weight loss improves insulin resistance and hyperandrogenism, resulting in improvement of clinical symptoms. Since lean women with PCOS do not have the option of weight loss, it is important to know weather diet composition and meal timing distribution may influence glucose metabolism and hyperandrogenism.

We hypothesized that a timing pattern of increased nutrient intake of protein and carbohydrates in the morning, with decreased caloric intake at night would improve insulin sensitivity and hyperandrogenism in lean women with PCOS.

Objective:The objective of this study is to investigate the effects of two isocaloric diets with different meal timing distribution on insulin resistance and hyperandrogenism in lean PCOS women.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 60
• Est. completion date: June 2015
• Est. primary completion date: June 2012
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Subjects =18 and =45 years of age

2. Lean women with PCOS (BMI: = 25 kg/m2)

3. Signed informed consent

4. Exclusion of late-onset adrenal hyperplasia by a fasting serum 17- hydroxy progesterone concentration below 200 ng/dl.

5. Acceptable health based on interview, medical history, physical examination, and laboratory tests (SMA20 and CBC).

6. Not dieting and no change in body weight >10 lb = 4.5 kg within the last 6 months

7. Stable physical activity pattern during the three months immediately preceding study initiation

8. Hyperandrogenemia (elevated free testosterone).

9. Normal liver and kidney function

10. Fasting blood glucose <110 mg/dl.

11. No metabolic disease

12. Usually wakes up between 05:00 and 07:00 and goes to sleep between 22:00 and 24:00.

13. Normal TSH and FT4 levels and serum prolactin

14. Acceptable health based on interview, medical history, physical examination, and laboratory tests

Exclusion Criteria:

1. Diabetes mellitus diagnosed by fasting glucose or a 2-hour OGTT, or fasting glucose > 110 mg/dl

2. Clinically significant pulmonary, cardiac, renal, hepatic, neurologic, psychiatric, infectious, malignant disease (other than skin cancer).

3. Current use of oral contraceptives

4. Serum creatinine level > 1.5 mg/dl

5. Abnormal liver function tests defined as an increase by a factor of at least 2 above the upper normal limit of alanine aminotransferase and/or aspartate

6. Any physiologic or mechanical problems preventing dietary adherence

7. Pregnant or lactating

8. Participating in another dietary program or use of weight-loss medications

9. Documented or suspected history (within one year) of illicit drug abuse or alcoholism.

10. Use of psychotropic or anoretic medication during the month immediately prior to study onset

11. Night or rotating shift work

12. Jet lag during the 2 week period immediately prior to study onset

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Hyperandrogenism
• Insulin Resistance
• Polycystic Ovary Syndrome

Intervention

Other:
• Dietary intervention
High Calorie breakfast and high calorie dinner

Locations

Country	Name	City	State
Israel	Daniela Jakubowicz	Holon	Tel Aviv

Sponsors (1)

Lead Sponsor	Collaborator
Tel Aviv University

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	hyperandrogenism	Androgens will be evaluate at baseline and after one of two isocaloric diet that differe in meal timing distribution	90 days	No
Secondary	glucose metabolism	Glucose metabolism will be evaluated at baseline and after one of two isocaloric diets that differ in meal timing distribution	90 days	No