Polynut: Effect of Modifications of Nutritional Intake Upon Reproductive Hormones in Normal Women

Sponsor
Centre Hospitalier Universitaire Vaudois (Other)
Overall Status
Completed
CT.gov ID
NCT02233283
Collaborator
(none)
9
1
4
17
0.5

Study Details

Study Description

Brief Summary

Undernutrition has a known and well recognized negative impact on reproductive hormones, and ultimately fertility. In contrast, much less is known regarding the potential effects of overnutrition on the same hormones. Epidemiological data suggest that overnutrition might have a deleterious impact as well on the fertile potential of affected women, but very little is known about the mechanisms implicated. Such knowledge may be of importance, given the increasing prevalence of overweight and obesity worldwide.

Condition or Disease Intervention/Treatment Phase
  • Other: Clamp
  • Other: Hypercaloric diet
  • Other: Basal
  • Other: Isocaloric diet
N/A

Detailed Description

In the present study, the investigators will perform a very detailed study of the minute to minute regulation of hormones of the neuroendocrine reproductive axis in normal young female volunteers. These studies will initially be performed at base line during isocaloric diet, where the stimulation of LH secretion by exogenous insulin will be tested during hyperinsulinemic eugylcemic clamp studies.

The same studies will then be repeated after a period of one month of controlled hypercaloric diet, where volunteers will receive an excess of approximately 30% KCal compared to their calculated daily energy expenditure. it is anticipated that such hypercaloric nutrition will induce a significant decrease in normal insulin sensitivity of these volunteers. Thus, the effect of changing whole body insulin sensitivity on the fine regulation of neuroendocrine reproductive hormones will be evaluated.

Study Design

Study Type:
Interventional
Actual Enrollment :
9 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Effect of Metabolic Variations Upon the Activity of the Neuroendocrine Reproductive Axis in Normal Female Volunteers
Study Start Date :
Jan 1, 2014
Actual Primary Completion Date :
Dec 1, 2014
Actual Study Completion Date :
Jun 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Hypercaloric diet and basal

Volunteers fed a hypercaloric diet for one month will be submitted to a fasting period of ten hours duration

Other: Hypercaloric diet
Hypercaloric diet will be conducted during one month, and designed to provide 30% excess in calories compared to daily requirements. It will consist in a high fat, high carbohydrates diet.
Other Names:
  • Overfeeding
  • Other: Basal
    Keeping the volunteers in the fasting state overnight and for the entire duration of the experiment (10 hours)
    Other Names:
  • Fasting
  • Experimental: Hypercaloric diet and clamp

    Volunteers fed a hypercaloric diet for one month will be submitted to a hyperinsulinemic and euglycemic clamp of ten hours duration

    Other: Clamp
    Volunteers will be submitted to hyperinsulinemic, euglycemic clamp studies of 10 hours duration.
    Other Names:
  • Hyperinsulinemic and euglycemic clamp study
  • Other: Hypercaloric diet
    Hypercaloric diet will be conducted during one month, and designed to provide 30% excess in calories compared to daily requirements. It will consist in a high fat, high carbohydrates diet.
    Other Names:
  • Overfeeding
  • Active Comparator: Isocaloric diet and basal

    Volunteers fed a isocaloric diet for one month will be submitted to a fasting period of ten hours duration

    Other: Basal
    Keeping the volunteers in the fasting state overnight and for the entire duration of the experiment (10 hours)
    Other Names:
  • Fasting
  • Other: Isocaloric diet
    Isocaloric diet will conducted for one month, and designed to provide the calculated daily energy needs
    Other Names:
  • Controlled diet
  • Experimental: Isocaloric diet and clamp

    Volunteers fed a isocaloric diet for one month will be submitted to a hyperinsulinemic and euglycemic clamp of ten hours duration

    Other: Clamp
    Volunteers will be submitted to hyperinsulinemic, euglycemic clamp studies of 10 hours duration.
    Other Names:
  • Hyperinsulinemic and euglycemic clamp study
  • Other: Isocaloric diet
    Isocaloric diet will conducted for one month, and designed to provide the calculated daily energy needs
    Other Names:
  • Controlled diet
  • Outcome Measures

    Primary Outcome Measures

    1. Luteinizing hormone secretion [Every ten minutes for 10 hours]

      The pulsatility of LH will be assessed by measuring LH levels in blood sample obtained every ten minutes over the entire study period (12 hours).

    Secondary Outcome Measures

    1. Insulin sensitivity [10 hours]

      Insulin sensitivity will be defined as the rate of glucose infusion required to maintain euglycemia during the hyperinsulinemic clamp

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 30 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    normally cycling young (between 18 and 30 yo) female, with a BMI between 20 and 25 kg/m2.

    -

    Exclusion Criteria:
    • Personal history of endocrine dysfunction (any kind)

    • Hormonal contraception

    • Pregnancy

    • Food allergy (any kind)

    • Intense physical activity (>4 hrs/week)

    • Smoking

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Clinical Research Center, University Hospital Lausanne Vaud Switzerland 1011

    Sponsors and Collaborators

    • Centre Hospitalier Universitaire Vaudois

    Investigators

    • Principal Investigator: Francois P Pralong, MD, Centre Hospitalier Universitaire Vaudois

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Francois Pralong, Full professor and Head, Service of Endocrinology, Diabetology and Metabolism, Centre Hospitalier Universitaire Vaudois
    ClinicalTrials.gov Identifier:
    NCT02233283
    Other Study ID Numbers:
    • 43/13
    • 320030_141065
    First Posted:
    Sep 8, 2014
    Last Update Posted:
    Aug 21, 2015
    Last Verified:
    Aug 1, 2015
    Keywords provided by Francois Pralong, Full professor and Head, Service of Endocrinology, Diabetology and Metabolism, Centre Hospitalier Universitaire Vaudois

    Study Results

    No Results Posted as of Aug 21, 2015