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Effect of the Glycemic Index of Diet on Metabolic and Reproductive Parameters in Overweight and Obese Infertile Women

Primary Purpose

Female Infertility, Obesity

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Low Glycemic Index Diet Group
Conventional Diet Group
Sponsored by
Hospital de Clinicas de Porto Alegre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Female Infertility focused on measuring female infertility, glycemic index, leptin, ghrelin, overweight, obesity, in vitro fertilization

Eligibility Criteria

18 Years - 35 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnose of female infertility and indication for treatment with in vitro fertilization
  • Body Mass Index (BMI) equal or greater than 30 kg/m² or BMI > 25 kg/m² with increased waist circumference (> 80 cm);
  • Being not treated (diet) for weight loss/gain and maintaining stable body weight in the three months prior to the study;
  • Not having stomach/digestive problems
  • Not having the knowledge of cardiovascular disease history;
  • Non-smokers;
  • Not using any medication.

Exclusion Criteria:

  • Patients with BMI equal or higher than 40 kg/m² (morbid obesity)
  • Patients who are already receiving some type of nutritional intervention
  • Patients with co-morbidities that may interfere with reproductive capacity (genetic and/or endocrine disorders, diabetes mellitus, cancer, liver or kidney failure), alcoholics, individuals who have contact (work) with heavy metals or chemicals (exposure to solvents and pesticides)
  • Lack of adherence to the proposed dietary treatment

Sites / Locations

  • Hospital de Clínicas de Porto Alegre

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

No Intervention

Arm Label

Low Glycemic Index Diet Group

Conventional Diet Group

Control Group

Arm Description

Patients will follow a treatment with a hypocaloric diet with low glycemic index/load for 12 weeks, immediately before the in vitro fertilization cycle.

Patients will follow a treatment with a hypocaloric diet with high glycemic index/load for 12 weeks, immediately before the in vitro fertilization cycle.

Patients will follow their usual diet for 12 weeks, immediately before the in vitro fertilization cycle.

Outcomes

Primary Outcome Measures

Clinical Pregnancy Rate
Clinical Pregnancy will be considered as pregnancy diagnosed by ultrasound visualization of one or more gestational sacs or definitive clinical signs of pregnancy.

Secondary Outcome Measures

HOMA-IR index (Homeostasis Model Assessment)
The HOMA-IR index will be obtained by the following formula: fasting glucose (mg/dl/18) x fasting insulin (U/mL)/22.5.
Acylated Ghrelin Levels (pg/dL)
The levels of acylated ghrelin will be determined by enzyme immunoassay (SPI BIO, Montigny le Bretonneux, France) using a plate reader (Biochrom Anthos MultiRead 400, Biochrom Ltd., Cambridge, UK).
Leptin Levels (ng/mL)
The levels of leptin will be determined by enzyme immunoassay (SPI BIO, Montigny le Bretonneux, France) using a plate reader (Biochrom Anthos MultiRead 400, Biochrom Ltd., Cambridge, UK).
Body Fat Percentage (%)
The body fat percentage will be determined measuring the skinfolds at seven sites (triceps, subscapular, suprailiac, axillary, pectoral, abdomen and thigh) using a standardized technique of measurement and determination.
Number of Oocytes Retrieved
Women will follow a pre-established protocol of ovarian stimulation as part of the preparation for the in vitro fertilization cycle. The evolution of oocytes development will be accompanied by the medical team using the ultrasound technique and when at least one oocyte reach the average size of 17 mm the puncture of oocytes by aspiration will be held.
Percentage of Fertilized Oocytes (%)
The percentage of fertilized oocytes will be obtained using the following formula: number of embryos/ total number of oocytes x 100.
Embryo Quality
Embryo quality will be determined by the Embryonic Score Calculation - ESC, where embryos with score 4, are considered the best quality.

Full Information

First Posted
April 7, 2015
Last Updated
April 14, 2015
Sponsor
Hospital de Clinicas de Porto Alegre
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Conselho Nacional de Desenvolvimento Científico e Tecnológico
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1. Study Identification

Unique Protocol Identification Number
NCT02416960
Brief Title
Effect of the Glycemic Index of Diet on Metabolic and Reproductive Parameters in Overweight and Obese Infertile Women
Official Title
Effect of a Hypocaloric Diet With Different Glycemic Indexes on Ghrelin and Leptin Levels, Metabolic Parameters, and Reproductive Outcomes in Overweight and Obese Infertile Women: A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital de Clinicas de Porto Alegre
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Conselho Nacional de Desenvolvimento Científico e Tecnológico

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Infertility has been currently recognized as a disorder related to obesity. Among several metabolic changes associated with obesity, insulin resistance appears to be linked to hormonal disorders that affect reproductive system. Leptin and ghrelin are hormones involved in energy balance regulation and are also associated with reproductive system regulation, but its relationship with infertility is scarce. The aim of this study is to determine the effect of a hypocaloric diet with different glycemic indexes on ghrelin and leptin levels, hormonal, metabolic and reproductive parameters in infertile overweight or obese women candidates to in vitro fertilization. The patients who meet the inclusion criteria and accept to participate in the study, will be allocated in one of the following groups: Hypocaloric Low Glycemic Index diet group; Hypocaloric Conventional diet group or Control group (maintenance of usual diet) and follow the study protocol for 12 week. Immediately after the end of the diet protocol, the patients will be submitted to the in vitro fertilization treatment.
Detailed Description
Infertility has been currently recognized as a disorder related to obesity. Among several metabolic changes associated with obesity, insulin resistance appears to be linked to hormonal disorders that affect reproductive system. Leptin and ghrelin are hormones involved in energy balance regulation and are also associated with reproductive system regulation, but its relationship with infertility is scarce. The aim of this study is to determine the effect of a hypocaloric diet with different glycemic indexes on ghrelin and leptin levels, hormonal, metabolic and reproductive parameters in infertile overweight or obese women candidates to in vitro fertilization. Infertile women with grade I and II obesity, or pre-obesity with increased waist circumference will be recruited. Patients will be assigned to Hypocaloric Low Glycemic Index diet group; Hypocaloric Conventional diet group or Control group (maintenance of usual diet), and will follow the protocol for 12 weeks. The two intervention diets will be similar in terms of caloric intake and macronutrient distribution and different in terms of carbohydrates quality (index and glycemic load). Immediately after the end of the diet protocol, the patients will be submitted to the in vitro fertilization treatment. Before and after the intervention anthropometric measurements (weight, height, body mass index, waist and hip circumference) and body composition (body fat percentage determined by the measurement of seven skinfolds) will be evaluated as well as biochemical parameters: leptin, acylated ghrelin, glucose, insulin, serum lipids (total cholesterol and lipoproteins, and triglycerides), sex hormones - follicle stimulating hormone (FSH), luteinizing hormone (LH), estradiol, progesterone, prolactin, testosterone and sex hormone binding globulin (SHBG). Primary outcome: clinical pregnancy rate. Secondary outcomes: HOMA-IR (Homeostasis Model Assessment), acylated ghrelin and leptin levels, body fat percentage, number of oocytes retrieved, percentage of fertilized oocytes and embryo quality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Female Infertility, Obesity
Keywords
female infertility, glycemic index, leptin, ghrelin, overweight, obesity, in vitro fertilization

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Low Glycemic Index Diet Group
Arm Type
Experimental
Arm Description
Patients will follow a treatment with a hypocaloric diet with low glycemic index/load for 12 weeks, immediately before the in vitro fertilization cycle.
Arm Title
Conventional Diet Group
Arm Type
Active Comparator
Arm Description
Patients will follow a treatment with a hypocaloric diet with high glycemic index/load for 12 weeks, immediately before the in vitro fertilization cycle.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Patients will follow their usual diet for 12 weeks, immediately before the in vitro fertilization cycle.
Intervention Type
Other
Intervention Name(s)
Low Glycemic Index Diet Group
Intervention Description
This diet will be designed as a moderate reduced-energy, moderate-to-high fiber, low glycemic index/load diet.
Intervention Type
Other
Intervention Name(s)
Conventional Diet Group
Intervention Description
This diet will be designed as a moderate reduced-energy, moderate-to-high fiber, high glycemic index/load diet.
Primary Outcome Measure Information:
Title
Clinical Pregnancy Rate
Description
Clinical Pregnancy will be considered as pregnancy diagnosed by ultrasound visualization of one or more gestational sacs or definitive clinical signs of pregnancy.
Time Frame
up to 18 weeks - in average, two weeks after the end of the in vitro fertilization cycle
Secondary Outcome Measure Information:
Title
HOMA-IR index (Homeostasis Model Assessment)
Description
The HOMA-IR index will be obtained by the following formula: fasting glucose (mg/dl/18) x fasting insulin (U/mL)/22.5.
Time Frame
baseline and 12 weeks
Title
Acylated Ghrelin Levels (pg/dL)
Description
The levels of acylated ghrelin will be determined by enzyme immunoassay (SPI BIO, Montigny le Bretonneux, France) using a plate reader (Biochrom Anthos MultiRead 400, Biochrom Ltd., Cambridge, UK).
Time Frame
baseline and 12 weeks
Title
Leptin Levels (ng/mL)
Description
The levels of leptin will be determined by enzyme immunoassay (SPI BIO, Montigny le Bretonneux, France) using a plate reader (Biochrom Anthos MultiRead 400, Biochrom Ltd., Cambridge, UK).
Time Frame
baseline and 12 weeks
Title
Body Fat Percentage (%)
Description
The body fat percentage will be determined measuring the skinfolds at seven sites (triceps, subscapular, suprailiac, axillary, pectoral, abdomen and thigh) using a standardized technique of measurement and determination.
Time Frame
baseline and 12 weeks
Title
Number of Oocytes Retrieved
Description
Women will follow a pre-established protocol of ovarian stimulation as part of the preparation for the in vitro fertilization cycle. The evolution of oocytes development will be accompanied by the medical team using the ultrasound technique and when at least one oocyte reach the average size of 17 mm the puncture of oocytes by aspiration will be held.
Time Frame
between 12 and 16 weeks, during the in vitro fertilization cycle
Title
Percentage of Fertilized Oocytes (%)
Description
The percentage of fertilized oocytes will be obtained using the following formula: number of embryos/ total number of oocytes x 100.
Time Frame
between 12 and 16 weeks, during the in vitro fertilization cycle
Title
Embryo Quality
Description
Embryo quality will be determined by the Embryonic Score Calculation - ESC, where embryos with score 4, are considered the best quality.
Time Frame
between 12 and 16 weeks, during the in vitro fertilization cycle

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnose of female infertility and indication for treatment with in vitro fertilization Body Mass Index (BMI) equal or greater than 30 kg/m² or BMI > 25 kg/m² with increased waist circumference (> 80 cm); Being not treated (diet) for weight loss/gain and maintaining stable body weight in the three months prior to the study; Not having stomach/digestive problems Not having the knowledge of cardiovascular disease history; Non-smokers; Not using any medication. Exclusion Criteria: Patients with BMI equal or higher than 40 kg/m² (morbid obesity) Patients who are already receiving some type of nutritional intervention Patients with co-morbidities that may interfere with reproductive capacity (genetic and/or endocrine disorders, diabetes mellitus, cancer, liver or kidney failure), alcoholics, individuals who have contact (work) with heavy metals or chemicals (exposure to solvents and pesticides) Lack of adherence to the proposed dietary treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cileide C Moulin, PhD
Organizational Affiliation
UFRGS/HCPA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de Clínicas de Porto Alegre
City
Porto Alegre
State/Province
RS
Country
Brazil

12. IPD Sharing Statement

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Citation
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Results Reference
derived

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Effect of the Glycemic Index of Diet on Metabolic and Reproductive Parameters in Overweight and Obese Infertile Women

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