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Effect of Dietary Modifacation on Microbiota in Overweight and Obese Polycystic Ovary Syndrome Patients

P

Poznan University of Medical Sciences (PUMS)

Status and phase

Unknown
Phase 4

Conditions

PCOS

Treatments

Dietary Supplement: Dietary and life style modification and probiotic Sanprobi Super Formula
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT03325023
PoznanUMS5

Details and patient eligibility

About

Polycystic ovary syndrome (PCOS) is the most common endocrinopathy affecting women of reproductive age. The pathogenesis of PCOS is not fully understood. The intestinal microbiota are believed to be associated with the development of insulin resistance and obesity, and therefore contributing to the development of PCOS. Incresed permeability of the intestinal mucosal barier and absorbtion of lipoproteinase (LPS) from G (-) bacteria promotes chronic inflammation and may lead to insulin resistance.

Approximately 50-60% of women suffering from PCOS are obese. It is known that lifestyle modification and body mass reduction improves endocrine parameters and restores ovulatory menstrual cycles in most patients. Currently, the use of probiotics and prebiotics is playing an increasingly important role in the treatment of obesity through the modulation of intestinal microflora.

The objectives of the study are based on the following assumptions:

  1. Insulin resistance and compensatory hyperinsulinemia are important aspects in the pathogenesis of PCOS and co-morbidity of cardiovascular disease.
  2. Aberrations in the intestinal microflora are associated with the development of obesity and insulin resistance.
  3. Dietary modification combined with probiotic supplementation improves endocrine and metabolic profiles in women with PCOS.

Full description

Polycystic ovary syndrome (PCOS) is the most common endocrinopathy affecting women of reproductive age. The pathogenesis of PCOS is not fully understood. The intestinal microbiota are believed to be associated with the development of insulin resistance and obesity, and therefore contributing to the development of PCOS. Incresed permeability of the intestinal mucosal barier and absorbtion of lipoproteinase (LPS) from G (-) bacteria promotes chronic inflammation and may lead to insulin resistance.

The microbiome consists of a complex community of microorganisms that live in the digestive tract. Intestinal microflora is colonized by various microorganisms, with the largest groups consisting of the Firmicutes, Bacteroides, Actinobacteria and Proteobacteria. Intestinal microflora has a beneficial effect on the host by competing with pathogenic bacteria, protecting the inegrity of the intestinal mucosal barier and stimulating the immune system. Some human gut microorganisms are involved In fermenting dietary fiber into short-chain fatty acids (SCFAs), such as acetic acid and butyric acid, which are then absorbed by the host. The most beneficial species of microbiota are Lactobacillus and Bifidobacterium.

Approximately 50-60% of women suffering from PCOS are obese. It is known that lifestyle modification and body mass reduction improves endocrine parameters and restores ovulatory menstrual cycles in most patients. Currently, the use of probiotics and prebiotics is playing an increasingly important role in the treatment of obesity through the modulation of intestinal microflora.

The objectives of the study are based on the following assumptions:

  1. Insulin resistance and compensatory hyperinsulinemia are important aspects in the pathogenesis of PCOS and co-morbidity of cardiovascular disease.
  2. Aberrations in the intestinal microflora are associated with the development of obesity and insulin resistance.
  3. Dietary modification combined with probiotic supplementation improves endocrine and metabolic profiles in women with PCOS.

Enrollment

80 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Written consent for participation in the clinical trial

  2. Age 18 to 45 years Irregular menstruation (> 35 days) or secondary amenorrhea> 3 months

  3. Hyperandrogenism (hirsutism and / or acne) and / or hyperandrogenemia (total serum testosterone> 0.5 ng / mL) 5. BMI > 25

Exclusion criteria

  1. Ovarian cancer, adrenal gland tumor, endometrial cancer, cervical cancer, breast cancer
  2. Congenital adrenal hyperplasia (17-OH-progesterone> 2.5 ng / mL)
  3. Clinically diagnosed Cushing's disease, acromegaly, gigantism
  4. Type I or II diabetes
  5. Unexplained bleeding from the genital tract
  6. Hormone treatment within the last 2 months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 2 patient groups, including a placebo group

Active Comparator:
Active Comparator group
Description:
Dietary modification + Probiotic supplementation (Sanprobi Super Formula)
Treatment:
Dietary Supplement: Dietary and life style modification and probiotic Sanprobi Super Formula
Placebo Comparator
Placebo Comparator group
Description:
Dietary modification + placebo.
Treatment:
Other: Placebo

Trial contacts and locations

1

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Central trial contact

Beata Banaszewska, MD PhD; Anna Kubiak

Data sourced from clinicaltrials.gov

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