Body Fat as Determinant of Female Gonadal Dysfunction

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СтатусРегрутирање

Спонзори

Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal

Соработници

Instituto de Salud Carlos III

University of Alcala

КЛИНИЧКО ИСПИТУВАЊЕ: NCT03841981

BioSeek: nct03841981

Клучни зборови

Апстракт

Reproduction requires from women enough energy depots to warrant an adequate nutritional supply to the fetus. Hence, adipose tissue is able to communicate with female hypothalamic-pituitary-ovary axis. The hypothesis of the project is that abnormalities in the quantity (absolute and relative to lean body mass), distribution and/or function of adipose tissue are associated with functional forms of female gonadal dysfunction in predisposed women, in a spectrum of anomalies that go from hypothalamic amenorrhea to the polycystic ovary syndrome (PCOS). To challenge this hypothesis, the investigators will study 5 groups of 10 women each: women with exercise-associated hypothalamic amenorrhea, women without ovulatory dysfunction that exercise equally, non-hyperandrogenic patients with PCOS, hyperandrogenic patients with PCOS, and healthy control women comparable to those with PCOS. The aims of the study will be:

Primary objective: To identify novel signalling factors originating from adipose tissue and muscle using targeted and nontargeted evaluation of the proteome and of gene expression of superficial subcutaneous fat, deep subcutaneous fat (which mimics visceral adipose tissue) and skeletal muscle.

Secondary objectives:

1. To study the serum adipokine profile - including those identified by the primary objective - and circulating gut hormones during fasting and after a glucose load in the 5 groups of women, and their associations with sexual hormones and body fat distribution.

2. To study body composition and body fat distribution in these women and their relationships with:

2.1, Sex steroid profiles.

2.2. Classic cardiovascular risk factors: carbohydrate metabolism, lipid profiles and blood pressure.

2.3 Markers of low-grade chronic inflammation.

2.4. Oxidative stress markers.

2.5. Cardiovascular autonomic function.

2.6. Surrogate markers of subclinical atherosclerosis.

2.7. Circulating concentrations of endocrine disruptors.

2.8. Oral and gut microbiome.

The results will provide a better understanding of the mechanisms linking body energy depots with the female reproductive axis and, hopefully, the identification of potential biomarkers for the diagnosis and treatment of the disorders studied here.

Датуми

Последен пат проверено:	06/30/2020
Прво доставено:	02/07/2019
Поднесено е проценето запишување:	02/11/2019
Прво објавено:	02/14/2019
Последното ажурирање е доставено:	07/20/2020
Последно ажурирање објавено:	07/21/2020
Крај на датумот на започнување на студијата:	01/30/2020
Проценет датум на примарно завршување:	06/30/2021
Проценет датум на завршување на студијата:	12/30/2021

Состојба или болест

Polycystic Ovary Syndrome

Hypothalamic Amenorrhea

Интервенција / третман

Diagnostic Test: Anthropometric and physical examination

Diagnostic Test: Indirect calorimetry, accelerometer and seven-day dietary recall

Diagnostic Test: Biochemical, hormonal and metabolic phenotyping

Diagnostic Test: Sonographic studies

Diagnostic Test: 24-hour Ambulatory blood pressure monitoring

Procedure: Percutaneous biopsy

Diagnostic Test: Cardiovascular autonomic function studies

Diagnostic Test: Oral smear and feces specimen

Фаза

Групи за раце

Рака	Интервенција / третман
I- Hypothalamic amenorrhea 10 women with exercise-associated hypothalamic amenorrhea
II- Hyperandrogenic polycystic ovary syndrome 5 lean women with hyperandrogenic polycystic ovary syndrome. 5 women with weight excess and hyperandrogenic polycystic ovary syndrome.
III- Non-hyperandrogenic polycystic ovary syndrome 5 lean women with non-hyperandrogenic polycystic ovary syndrome 5 women with weight excess and non-hyperandrogenic polycystic ovary syndrome
IV- Trained women without ovulatory dysfunction 10 women who exercise as intensively as women with exercise-associated hypothalamic amenorrhea but with normal ovulatory cycles.
V- Non-hyperandrogenic healthy women 10 women matched by age and body mass index with women with polycystic ovary syndrome who do not perform physical activity on a regular basis

Критериуми за подобност

Возраст подобни за студии	18 Years До 18 Years
Полови квалификувани за студии	Female
Метод на земање примероци	Non-Probability Sample
Прифаќа здрави волонтери	Да
Критериуми	Inclusion Criteria Group I - Body mass index between 18.5 and 25.0 kg/m2. - Group 1 ovulatory dysfunction [World Health Organization (WHO) classification]. - Normal/low gonadotrophin levels [follicle-stimulating hormone (FSH) and luteinizing (LH) < 10 IU/l] and low estradiol (< 50 pg/ml). - Moderate-vigorous intensity physical activity (> 5 hours per week) plus low energy availability (< 30 kcal/per kg of lean mass). - Exclusion of secondary etiologies - Informed consent signed. Group II: - Polycystic ovary syndrome phenotype I, II and III [National Institute of Health (NIH)-2012] with hyperandrogenemia (http://prevention.nih.gov/workshops/2012/resources.aspx). - Body mass index between 18.5 and 40.0 kg/m2. - Informed consent signed. Group III: - Polycystic ovary syndrome phenotype IV (NIH-2012) (http://prevention.nih.gov/workshops/2012/resources.aspx). - Body mass index between 18.5 and 40.0 kg/m2. - Informed consent signed. Group IV: - Body mass index between 18.5 and 25.0 kg/m2. - Regular menses. - Normal gonadotropins and estradiol levels at follicular phase. - Moderate-vigorous intensity physical activity (> 5 hours per week) with normal energy availability (> 30 kcal/per kg of lean mass). - Informed consent signed. Group V: - No signs or symptoms of hyperandrogenism. - No exercise or mild intensity physical activity. - Regular menses. - Body mass index between 18.5 and 40.0 kg/m2. - Informed consent signed. Exclusion Criteria (Groups I-V) - Oral drugs interfering with ovulation (glucocorticoids, antipsychotics, antidepressants, contraceptives, sex steroids and/or opioids) for the previous 6 months to study inclusion. - Current pregnancy or lactation, or during the previous 6 months to study inclusion. - Asherman's syndrome or outflow tract disorders. - Current smoking or alcohol intake > 40 g per day. - Previous diagnosis of glucose intolerance, hypertension, dyslipidemia, known heart or lung diseases, kidney disease, liver disease, celiac disease or any other malabsorptive condition, chronic inflammatory disease or malignancy.

Исход

Мерки на примарниот исход

1. Adipokine and myokine signaling identification [Up to 5 years]

Секундарни мерки на исходот

1. Circulating adipokine profile [Up to 5 years]

At fasting and after an oral glucose challenge: Circulating concentrations of Leptin, Adiponectin, Chemerin, Lipocalin-2, Adipsin, Plasminogen Activator Inhibitor (PAI)-1, Monocyte Chemoattractant Protein (MCP)-1, and Soluble Leptin Receptor by multianalyte profiling on the Luminex Magpix system (Luminex Technologies, Austin, USA.).

2. Appetite regulation hormonal profile [Up to 5 years]

At fasting and after an oral glucose challenge: Circulating concentrations of Amylin, C-Peptide, Ghrelin, Gastric Inhibitory Peptide (GIP), Glucagon-Like Peptide (GLP)-1, Glucagon, IL-6, Insulin, Pancreatic Polypeptide (PP), Peptide YY, Tumor Necrosis Factor (TNF)-α by multianalyte profiling on the Luminex Magpix system (Luminex Technologies, Austin, USA.).

3. Association between body mass index and sex steroids [Up to 5 years]

Body mass index in in kg/m^2. Sex steroids (including circulating total testosterone, estradiol, androstenedione, dehydroepiandrosterone-sulphate and estrone) measured by liquid chromatography tandem mass spectrometry (LC-MS/MS). Free testosterone will be calculated from total testosterone and sex hormone binding globulin levels.

4. Association between percentage of fat mass with respect to total body weight and sex steroids [Up to 5 years]

Fat mass% by bioelectric impedanciometry and DEXA. Sex steroids (including circulating total testosterone, estradiol, androstenedione, dehydroepiandrosterone-sulphate and estrone) measured by liquid chromatography tandem mass spectrometry (LC-MS/MS). Free testosterone will be calculated from total testosterone and sex hormone binding globulin levels.

5. Association between percentage of lean mass with respect to total body weight and sex steroids [Up to 5 years]

Lean mass% by bioelectric impedanciometry and DEXA. Sex steroids (including circulating total testosterone, estradiol, androstenedione, dehydroepiandrosterone-sulphate and estrone) measured by liquid chromatography tandem mass spectrometry (LC-MS/MS). Free testosterone will be calculated from total testosterone and sex hormone binding globulin levels.

6. Association between body fat depots and sex steroids [Up to 5 years]

Adipose tissue depots will be estimated using a Toshiba Nemio XG SSA-580A Diagnostic Ultrasound System. Minimum sc and preperitoneal fat thicknesses will be measured at the level of the xyphoid process. Maximum sc fat thickness will be measured at the level of the umbilicus. Intraperitoneal fat thickness will be measured placing a probe transversally in the midline of abdomen, 2 cm above the umbilicus. Three measures of ip fat thickness will be obtained: the distance from the fascia of rectus abdominis muscle to the vertebral column, the distance from the peritoneum to the vertebral column, and the distance from the linea alba to the vertebral column. Perirenal fat thickness will be estimated as the distance from the perirenal fascia to the renal surface. Sex steroids will be measured as previously described.

7. Association between body composition, sex steroids, and insulin resistance. [Up to 5 years]

Fat mass, lean mass and body fat depots will be measured as previously described. Fasting glucose and insulin levels will be used for calculating the homeostasis model assessment of insulin resistance (HOMA-IR), and the composite insulin sensitivity index will be estimated from the glucose and insulin concentrations measured during the oral glucose tolerance test. Sex steroids will be measured as previously described.

8. Association between body composition, sex steroids, and lipids. [Up to 5 years]

Fat mass, lean mass and body fat depots will be measured as previously described. Circulating HDL-cholesterol and phospholipid levels will be measured by enzymatic methods after precipitation of plasma with phosphotungstic acid and Mg2+. Total cholesterol and triglyceride levels will be determined by enzymatic methods. LDL-cholesterol concentrations will be estimated by Friedewald's equation. Circulating apolipoprotein (Apo) AI, Apo B100, and lipoprotein (a) levels will be determined by kinetic immunonephelometry. Sex steroids will be measured as previously described.

9. Association between body composition, sex steroids, and office blood pressure. [Up to 5 years]

Fat mass, lean mass and body fat depots will be measured as previously described. Office blood pressure will be determined as the mean of three manual sphygmomanometer readings in the sitting position. Sex steroids will be measured as previously described.

10. Association between body composition, sex steroids, and ambulatory blood pressure monitoring parameters. [Up to 5 years]

Fat mass, lean mass and body fat depots will be measured as previously described. Twenty-four-hour ambulatory blood pressure monitoring will be performed using an A&D TM2430EX oscillometric device (A&D Co., Ltd., Tokyo, Japan). The cuff (12 × 22 cm for lean participants, 14 × 30 cm for overweight or obese participants) will placed on the nondominant arm in every woman. The period from 0700 to 2300 h will be considered daytime, and from 2300 until 0700 h the next day will be considered nighttime, reflecting the usual sleeping habits of Spaniards. Systolic, diastolic, and mean blood pressure as well as heart rate will be measured every 20 min during daytime and every 30 min during nighttime. Sex steroids will be measured as previously described.

11. Association between body composition, sex steroids, and cardiovascular autonomic function tests. [Up to 5 years]

Fat mass, lean mass and body fat depots will be measured as previously described. Cardiovascular autonomic function will be assessed by the blood pressure and heart rate responses to active standing, and Ewing and Clarke's tests. Sex steroids will be measured as previously described.

12. Association between body composition, sex steroids, and carotid intima-media thickness. [Up to 5 years]

Fat mass, lean mass and body fat depots will be measured as previously described. Imaging will be conducted using a high-resolution 7.5-MHz phased-array transducer by the same trained operator in all the participants. Sex steroids will be measured as previously described.

13. Association between body composition, sex steroids, and oxidative stress. [Up to 5 years]

Fat mass, lean mass and body fat depots will be measured as previously described. Oxidative stress profile will be measured by enzymatic assays: Plasma thiobarbituric acid reactive substances, total antioxidant capacity, nitrotyrosine, protein carbonyl groups and erythrocyte glutathione peroxidase levels. Sex steroids will be measured as previously described.

14. Association between body composition, sex steroids, and microbiome [Up to 5 years]

Participants will be instructed to collect fecal and salivary samples. DNA samples wil be used for massive sequencing of 16S ribosomal DNA (rDNA) amplicons in a MiSeq platform (Illumina). The bacterial diversity will be estimated by using Shannon, Chao 1, Jaccard, and Sorensen indexes with their SDs. Taxonomic affiliations will be assigned by using the RDP_classifier from the Ribosomal Database Project (RDP), and readings with RDP score value <0.8 will be assigned to the upper taxonomic rank, leaving the last rank as unidentified. Sex steroids will be measured as previously described.

Body Fat as Determinant of Female Gonadal Dysfunction

Клучни зборови

alpha glucose

inflammation

amenorrhea

атеросклероза

carbohydrate