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1.
J Assist Reprod Genet ; 35(6): 1019-1025, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29619608

ABSTRACT

PURPOSE: To calculate the concentrations of interleukin 15 (IL-15) in follicular fluid (FF) and evaluate their relation with oocyte maturation, follicle size, and patients' body mass index (BMI) and age. METHODS: Follicular fluid specimens were obtained from 56 subfertile women undergoing intracytoplasmic sperm injection (ICSI) during oocyte retrieval for measurement of IL-15 concentrations with ELISA. Wilcoxon's test and Pearson's correlation coefficient were used to correlate FF concentrations of IL-15 with follicular size and stage of oocyte maturation, along with patients' BMI and age. RESULTS: IL-15 concentrations in FF of follicles with immature oocytes were significantly greater than those from follicles with mature ones (median 5.333 vs. 3.250 pg/ml, respectively, p < 0.001). There was a significant negative correlation between IL-15 concentrations and follicle size (r = - 0.333, p = 0.003). No significant correlation was observed between IL-15 concentrations and patients' BMI and age (p > 0.05). CONCLUSIONS: IL-15 concentrations in FF are adversely related with the size of the follicles and the maturity of the corresponding retrieved oocytes in a cohort of expected normal responders undergoing intracytoplasmic sperm injection (ICSI). Follicular fluid concentrations of IL-15 should be investigated as a possible predictive factor for oocyte maturity.


Subject(s)
Follicular Fluid/metabolism , In Vitro Oocyte Maturation Techniques , Infertility, Female/physiopathology , Interleukin-15/metabolism , Ovulation Induction , Pregnancy Outcome , Sperm Injections, Intracytoplasmic , Adult , Cohort Studies , Cross-Sectional Studies , Female , Humans , Middle Aged , Oogenesis , Pregnancy , Young Adult
3.
Ann N Y Acad Sci ; 900: 203-12, 2000.
Article in English | MEDLINE | ID: mdl-10818407

ABSTRACT

The heterogeneous origin of polycystic ovary syndrome (PCOS) has been demonstrated by several studies. Abnormalities in steroidogenesis and metabolism are present, but the exact link between these two pathologic features remains to be clarified. In clinical practice, more than one therapeutic approach for the treatment of this syndrome has been proposed over the last few decades. Because hyperandrogenism and hyperinsulinemia contribute to a different degree to the phenotype of PCOS, therapeutic efforts have focused on agents that could treat or modify the clinical manifestations of these disorders. Antiandrogens as a sole treatment or combined with oral contraceptives are considered the treatment of choice for the manifestations of hyperandrogenemia, but there is no agreement about their efficacy on the metabolic sequelae of PCOS (insulin resistance, hyperinsulinemia, dislipidemia). Furthermore, the improvement of insulin sensitivity by insulin sensitizers may be of therapeutic value directly and/or indirectly in the management of clinical manifestations of hyperinsulinemia and hyperandrogenemia.


Subject(s)
Androgen Antagonists/therapeutic use , Hypoglycemic Agents/therapeutic use , Insulin Resistance , Polycystic Ovary Syndrome/drug therapy , Thiazolidinediones , Androgen Antagonists/adverse effects , Chromans/adverse effects , Chromans/therapeutic use , Female , Humans , Hypoglycemic Agents/adverse effects , Metformin/adverse effects , Metformin/therapeutic use , Polycystic Ovary Syndrome/metabolism , Pregnancy , Thiazoles/adverse effects , Thiazoles/therapeutic use , Troglitazone
4.
J Clin Endocrinol Metab ; 84(11): 4006-11, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10566641

ABSTRACT

Polycystic ovary syndrome (PCOS) is characterized by hyperandrogenism, chronic anovulation, and oligomenorrhea (O/M). PCOS has variable clinical phenotypes, biochemical features, and metabolic abnormalities. To determine the prevalence of PCOS in the Greek population as well as the metabolic parameters, we performed a cross-sectional study of 192 women of reproductive age (17-45 yr), living on the Greek island of Lesbos. They were divided into 4 groups according to the presence of hirsutism (defined as a Ferriman-Gallwey score > or = 6) and O/M: group N (n = 108), regular menses and absence of hirsutism; group 1 (n = 56), regular menses and hirsutism; group 2 (n = 10), O/M and absence of hirsutism; and group 3 (n = 18), O/M and hirsutism. Body mass index, waist to hip ratio, and mean blood pressure did not differ among the studied groups. Hormonal profile was assessed by measuring free testosterone (FT). The prevalence of PCOS, defined by the presence of O/M and biochemical hyperandrogenism (FT > or = 95th percentile of the normal women), was estimated to be 6.77% (13 women of 192). Higher FT levels were observed in group 3 (O/M and hirsutism) compared with groups N (P < 0.00001) and 1 (P < 0.0001) and in groups 1 (hirsutism) and 2 (O/M) compared with group N (P < 0.0001 and P < 0.005, respectively). Sex hormone-binding globulin levels were lower in women with PCOS and in groups 1 and 3 than those in group N (P < 0.002, P < 0.02, and P < 0.002, respectively) independently of the body mass index. The metabolic profile was investigated by measurements of fasting glucose (FG), fasting insulin (FI), and estimation of the fasting glucose to insulin ratio (FG:I ratio). After covariance adjusted for the BMI, FI levels were higher in group 3 and in women with PCOS than in the normal (P < 0.005 and P < 0.002, respectively) and the hirsute (P < 0.05 and P < 0.02, respectively) women, whereas FG levels did not differ among the studied groups. The FG:I ratio was lower in group 3, group 1, and in women with PCOS than in normal women (P < 0.05). Finally, a high incidence of family history of diabetes mellitus (P = 0.001) and menstrual disorders (P = 0.01) was observed in women with PCOS, in contrast to the normal and hirsute women. In conclusion, PCOS appears to be a particularly common endocrine disorder in the Greek population under study (prevalence, 6.77%); furthermore, it is associated with certain metabolic abnormalities. These data also suggest that the severity of the fasting hyperinsulinemia is associated with the severity of the clinical phenotype of hyperandrogenism independently of obesity.


Subject(s)
Hormones/blood , Polycystic Ovary Syndrome/epidemiology , Polycystic Ovary Syndrome/physiopathology , Adolescent , Adult , Blood Glucose/analysis , Body Constitution , Body Mass Index , Diabetes Mellitus/genetics , Fasting , Female , Greece/epidemiology , Hirsutism/epidemiology , Humans , Insulin/blood , Male , Menstruation , Middle Aged , Oligomenorrhea , Polycystic Ovary Syndrome/genetics , Testosterone/blood
5.
Fertil Steril ; 71(3): 431-5, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10065777

ABSTRACT

OBJECTIVE: To investigate the frequency of T-->C substitution (-34 bp) of gene CYP17 promoter in Greek patients with polycystic ovary syndrome (PCOS) and to elucidate its role in the pathogenesis of the syndrome. DESIGN: Follow-up study. SETTING: Academic research setting. PATIENT(S): Fifty patients with PCOS and 50 healthy women. INTERVENTION(S): Body mass index and the waist-hip ratio were determined for each woman. Blood samples were obtained for DNA analysis and hormone estimates. MAIN OUTCOME MEASURE(S): Serum total T levels. RESULT(S): Seventeen patients (34%) did not carry the base pair substitution (genotype A1A1) and their mean (+/- SD) total T level was 75.7+/-32.2 ngl/dL, 29 patients (58%) were heterozygous carriers of the A2 allele (genotype A1A2) and their mean total T level was 77.8+/-29.9 ng/dL, and 4 patients (8%) carried the A2 allele in homozygosity (genotype A2A2) and their mean total T level was 87.0+/-2.8 ngl/dL. Twenty-two controls had the genotype A1A1 (44%) and their mean total T level was 39.1+/-15.5 ng/dL, whereas 28 (56%) had the genotype A1A2 and their mean total T level was 44.9+/-22.1 ng/dL. Homozygosity of the polymorphic A2 allele was not observed in controls, and this difference (8% versus 0%) was statistically significant. CONCLUSION(S): Although this base pair substitution is not the primary genetic defect in PCOS, it may aggravate the clinical picture of hyperandrogenemia, particularly when homozygosity exists.


Subject(s)
Polycystic Ovary Syndrome/genetics , Steroid 17-alpha-Hydroxylase/genetics , Adult , Alleles , DNA/analysis , Female , Genotype , Greece/epidemiology , Humans , Point Mutation , Polycystic Ovary Syndrome/blood , Polycystic Ovary Syndrome/epidemiology , Polymerase Chain Reaction , Polymorphism, Genetic , Steroid 17-alpha-Hydroxylase/blood
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