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1.
Gynecol Endocrinol ; 19(2): 88-96, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15624270

ABSTRACT

A longitudinal prospective study was conducted in 21 women with polycistic ovary syndrome (PCOS), aged 27.20 +/- 5.02 years and treated with metformin (1500 mg/day)for 8 weeks. The patients were assessed for spontaneous menstruation, weight, body mass index (BMI), waist circumference, waist/hip ratio (WHR), glucose and insulin concentrations under fasting conditions and after a 75-g glucose tolerance test, lipid profile, testosterone, androstenedione, dehydroepiandrosterone sulfate, sex-hormone binding globulin (SHBG), and insulin-like growth factor (IGF)-I. Spontaneous menstruation was observed in 81% of the women treated with metformin, with no changes in weight or BMI. Waist measurement and the WHR were reduced. The quantitative insulin sensitivity check index (QUICKI) improved from 0.33 +/- 0.03 to 0.35 +/- 0.04 (p < 0.005), and serum total cholesterol and low-density lipoprotein-cholesterol were reduced, while high-density lipoprotein-cholesterol was increased. Serum testosterone concentrations were also reduced. There were no differences in serum triglycerides, SHBG or IGF-I. The occurrence of spontaneous menstruation and changes in the pattern of body fat distribution, the reduction in serum testosterone concentrations, the improvement in lipid profile and the reduction of insulinemia with the use of metformin permit us to conclude that treatment with this drug is of benefit to women with PCOS.


Subject(s)
Hypoglycemic Agents/therapeutic use , Metformin/therapeutic use , Polycystic Ovary Syndrome/drug therapy , Adolescent , Adult , Blood Glucose/analysis , Body Mass Index , Body Weight , Female , Glucose Tolerance Test , Humans , Insulin/blood , Insulin-Like Growth Factor I/analysis , Lipids/blood , Longitudinal Studies , Menstruation , Prospective Studies , Sex Hormone-Binding Globulin/analysis , Testosterone/blood , Waist-Hip Ratio
2.
J Assist Reprod Genet ; 18(8): 413-6, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11599460

ABSTRACT

PURPOSE: Intrauterine insemination (IUI) is a method for the treatment of marital infertility involving the intrauterine or fallopian deposition of washed spermatozoa, depending on the amount of inseminated semen. In view of the divergent opinions about the inseminated volume, the objective of this study was to compare the two techniques (3.0 mL or 0.5 mL) in two groups of patients. METHODS: We performed 164 cycles of ovulation induction followed by IUI. The patients were divided into two groups according to the technique used. Group low volume--50 cycles and 0.5 mL of inseminated semen; Group high volume--114 cycles and 3.0 mL of inseminated semen. The cycle was monitored on the basis of endometrial thickness and follicular development measured by transvaginal ultrasound. Human chorionic gonadotrophin (hCG) was administered in the presence of a follicle measuring 18 mm in mean diameter. The procedure was performed after sperm washing using a discontinuous PureSperm gradient, 40 h later. RESULTS: We obtained a similar clinical pregnancy rate for the two groups (14.0% for Group low volume and 15.7% for Group high volume). There was one abortion in each group. We detected no interference by any etiology of infertility or by the total motile recovered sperm with pregnancy rate. CONCLUSIONS: The results did not demonstrate superiority of one method over the other, with both therapeutic alternatives being satisfactory for the treatment of infertile couples.


Subject(s)
Insemination, Artificial/methods , Semen , Adult , Female , Humans , Infertility, Female/therapy , Infertility, Male/therapy , Male , Pregnancy , Pregnancy Rate , Prospective Studies
3.
J Assist Reprod Genet ; 16(9): 500-3, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10530406

ABSTRACT

PURPOSE: The objective of the present study was to determine the prevalence of endometriosis among the relatives of patients with confirmed endometriosis. METHODS: We analyzed the prevalence of endometriosis among first-, second-, and third-degree relatives in a group of 101 patients with varying symptoms related to endometriosis seen at two public hospitals and submitted to laparoscopy and/or laparotomy. The control group consisted of 43 women submitted to laparoscopy without a diagnosis of endometriosis. RESULTS: Among the patients with endometriosis, we detected nine families with a positive history of endometriosis, comprising one mother, six sisters, three aunts, and two cousins, as opposed to no case among the controls. CONCLUSIONS: These data confirm a familial tendency for endometriosis and suggest that this disorder has a genetic basis.


Subject(s)
Endometriosis/epidemiology , Endometriosis/genetics , Adult , Female , Humans , Middle Aged , Pedigree , Prevalence , Risk Assessment
4.
Gynecol Endocrinol ; 9(1): 45-50, 1995 Mar.
Article in English | MEDLINE | ID: mdl-7793299

ABSTRACT

Insulin resistance has been reported to be associated with hyperandrogenism and polycystic ovaries. To study the prevalence of insulin resistance in patients with polycystic ovary syndrome (PCO) and the correlation between hyperinsulinemia and hyperandrogenism, 48 patients were divided into four groups: group 1, non-obese ovulatory women (n = 10); group 2, obese ovulatory women (n = 9); group 3, non-obese women with PCO (n = 14); group 4, obese women with PCO (n = 15). Each patient was submitted to an oral glucose tolerance test (OGTT). Glucose, insulin, androstenedione and testosterone levels were determined and the blood glucose and insulin response of women with PCO and normal women were compared. Glucose intolerance was observed in group 3 (28.6%) and group 4 (40%) but not in groups 1 or 2, and hyperinsulinemia was observed in group 2 (66.7%), group 3 (64.3%) and group 4 (86.6%). There was a correlation between androstenedione and testosterone levels and insulinemia in group 4. There was also a high prevalence of insulin resistance in patients with PCO regardless of obesity, and hyperandrogenism-aggravated insulin resistance.


Subject(s)
Hyperandrogenism/complications , Insulin/metabolism , Obesity/complications , Polycystic Ovary Syndrome/complications , Adolescent , Adult , Androstenedione/blood , Blood Glucose/metabolism , Female , Glucose Tolerance Test , Humans , Hyperandrogenism/physiopathology , Insulin Resistance , Insulin Secretion , Obesity/physiopathology , Polycystic Ovary Syndrome/physiopathology , Testosterone/blood
6.
Int J Fertil Menopausal Stud ; 38(3): 152-9, 1993.
Article in English | MEDLINE | ID: mdl-8348163

ABSTRACT

OBJECTIVE: Use of a low, fixed dose of purified FSH to induce ovulation in polycystic ovarian syndrome. DESIGN: Fixed protocol, using 75 IU/day of "pure" FSH starting on day 1-5 of menses. SETTING: University outpatient clinic. PATIENTS AND INTERVENTIONS: Seventeen patients, aged 18-38, with clomiphene-resistant polycystic ovarian syndrome, for 23 cycles. All received 50 mg medroxyprogesterone to induce menstrual flow. "Pure" FSH given i.m. for eight to ten days. If follicle reached > or = 18 mm, hCG (5,000 IU) was given, in one-half of cases, in a single dose to induce rupture. MAIN OUTCOME MEASURES: Hormonal measurements (plasma LH, FSH, estradiol, testosterone, progesterone); daily, LH/FSH ratio; daily abdominal sonogram. RESULTS: I: No follicular growth (3 cycles; 13%); II: Inadequate follicular growth (< or = 14 mm--6 cycles; 26%); IIIa: Follicle > or = 18 mm, hCG given; 100% ovulatory; IIIb: Follicle > or = 18 mm, no hCG given; 2/7 ovulatory. Hyperstimulation: one (moderate) in IIIa; one (mild) in IIIb. CONCLUSIONS: Fixed protocol of low-dose, "pure" FSH produces good results, especially combined with hCG, which is effective up to 48 hours after last injection of FSH.


Subject(s)
Follicle Stimulating Hormone/therapeutic use , Ovulation Induction/methods , Polycystic Ovary Syndrome/drug therapy , Adolescent , Adult , Chorionic Gonadotropin/therapeutic use , Drug Therapy, Combination , Estradiol/blood , Female , Follicle Stimulating Hormone/administration & dosage , Follicle Stimulating Hormone/blood , Follicle Stimulating Hormone/pharmacology , Humans , Infertility/drug therapy , Infertility/etiology , Injections, Intramuscular , Luteinizing Hormone/blood , Male , Medroxyprogesterone/therapeutic use , Ovarian Follicle/drug effects , Ovarian Follicle/physiology , Polycystic Ovary Syndrome/complications , Progesterone/blood , Testosterone/blood , Treatment Outcome
7.
Gynecol Obstet Invest ; 36(4): 221-5, 1993.
Article in English | MEDLINE | ID: mdl-8300006

ABSTRACT

An enzyme-linked immunosorbent assay was developed for the detection of anticardiolipin antibody (ACA) in habitual aborters. Results above the 98th percentile of a distribution of 100 blood donors were considered to be positive. Specific binding index for ACA was higher in 20 patients with at least 3 consecutive spontaneous abortions (group A) than in 20 women with at least one live birth without pregnancy wastage (group B). ACA was detected in 4 patients of group A and in none of the women of group B. Most of the pregnancy wastages occurred after the first trimester in ACA-positive patients and during the first trimester in ACA-negative patients.


Subject(s)
Abortion, Habitual/immunology , Antibodies, Anticardiolipin/blood , Enzyme-Linked Immunosorbent Assay/methods , Abortion, Habitual/blood , Adult , Female , Humans , Lupus Erythematosus, Systemic/blood , Lupus Erythematosus, Systemic/immunology , Male , Pregnancy , Reference Values
8.
Fertil Steril ; 58(3): 504-7, 1992 Sep.
Article in English | MEDLINE | ID: mdl-1521643

ABSTRACT

OBJECTIVE: To evaluate the effects of clomiphene citrate (CC) on pituitary luteinizing hormone (LH) and follicle-stimulating hormone (FSH) release in hypoestrogenic women and in the same women after treatment with ethinyl estradiol (EE2). DESIGN: The study was of a prospective nature and was conducted on selected patients. SETTING: Volunteer women were studied in a tertiary care public hospital. PATIENTS: The 10 patients studied were selected on the basis of hypogonadal status (menopause, premature ovarian failure, or gonadal dysgenesis and Turner phenotype) and no hormonal treatment. INTERVENTIONS: Gonadotropin-releasing hormone (GnRH) was continually infused at the dose of 0.2 micrograms/min for 4 hours before and after the use of CC and/or EE2. MAIN OUTCOME MEASURE: The study was performed with the objective of determining the effect of estrogen (E) levels on the action of CC on in vivo gonadotropin release. RESULTS: In the presence of hypoestrogenic conditions, CC had no pituitary action. However, after EE2 treatment CC promoted greater FSH release and a significant inhibition of LH release from the pituitary. CONCLUSION: Clomiphene citrate needs a basal E level to be able to act on the pituitary. In normoestrogenic states and under GnRH stimulation, CC preferentially promotes FSH release while presenting a predominantly inhibitory effect on LH release.


Subject(s)
Clomiphene/pharmacology , Ethinyl Estradiol/pharmacology , Follicle Stimulating Hormone/metabolism , Luteinizing Hormone/metabolism , Pituitary Gland, Anterior/metabolism , Female , Gonadotropin-Releasing Hormone , Humans , Pituitary Gland, Anterior/drug effects , Prospective Studies
9.
Gynecol Obstet Invest ; 30(3): 186-8, 1990.
Article in English | MEDLINE | ID: mdl-2265807

ABSTRACT

A rare case of microscopic gonadoblastoma associated with gonadal fibroadenoma in a patient with gonadal dysgenesis and Turner phenotype is reported. The higher incidence of tumor pathologies in patients with gonadal dysgenesis presenting a Y chromosome in their karyotype is discussed, and the need for judicious microscopic analysis of the gonadal streaks of these patients for the detection of possible incipient tumors is emphasized.


Subject(s)
Adenofibroma/pathology , Dysgerminoma/pathology , Neoplasms, Multiple Primary/pathology , Turner Syndrome/pathology , Adolescent , Female , Gonads/pathology , Humans , Phenotype , Turner Syndrome/complications , Turner Syndrome/genetics
10.
Gynecol Endocrinol ; 3(3): 193-202, 1989 Sep.
Article in English | MEDLINE | ID: mdl-2686353

ABSTRACT

The effect of luteinizing hormone-releasing hormone (LHRH) on LH release was studied in 5 menopausal women injected with progesterone. Each patient received 2 x 100 micrograms doses of LHRH administered intravenously 120 minutes apart under the following conditions: without any previous treatment (test 1); 16 hours after intramuscular injection of 10 mg progesterone (test 2); after 3-4 weeks of oral treatment with 50 micrograms/day of ethinyl estradiol (EE2) (test 3); 16 hours after intramuscular injection of 10 mg progesterone following treatment with 50 micrograms/day oral EE2 for 3-4 weeks (test 4). The interval between tests was at least 1 month. Progesterone decreased the total plasma hormonal increment (PHIt) of hypogonadal women, with a reduction in plasma hormonal increment both after the 1st stimulus (PHI1) and after the 2nd stimulus (PHI2), whereas estradiol increased PHIt, mainly due to an increase of PHI2. The administration of progesterone to hypogonadal women previously treated with EE2 maintained the increased PHIt caused by the latter, but not owing to a greater increase in PHI1.


Subject(s)
Ethinyl Estradiol/pharmacology , Gonadotropin-Releasing Hormone/pharmacology , Menopause/drug effects , Pituitary Gland/drug effects , Progesterone/pharmacology , Drug Interactions , Female , Humans , Luteinizing Hormone/metabolism , Menopause/metabolism , Middle Aged , Pituitary Gland/metabolism
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