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1.
HIV Clin Trials ; 7(4): 184-93, 2006.
Article in English | MEDLINE | ID: mdl-17065030

ABSTRACT

PURPOSE: We investigated the evolution of serum lipid levels in HIV-infected pregnant women and the potential effect of antiretroviral treatment during pregnancy using data from a national surveillance study. METHOD: Fasting lipid measurements collected during routine care in pregnancy were used, analyzing longitudinal changes and differences in lipid values at each trimester by protease inhibitors (PIs) and stavudine use. Multivariate analyses were used to control for simultaneous factors potentially leading to hyperlipidemia. Study population included 248 women. RESULTS: Lipid values increased progressively and significantly during pregnancy: mean increases between the first and third trimesters were 141.6 mg/dL for triglycerides (p < .001), 60.8 mg/dL for total cholesterol (p < .001), 13.7 mg/dL for HDL cholesterol (p < .001), and 17.8 mg/dL for LDL cholesterol (p = .001). At all trimesters, women on PIs had significantly higher triglyceride values compared to women not on PIs. The effect of PIs on cholesterol levels was less consistent. Stavudine showed a dyslipidemic effect at first trimester only. Multivariate analyses confirmed these observations and suggested a potential role of other cofactors in the development of hyperlipidemia during pregnancy. CONCLUSION: The changes observed point to the need to further explore the causes and the clinical correlates of hyperlipidemia during pregnancy in women with HIV.


Subject(s)
HIV Infections/blood , HIV Infections/drug therapy , HIV Protease Inhibitors/pharmacology , HIV-1 , Lipid Metabolism , Pregnancy Complications, Infectious/blood , Adult , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Female , HIV Protease Inhibitors/therapeutic use , Humans , Hyperlipidemias/blood , Italy , Lipid Metabolism/drug effects , Logistic Models , Population Surveillance , Pregnancy , Pregnancy Trimesters/blood , Stavudine/pharmacology , Stavudine/therapeutic use , Treatment Outcome , Triglycerides/blood
2.
Eur J Endocrinol ; 138(4): 379-82, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9578503

ABSTRACT

OBJECTIVE: To evaluate the effect of passive smoking on thyroid function in infants. DESIGN AND METHODS: Cord serum tri-iodiothyronine (T3), free T3 (fT3), thyroxine (T4), free T4 (fT4), TSH, thyroxine binding globulin (TBG), thyroglobulin (TG) and cord plasma thiocyanate were measured at birth, and serum TG and thiocyanate after 1 year of life, in 18 infants born from parents who did not smoke (group A), in 18 infants with a father who smoked (group B) and in 18 infants with parents both being smokers (group C). RESULTS: No significant differences were observed in cord serum concentrations of T3, fT3, T4, fT4, TSH and TBG among the three groups. Median (range) TG concentrations (ng/ml) were 30.2 (5.0-102.0), 56.3 (20.5-208.0) and 76.0 (26.0-199.0) at birth (P=0.009 for groups A and B compared; P=0.0002 for groups A and C compared), and 14.9 (5.4-32.0), 19.5 (10.0-57.5) and 20.0 (14.0-40.7) at 1 year (P=0.017 for groups A and C compared), in the three groups respectively, and thiocyanate concentrations (mmol/l) were 3.3 (0.0-51.4), 12.9 (0.0-122.2) and 27.8 (3.3-184.5) at birth (P=0.015 for groups A and C compared), and 3.1 (0.0-32.7), 6.0 (0.0-47.3) and 20.3 (0.0-230.8) at 1 year (P=0.01 for groups A and C compared) in the three groups respectively. CONCLUSIONS: TG and thiocyanate concentrations at birth and at 1 year of age in infants of smoking parents are greater than in infants with non-smoking parents. These results indicate that the change in thyroid function as evaluated by serum TG concentrations observed at birth can persist at least for 1 year if the exposure to passive smoking from both parents is continued. Increased TG concentrations may be due to a direct effect of thiocyanate on the thyroid gland.


Subject(s)
Fetal Blood/metabolism , Thyroid Gland/physiopathology , Thyroid Hormones/blood , Tobacco Smoke Pollution/adverse effects , Analysis of Variance , Humans , Infant , Infant, Newborn , Risk Factors
3.
Minerva Ginecol ; 46(12): 645-50, 1994 Dec.
Article in Italian | MEDLINE | ID: mdl-7885608

ABSTRACT

OBJECTIVE: to investigate the efficacy of a gonadotropin-releasing hormone analogue (GN-RH-a) in combination with human menopausal menotropin (hMG) for in-vitro fertilization. METHODS: 30 infertile women aged 32 to 37 years received a combined treatment with a long-acting slow-releasing Gn-RH-a and hMG to perform ovarian stimulation in a program of in-vitro fertilization. Serum levels of Follicle Stimulating Hormone (FSH), Luteinizing Hormone (LH), 17-beta-estradiol (E2), Progesterone (P), were evaluated and transvaginal ultrasonographic examinations were performed during the treatment to assess the ovarian volume, the mean number and diameter of growing follicles and the endometrial morphology and thickness. Oocyte retrieval was performed by transvaginal-ultrasound-guided approach, 24-36 hours after the administration of human chorionic gonadotropin (hCG). RESULTS: our data suggest that the combined use of Gn-RH-a and exogenous gonadotropins is associated with a more uniform ovarian response and with the absence of premature LH discharge. Moreover, the Gn-RH-a as polymer implant provides a controlled delivery per day over a one-month period and avoids the inconvenience of a daily administration. CONCLUSIONS: this kind of Gn-RH-a formulation, in in-vitro fertilization programs, appears very effective in inducing a reversible hypogonadic state, easy to manage and well tolerated by the patient. Its association with exogenous gonadotropins appears to be effective in increasing the success rate of good quality oocyte retrieval.


Subject(s)
Embryo Transfer , Fertilization in Vitro , Gonadotropins/therapeutic use , Goserelin/therapeutic use , Ovarian Follicle/drug effects , Ovarian Follicle/physiology , Ovulation Induction , Adult , Drug Therapy, Combination , Female , Humans , Time Factors
4.
Rev Fr Gynecol Obstet ; 84(11): 725-30, 1989 Nov.
Article in French | MEDLINE | ID: mdl-2513632

ABSTRACT

Between 1983 and 1988, 40 patients with Turner's syndrome, aged 8 to 26 years, underwent serial pelvic ultrasonography, in order to evaluate the morphofunctional parameters of the internal genital apparatus and correlate them with the karyotype and gonadotropin levels. Correlation of uterine and gonadal sonograms (site, size and echogenic potential) with the karyotype and the gonadotropin assays, permits the definition of each case and a personalized therapeutic approach as well as a control of its efficacy and/or its side-effects.


Subject(s)
Ovary/pathology , Turner Syndrome/diagnosis , Ultrasonography , Uterus/pathology , Adolescent , Adult , Child , Female , Follicle Stimulating Hormone/blood , Follow-Up Studies , Humans , Karyotyping , Luteinizing Hormone/blood , Turner Syndrome/blood , Turner Syndrome/genetics , Turner Syndrome/pathology
6.
Biol Res Pregnancy Perinatol ; 8(2 2D Half): 60-4, 1987.
Article in English | MEDLINE | ID: mdl-3427137

ABSTRACT

To study physiological variations in serum growth factors during peripartal period, we have measured levels of a serum growth-promoting activity (thymidine activity, TA) and radioimmunoassayable somatomedin C (Sm-C) during labor in 39 women who delivered spontaneously (group A), by caesarean section (group B) and by legal abortion (LA) (group C). TA values were higher in the group A than in the group B and C, suggesting an important effect of uterine contractions in TA generation. A major role in Sm-C production seems to be played by the length of gestation since Sm-C concentrations were significantly higher in mothers delivered by caesarean section than in LA women. During labor influence of estrogens and progesterone in growth factor production seems unlikely because of the lack of correlation with TA and Sm-C levels. The lower TA values in placental flow than in the capillary blood of newborn suggest that serum growth factors, measured as TA, are produced by the newborn and do not cross through the placenta. These data suggest that the absolute dependence of the fetus on the mother does not preclude instances of fetal autonomy.


Subject(s)
Growth Substances/blood , Pregnancy/blood , Abortion, Legal , Adult , Cesarean Section , Estradiol/blood , Female , Fetal Blood/metabolism , Humans , Insulin-Like Growth Factor I/blood , Progesterone/blood , Radioimmunoassay , Thymidine
11.
Am J Obstet Gynecol ; 131(7): 792-6, 1978 Aug 01.
Article in English | MEDLINE | ID: mdl-567429

ABSTRACT

The results obtained with intermittent bromocryptine treatment from the fifth day after the beginning of menstruation until the second day after the basal temperature rise, in 14 women with hyperprolactinemic amenorrhea-galactorrhea and in whom menses had previously been induced by continuous treatment, are presented. All women had menses without reappearance of galactorrhea; serum FSH, LH, estradiol, and progesterone followed a normal physiologic trend. Only prolactin rose again in the second phase of the cycle, in which lower levels of progesterone were also found, but without any significant interference in the clinical and hormonal trend. It is stressed that administration of bromocryptine during the first part of the cycle might substitute for continuous administration, thereby reducing drug consumption and hence possible side-effects as well as the cost of treatment.


Subject(s)
Amenorrhea/drug therapy , Bromocriptine/administration & dosage , Prolactin/blood , Amenorrhea/complications , Bromocriptine/therapeutic use , Drug Administration Schedule , Estradiol/blood , Female , Follicle Stimulating Hormone/blood , Galactorrhea/complications , Galactorrhea/drug therapy , Humans , Luteinizing Hormone/blood , Pregnancy , Progesterone/blood
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