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1.
Minerva Obstet Gynecol ; 75(1): 1-6, 2023 Feb.
Article in English | MEDLINE | ID: mdl-34047526

ABSTRACT

BACKGROUND: This prospective observational study aimed to assess the association between maternal abdominal subcutaneous and visceral fat thickness measured with ultrasound scan during the first trimester and the risk of developing gestational diabetes mellitus (GDM). METHODS: We recruited 43 non-diabetic women with singleton pregnancy between 11 and 14 week of gestation and evaluated ultrasonographic measurements of subcutaneous fat thickness (SFT) and preperitoneal fat (PF) above the umbilicus. During the 2nd trimester, GDM screening was performed by 75 g two-hour oral glucose tolerance test (OGTT) and diagnosis was made when one or more plasma glucose values meets or exceeds the values indicated by International Association of the Diabetes and Pregnancy Study Groups (IADPSG). RESULTS: Among the 43 woman, 8 developed GDM (18.6%). Of these 37,5% (N.=3) had been diagnosed with GDM during a previous pregnancy, with a statistically significant correlation (P=0.035). Mean SFT for all patients was significantly higher in the GDM group compared to non-GDM group (27.30±8.78 mm vs. 18.56±9.99 mm; P=0.049). Mean PF for all women showed a statistically significant correlation with GDM (13.27±9.07 mm for non GDM group vs. 23.52±10.24 mm for GDM group; P=0.038). CONCLUSIONS: Abdominal adiposity, both subcutaneous and visceral, seem to be a suitable predictor of GDM in early pregnancy and it can be easily assessed during a first trimester routine ultrasound, although further studies are needed to evaluate their role in the screening protocols.


Subject(s)
Diabetes, Gestational , Pregnancy in Diabetics , Pregnancy , Humans , Female , Diabetes, Gestational/diagnostic imaging , Pregnancy Trimester, First , Prospective Studies , Glucose Tolerance Test , Adipose Tissue/diagnostic imaging
2.
Taiwan J Obstet Gynecol ; 59(1): 120-122, 2020 Jan.
Article in English | MEDLINE | ID: mdl-32039778

ABSTRACT

OBJECTIVE: To report cases of use of chelation therapy during pregnancy which resulted in favorable outcomes for the babies. MATERIALS AND METHODS: In this retrospective cohort study, we described the evolution and outcome of 9 pregnancies in Italian thalassemic women who received deferoxamine (DFO) inadvertently during early pregnancy. RESULTS: The use of deferoxamine during first trimester did not lead to adverse effects on the fetus or cause major complications for the gestation, although an increase in iron burden was observed after suspending chelation therapy. CONCLUSION: In our experience, iron-chelation therapy might be administrated in pregnancy where the benefits to the mother outweigh the potential risks to the baby.


Subject(s)
Chelation Therapy/adverse effects , Deferoxamine/adverse effects , Maternal Exposure/adverse effects , Pregnancy Complications, Hematologic/drug therapy , Siderophores/adverse effects , beta-Thalassemia/drug therapy , Adult , Deferoxamine/administration & dosage , Female , Humans , Live Birth , Maternal-Fetal Exchange/drug effects , Pregnancy , Pregnancy Trimester, First , Retrospective Studies , Siderophores/administration & dosage
3.
Indian J Med Res ; 152(5): 449-455, 2020 11.
Article in English | MEDLINE | ID: mdl-33707386

ABSTRACT

Malaria in pregnancy is an important cause of maternal and foetal morbidity and is a potentially life-threatening infection. With ever-growing global exchanges, imported malaria in pregnancy is becoming an issue of concern in non-endemic countries where women, because of low immunity, have higher risk of severe diseases and death. Malaria in pregnancy is a dangerous condition which can be associated with important consequences for both mother and child such as stillbirth, low birth weight, maternal anaemia. In non-endemic-countries it is more frequent in its severe form which can lead to maternal death if not treated adequately. Specific anti-malarial interventions such as the use of repellents and insecticide treated bed nets in addition to chemoprophylaxis should be used by pregnant women if they are travelling to endemic areas. In cases of confirmed infection, specific treatment regimens vary according to gestational age and the presence of complications. Malaria should be considered a global health problem, increasingly involving western countries. Clinicians all over the world need to be prepared for this emerging disease both in terms of prevention and therapy.


Subject(s)
Antimalarials , Malaria, Falciparum , Malaria , Pregnancy Complications, Infectious , Antimalarials/therapeutic use , Child , Female , Humans , Infant, Newborn , Malaria/diagnosis , Malaria/drug therapy , Malaria/epidemiology , Malaria, Falciparum/drug therapy , Pregnancy , Pregnancy Complications, Infectious/drug therapy , Pregnant Women , Travel
4.
J Gynecol Oncol ; 30(3): e46, 2019 May.
Article in English | MEDLINE | ID: mdl-30887763

ABSTRACT

This extensive review summarizes clinical evidence on immunotherapy and targeted therapy currently available for endometrial cancer (EC) and reports the results of the clinical trials and ongoing studies. The research was carried out collecting preclinical and clinical findings using keywords such as immune environment, tumor infiltrating lymphocytes, programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) expression, immune checkpoint inhibitors, anti-PD-1/PD-L1 antibodies and others' on PubMed. Finally, we looked for the ongoing immunotherapy trials on ClinicalTrials.gov. EC is the fourth most common malignancy in women in developed countries. Despite medical and surgical treatments, survival has not improved in the last decade and death rates have increased for uterine cancer in women. Therefore, identification of clinically significant prognostic risk factors and formulation of new rational therapeutic regimens have great significance for enhancing the survival rate and improving the outcome in patients with advanced or metastatic disease. The identification of genetic alterations, including somatic mutations and microsatellite instability, and the definition of intracellular signaling pathways alterations that have a major role in in tumorigenesis is leading to the development of new therapeutic options for immunotherapy and targeted therapy.


Subject(s)
Endometrial Neoplasms/therapy , Immunotherapy/methods , Immunotherapy/trends , Antibodies, Monoclonal/therapeutic use , Endometrial Neoplasms/genetics , Endometrial Neoplasms/immunology , Endometrial Neoplasms/pathology , Female , Humans , Molecular Targeted Therapy/methods , Molecular Targeted Therapy/trends , Tumor Microenvironment/genetics , Tumor Microenvironment/immunology
5.
Gynecol Endocrinol ; 34(9): 729-733, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29726290

ABSTRACT

Alpha-Lipoic acid (ALA) is a natural antioxidant synthetized by plants and animals, identified as a catalytic agent for oxidative decarboxylation of pyruvate and α-ketoglutarate. In this review, we analyzed the action of ALA in gynecology and obstetrics focusing in particular on neuropathic pain and antioxidant and anti-inflammatory action. A comprehensive literature search was performed in PubMed and Cochrane Library for retrieving articles in English language on the antioxidant and anti-inflammatory effects of ALA in gynecological and obstetrical conditions. ALA reduces oxidative stress and insulin resistance in women with polycystic ovary syndrome (PCOS). The association of N-acetyl cysteine (NAC), alpha-lipoic acid (ALA), and bromelain (Br) is used for prevention and treatment of endometriosis. In association with omega-3 polyunsaturated fatty acids (n-3 PUFAs) with amitriptyline is used for treatment of vestibulodynia/painful bladder syndrome (VBD/PBS). A promising area of research is ALA supplementation in patients with threatened miscarriage to improve the subchorionic hematoma resorption. Furthermore, ALA could be used in prevention of diabetic embryopathy and premature rupture of fetal membranes induced by inflamation. In conclusion, ALA can be safely used for treatment of neuropatic pain and as a dietary support during pregnancy.


Subject(s)
Antioxidants/pharmacology , Oxidative Stress/drug effects , Thioctic Acid/pharmacology , Abortion, Threatened/prevention & control , Dietary Supplements , Female , Gynecology , Humans , Obstetrics , Polycystic Ovary Syndrome/metabolism , Pregnancy
6.
Gynecol Endocrinol ; 34(8): 666-669, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29463148

ABSTRACT

The aim of this study was to assess the effectiveness of ospemifene in the improvement of sexual function in postmenopausal women with vulvovaginal atrophy (VVA) affected by overactive bladder syndrome (OAB) or urge urinary incontinence (UUI). One hundred five postmenopausal patients with VVA affected by OAB and/or UUI were enrolled for the study. All patients received ospemifene 60 mg for 12 weeks. Clinical examination, 3-d voiding diary and the vaginal health index (VHI) were performed at baseline and at 12 weeks. Patients completed the OAB-Q SF, FSFI, FSDS, and SF-36 questionnaires. The patient's satisfaction was also calculated. After 12 weeks, the reduction of urinary symptoms was observed. The OAB-Q symptoms, OAB-Q (HRQL) score were (55.34 ± 13.54 vs. 23.22 ± 9.76; p < .0001) and (22.45 ± 9.78 vs. 70.56 ± 15.49; p < .0001), before and after treatment. SF-36 questionnaire showed a significant improvement (p < .0001). VHI score increased and the women who regularly practice sexual activity increased after treatment. The total FSFI score increased significantly and the FSDS score changed after 12 weeks (p < .0001). The PGI-I after 12 weeks showed a total success rate of 90.5%. Ospemifene is an effective potential therapy for postmenopausal women with VVA affected by OAB or UUI improving sexual function and quality of life.


Subject(s)
Selective Estrogen Receptor Modulators/therapeutic use , Sexuality/drug effects , Tamoxifen/analogs & derivatives , Urinary Bladder, Overactive/drug therapy , Vaginal Diseases/drug therapy , Aged , Atrophy , Female , Humans , Middle Aged , Postmenopause , Selective Estrogen Receptor Modulators/pharmacology , Tamoxifen/pharmacology , Tamoxifen/therapeutic use , Urinary Bladder, Overactive/complications , Vagina/pathology , Vaginal Diseases/complications
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