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We conducted this meta-analysis of randomized controlled trials (RCTs) with the aim of assessing the effect of 17β-estradiol plus norethisterone acetate on estradiol, testosterone, IGF-1, and SHBG in postmenopausal women. To our knowledge, this is the first meta-analysis of RCTs to assess these effects. Databases including the Web of Science, PubMed/Medline, Scopus, and EMBASE were searched to identify publications up to July 2024. The results were reported as weighted mean difference (WMD) and 95% confidence intervals (CI) generated by using a random-effects model according to the Der-Simonian-Laird model. Fifteen publications were included in current meta-analysis. Overall results from the random-effects model manifested a significant increase in estradiol (WMD: 55.30 pg/ml, 95% CI: 39.32, 7128, p<0.001) and SHBG (WMD: 18.48 nmol/l, 95% CI: 3.64, 33.33, p=0.015) levels, a significant decrease in FSH (WMD: -41.55 IU/l, 95% CI: -53.17, -29.92, p<0.001) and testosterone (WMD: -4.29 ng/dl, 95% CI: -5.38, -3.21, p=0.000) levels, and a non-significant decrease in IGF-1 levels (WMD: -9.70 μg/l, 95% CI: -34.21, 14.80, p=0.438) after treatment with 17β-estradiol plus norethisterone acetate on postmenopausal women. In conclusion, 17β-estradiol plus norethisterone acetate in postmenopausal women increases estradiol and SHBG concentrations and decreases FSH and testosterone concentrations, with no statistically significant effect on IGF-1.
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http://dx.doi.org/10.1055/a-2531-9363 | DOI Listing |
BMJ Case Rep
September 2025
Medical Gastroenterology, All India Institute of Medical Science Bhopal, Bhopal, MP, India.
We report a case of a female in her mid-40s diagnosed as norethisterone-induced liver injury. Our patient presented to the medical gastroenterology clinic with an incidental finding of progressively increasing transaminases. A detailed evaluation strongly supported our suspicion of progestin-induced liver disease with prompt reversal after discontinuation of norethisterone.
View Article and Find Full Text PDFExp Ther Med
October 2025
Department of Surgery, Shanghai Jiading District Hospital of Traditional Chinese Medicine, Shanghai 201800, P.R. China.
The aim of the present study was to characterize the metabolomic signatures associated with colorectal polyps (CPs) in the gut. A metabolomics analysis was conducted on fecal samples collected from patients diagnosed with CPs as well as from healthy participants. A total of 60 participants were selected for analysis, including 30 patients diagnosed with CPs (CP group) and 30 healthy individuals serving as controls [healthy control (HC) group].
View Article and Find Full Text PDFAm J Obstet Gynecol
August 2025
Department of Obstetrics and Gynecology, Ribeirao Preto Medical School, University of São Paulo. Avenida Bandeirantes, 3900 - Campus Universitário - Monte Alegre, CEP 14049-900, Ribeirão Preto, SP, Brazil. Electronic address:
Background: Additional progestogens are often used in some countries to stop prolonged bleeding in etonogestrel implant users, although no evidence currently supports this practice.
Objective: To evaluate the efficacy and safety of oral norethisterone acetate (NETA), also known as norethindrone acetate, at a dose of 10 mg/day for prolonged bleeding associated with etonogestrel implant use.
Study Design: IMPLANET is a randomized, controlled, blinded, multicenter trial conducted in Brazil.
Biomedicines
July 2025
Osteoporosis Group of the Spanish Association for the Study of Menopause (AEEM), University Hospital of Jaén, 23007 Jaén, Spain.
Uterine fibroids (UFs) and endometriosis are gynecological conditions that significantly increase morbidity among women of reproductive age. Relugolix, a novel gonadotropin-releasing hormone receptor antagonist, is approved in combined therapy for the management of symptoms related to these disorders. However, its potential impact on bone mineral density (BMD) and osteoporosis risk should be considered when using a gonadotropin-releasing hormone (GnRH) antagonist.
View Article and Find Full Text PDFJ Org Chem
August 2025
Centre of Biomedical Research, Sanjay Gandhi Post-Graduate Institute of Medical Sciences Campus, Raebareli Road, Lucknow 226014, India.
The first regio- and stereospecific nucleophilic azidation at the tertiary C3-(sp-carbon) center of spiroaziridine oxindoles is developed using inexpensive trimethylsilyl azide (TMS-azide) under catalyst-free and ambient conditions for the exclusive synthesis of 3-azido oxindoles with excellent yield and enantioselectivity (ee up to >99%). The method is robust and scalable. 3-Azido oxindole is employed to synthesize 3-amino- and 3-triazole oxindoles via Staudinger reduction and click chemistry, respectively.
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