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1.
Hum Reprod ; 30(9): 2178-83, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26202923

RESUMO

STUDY QUESTION: Should fasting glucose (FG) or an oral glucose tolerance test (OGTT) be used to screen for dysglycaemia in women with polycystic ovary syndrome (PCOS)? SUMMARY ANSWER: A full OGTT should be recommended as the screening method for dysglycaemia in women with PCOS, regardless of BMI or family history of diabetes mellitus (DM). STUDY DESIGN, SIZE, DURATION: A cross-sectional study on 467 Chinese women diagnosed with PCOS by the Rotterdam criteria between January 2010 to December 2013. PARTICIPANTS, SETTING, METHODS: The study was done at a university hospital in Hong Kong. All subjects underwent a 75 g OGTT after overnight fasting. We evaluated the performance of FG alone, when compared with the full OGTT, in identifying subjects with dysglycaemia (prediabetes or DM, according to the 2010 diagnostic criteria of the American Diabetes Association). MAIN RESULTS AND THE ROLE OF CHANCE: Of the 467 subjects, 58 (12.4%) had dysglycaemia, among which 46 (9.8%) had prediabetes and 12 (2.6%) had DM, including 4 with known DM. Of the 46 subjects with prediabetes, 25 (54.3%) had normal FG and of the 8 subjects with screened DM in this study, 1 (12.5%) had normal FG. The sensitivity of FG alone in screening for prediabetes, DM and overall dysglycaemia were 45.7, 87.5 and 48.1%, respectively, i.e. missing 54.3% of prediabetes and 12.5% of DM cases as defined by the OGTT. Among the 54 subjects with screened dysglycaemia, 20 (37.0%) had BMI < 25 kg/m(2) and 35 (64.8%) had no family history of DM. LIMITATIONS, REASONS FOR CAUTION: We only reported on the biochemical diagnosis of DM based on a single time point. In clinical practice, confirmatory results at another time point is required for definitive diagnosis in asymptomatic subjects. WIDER IMPLICATIONS OF THE FINDINGS: There is an ongoing debate as to whether FG or an OGTT should be used as a screening method for dysglycaemia in women with PCOS. Some guidelines also recommend glucose screening only in those who are overweight and/or having family history of diabetes (DM). There have been scarce data on this issue in the Chinese population, which the current study aims at addressing. STUDY FUNDING/COMPETING INTERESTS: The study was supported by a research grant from the Hong Kong Obstetrical and Gynaecological Trust Fund, as well as internal research funding of the Department of Obstetrics and Gynaecology, The University of Hong Kong. All authors have no competing interests.


Assuntos
Glicemia/metabolismo , Transtornos do Metabolismo de Glucose/diagnóstico , Síndrome do Ovário Policístico/complicações , Adulto , Diabetes Mellitus/diagnóstico , Diabetes Mellitus/etiologia , Feminino , Transtornos do Metabolismo de Glucose/etiologia , Teste de Tolerância a Glucose , Hong Kong , Humanos , Estado Pré-Diabético/diagnóstico , Estado Pré-Diabético/etiologia
2.
Ultrasound Obstet Gynecol ; 40(4): 392-7, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22302719

RESUMO

OBJECTIVE: We previously demonstrated that a sequential regimen of letrozole and misoprostol resulted in a marked reduction in the serum estradiol concentration and in a higher efficacy of first-trimester termination of pregnancy than misoprostol alone. The aim of this study was to evaluate the effect of letrozole on uterine artery Doppler flow indices during early pregnancy. METHODS: This was a randomized controlled trial. Thirty women requesting termination of pregnancy up to 63 days' gestation were randomized into two groups: a letrozole group receiving 10 mg of letrozole, daily, for 3 days, and a control group receiving a placebo for 3 days. Serum estradiol, progesterone and human chorionic gonadotropin (hCG) concentrations were measured before drug administration and then daily for 6 days. Ultrasound scanning for fetal viability and measurement of the pulsatility (PI) and resistance (RI) indices of the uterine arteries was performed before drug administration, and then on day 3 and day 7 after starting letrozole or placebo. All pregnancies were terminated by surgical evacuation on day 7 or day 8. RESULTS: Uterine artery PI and RI decreased significantly in the letrozole group, but not in the control group. Serum estradiol concentrations were significantly lower in the letrozole group than in the control group from day 2 onwards. Serum progesterone and hCG concentrations were comparable for the two groups throughout the 7 days. There were significantly more women in the letrozole group with vaginal bleeding. CONCLUSION: We have demonstrated that the use of letrozole in the first trimester of pregnancy suppresses serum estradiol levels but results in an increase in blood flow to the uterus. Further studies should be carried out to elucidate the mechanism of letrozole pretreatment in medical abortion.


Assuntos
Abortivos não Esteroides/farmacologia , Aborto Induzido/métodos , Nitrilas/farmacologia , Fluxo Pulsátil/efeitos dos fármacos , Triazóis/farmacologia , Artéria Uterina/efeitos dos fármacos , Artéria Uterina/diagnóstico por imagem , Hemorragia Uterina/induzido quimicamente , Abortivos não Esteroides/administração & dosagem , Abortivos não Esteroides/efeitos adversos , Adulto , Gonadotropina Coriônica/sangue , Estradiol/sangue , Feminino , Hong Kong/epidemiologia , Humanos , Letrozol , Pessoa de Meia-Idade , Nitrilas/administração & dosagem , Gravidez , Primeiro Trimestre da Gravidez , Cuidados Pré-Operatórios , Progesterona/sangue , Resultado do Tratamento , Triazóis/administração & dosagem , Ultrassonografia Doppler , Artéria Uterina/fisiopatologia
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