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Effectiveness and safety assessment of drospirenone/ethinyl estradiol tablet in treatment of PCOS patients: a single center, prospective, observational study

机译:双孢润酮/乙酸乙烯雌二醇片治疗PCOS患者的有效性和安全评估:单一中心,前瞻性,观测研究

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To investigate the effectiveness and safety of 3?mg drospirenone and 20?μg ethinyl estradiol tablet (3?mg DRSP/20?μg EE) in the treatment of polycystic ovary syndrome (PCOS). This single center, prospective observational study was conducted in 140 patients with PCOS. They were prescribed 3?mg DRSP/20?μg EE in a 24/4/ regimen for 3?months. Patients were instructed to take oral DRSP/EE tablets (once daily) on the 2nd day of menstruation, for 28 consecutive days for 1?cycle. After 3?months of treatment, anthropometric assessments along with variations in sex hormones related index, glucolipid metabolic index, changes in bilateral ovarian volume, as well as adverse effect of the combination were evaluated. When compared to baseline, body mass index (BMI, 22.07?±?4.09 vs. 21.35?±?3.22, p??0.001) and waist hip ratio (WHR, 0.86?±?0.07 vs. 0.854?±?0.06, p?=?0.026) decreased significantly after treatment. Sex-hormones such as luteinizing hormone (LH) (10.88 vs. 5.81?U/L), testosterone (T) (1.85 vs. 1.51?nmol/L) and free androgen index (FAI) (5.37 vs. 1.50) decreased significantly after treatment (p??0.001). Follicular stimulating hormone (FSH) increased significantly at 3?months as compared to before treatment (5.13 vs. 5.42?U/L, p?=?0.009). Plasma insulin (11.03 vs. 11.10?pmol/L), fasting (4.97 vs. 4.93?mmol/L) and 2?h-blood glucose levels (7.18 vs. 7.04?mmol/L) did not change when compared to baseline. Plasma triglycerides (TG, 1.32 vs. 1.65?mmol/L) significantly increased 3?months after treatment when compared to before treatment (p??0.001). However, high density lipoprotein-cholesterol (HDL-C) levels increased significantly after treatment (1.41 vs. 1.57?mmol/L, p??0.001). It was seen that, when compared to baseline, bilateral ovarian volume (left and right) was significantly lower after treatment (p??0.05). It was seen that 81 patients reported no adverse reactions. Of the common discomforts reported, breast swelling and pain, gastrointestinal disorder and dizziness and headache were most frequent. Treatment of PCOS patients with3 mg DRSP/20?μg EE has shown beneficial hormonal and lipid profile along with considerable safety profile. Chinese Clinical Trial Registry ChiCTR1900022001, March 2019, retrospectively registered.
机译:研究3?Mg替代罗酮和20μl乙炔雌二醇片(3〜Mg DRSP /20≤μgEE)的效果和安全性在治疗多囊卵巢综合征(PCOS)中。该单一中心,前瞻性观察研究是在140例PCOS患者中进行的。它们在3〜4/4℃的24/4 / 4个月中被规定3?mg DRSP / 20?μgee。指示患者在月经的第二天服用口服DRSP / EE片剂(每日一次),连续28天进行1个?循环。在3个月的治疗后,人类测量评估以及性激素相关指数的变化,评估了双侧卵巢体积的变化,以及对组合的不利影响。与基线相比,体重指数(BMI,22.07?±4.09与21.35?±3.22,P?0.001)和腰臀比(WHR,0.86?±0.07 Vs.0.854?±0.06, p?= 0.026)治疗后显着降低。性激素如叶英激素(LH)(10.88 vs.5.81?U / L),睾酮(T)(1.85 vs.1.51?Nmol / L)和自由雄激素指数(Fai)(5.37与1.50)显着下降治疗后(P?<〜0.001)。与治疗前3个月(5.13对5.42?U / L,P?0.009)相比,卵泡刺激激素(FSH)在3个月内显着增加血浆胰岛素(11.03 vs.11.10?pmol / L),禁食(4.97 vs.4.93?mmol / l)和2?H血糖水平(7.18 vs.04?mmol / l)在与基线相比没有变化。血浆甘油三酯(Tg,1.32与1.65?mmol / l)显着增加3?治疗后的治疗后有显着增加3?治疗前(p?<0.001)。然而,处理后,高密度脂蛋白 - 胆固醇(HDL-C)水平显着增加(1.41 vs.1.57?mmol / L,p?<0.001)。有人看出来,与基线相比,治疗后双侧卵巢体积(左右)显着降低(P?<?0.05)。有人认为,81名患者报告没有不良反应。报道的常见不适,乳腺肿胀和疼痛,胃肠疾病和头晕和头痛最常见。用3mg DRSP /20Ω患者的PCOS患者的治疗均显示有益激素和脂质型材以及相当大的安全性。中国临床试验登记册CHICTR1900022001,2019年3月,回顾性注册。

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