Succinate-Based Dietary Supplement for Menopausal Symptoms: A Pooled Analysis of Two Identical Randomized, Double-Blind, Placebo-Controlled Clinical Trials.

IF 1.6 Q3 OBSTETRICS & GYNECOLOGY Obstetrics and Gynecology International Pub Date : 2019-10-31 eCollection Date: 2019-01-01 DOI:10.1155/2019/1572196
Viktor E Radzinsky, Yulia Uspenskaya, Lee P Shulman, Irina V Kuznetsova
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引用次数: 3

Abstract

Background: To evaluate the efficacy of a succinate-based dietary supplement (SBDS; Amberen) in symptomatic menopausal women using a larger sample size derived by pooling data from two identical trials.

Methods: Raw data were pooled from two identical randomized, multicenter, double-blinded, placebo-controlled, 90-day clinical trials. Women aged 42-60 years with mild to moderate vasomotor and psychosomatic menopausal symptoms were included (114 in the treatment group and 113 in the placebo group). Symptoms were assessed by the Greene Climacteric Scale and State-Trait Anxiety Inventory. Changes in body mass index, body weight, waist and hip circumferences, and plasma levels of follicle stimulating hormone, luteinizing hormone, estradiol, leptin, and apolipoproteins A1 and B were also evaluated.

Results: SBDS use resulted in significant improvements in several endpoints including alleviation of 16 of 21 menopausal symptoms (p ≤ 0.05, Greene Scale) and a decrease in anxiety (p < 0.0001, State-Trait Anxiety Inventory) when compared to placebo. Significant reductions were observed in weight, body mass index, and waist and hip circumferences in the supplement cohort. Evaluation of physiological parameters showed a significant increase in serum estradiol levels compared to baseline (p < 0.0001) among users of the SBDS. Levels of follicle stimulating hormone and luteinizing hormone decreased slightly in both groups, without significant differences between the groups. Leptin levels decreased with statistical significance in the SBDS cohort compared to placebo (p=0.027). For those with initial leptin concentrations above the reference range, leptin decreased significantly in the SBDS group compared to the baseline (p < 0.0001) and to placebo (p=0.027).

Conclusions: The pooled analysis reaffirms the outcomes from the individual trials. A nonhormonal, succinate-based dietary supplement is shown to relieve menopausal symptoms when compared to a placebo regimen in a randomized, double-blinded clinical trial.

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琥珀酸酯膳食补充剂治疗更年期症状:两项相同的随机、双盲、安慰剂对照临床试验的汇总分析。
背景:通过汇集两项相同试验的数据,使用更大的样本量来评估基于琥珀酸的膳食补充剂(SBDS;Amberen)对有症状的更年期妇女的疗效。方法:从两个相同的随机、多中心、双盲、安慰剂对照的90天临床试验中收集原始数据。纳入年龄为42-60岁、有轻度至中度血管舒缩和心身更年期症状的女性(治疗组114例,安慰剂组113例)。症状评估采用格林更年期症状量表和状态-特质焦虑量表。还评估了体重指数、体重、腰围和臀围以及血浆促卵泡激素、黄体生成素、雌二醇、瘦素和载脂蛋白A1和B水平的变化。结果:与安慰剂相比,SBDS的使用在几个终点上有显著改善,包括缓解了21种更年期症状中的16种(p≤0.05,格林量表)和减少了焦虑(p<0.0001,状态-特质焦虑量表)。在补充剂队列中,观察到体重、体重指数以及腰围和臀围显著下降。生理参数评估显示,与基线相比,SBDS使用者的血清雌二醇水平显著升高(p<0.0001)。两组的卵泡刺激素和黄体生成素水平均略有下降,两组之间无显著差异。与安慰剂相比,SBDS队列中的瘦素水平下降具有统计学意义(p=0.027)。对于初始瘦素浓度高于参考范围的患者,SBDS组的瘦素水平与基线(p<0.0001)和安慰剂(p=0.027)相比显著下降。结论:汇总分析重申了个体试验的结果。在一项随机、双盲临床试验中,与安慰剂方案相比,以琥珀酸为基础的非均衡膳食补充剂可以缓解更年期症状。
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来源期刊
Obstetrics and Gynecology International
Obstetrics and Gynecology International OBSTETRICS & GYNECOLOGY-
CiteScore
3.60
自引率
0.00%
发文量
26
审稿时长
19 weeks
期刊介绍: Obstetrics and Gynecology International is a peer-reviewed, Open Access journal that aims to provide a forum for scientists and clinical professionals working in obstetrics and gynecology. The journal publishes original research articles, review articles, and clinical studies related to obstetrics, maternal-fetal medicine, general gynecology, gynecologic oncology, uro-gynecology, reproductive medicine and infertility, reproductive endocrinology, and sexual medicine.
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