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α-环糊精对糖尿病前期患者胆固醇控制的影响和水解人参提取物对血糖控制的影响:一项随机临床试验。

Effects of α-Cyclodextrin on Cholesterol Control and Hydrolyzed Ginseng Extract on Glycemic Control in People With Prediabetes: A Randomized Clinical Trial.

机构信息

The Boden Collaboration, Charles Perkins Centre, The University of Sydney, Sydney, Australia.

Metabolism and Obesity Services, Royal Prince Alfred Hospital, Camperdown, Australia.

出版信息

JAMA Netw Open. 2020 Nov 2;3(11):e2023491. doi: 10.1001/jamanetworkopen.2020.23491.

Abstract

IMPORTANCE

Effective strategies for preventing type 2 diabetes are needed. Many people turn to complementary medicines, but there is little well-conducted scientific evidence to support their use.

OBJECTIVE

To assess the efficacy of α-cyclodextrin for cholesterol control and that of hydrolyzed ginseng for glycemic control in people with prediabetes and overweight or obesity.

DESIGN, SETTING, AND PARTICIPANTS: This 6-month double-blind, placebo-controlled, randomized clinical trial, with a 2 × 2 factorial design, was conducted between July 2015 and October 2018 at 2 locations in Sydney, Australia. Eligible participants were aged 18 years or older, had a body mass index (weight in kilograms divided by height in meters squared) of 25 or higher, and had prediabetes within 6 months of study entry according to the American Diabetes Association guidelines. Data analysis was performed from May to August 2019.

INTERVENTIONS

Participants were randomized to 1 of 4 groups to take active or placebo versions of each supplement (α-cyclodextrin plus hydrolyzed ginseng, α-cyclodextrin plus placebo, placebo plus hydrolyzed ginseng, or placebo plus placebo) for 6 months. All participants received dietetic advice for weight loss.

MAIN OUTCOMES AND MEASURES

The primary outcomes were the differences in total cholesterol and fasting plasma glucose between groups after 6 months. The primary analysis used the intention-to-treat principle. Multiple predetermined subsample analyses were conducted.

RESULTS

A total of 401 participants were eligible for the study (248 women [62%]; mean [SD] age, 53.5 [10.2] years; mean [SD] body mass index, 34.6 [6.2]). One hundred one patients were randomized to receive α-cyclodextrin plus hydrolyzed ginseng, 99 were randomized to receive α-cyclodextrin plus placebo, 101 were randomized to receive placebo plus hydrolyzed ginseng, and 100 were randomized to receive placebo plus placebo. For 200 participants taking α-cyclodextrin compared with 201 participants taking placebo, there was no difference in total cholesterol after 6 months (-1.5 mg/dL; 95% CI, -6.6 to 3.5 mg/dL; P = .51). For 202 participants taking hydrolyzed ginseng compared with 199 participants taking placebo, there was no difference in fasting plasma glucose after 6 months (0.0 mg/dL; 95% CI, -1.6 to 1.8 mg/dL; P = .95). Use of α-cyclodextrin was associated with constipation (16 participants vs 4 participants; P = .006) and cough (8 participants vs 1 participant; P = .02). Use of hydrolyzed ginseng was associated with rash and pruritus (13 participants vs 2 participants; P = .006). Only 37 of 401 participants (9.2%) experienced these adverse events.

CONCLUSIONS AND RELEVANCE

Although they are safe for use, there was no benefit found for either α-cyclodextrin for cholesterol control or hydrolyzed ginseng for glycemic control in people with prediabetes and overweight or obesity.

TRIAL REGISTRATION

Australian New Zealand Clinical Trials Registry Identifier: ACTRN12614001302640.

摘要

重要性

需要有效的策略来预防 2 型糖尿病。许多人求助于补充药物,但很少有经过精心设计的科学证据支持它们的使用。

目的

评估 α-环糊精在控制胆固醇和水解人参在控制血糖方面的疗效,适用于患有前驱糖尿病和超重或肥胖的人群。

设计、地点和参与者:这是一项为期 6 个月的双盲、安慰剂对照、随机临床试验,采用 2×2 析因设计,于 2015 年 7 月至 2018 年 10 月在澳大利亚悉尼的 2 个地点进行。合格的参与者年龄在 18 岁或以上,体重指数(体重以千克为单位除以身高以米为单位)为 25 或更高,并且根据美国糖尿病协会的指南,在研究开始后 6 个月内患有前驱糖尿病。数据分析于 2019 年 5 月至 8 月进行。

干预措施

参与者被随机分配到 4 组中的 1 组,服用每种补充剂(α-环糊精加水解人参、α-环糊精加安慰剂、安慰剂加水解人参或安慰剂加安慰剂)的活性或安慰剂版本,持续 6 个月。所有参与者都接受了减肥的饮食建议。

主要结果和测量

主要结果是 6 个月后各组总胆固醇和空腹血浆葡萄糖之间的差异。主要分析采用意向治疗原则。进行了多个预定的亚样本分析。

结果

共有 401 名符合研究条件的参与者(248 名女性[62%];平均[标准差]年龄为 53.5[10.2]岁;平均[标准差]体重指数为 34.6[6.2])。101 名患者被随机分配接受 α-环糊精加水解人参,99 名患者被随机分配接受 α-环糊精加安慰剂,101 名患者被随机分配接受安慰剂加水解人参,100 名患者被随机分配接受安慰剂加安慰剂。与服用安慰剂的 200 名参与者相比,服用 α-环糊精的 201 名参与者 6 个月后总胆固醇没有差异(-1.5 毫克/分升;95%置信区间,-6.6 至 3.5 毫克/分升;P=0.51)。与服用安慰剂的 202 名参与者相比,服用水解人参的 199 名参与者 6 个月后空腹血糖没有差异(0.0 毫克/分升;95%置信区间,-1.6 至 1.8 毫克/分升;P=0.95)。使用 α-环糊精与便秘(16 名参与者与 4 名参与者;P=0.006)和咳嗽(8 名参与者与 1 名参与者;P=0.02)有关。使用水解人参与皮疹和瘙痒(13 名参与者与 2 名参与者;P=0.006)有关。401 名参与者中只有 37 名(9.2%)出现这些不良事件。

结论和相关性

尽管它们的使用是安全的,但在患有前驱糖尿病和超重或肥胖的人群中,α-环糊精对控制胆固醇或水解人参对控制血糖均无益处。

试验注册

澳大利亚和新西兰临床试验注册中心标识符:ACTRN12614001302640。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c2c/7672512/09ed65b41469/jamanetwopen-e2023491-g001.jpg

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