Suppr超能文献

聚葡萄糖胺减肥功效——在一项随机双盲、安慰剂对照临床研究中得到证实。

Efficacy of polyglucosamine for weight loss-confirmed in a randomized double-blind, placebo-controlled clinical investigation.

作者信息

Pokhis Karina, Bitterlich Norman, Cornelli Umberto, Cassano Giuseppina

机构信息

Salztal Klinik GmbH, Parkstrasse 18, D-63628 Bad Soden-Salmünster, Germany.

Medizin & Service GmbH, Abt. Biostatistik, Boettcherstr. 10, D-09117 Chemnitz, Germany.

出版信息

BMC Obes. 2015 Jun 10;2:25. doi: 10.1186/s40608-015-0053-5. eCollection 2015.

Abstract

BACKGROUND

The purpose of this clinical study was to ascertain whether low molecular weight chitosan polyglucosamine is able to produce significantly better weight loss than placebo.

METHOD

115 participants were included in the study. We used a two-center randomized, double blind, placebo-controlled design. The participants followed a standard treatment (ST), which included the combination of a low-calorie diet achieved through creating a daily calorie deficit (500 cal) and an increased daily physical activity (7 MET-h/week). They were randomized to receive standard treatment plus placebo (ST + PL) or standard treatment plus polyglucosamine (ST + PG), respectively. Participants were instructed to take 2 × 2 tablets before the two meals containing the highest fat content for at least 24 weeks. Body weight, BMI, waist circumference and the time needed for a 5 % body weight reduction (5R) were taken as main variables.

RESULTS

The average weight loss over a period of 25 weeks in the ITT population was 5.8 ± 4.09 kg in the ST + PG group versus 4.0 ± 2.94 kg in the ST + PL (pU = 0.023; pt = 0.010). After 25 weeks, 34 participants achieved 5R in the ST + PG group (64.1 %) compared to only 23 participants in the ST + PL group (42.6 %) (ITT) (p Fisher = 0.033). Weight loss through hypo-caloric diets have been found to be effective. The additional effect of PG in combination with standard treatment is able to produce significantly better weight loss than placebo.

CONCLUSIONS

Participants treated with ST + PG showed a significant amount of weight loss, an additional 1.8 kg, compared to controls treated with ST + PL.

TRIAL REGISTRATION

Trial Registration at ClinicalTrials.gov: NCT02410785 Registered 07 April 2015.

摘要

背景

本临床研究的目的是确定低分子量壳聚糖聚葡萄糖胺是否能比安慰剂产生显著更好的体重减轻效果。

方法

115名参与者纳入本研究。我们采用双中心随机、双盲、安慰剂对照设计。参与者遵循标准治疗(ST),包括通过每日热量缺口(500卡路里)实现低热量饮食与增加每日体力活动(7代谢当量小时/周)相结合。他们被随机分为分别接受标准治疗加安慰剂(ST + PL)或标准治疗加聚葡萄糖胺(ST + PG)。参与者被指示在含脂肪量最高的两餐之前服用2×2片药物,持续至少24周。体重、体重指数、腰围以及减轻5%体重所需时间(5R)作为主要变量。

结果

在意向性分析人群中,25周期间ST + PG组平均体重减轻5.8±4.09千克,而ST + PL组为4.0±2.94千克(pU = 0.023;pt = 0.010)。25周后,ST + PG组有34名参与者实现5R(64.1%),而ST + PL组只有23名参与者(42.6%)(意向性分析)(p费舍尔检验 = 0.033)。通过低热量饮食实现体重减轻已被证明是有效的。PG与标准治疗联合使用的额外效果能比安慰剂产生显著更好的体重减轻效果。

结论

与接受ST + PL治疗的对照组相比,接受ST + PG治疗的参与者体重显著减轻,额外减轻了1.8千克。

试验注册

在ClinicalTrials.gov上的试验注册:NCT02410785,于2015年4月7日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2fa/4511026/5021cf9a0253/40608_2015_53_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验