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度拉糖肽可减少伴有暴饮暴食症的2型糖尿病患者的暴饮暴食发作:一项试点研究。

Dulaglutide reduces binge episodes in type 2 diabetic patients with binge eating disorder: A pilot study.

作者信息

Da Porto Andrea, Casarsa Viviana, Colussi Gianluca, Catena Cristiana, Cavarape Alessandro, Sechi Leonardo

机构信息

Internal Medicine, University of Udine, Italy.

Internal Medicine, University of Udine, Italy.

出版信息

Diabetes Metab Syndr. 2020 Jul-Aug;14(4):289-292. doi: 10.1016/j.dsx.2020.03.009. Epub 2020 Mar 31.

Abstract

AIMS

Binge eating disorder (BED) is the most common eating disorder in the United States and Europe and is associated with obesity and type 2 diabetes (T2D). Presence and severity of BED have been associated with worse metabolic control and greater BMI in T2D patients. Glucagon Like Peptide-1 (GLP1) receptors are present in central nervous system areas involved in appetite regulation and treatment with GLP-1 receptor agonists modulates appetite and reward-related brain areas in humans. We evaluated the effects of treatment with dulaglutide on eating behavior in T2D outpatients with BED.

METHODS

This was a pilot open label, prospective controlled study. Inclusion criteria were: Age ≤65, HbA1c between 7.5 and 9% on metformin therapy alone, normal renal function and diagnosis of BED. Patients were randomly assigned to receive either Dulaglutide 1,5 mg/sett or Gliclazide 60 mg for 12 weeks. We evaluated baseline binge eating scale score (BES), weight, BMI, percentage fat mass, HbA1c and their changes after treatment. A multivariate linear regression model was used to verify the association between Δ BES from baseline with Δ Hba1c and variation of anthropometric parameters after treatment.

RESULTS

After 12 weeks patients treated with dulaglutide had grater reduction of binge eating behaviour (p < 0.0001), body weight (p < 0,0001), BMI (p < 0.0001), percentage fat mass (p < 0.0001) and HbA1c (p = 0.009) than patients treated with gliclazide. Reduction in BES was associated with reduction in body weight (p < 0.0001) and HbA1c (p = 0.033).

CONCLUSION

Dulaglutide treatment reduces binge eating behaviour in T2D patients with BED.

摘要

目的

暴饮暴食症(BED)是美国和欧洲最常见的饮食失调症,与肥胖症和2型糖尿病(T2D)相关。BED的存在和严重程度与T2D患者较差的代谢控制和更高的体重指数(BMI)有关。胰高血糖素样肽-1(GLP1)受体存在于参与食欲调节的中枢神经系统区域,用GLP-1受体激动剂治疗可调节人类的食欲和与奖赏相关的脑区。我们评估了度拉糖肽治疗对患有BED的T2D门诊患者饮食行为的影响。

方法

这是一项开放性标签的前瞻性对照试验研究。纳入标准为:年龄≤65岁,仅接受二甲双胍治疗时糖化血红蛋白(HbA1c)在7.5%至9%之间,肾功能正常且诊断为BED。患者被随机分配接受1.5mg/周的度拉糖肽或60mg的格列齐特治疗12周。我们评估了基线暴饮暴食量表评分(BES)、体重、BMI、体脂百分比、HbA1c及其治疗后的变化。使用多元线性回归模型来验证治疗后基线BES的变化与HbA1c变化以及人体测量参数变化之间的关联。

结果

治疗12周后,与接受格列齐特治疗的患者相比,接受度拉糖肽治疗的患者在暴饮暴食行为(p<0.0001)、体重(p<0.0001)、BMI(p<0.0001)、体脂百分比(p<0.0001)和HbA1c(p=0.009)方面的降低幅度更大。BES的降低与体重(p<0.0001)和HbA1c(p=0.033)的降低相关。

结论

度拉糖肽治疗可减少患有BED的T2D患者的暴饮暴食行为。

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