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Protein kinase C pathway mediates the protective effects of glucagon-like peptide-1 on the apoptosis of islet β-cells.蛋白激酶C通路介导胰高血糖素样肽-1对胰岛β细胞凋亡的保护作用。
Mol Med Rep. 2015 Nov;12(5):7589-94. doi: 10.3892/mmr.2015.4355. Epub 2015 Sep 24.
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Incretin physiology and pathophysiology from an Asian perspective.从亚洲视角看肠促胰岛素的生理学与病理生理学
J Diabetes Investig. 2015 Sep;6(5):495-507. doi: 10.1111/jdi.12305. Epub 2014 Dec 17.
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THE INCREASE OF DAIRY INTAKE IS THE MAIN DIETARY FACTOR ASSOCIATED WITH REDUCTION OF BODY WEIGHT IN OVERWEIGHT ADULTS AFTER LIFESTYLE CHANGE PROGRAM.在生活方式改变计划后,乳制品摄入量的增加是与超重成年人体重减轻相关的主要饮食因素。
Nutr Hosp. 2015 Sep 1;32(3):1042-9. doi: 10.3305/nh.2015.32.3.9345.
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The potential of phototherapy to reduce body fat, insulin resistance and "metabolic inflexibility" related to obesity in women undergoing weight loss treatment.光疗法对于正在接受减肥治疗的女性减少体脂、胰岛素抵抗以及与肥胖相关的“代谢灵活性受损”的潜力。
Lasers Surg Med. 2015 Oct;47(8):634-42. doi: 10.1002/lsm.22395. Epub 2015 Jul 29.
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MARCH2: comparative assessment of therapeutic effects of acarbose and metformin in newly diagnosed type 2 diabetes patients.MARCH2:阿卡波糖与二甲双胍对新诊断2型糖尿病患者治疗效果的比较评估
PLoS One. 2014 Aug 22;9(8):e105698. doi: 10.1371/journal.pone.0105698. eCollection 2014.
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Exenatide once weekly versus insulin glargine for type 2 diabetes (DURATION-3): 3-year results of an open-label randomised trial.度拉糖肽每周 1 次对比甘精胰岛素治疗 2 型糖尿病 (DURATION-3): 一项开放标签随机试验的 3 年结果。
Lancet Diabetes Endocrinol. 2014 Jun;2(6):464-73. doi: 10.1016/S2213-8587(14)70029-4. Epub 2014 Apr 4.
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Differences in the HbA1c-lowering efficacy of glucagon-like peptide-1 analogues between Asians and non-Asians: a systematic review and meta-analysis.亚洲人与非亚洲人之间胰高血糖素样肽-1类似物降低糖化血红蛋白(HbA1c)疗效的差异:一项系统评价和荟萃分析。
Diabetes Obes Metab. 2014 Oct;16(10):900-9. doi: 10.1111/dom.12293. Epub 2014 Apr 15.
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Global estimates of diabetes prevalence for 2013 and projections for 2035.全球 2013 年糖尿病患病率估计值及 2035 年预测值。
Diabetes Res Clin Pract. 2014 Feb;103(2):137-49. doi: 10.1016/j.diabres.2013.11.002. Epub 2013 Dec 1.
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Metformin and liraglutide ameliorate high glucose-induced oxidative stress via inhibition of PKC-NAD(P)H oxidase pathway in human aortic endothelial cells.二甲双胍和利拉鲁肽通过抑制蛋白激酶 C-烟酰胺腺嘌呤二核苷酸(NAD(P)H)氧化酶途径改善人主动脉内皮细胞高糖诱导的氧化应激。
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Internet interventions to support lifestyle modification for diabetes management: a systematic review of the evidence.支持糖尿病管理中生活方式改变的互联网干预措施:证据的系统评价
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艾塞那肽与二甲双胍单药治疗新诊断2型糖尿病超重/肥胖患者的比较

Comparison of Exenatide and Metformin Monotherapy in Overweight/Obese Patients with Newly Diagnosed Type 2 Diabetes.

作者信息

Liu Jia, Hu Yanjin, Xu Yuan, Jia Yumei, Miao Li, Wang Guang

机构信息

Department of Endocrinology, Beijing Chao-Yang Hospital, Capital Medical University, No. 8, Gongti South Road, Chaoyang District, Beijing 100020, China.

出版信息

Int J Endocrinol. 2017;2017:9401606. doi: 10.1155/2017/9401606. Epub 2017 Nov 20.

DOI:10.1155/2017/9401606
PMID:29358950
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5735665/
Abstract

AIMS

The present study assessed the therapeutic effect of exenatide and metformin as the initial therapy on overweight/obese patients with newly diagnosed type 2 diabetes (T2D).

METHODS

The prospective, nonrandomized, interventional study enrolled a total of 230 overweight or obese patients with newly diagnosed T2D who were administrated exenatide or metformin hydrochloride for 12 weeks.

RESULTS

224/230 patients, including 106 in the exenatide group and 118 in the metformin group, completed the 12-week treatment. Both exenatide and metformin significantly decreased the HbA1c levels in overweight/obese patients with newly diagnosed T2D (all < 0.05). The reduction in HbA1c and the proportion of patients with HbA1c < 7.0% (53 mmol/mol) were higher in the exenatide group than in the metformin group (all < 0.05). The exenatide treatment caused a greater decline in the body weight and BMI as compared to the metformin treatment (all < 0.01). The exenatide treatment ( = 0.41, < 0.01) and baseline HbA1c level ( = -0.84, < 0.01) were independent influencing factors for the decrease in HbA1c level.

CONCLUSIONS

For an initial therapy in overweight/obese patients with newly diagnosed T2D, exenatide causes a better glycemic control than metformin. This trial is registered with NCT03297879.

摘要

目的

本研究评估艾塞那肽和二甲双胍作为初始治疗对新诊断的2型糖尿病(T2D)超重/肥胖患者的治疗效果。

方法

这项前瞻性、非随机、干预性研究共纳入230例新诊断的T2D超重或肥胖患者,给予艾塞那肽或盐酸二甲双胍治疗12周。

结果

224/230例患者完成了12周治疗,其中艾塞那肽组106例,二甲双胍组118例。艾塞那肽和二甲双胍均显著降低了新诊断的T2D超重/肥胖患者的糖化血红蛋白(HbA1c)水平(均P<0.05)。艾塞那肽组HbA1c的降低幅度及HbA1c<7.0%(53 mmol/mol)的患者比例高于二甲双胍组(均P<0.05)。与二甲双胍治疗相比,艾塞那肽治疗导致体重和体重指数(BMI)下降幅度更大(均P<0.01)。艾塞那肽治疗(β=0.41,P<0.01)和基线HbA1c水平(β=-0.84,P<0.01)是HbA1c水平降低的独立影响因素。

结论

对于新诊断的T2D超重/肥胖患者的初始治疗,艾塞那肽比二甲双胍能更好地控制血糖。本试验已在ClinicalTrials.gov注册,注册号为NCT03297879。