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二甲双胍治疗的 2 型糖尿病患者中,尽管血糖控制更好,但合用艾塞那肽和达格列净对降低肝细胞脂质没有额外作用:EXENDA,一项 24 周前瞻性随机安慰剂对照先导试验。

Combined exenatide and dapagliflozin has no additive effects on reduction of hepatocellular lipids despite better glycaemic control in patients with type 2 diabetes mellitus treated with metformin: EXENDA, a 24-week, prospective, randomized, placebo-controlled pilot trial.

机构信息

Gender Medicine Unit, Division of Endocrinology and Metabolism, Department of Medicine III, Medical University Vienna, Vienna, Austria.

Department of Biomedical Imaging and Image-Guided Therapy, High-Field MR Center, Medical University of Vienna, Vienna, Austria.

出版信息

Diabetes Obes Metab. 2021 May;23(5):1129-1139. doi: 10.1111/dom.14319. Epub 2021 Feb 10.

DOI:10.1111/dom.14319
PMID:33464703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8247845/
Abstract

AIMS

To investigate the potential synergistic effects of combined exenatide (EXE) and dapagliflozin (DAPA) versus (PLAC) placebo and DAPA on hepatocellular lipid (HCL) reduction after 24 weeks of treatment.

MATERIALS AND METHODS

Thirty patients with type 2 diabetes were randomized to weekly EXE and daily DAPA (n = 16) or weekly PLAC and daily DAPA (n = 14). Inclusion criteria were glycated haemoglobin (HbA1c) 48 to 97 mmol/mol (6.5-11%), age 18 to 75 years, body mass index (BMI) ≥25 kg/m and metformin ≥1000 mg. The primary endpoint, HCL levels, were measured at baseline and after 24 weeks of treatment using magnetic resonance spectroscopy. Between-group effects were analysed using general linear models, adjusted for baseline outcome variables, age, sex and BMI. Within-group differences were assessed using a paired t-test.

RESULTS

After 24 weeks, HCLs were reduced in both treatment groups (absolute change from baseline: EXE + DAPA -4.4%, 95% confidence interval [CI] -8.2, -0.7, P < 0.05; PLAC + DAPA -3.9%, 95% CI -6.0, -1.7, P < 0.01; relative change: EXE + DAPA -35.6%, PLAC + DAPA -32.3%) with no difference between groups. Similar findings were observed for subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT). HbA1c (EXE + DAPA -17.8 mmol/mol, [95% CI -24.8, -10.8], P <0.001; PLAC + DAPA -6.9 mmol/mol, [95% CI -10.5, -3.3], P = 0.001) and fasting glucose significantly decreased in both groups, although EXE + DAPA achieved better glycaemic control than PLAC + DAPA (adjusted difference: HbA1c -6.0 mmol/mol [95% CI -9.7, -2.2], P < 0.01). Body weight was reduced in both treatment groups (EXE + DAPA -7.3 kg, 95% CI -9.9, -4.8, P <0.001; PLAC + DAPA -4.6 kg, 95% CI -7.4, -1.8, P <0.01) with comparable results between groups. Changes in HCLs and weight, hip and waist circumference, VAT and SAT were positively associated.

CONCLUSION

After 24 weeks, HCLs were significantly but comparably reduced in the EXE + DAPA and PLAC + DAPA groups, despite significantly better glycaemic control in the combined group EXE + DAPA. Changes in HCLs were associated with weight loss and reduction of visceral adiposity, but not with glucose control. Further studies are necessary to evaluate possible additional long-term effects of a combined treatment.

摘要

目的

研究联合使用艾塞那肽(EXE)和达格列净(DAPA)与(PLAC)安慰剂和 DAPA 对 24 周治疗后肝细胞脂质(HCL)减少的潜在协同作用。

材料和方法

30 名 2 型糖尿病患者被随机分为每周 EXE 和每日 DAPA(n = 16)或每周 PLAC 和每日 DAPA(n = 14)。纳入标准为糖化血红蛋白(HbA1c)48 至 97mmol/mol(6.5-11%),年龄 18 至 75 岁,体重指数(BMI)≥25kg/m2 和二甲双胍≥1000mg。主要终点为使用磁共振波谱法测量基线和 24 周治疗后的 HCL 水平。使用一般线性模型分析组间效应,根据基线结局变量、年龄、性别和 BMI 进行调整。使用配对 t 检验评估组内差异。

结果

24 周后,两组 HCL 均降低(从基线的绝对变化:EXE+DAPA -4.4%,95%置信区间 [CI] -8.2,-0.7,P<0.05;PLAC+DAPA -3.9%,95% CI -6.0,-1.7,P<0.01;相对变化:EXE+DAPA -35.6%,PLAC+DAPA -32.3%),但两组之间无差异。皮下脂肪组织(SAT)和内脏脂肪组织(VAT)也观察到类似的发现。HbA1c(EXE+DAPA -17.8mmol/mol,95% CI -24.8,-10.8,P<0.001;PLAC+DAPA -6.9mmol/mol,95% CI -10.5,-3.3,P = 0.001)和空腹血糖均显著降低,但 EXE+DAPA 组的血糖控制优于 PLAC+DAPA 组(调整后的差异:HbA1c -6.0mmol/mol,95% CI -9.7,-2.2,P<0.01)。两组体重均减轻(EXE+DAPA -7.3kg,95% CI -9.9,-4.8,P<0.001;PLAC+DAPA -4.6kg,95% CI -7.4,-1.8,P<0.01),但两组之间结果相似。HCL 变化与体重、臀部和腰围、VAT 和 SAT 的变化呈正相关。

结论

24 周后,尽管 EXE+DAPA 联合组的血糖控制明显更好,但 EXE+DAPA 和 PLAC+DAPA 组的 HCL 均显著但相当程度地降低。HCL 的变化与体重减轻和内脏脂肪减少有关,但与血糖控制无关。需要进一步研究以评估联合治疗的可能的长期影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c85/8247845/91f30f7ce657/DOM-23-1129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c85/8247845/440620b1e159/DOM-23-1129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c85/8247845/91f30f7ce657/DOM-23-1129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c85/8247845/440620b1e159/DOM-23-1129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c85/8247845/91f30f7ce657/DOM-23-1129-g002.jpg

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