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达格列净对2型糖尿病患者血清代谢组的影响。

Effect of dapagliflozin on the serum metabolome in patients with type 2 diabetes mellitus.

作者信息

Filippas-Ntekouan Sempastian, Dimou Aikaterini, Dafopoulos Panagiotis, Kostara Christina, Bairaktari Eleni, Chasapi Styliani, Spyroulias Georgios, Koufakis Theoharis, Koutsovasilis Anastasios, Tsimihodimos Vasileios

机构信息

Department of Internal Medicine, University of Ioannina, Stavrou Niarchou Avenue, Ioannina, 45500 Greece.

Laboratory of Clinical Chemistry, University of Ioannina, Ioannina, Greece.

出版信息

J Diabetes Metab Disord. 2024 Dec 16;24(1):4. doi: 10.1007/s40200-024-01508-1. eCollection 2025 Jun.

Abstract

OBJECTIVES

SGLT-2 inhibitors have been shown to exert cardio- and renoprotective actions. We aimed to investigate the underlying mechanisms using H-NMR based metabolomics in patients with type-2 diabetes mellitus who received dapagliflozin.

METHODS

50 patients with type 2 diabetes mellitus, inadequately controlled on metformin monotherapy (HbA1c > 7%) received dapagliflozin for 3 months and 30 matched patients received insulin degludec for 3 months. Clinical and laboratory values, as well as H-NMR based metabolomics were assessed before treatment and after completion of 3 months of treatment.

RESULTS

Dapagliflozin reduced weight, body mass index, systolic and diastolic blood pressure significantly. Using H-NMR based metabolomics, the dapagliflozin group showed a good separation with a degree of overlap before and after treatment initiation. Regarding targeted metabolomics, dapagliflozin increased serum ketone, citrate and tryptophan levels compared with insulin. On the other hand, serum taurine, threonine and mannose levels were significantly decreased following dapagliflozin administration.

CONCLUSIONS

Dapagliflozin led to a small, but significant change in serum metabolome. The observed changes may indicate improvement in energy metabolism, reduction in inflammatory activity and decreased insulin resistance which may provide further evidence of the agent's observed cardiac and renal protection. The study was registered with ClinicalTrials.gov

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s40200-024-01508-1.

摘要

目的

已证实钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂具有心脏和肾脏保护作用。我们旨在利用基于氢核磁共振(H-NMR)的代谢组学技术,研究接受达格列净治疗的2型糖尿病患者的潜在机制。

方法

50例接受二甲双胍单药治疗但控制不佳(糖化血红蛋白>7%)的2型糖尿病患者接受达格列净治疗3个月,30例匹配的患者接受德谷胰岛素治疗3个月。在治疗前和完成3个月治疗后,评估临床和实验室指标以及基于H-NMR的代谢组学情况。

结果

达格列净显著降低了体重、体重指数、收缩压和舒张压。利用基于H-NMR的代谢组学技术,达格列净组在治疗开始前后表现出良好的分离,且有一定程度的重叠。关于靶向代谢组学,与胰岛素相比,达格列净提高了血清酮、柠檬酸和色氨酸水平。另一方面,服用达格列净后血清牛磺酸、苏氨酸和甘露糖水平显著降低。

结论

达格列净导致血清代谢组发生了微小但显著的变化。观察到的变化可能表明能量代谢改善、炎症活动减轻和胰岛素抵抗降低,这可能为该药物所观察到的心脏和肾脏保护作用提供进一步证据。该研究已在ClinicalTrials.gov注册。

补充信息

在线版本包含可在10.1007/s40200-024-01508-1获取的补充材料。

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