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增加二甲双胍的剂量可以抑制全身循环中促炎细胞因子的水平,并可能有助于其有益作用。

Increased metformin dosage suppresses pro-inflammatory cytokine levels in systemic circulation and might contribute to its beneficial effects.

机构信息

Department of Biomedical Sciences, College of Health and Allied Sciences, School of Allied Health Sciences, University of Cape Coast, Cape Coast, Ghana.

Department of Molecular Medicine. School of Medical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

出版信息

J Immunoassay Immunochem. 2021 May 4;42(3):252-264. doi: 10.1080/15321819.2020.1862861. Epub 2021 Jan 14.

Abstract

Type 2 Diabetes Mellitus (T2DM) is a metabolic disorder, characterized by persistent elevation of blood glucose either due to insulin resistance or insulin insufficiency. Metformin is the recommended first choice of drug for the management of T2DM and is known to improve insulin sensitivity and prevents hyperglycemia by reducing chronic inflammation. T-helper type 1 (Th1) and type 17 (Th17) cells, are important pro-inflammatory CD4 T cell subsets secreting TNF-α, and INF-γ (Th1), and interleukin 17 (Th17). These cytokines have been shown to play a crucial role in inflammation, insulin resistance, and the development of T2DM. Here, we explore the effect of different metformin dosages on pro-inflammatory cytokine (TNF-α, INF-γ, GM-CSF and IL-17) levels in systemic circulation among T2DM patients in Ghana, since inflammatory responses and cytokines play significant roles in the pathogenesis and progression of T2DM patients on metformin. Two hundred and nine (209) consenting T2DM patients receiving treatment at the Diabetic unit of the Komfo Anokye Teaching Hospital (KATH) in the Ashanti region of Ghana were recruited in a hospital-based cross-sectional study design. Blood samples were collected and serum obtained from each participant were analyzed for the concentrations of TNF-α, INF-γ, GM-CSF and IL-17 cytokine levels by solid-phase sandwich ELISA. We observed that participants on 3000 mg/day dose of metformin had significantly lower levels of TNF-α ( < .001) and IFN-γ ( = .014) compared to those on other dosages (1000 mg and 2000 mg/day). However, GM-CSF and IL-17 levels were not affected by increased metformin dosages. After adjusting for age, gender, dose and duration of metformin use, we observed that participants who took higher doses of metformin had significantly reduced levels of TNF-α (β = -0.0297, 95% CI = (-0.005 to -0.002) < .001. Metformin dosage independently predicted reduced TNF-α levels with 14.4% variations in the metformin dosage levels. Increased metformin dosage suppresses TNF-α levels in systemic circulation and hence might contribute to its beneficial effects.

摘要

2 型糖尿病(T2DM)是一种代谢紊乱,其特征是由于胰岛素抵抗或胰岛素不足而导致血糖持续升高。二甲双胍是治疗 T2DM 的首选药物,已知其可通过降低慢性炎症来提高胰岛素敏感性并预防高血糖。辅助性 T 细胞 1 型(Th1)和 17 型(Th17)细胞是分泌 TNF-α和 INF-γ(Th1)和白细胞介素 17(Th17)的重要促炎 CD4 T 细胞亚群。这些细胞因子已被证明在炎症、胰岛素抵抗和 T2DM 的发展中发挥着关键作用。在这里,我们研究了不同剂量的二甲双胍对加纳 T2DM 患者全身循环中促炎细胞因子(TNF-α、INF-γ、GM-CSF 和 IL-17)水平的影响,因为炎症反应和细胞因子在 T2DM 患者的发病机制和进展中起着重要作用。我们在加纳阿散蒂地区科福阿南耶教学医院(KATH)的糖尿病科进行了一项基于医院的横断面研究,共招募了 209 名同意接受治疗的 T2DM 患者。采集每个参与者的血液样本,并从血清中分析 TNF-α、INF-γ、GM-CSF 和 IL-17 细胞因子水平,采用固相夹心 ELISA 法。我们观察到,每天服用 3000 毫克二甲双胍的参与者的 TNF-α(<0.001)和 IFN-γ(=0.014)水平明显低于其他剂量(1000 毫克和 2000 毫克/天)。然而,GM-CSF 和 IL-17 水平不受增加的二甲双胍剂量影响。调整年龄、性别、二甲双胍剂量和使用时间后,我们观察到服用较高剂量二甲双胍的参与者 TNF-α水平显著降低(β=-0.0297,95%CI=(-0.005 至 -0.002)<0.001)。二甲双胍剂量独立预测了 TNF-α水平的降低,二甲双胍剂量水平变化了 14.4%。增加二甲双胍剂量可抑制全身循环中的 TNF-α水平,从而可能有助于其有益作用。

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