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二甲双胍和胰岛素联合治疗对 2 型糖尿病患者单核细胞趋化蛋白-1 和组织蛋白酶 D 的影响。

Effect of metformin and insulin combination on monocyte chemoattractant protein-1 and cathepsin-D in type 2 diabetes mellitus.

机构信息

Department of Pharmacology, Lady Hardinge Medical College & Smt. S.K. Hospital, New Delhi, 110 001, India.

Department of Ophthalmology, Lady Hardinge Medical College & Smt. S.K. Hospital, New Delhi, 110 001, India.

出版信息

Diabetes Metab Syndr. 2020 Nov-Dec;14(6):1703-1710. doi: 10.1016/j.dsx.2020.08.016. Epub 2020 Aug 25.

DOI:10.1016/j.dsx.2020.08.016
PMID:32911202
Abstract

BACKGROUND AND AIMS

Monocyte chemoattractant protein-1 (MCP-1) and cathepsin-D are progressively raised in type 2 diabetes mellitus (T2DM) with both non proliferative and proliferative retinal disease. This study aimed to evaluate the effect of antidiabetic medications on MCP-1 and cathepsin-D.

METHODS

60 patients of T2DM without retinopathy and 60 of diabetic retinopathy were enrolled to receive metformin (500 mg-1000 mg) combined with either glimepiride (1 mg-2 mg) or insulin. The effect of antidiabetic medications on serum MCP-1 and cathepsin-D was assessed.

RESULTS

Mean MCP-1 (pg/ml) and cathepsin-D (ng/ml) levels were significantly lower in patients of T2DM with and without retinopathy treated with metformin + insulin (468.52 ± 272.84 vs 234.30 ± 180.58; p < 0.01 and 460.15 ± 128.52 vs 517.33 ± 213.49; p = 0.214) as compared to patients treated with metformin + glimepiride (1434.02 ± 105.27 vs 1256.27 ± 76.76; p < 0.01 and 1689.36 ± 752.57 vs 919.69 ± 675.05; p = < 0.01). No significant correlation of MCP-1 and cathepsin-D with HbA1c, fasting and post prandial blood glucose were found.

CONCLUSION

Patients treated with metformin and insulin combination had lower serum MCP-1 and cathepsin-D levels which suggests that this combination may be more effective in reducing the progression of diabetic retinopathy. (CTRI/2018/05/013601).

摘要

背景与目的

单核细胞趋化蛋白-1(MCP-1)和组织蛋白酶-D 在 2 型糖尿病(T2DM)中逐渐升高,无论是否存在非增殖性和增殖性视网膜病变。本研究旨在评估抗糖尿病药物对 MCP-1 和组织蛋白酶-D 的影响。

方法

纳入 60 例无视网膜病变的 T2DM 患者和 60 例糖尿病视网膜病变患者,分别接受二甲双胍(500mg-1000mg)联合格列美脲(1mg-2mg)或胰岛素治疗。评估抗糖尿病药物对血清 MCP-1 和组织蛋白酶-D 的影响。

结果

与接受二甲双胍+格列美脲治疗的患者相比,接受二甲双胍+胰岛素治疗的 T2DM 伴或不伴视网膜病变患者的 MCP-1(pg/ml)和组织蛋白酶-D(ng/ml)水平均显著降低(468.52±272.84 对 234.30±180.58;p<0.01 和 460.15±128.52 对 517.33±213.49;p=0.214)。与接受二甲双胍+格列美脲治疗的患者相比,接受二甲双胍+胰岛素治疗的患者的 MCP-1(pg/ml)和组织蛋白酶-D(ng/ml)水平也显著降低(1434.02±105.27 对 1256.27±76.76;p<0.01 和 1689.36±752.57 对 919.69±675.05;p<0.01)。MCP-1 和组织蛋白酶-D 与 HbA1c、空腹和餐后血糖均无显著相关性。

结论

接受二甲双胍和胰岛素联合治疗的患者血清 MCP-1 和组织蛋白酶-D 水平较低,这表明这种联合治疗可能更有效地减缓糖尿病视网膜病变的进展。(临床试验注册号:CTRI/2018/05/013601)。

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