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利拉鲁肽相较于二甲双胍可降低新发 2 型糖尿病患者的非酯化游离脂肪酸和可溶性血管细胞黏附分子-1。

Liraglutide suppresses non-esterified free fatty acids and soluble vascular cell adhesion molecule-1 compared with metformin in patients with recent-onset type 2 diabetes.

机构信息

Department of Endocrinology and Metabolism, Zhongshan Hospital Xiamen University, 201-209 Hubin South Road, Xiamen, 361004, People's Republic of China.

Guangzhou Medicine University Second Affiliated Hospital, 250-296 Changgang East Road, Guangzhou, 510260, People's Republic of China.

出版信息

Cardiovasc Diabetol. 2018 Apr 10;17(1):53. doi: 10.1186/s12933-018-0701-4.

Abstract

BACKGROUND

It has been suggested that liraglutide could have an impact on glucose and lipid metabolism disorder and adhesion molecule activation, which may play important roles in the vascular damage of diabetes. In this study, we examined the effects of liraglutide versus metformin on non-esterified free fatty acids, beta-cell insulin secretion, and adhesion molecule levels in patients with recent-onset type 2 diabetes mellitus.

METHODS

In this study, 60 patients newly diagnosed with type 2 diabetes mellitus (mean age 33.97 ± 5.67 years) were randomly assigned to receive once-daily subcutaneous liraglutide or oral metformin. Before the study and after the 8-week treatment period, a 75 g oral glucose tolerance test was performed. Plasma glucose, lipids and lipoprotein, plasma insulin, glycaemic and insulin responses, non-esterified free fatty acids (NEFA), and soluble vascular cell adhesion molecule-1 (sVCAM-1) levels were evaluated.

RESULTS

After 8 weeks, 120 min of NEFA (155 ± 125 vs 99 ± 73 µmol/L, P = 0.026) and the levels of sVCAM-1 (465 ± 136 vs 382 ± 131 ng/ml, P = 0.013) significantly decreased, while the early phase insulin secretion index (24.94 [7.78, 38.89] vs. 31.13 [17.67, 59.09], P = 0.031), fasting plasma insulin (104 [51, 123] vs 113 [54, 171] mIU/L, P = 0.015), 60 min plasma insulin (326 [165, 441] vs 471 [334, 717] mIU/L, P = 0.005), 120 min plasma insulin (401 [193, 560] vs 500 [367, 960] mIU/L, P = 0.047), and insulin area under the curve (AUCins) (648 [321, 742] vs 738 [451, 1118] mIU/L, P = 0.005) remarkably increased for patients in the liraglutide treatment group. The levels of sVCAM-1 dramatically decreased after 8 weeks of liraglutide treatment (503 ± 182 vs 382 ± 131 ng/ml, P = 0.046) compared to that of the metformin treatment group. At the same time, the differences before and after liraglutide treatment in 120 min of NEFA (- 32 [- 96, - 5] vs 5 [- 35, 38] µmol/L, P = 0.033) and AUCins (738 [451, 1118] vs 594 [357, 1216] mIU/L, P = 0.014) were remarkably enhanced compared to that of the metformin therapy. Nevertheless, there were no significant differences in fasting NEFA after liraglutide or metformin treatment. The reduction of 120 min NEFA (ΔNEFA) was positively correlated with the decrease of sVCAM-1 (ΔsVCAM-1) after 8 weeks of liraglutide treatment (r = 0.523, P = 0.003).

CONCLUSIONS

Our results demonstrate that liraglutide administration is more effective than metformin in reducing 120 min NEFA and suppressing sVCAM-1 levels for recent-onset type 2 diabetes mellitus. We suggest that this outcome may be because liraglutide is associated with potentiating insulin secretion capacity, inhibiting vascular inflammatory cytokines, and antagonizing atherosclerosis.

摘要

背景

已有研究表明,利拉鲁肽可能对葡萄糖和脂质代谢紊乱及黏附分子激活具有影响,这可能在糖尿病血管损伤中发挥重要作用。本研究旨在观察利拉鲁肽和二甲双胍对初发 2 型糖尿病患者非酯化游离脂肪酸、β细胞胰岛素分泌和黏附分子水平的影响。

方法

本研究纳入 60 例初诊 2 型糖尿病患者(平均年龄 33.97±5.67 岁),随机接受每日 1 次皮下注射利拉鲁肽或口服二甲双胍治疗。在研究前和 8 周治疗后,进行 75 g 口服葡萄糖耐量试验。评估血浆葡萄糖、血脂和脂蛋白、血浆胰岛素、血糖和胰岛素反应、非酯化游离脂肪酸(NEFA)和可溶性血管细胞黏附分子-1(sVCAM-1)水平。

结果

8 周后,利拉鲁肽组 120 min 的 NEFA(155±125 vs 99±73 μmol/L,P=0.026)和 sVCAM-1 水平(465±136 vs 382±131 ng/ml,P=0.013)显著降低,而早期胰岛素分泌指数(24.94[7.78, 38.89] vs. 31.13[17.67, 59.09],P=0.031)、空腹血浆胰岛素(104[51, 123] vs 113[54, 171] mIU/L,P=0.015)、60 min 血浆胰岛素(326[165, 441] vs 471[334, 717] mIU/L,P=0.005)、120 min 血浆胰岛素(401[193, 560] vs 500[367, 960] mIU/L,P=0.047)和胰岛素曲线下面积(AUCins)(648[321, 742] vs 738[451, 1118] mIU/L,P=0.005)显著增加。利拉鲁肽治疗 8 周后,sVCAM-1 水平(503±182 vs 382±131 ng/ml,P=0.046)显著降低。同时,与二甲双胍治疗相比,利拉鲁肽治疗后 120 min 的 NEFA(-32[-96, -5] vs 5[-35, 38] μmol/L,P=0.033)和 AUCins(738[451, 1118] vs 594[357, 1216] mIU/L,P=0.014)的变化显著增强。然而,利拉鲁肽或二甲双胍治疗后空腹 NEFA 无显著差异。利拉鲁肽治疗 8 周后,120 min 的 NEFA 降低(ΔNEFA)与 sVCAM-1 降低(ΔsVCAM-1)呈正相关(r=0.523,P=0.003)。

结论

本研究表明,利拉鲁肽在降低初发 2 型糖尿病患者 120 min 的 NEFA 和抑制 sVCAM-1 水平方面比二甲双胍更有效。我们推测,这可能是因为利拉鲁肽能增强胰岛素分泌能力、抑制血管炎症细胞因子和拮抗动脉粥样硬化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd7a/5891985/21ebaa605304/12933_2018_701_Fig1_HTML.jpg

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