出 处:《中华老年医学杂志》2018年第10期1069-1072,共4页Chinese Journal of Geriatrics
基 金:国家自然科学基金(61151003);河南省科技攻关计划项目(142300410053)
摘 要:目的探讨利格列汀对2型糖尿病(T2DM)患者轻度认知功能障碍(MCI)的影响及可能机制。方法前瞻性研究,应用蒙特利尔认知评估量表(MoCA)对2016年12月至2017年6月就诊于我院的T2DM患者进行认知功能筛查,选取98例老年T2DMMCI患者,随机数字表法分为利格列汀药物组(利格列汀±二甲双胍)50例和非利格列汀药物组(格列奇特±二甲双胍)48例,于用药前和用药24周后分别比较MoCA评分、空腹血糖、糖化血红蛋白、血脂、血清β淀粉样蛋白(Aβ)1—42含量,稳态模型评估胰岛素抵抗指数(HOMA—IR)。结果利格列汀组干预24周后与治疗前比较,空腹血糖[(7.29±1.00)mmol/L比(9.16±1.60)mmol/L,P〈0.05],糖化血红蛋白[(7.19±0.99)%比(9.36±1.07)%,P〈0.05]、HOMA-IR[(3.05±1.12)比(4.05±1.30),P〈0.05]、Aβ1—42[(0.463±0.093)g/L比(0.528±0.110)g/L,P〈0.05]均降低;MoCA评分[(24.48±1.18)分比(23.22±1.37)分,P〈0.05]提高。非利格列汀组干预24周后与治疗前比较,空腹血糖、糖化血红蛋白均降低(P〈0.05);HOMA—IR、Aβ1~42差异无统计学意义(P〉0.05)。利格列汀组干预24周后与非利格列汀组干预24周后比较,HOMA-IR、Aβ1—42降低(P〈0.05),MoCA评分提高,差异有统计学意义(P〈0.05)。结论利格列汀可改善老年T2DM患者认知功能,可能与其降低血清AB含量及改善胰岛素抵抗有关。DDP-4酶抑制剂可能是将来治疗糖尿病患者认知功能障碍的理想药物。Objective To investigate the effect and its underlying mechanism of Linagliptin on mild cognitive impairment(MCI)in elderly type 2 diabetes mellitus (T2DM) patients. Methods Montreal Cognitive Assessment (MoCA)scale was used to prospectively screen T2DM patients for MCI in our hospital from December 2016 to June 2017,and a total of 98 elderly T2DM patients with MCI were recruited. They were randomly divided into the linagliptin group(Linagliptin + metformin, n=50)and the non-linagliptin group (gliclazide + metformin, n = 48). Serum fasting plasma glucose (FPG), glycosylated hemoglobin( HbAle), blood lipids and amyloid Q-protein 1-42 (Aβ1-42)levels were determined, and MoCA score and homeostasis model assessment of insulin resistance(HOMA-IR)were calculated,and were compared between the two groups before and after 24 weeks of treatment. Results In the linagliptin group, serum FPG, HbAlc, HOMA-IR, Aβ1-42 levels were significantly decreased and MoCA score was increased after 24 weeks of treatment as compared with pre-treatment [(7.29±1.00)mmol/Lvs. (9.16±1.60)mmol/L,(7.19±0.99)% vs. (9.36±1.07)%,(3.05± 1.12) vs. (4. 05±1.30) ,(0. 463±0. 093)g/L vs. (0. 528±0. 110)g/L, (24.48±1.18) vs. (23.22± 1.37) ,all P〈0.05]. In the non-linagliptin group as control, FPG and HbAlc levels were decreased after 24 weeks of treatment as compared with pre-treatment[(7.23 ± 1.09)mmol/L vs. (9.20± 1.75) mmol/L,(7.23± 1.03)M vs. (9.69±1.18)],both P〈0. 05],while there was no significant difference in HOMA-IR,Aβ1-42 level and MoCA score[(3. 95± 1.00) vs. (4. 19± 1.13), (0. 517± 0. 113)g/L vs. (0. 526±0. 119)g/L,(23.21±1.18) vs. (23. 00±1.32),all P〉0.05]. It is worth to pay close attention to the key discovery of this paper that HOMA-IR and Aβ1-42 levels were significantly lower and MoCA score was significantly higher in the linagliptin group than in the non-linagliptin group after 24 weeks of
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