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2型糖尿病与阿尔茨海默病。

Type 2 diabetes mellitus and Alzheimer's disease.

作者信息

Barbagallo Mario, Dominguez Ligia J

机构信息

Mario Barbagallo, Ligia J Dominguez, Geriatric Unit, Department DIBIMIS, University of Palermo, 90127 Palermo, Italy.

出版信息

World J Diabetes. 2014 Dec 15;5(6):889-93. doi: 10.4239/wjd.v5.i6.889.

Abstract

Epidemiological and biological evidences support a link between type 2 diabetes mellitus (DM2) and Alzheimer's disease (AD). Persons with diabetes have a higher incidence of cognitive decline and an increased risk of developing all types of dementia. Cognitive deficits in persons with diabetes mainly affect the areas of psychomotor efficiency, attention, learning and memory, mental flexibility and speed, and executive function. The strong epidemiological association has suggested the existence of a physiopathological link. The determinants of the accelerated cognitive decline in DM2, however, are less clear. Increased cortical and subcortical atrophy have been evidenced after controlling for diabetic vascular disease and inadequate cerebral circulation. Most recent studies have focused on the role of insulin and insulin resistance as possible links between diabetes and AD. Disturbances in brain insulin signaling mechanisms may contribute to the molecular, biochemical, and histopathological lesions in AD. Hyperglycemia itself is a risk factor for cognitive dysfunction and dementia. Hypoglycemia may also have deleterious effects on cognitive function. Recurrent symptomatic and asymptomatic hypoglycemic episodes have been suggested to cause sub-clinical brain damage, and permanent cognitive impairment. Future trials are required to clarify the mechanistic link, to address the question whether cognitive decline may be prevented by an adequate metabolic control, and to elucidate the role of drugs that may cause hypoglycemic episodes.

摘要

流行病学和生物学证据支持2型糖尿病(DM2)与阿尔茨海默病(AD)之间存在联系。糖尿病患者认知功能下降的发生率较高,患各类痴呆症的风险也增加。糖尿病患者的认知缺陷主要影响心理运动效率、注意力、学习和记忆、心理灵活性和速度以及执行功能等方面。这种强大的流行病学关联表明存在生理病理联系。然而,DM2中认知功能加速下降的决定因素尚不清楚。在控制糖尿病血管疾病和脑循环不足后,已证实皮质和皮质下萎缩增加。最近的研究集中在胰岛素和胰岛素抵抗作为糖尿病与AD之间可能联系的作用。脑胰岛素信号机制紊乱可能导致AD中的分子、生化和组织病理学病变。高血糖本身是认知功能障碍和痴呆的危险因素。低血糖也可能对认知功能产生有害影响。反复出现的有症状和无症状低血糖发作被认为会导致亚临床脑损伤和永久性认知障碍。需要未来的试验来阐明这种机制联系,解决是否可以通过适当的代谢控制预防认知功能下降的问题,并阐明可能导致低血糖发作的药物的作用。

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