Type 2 Diabetes Mellitus, Platelet Activation and Alzheimer's Disease: A Possible Connection.

IF 2 Q3 CLINICAL NEUROLOGY Clinical Neuropsychiatry Pub Date : 2022-12-01 DOI:10.36131/cnfioritieditore20220604
Manuel Glauco Carbone, Nunzio Pomara, Camilla Callegari, Donatella Marazziti, Bruno Pietro Imbimbo
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引用次数: 2

Abstract

Type 2 diabetes mellitus DM (T2DM) is associated with a 70% increased risk for dementia, including Alzheimer's disease (AD). Insulin resistance has been proposed to play a pivotal role in both T2DM and AD and the concept of "brain insulin resistance" has been suggested as an interpretation to the growing literature regarding cognitive impairment and T2DM. Subjects with T2DM present an abnormal platelet reactivity that together with insulin resistance, hyperglycaemia and dyslipidaemia effect the vascular wall by a series of events including endothelial dysfunction, oxidative stress and low-grade inflammation. Activated platelets directly contribute to cerebral amyloid angiopathy (CAA) by promoting the formation of β-amyloid (Aβ) aggregates and that Aβ, in turn, activates platelets, creating a feed-forward loop suggesting the involvement of platelets in the AD pathogenesis. Moreover, islet amyloid polypeptide deposition, co-localized with Aβ deposits, is a common finding in the brain of patients with T2DM. These observations raise the intriguing prospect that traditional or novel antiplatelet therapeutic strategies may alleviate fibril formation and could be used in the prevention or treatment of AD subjects with diabetes.

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2型糖尿病、血小板活化和阿尔茨海默病:可能的联系
2型糖尿病(T2DM)与痴呆症(包括阿尔茨海默病(AD))风险增加70%相关。胰岛素抵抗被认为在T2DM和AD中都起着关键作用,“脑胰岛素抵抗”的概念被认为是对越来越多的关于认知障碍和T2DM的文献的解释。T2DM患者血小板反应性异常,并伴有胰岛素抵抗、高血糖和血脂异常,通过内皮功能障碍、氧化应激和低度炎症等一系列事件影响血管壁。活化的血小板通过促进β-淀粉样蛋白(a β)聚集体的形成直接促进脑淀粉样血管病(CAA),而a β反过来激活血小板,形成一个前馈循环,表明血小板参与AD的发病机制。此外,胰岛淀粉样多肽沉积,与a β沉积共定位,是T2DM患者大脑中常见的发现。这些观察结果提出了一个有趣的前景,即传统的或新的抗血小板治疗策略可能会减轻原纤维的形成,并可用于预防或治疗AD合并糖尿病患者。
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来源期刊
Clinical Neuropsychiatry
Clinical Neuropsychiatry CLINICAL NEUROLOGY-
CiteScore
11.10
自引率
1.60%
发文量
0
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