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葡萄糖代谢的双重作用:大脑健康、血糖稳态与您的2型糖尿病患者

The double life of glucose metabolism: brain health, glycemic homeostasis, and your patients with type 2 diabetes.

作者信息

Schwartz Stanley S, Herman Mary E, Tun May Thet Hmu, Barone Eugenio, Butterfield D Allan

机构信息

University of Pennsylvania School of Medicine, 771 County Line Road, Villanova, PA, 19085, USA.

Social Alchemy: Building Physician Competency Across the Globe, 5 Ave Sur #36, Antigua, Sacatepéquez, Guatemala.

出版信息

BMC Med. 2024 Dec 18;22(1):582. doi: 10.1186/s12916-024-03763-8.

Abstract

The maintenance of cognitive function is essential for quality of life and health outcomes in later years. Cognitive impairment, however, remains an undervalued long-term complication of type 2 diabetes by patients and providers alike. The burden of sustained hyperglycemia includes not only cognitive deficits but also the onset and progression of dementia-related conditions, including Alzheimer's disease (AD). Recent research has shown that the brain maintains an independent glucose "microsystem"-evolved to ensure the availability of fuel for brain neurons without interruption by transient hypoglycemia. When this milieu is perturbed, brain hyperglycemia, brain glucotoxicity, and brain insulin resistance can ensue and interfere with insulin signaling, a key pathway to cognitive function and neuronal integrity. This newly understood brain homeostatic system operates semi-autonomously from the systemic glucoregulatory apparatus. Large-scale clinical studies have shown that systemic dysglycemia is also strongly associated with poorer cognitive outcomes, which can be mitigated through appropriate clinical management of plasma glucose levels. Moreover, these studies demonstrated that glucose-lowering agents are not equally effective at preventing cognitive dysfunction. Glucagon-like peptide-1 (GLP-1) receptor analogs and sodium glucose cotransporter 2 inhibitors (SGLT2is) appear to afford the greatest protection; metformin and dipeptidyl peptidase 4 inhibitors (DPP-4is) also significantly improved cognitive outcomes. Sulfonylureas (SUs) and exogenous insulin, on the other hand, do not provide the same protection and may actually worsen cognitive outcomes. In the creation of a treatment plan, comorbid cognitive conditions should be considered. These efficacious treatments create a new gold standard of managing hyperglycemia-one which is consistent with the "complication-centric prescribing" mandates issued in type 2 diabetes treatment guidelines. The increasing longevity enjoyed by our populace places the onus on clinical care to play the "long game" in using targeted treatments for glucose control in patients with, or at risk for, cognitive decline to maintain cognitive wellness later in life. This article reviews critical emerging data for scientists and trialists and translates new enhancements in patient care for practitioners.

摘要

认知功能的维持对于晚年的生活质量和健康结果至关重要。然而,认知障碍仍然是2型糖尿病被患者和医护人员同样低估的长期并发症。持续性高血糖的负担不仅包括认知缺陷,还包括与痴呆相关疾病(包括阿尔茨海默病(AD))的发生和进展。最近的研究表明,大脑维持着一个独立的葡萄糖“微系统”——其进化是为了确保脑神经元的燃料供应不受短暂低血糖的干扰。当这种环境受到干扰时,可能会出现脑高血糖、脑葡萄糖毒性和脑胰岛素抵抗,并干扰胰岛素信号传导,而胰岛素信号传导是认知功能和神经元完整性的关键途径。这个新认识的脑稳态系统在很大程度上独立于全身葡萄糖调节装置运行。大规模临床研究表明,全身血糖异常也与较差的认知结果密切相关,通过对血糖水平进行适当的临床管理可以减轻这种情况。此外,这些研究表明,降糖药物在预防认知功能障碍方面的效果并不相同。胰高血糖素样肽-1(GLP-1)受体类似物和钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)似乎提供了最大的保护作用;二甲双胍和二肽基肽酶4抑制剂(DPP-4i)也显著改善了认知结果。另一方面,磺脲类药物(SU)和外源性胰岛素不能提供同样的保护作用,实际上可能会使认知结果恶化。在制定治疗方案时,应考虑并存的认知状况。这些有效的治疗方法创造了一种管理高血糖的新金标准——这与2型糖尿病治疗指南中发布的“以并发症为中心的处方”要求相一致。我们人口寿命的延长使临床护理有责任在对认知功能下降或有认知功能下降风险的患者使用靶向治疗来控制血糖方面“着眼长远”,以在晚年维持认知健康。本文为科学家和试验人员综述了关键的新出现数据,并为从业者解读了患者护理方面的新改进措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ff/11657227/64e0cd5f22e4/12916_2024_3763_Fig1_HTML.jpg

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