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The Time Is Right for a New Classification System for Diabetes: Rationale and Implications of the beta-Cell-Centric Classification Schema

机译:新的糖尿病分类系统的时机已到:β细胞中心分类模式的原理和含义

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The current classification system presents challenges to the diagnosis and treatment of patients with diabetes mellitus (DM), in part due to its conflicting and confounding definitions of type 1 DM, type 2 DM, and latent autoimmune diabetes of adults (LADA). The current schema also lacks a foundation that readily incorporates advances in our understanding of the disease and its treatment. For appropriate and coherent therapy, we propose an alternate classification system. The beta-cell-centric classification of DM is a new approach that obviates the inherent and unintended confusions of the current system. The beta-cell-centric model presupposes that all DM originates from a final common denominator-the abnormal pancreatic beta-cell. It recognizes that interactions between genetically predisposed beta-cells with a number of factors, including insulin resistance (IR), susceptibility to environmental influences, and immune dysregulation/ inflammation, lead to the range of hyperglycemic phenotypes within the spectrum of DM. Individually or in concert, and often self-perpetuating, these factors contribute to beta-cell stress, dysfunction, or loss through at least 11 distinct pathways. Available, yet underutilized, treatments provide rational choices for personalized therapies that target the individual mediating pathways of hyperglycemia at work in any given patient, without the risk of drug-related hypoglycemia or weight gain or imposing further burden on the beta-cells. This article issues an urgent call for the review of the current DM classification system toward the consensus on a new, more useful system.
机译:当前的分类系统对糖尿病患者(DM)的诊断和治疗提出了挑战,部分原因是其对1型DM,2型DM和成人潜伏性自身免疫性糖尿病(LADA)的定义存在冲突和混淆。当前的方案还缺乏一个基础,无法将我们对疾病及其治疗方法的了解结合进去。为了进行适当且连贯的治疗,我们提出了一种替代分类系统。 DM的以β细胞为中心的分类是一种新方法,它消除了当前系统的内在和意料之外的混乱。以β细胞为中心的模型假定所有DM都来自最终的共同分母-异常的胰腺β细胞。它认识到遗传易感性β细胞与许多因素之间的相互作用,包括胰岛素抵抗(IR),对环境影响的敏感性以及免疫失调/炎症,导致DM频谱内的高血糖表型范围。这些因素单独或共同作用,并且经常自我延续,它们通过至少11种不同的途径导致β细胞应激,功能障碍或丧失。可用但尚未充分利用的治疗方法为针对个性化疗法的合理选择提供了选择,这些疗法针对任何给定患者工作中的高血糖个体调节途径,而没有与药物相关的低血糖或体重增加的风险,也不会给β细胞增加负担。本文紧急呼吁审查当前的DM分类系统,以期就新的,更有用的系统达成共识。

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