将肥胖在 T2DM 受试者胰岛素-葡萄糖调节系统中的作用纳入瘦素增强模型

MANOJA RAJALAKSHMI ARAVINDAKSHAN, Devleena Ghosh, Chittaranjan Mandal, Jit Sarkar, Sujay Krishna Maity, Partha Chakrabarti
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引用次数: 0

摘要

瘦素是一种源自脂肪细胞的激素,参与饱腹感和体重调节。它还通过调节葡萄糖代谢和能量平衡,在胰岛素-葡萄糖调节系统中发挥重要的调节作用。然而,现有的胰岛素-葡萄糖模型往往没有考虑体重指标(主要是体重指数(BMI)和血浆瘦素)的影响。为了解决这一局限性,我们建议在口服最小模型(OMM)的常微分方程(ODE)中增加一个方程,将瘦素以及补充项和参数纳入其中。通过估计模型参数,模型行为与 2 型糖尿病(T2DM)患者的葡萄糖、胰岛素和瘦素观测数据相一致。在模型行为的基础上,通过将体重指数和空腹瘦素值纳入口服葡萄糖耐量试验(OGTT)数据而制定的修订指数与现有指数具有更好的相关性。此外,还进行了参数敏感性分析,以研究模型参数对观测变量的影响。利用临床数据(不含瘦素)对增强模型进行了验证,结果表明与基础模型相比,增强模型更适合葡萄糖和胰岛素数据。该模型强调了瘦素、血糖和胰岛素浓度之间错综复杂的关联,有望为 T2DM 开发有针对性的干预和疗法。值得注意的是,该手稿首次引入了基于 ODE 的模型,将瘦素和体重指数纳入胰岛素-葡萄糖通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leptin augmented model to include the role of obesity in insulin-glucose regulatory system for T2DM subjects
Leptin is a fat cell-derived hormone involved in satiety and body weight regulation. It also plays a critical regulatory role in the insulin-glucose regulatory system by modulating glucose metabolism and energy homeostasis. However, existing insulin-glucose models often fail to consider the impact of body weight indicators mainly body mass index (BMI) and plasma leptin. To address this limitation, we propose augmenting the ordinary differential equations (ODE) of the Oral Minimal Model (OMM) with an additional equation, incorporating leptin as well as supplementary terms and parameters. By estimating the model parameters, the model behaviour is aligned with the observed data of glucose, insulin and leptin for individuals with type 2 diabetes mellitus (T2DM). Based on model behaviour, revised indices formulated from Oral Glucose Tolerance Test (OGTT) data by including BMI and fasting leptin values are found to have a better correlation with existing indices. Additionally, parameter sensitivity analysis is performed to investigate the influence of the model parameters on the observed variables. Validation of the augmented model with clinical data (without leptin) demonstrates a superior fit to glucose and insulin data compared to the base model. This model emphasizes the intricate associations between leptin, glucose, and insulin concentrations with a potential for developing targeted interventions and therapies for T2DM. Notably, this manuscript introduces the first ODE-based model that incorporates leptin and BMI in the insulin-glucose pathway.
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