口服葡萄糖耐量试验中胰高血糖素分泌模式的鉴定

Andrew Shahidehpour, Mudassir M. Rashid, Mohammad-Reza Askari, Mohammad Ahmadasas, A. Cinar
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摘要

胰高血糖素分泌受损是2型糖尿病(T2D)中葡萄糖耐受不良的主要组成部分。胰高血糖素分泌在个体和葡萄糖耐量诊断中表现出异质模式。胰高血糖素分泌模式范围的特征可以帮助临床医生根据胰高血糖素特征以及葡萄糖和胰岛素谱来个性化糖尿病护理。共有102名糖耐量正常、糖耐量受损和T2D的受试者在口服糖耐量试验中记录了他们的胰高血糖素谱。Shapelet分析用于识别早期胰高血糖素分泌最具描述性的模式,并采用光谱双聚类来识别相关受试者和Shapelet的双聚类。评估每组受试者的葡萄糖、胰岛素和胰高血糖素分泌的动态,以确定总体模式,并比较每组受试者的特征。选择三个簇来代表胰高血糖素的模式。根据口服碳水化合物摄入后的前30分钟是否存在极端情况来解释这三个集群的成员。集群1 (n = 23)在30分钟时最小,只有负趋势。集群2的最小值在10分钟,最大值在20分钟(n = 25)。第3组(n = 40)的平均空腹血糖最低(90.17 mg/dL),平均年龄最低(41.39岁),homa - β评分最高(87.5%);第2组的平均空腹血糖最高(102.56 mg/dL),平均年龄最高(53.16岁),homa - β评分最低(55.77%)。表征胰高血糖素动力学,除了葡萄糖和胰岛素,可以帮助个性化的治疗方法,并提供对潜在的血糖调节功能障碍的更深入的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Glucagon Secretion Patterns during an Oral Glucose Tolerance Test
Impaired glucagon secretion is a major component of glucose intolerance in type 2 diabetes mellitus (T2D). Glucagon secretion exhibits heterogenous patterns in individuals and across glucose tolerance diagnoses. Characterization of the range of glucagon secretion patterns can help clinicians personalize diabetes care based on glucagon characteristics in addition to glucose and insulin profiles. A total of 102 subjects with normal glucose tolerance, impaired glucose tolerance, and T2D had their glucagon profiles recorded in response to an oral glucose tolerance test. Shapelet analysis was used to identify the most descriptive patterns of early glucagon secretion, and spectral biclustering was employed to identify biclusters of associated subjects and shapelets. The dynamics of glucose, insulin, and glucagon secretion in each cluster were evaluated to identify overall patterns, and the characteristics of the subjects in each cluster were compared. Three clusters were chosen to represent the glucagon patterns. Membership in these three clusters was interpreted based on the presence or lack of extrema in the first 30 min after oral carbohydrate intake. Cluster 1 (n = 23) had a minimum at 30 min and only negative trends. Cluster 2 had a minimum at 10 min and a maximum at 20 min (n = 25). Cluster 3 (n = 40) had a maximum at 10 min and a minimum at 20 min. Subjects in cluster 1 had the lowest average fasting plasma glucose (90.17 mg/dL) and average age (41.39 years) and the highest HOMA-beta score (87.5%), while subjects in cluster 2 had the highest average fasting plasma glucose (102.56 mg/dL) and average age (53.16 years) and the lowest HOMA-beta score (55.77%). Characterization of glucagon dynamics, in addition to glucose and insulin, can aid in personalized treatment approaches and provide greater insight about the underlying dysfunction in glucose regulation.
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