The correlation between patients with type 2 diabetes mellitus and chronic microvascular complications during the glucose peak time


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The correlation between patients with type 2 diabetes mellitus and chronic microvascular complications during the glucose peak time

Introduction: To assess the Type 2 Diabetes Mellitus (T2DM) patients in association with Chronic Microvascular Complications at Glucose Peak Time and the association among chronic microvascular complications in T2DM patients and the glucose peak period in the typical steamed bread meal test.

Methods: Overall 1095 T2DM patients were classified as three groups: (1) Group G1: glucose peak time ≤ 1 h (n = 84), Group G2: 1 h < glucose peak time ≤ 2 h (n = 648) and Group G3: glucose peak time > 2 h (n = 363). The clinical characteristics, insulin characteristics and glucose peak time and chronic microvascular complications markers of patients in each group was analyzed and compared. Statistical analyses were performed using SPSS 23.0, employing chi-square tests, Kruskal-Wallis tests, one-way ANOVA, and binary logistic regression analysis, with significance set at P < 0.05.

Results: Age, length of disease, glycated hemoglobin (HbA1 c), urine albumin-creatinine ratio (UACR), and the number of patients with diabetic retinopathy (DR) increased (all P < 0.05) in those with postponed glucose peak time, while insulinogenic indexes, the AUC for C-p (AUCC-p), fasting, and 120-min C-peptide (C-p) decreased (all P < 0.05). Only age was connected to patients with diabetic kidney disease (DKD) independently in binary logistic regression analysis, although delayed glucose peak time was related to the presence of patients with DR. (all P < 0.05).

Conclusion: Delayed glucose peak time contributed to DR. Attention should be paid to condition of chronic microvascular complications in T2DM patients with a postponed peak glucose timing. © 2024 The Authors

Authors : Jiang Y.; Wang X.; Zhao X.; Sun Y.; Huang P.; Que Q.; Shi R.; Zhao X.; Lu H.; Gu Y.

Source : Elsevier Inc.

Article Information

Year 2024
Type Article
DOI 10.1016/j.jdiacomp.2024.108866
ISSN 10568727
Volume 38

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