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. 2017 Apr 14;8(42):73133-73143.
doi: 10.18632/oncotarget.17111. eCollection 2017 Sep 22.

Association of lower body mass index with increased glycemic variability in patients with newly diagnosed type 2 diabetes: a cross-sectional study in China

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Association of lower body mass index with increased glycemic variability in patients with newly diagnosed type 2 diabetes: a cross-sectional study in China

Jian Wang et al. Oncotarget. .

Abstract

Previous studies have indicated that the pathogenesis of diabetes differs between obese and lean patients. We investigated whether newly diagnosed Chinese diabetic patients with different body mass indices (BMIs) have different glycemic variability, and we assessed the relationship between BMI and glycemic variability. This was a cross-sectional study that included 169 newly diagnosed and drug-naïve type 2 diabetic patients (mean age, 51.33 ± 9.83 years; 110 men). The clinical factors and results of the 75-g oral glucose tolerance test were all recorded. Glycemic variability was assessed using continuous glucose monitoring. Compared with overweight or obese patients (BMI ≥ 24 kg/m2), underweight or normal-weight patients (BMI < 24 kg/m2) had higher levels of blood glucose fluctuation parameters, particularly in terms of mean amplitude of glycemic excursion (MAGE 6.64 ± 2.38 vs. 5.67 ± 2.05; P = 0.007) and postprandial glucose excursions (PPGEs) (PPGE at breakfast, 7.72 ± 2.79 vs. 6.79 ± 2.40, P = 0.028; PPGE at lunch, 5.53 ± 2.70 vs. 5.07 ± 2.40, P = 0.285; PPGE at dinner, 5.96 ± 2.24 vs. 4.87 ± 2.50, P = 0.008). BMI was negatively correlated with glycemic variability (r = -0.243, P = 0.002). On multiple linear regression analyses, BMI (β = -0.231, P = 0.013) and Insulin Secretion Sensitivity Index-2 (β = -0.204, P = 0.048) were two independent predictors of glycemic variability. In conclusion, lower BMI was associated with increased glycemic variability, characterized by elevated PPGEs, in newly diagnosed Chinese type 2 diabetic patients.

Keywords: body mass index; continuous glucose monitoring; glycemic variability; obesity; postprandial glucose excursion.

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Conflict of interest statement

CONFLICTS OF INTEREST The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1. Comparison of MAGE and PPGEs between underweight or normal-weight patients (Group A) and overweight or obese patients (Group B): using box-and-whisker plot
Abbreviations: MAGE, mean amplitude of glycemic excursions; PPGEs, postprandial glucose excursions. The box contained 50% of all values (from 25th to 75th percentile) and was divided by the horizontal bar of the median value (50th percentile). The whiskers showed the remainder of the distribution (1.5 × Inter Quartile Range). Outliers were shown as dots.
Figure 2
Figure 2. The relation between BMI and MAGE
Abbreviations: BMI, body mass index; MAGE, mean amplitude of glycemic excursions.Linear relation between BMI and MAGE was observed. The correlation coefficient was −0.243 (P = 0.002).

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