Laimer Markus, Melmer Andreas, Mader Julia K, Schütz-Fuhrmann Ingrid, Engels Heide-Rose, Götz Gabriele, Pfeifer Martin, Hermann Julia M, Stettler Christoph, Holl Reinhard W
Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Bern, Bern, Switzerland.
Department of Internal Medicine I, Medical University of Innsbruck, Innsbruck, Austria.
PLoS One. 2016 Mar 3;11(3):e0150604. doi: 10.1371/journal.pone.0150604. eCollection 2016.
Traditionally, basal rate profiles in continuous subcutaneous insulin infusion therapy are individually adapted to cover expected insulin requirements. However, whether this approach is indeed superior to a more constant BR profile has not been assessed so far. This study analysed the associations between variability of BR profiles and acute and chronic complications in adult type 1 diabetes mellitus.
BR profiles of 3118 female and 2427 male patients from the "Diabetes-Patienten-Verlaufsdokumentation" registry from Germany and Austria were analysed. Acute and chronic complications were recorded 6 months prior and after the most recently documented basal rate. The "variability index" was calculated as variation of basal rate intervals in percent and describes the excursions of the basal rate intervals from the median basal rate.
The variability Index correlated positively with severe hypoglycemia (r = .06; p<0.001), hypoglycemic coma (r = .05; p = 0.002), and microalbuminuria (r = 0.05; p = 0.006). In addition, a higher variability index was associated with higher frequency of diabetic ketoacidosis (r = .04; p = 0.029) in male adult patients. Logistic regression analysis adjusted for age, gender, duration of disease and total basal insulin confirmed significant correlations of the variability index with severe hypoglycemia (β = 0.013; p<0.001) and diabetic ketoacidosis (β = 0.012; p = 0.017).
Basal rate profiles with higher variability are associated with an increased frequency of acute complications in adults with type 1 diabetes.
传统上,持续皮下胰岛素输注治疗中的基础率曲线是根据预期的胰岛素需求进行个体化调整的。然而,到目前为止,这种方法是否确实优于更恒定的基础率曲线尚未得到评估。本研究分析了基础率曲线变异性与成年1型糖尿病急性和慢性并发症之间的关联。
分析了来自德国和奥地利“糖尿病患者病程记录”登记处的3118名女性和2427名男性患者的基础率曲线。在最近记录的基础率之前和之后6个月记录急性和慢性并发症。“变异指数”以基础率区间的变化百分比计算,描述基础率区间相对于基础率中位数的波动情况。
变异指数与严重低血糖(r = 0.06;p<0.001)、低血糖昏迷(r = 0.05;p = 0.002)和微量白蛋白尿(r = 0.05;p = 0.006)呈正相关。此外,在成年男性患者中,较高的变异指数与糖尿病酮症酸中毒的较高发生率相关(r = 0.04;p = 0.029)。经年龄、性别、病程和基础胰岛素总量校正的逻辑回归分析证实,变异指数与严重低血糖(β = 0.013;p<0.001)和糖尿病酮症酸中毒(β = 0.012;p = 0.017)存在显著相关性。
变异性较高的基础率曲线与成年1型糖尿病患者急性并发症的发生率增加有关。