Murase Y, Imagawa A, Hanafusa T, Iwahashi H, Uchigata Y, Kanatsuka A, Kawasaki E, Kobayashi T, Shimada A, Shimizu I, Maruyama T, Makino H
First Department of Internal Medicine, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, and Department of Metabolism/Diabetes and Clinical Nutrition, Nagasaki University Hospital of Medicine and Dentistry, Japan.
Diabetologia. 2007 Mar;50(3):531-7. doi: 10.1007/s00125-006-0575-y. Epub 2007 Jan 18.
AIMS/HYPOTHESIS: The aim of the present study was to assess the development of microangiopathy in patients with fulminant type 1 diabetes, a novel subtype of type 1B diabetes.
In a nationwide survey, we followed 41 patients with fulminant type 1 diabetes and 76 age- and sex-matched patients with type 1A diabetes for 5 years. The following data were recorded every 12 months after the onset of diabetes: seven-point blood glucose concentrations, HbA1c level, urinary albumin excretion, serum C-peptide level, blood pressure, daily dosages of insulin, frequency of severe hypoglycaemic episodes, and neurological and fundoscopic examination.
The 5-year cumulative incidence of microangiopathy was 24.4% in fulminant type 1 diabetes and 2.6% in type 1A diabetes. In longitudinal studies using the Kaplan-Meier method, the cumulative incidence of each form of microangiopathy was significantly higher in fulminant type 1 diabetes than in type 1A diabetes; retinopathy was 9.8% vs 0% (p=0.014), nephropathy 12.2% vs 2.6% (p=0.015) and neuropathy 12.2% vs 1.3% (p=0.010), respectively. Mean HbA1c levels were similar in the fulminant and type 1A diabetes groups during the follow-up periods. However, the mean M-value, mean insulin dosages and the frequency of severe hypoglycaemic episodes were significantly higher, and the mean postprandial C-peptide level was significantly lower in the fulminant type 1 diabetes group.
CONCLUSIONS/INTERPRETATION: These data suggest that patients with fulminant type 1 diabetes are a high-risk subgroup for diabetic microangiopathy associated with the lack of endogenous insulin secretion from the onset of diabetes.
目的/假设:本研究旨在评估暴发性1型糖尿病(1B型糖尿病的一种新型亚型)患者微血管病变的发展情况。
在一项全国性调查中,我们对41例暴发性1型糖尿病患者和76例年龄及性别匹配的1A型糖尿病患者进行了为期5年的随访。糖尿病发病后每隔12个月记录以下数据:七点血糖浓度、糖化血红蛋白水平、尿白蛋白排泄量、血清C肽水平、血压、胰岛素每日剂量、严重低血糖发作频率以及神经和眼底检查。
暴发性1型糖尿病患者微血管病变的5年累积发病率为24.4%,1A型糖尿病患者为2.6%。在使用Kaplan-Meier方法进行的纵向研究中,暴发性1型糖尿病患者每种微血管病变形式的累积发病率均显著高于1A型糖尿病患者;视网膜病变分别为9.8%和0%(p = 0.014),肾病为12.2%和2.6%(p = 0.015),神经病变为12.2%和1.3%(p = 0.010)。随访期间,暴发性糖尿病组和1A型糖尿病组的平均糖化血红蛋白水平相似。然而,暴发性1型糖尿病组的平均M值、平均胰岛素剂量和严重低血糖发作频率显著更高,餐后平均C肽水平显著更低。
结论/解读:这些数据表明,暴发性1型糖尿病患者是糖尿病微血管病变的高危亚组,与糖尿病发病时内源性胰岛素分泌缺乏有关。