Braun Doris, Konrad Daniel, Lang-Muritano Mariarosaria, Schoenle Eugen
Department of Endocrinology and Diabetology, University Children's Hospital, Steinwiesstrasse 75, Zurich, Switzerland.
Pediatr Diabetes. 2008 Aug;9(4 Pt 2):382-7. doi: 10.1111/j.1399-5448.2008.00371.x. Epub 2008 Mar 5.
To assess the effect of the insulin analog detemir on glycemic control and severe hypoglycemia in children and adolescents with type 1 diabetes.
A retrospective chart analysis was performed in 105 patients with type 1 diabetes after switching to insulin detemir between 2004 and 2007. In children below 12 yr of age (n = 53), evening neutral protomin hagedorn (NPH) insulin was replaced by insulin detemir if therapeutic goals were not reached and blood glucose levels were unpredictable or hardly controllable. In adolescents above 12 yr of age (n = 52), insulin detemir was started when changing to intensified insulin therapy.
In children below 12 yr of age, hemoglobin A1c (HbA1c) at start was 8.3 +/- 0.8% and after 12 months of treatment with insulin detemir significantly lowered (7.6 +/- 0.6%, p < 0.001). In the age-group above 12 yr of age at the start of the study, the improvement of HbA1c after 12 months of treatment was less pronounced (8.0 +/- 1.2 vs. 7.6 +/- 1.0%) but still significant (p < 0.01). The risk for severe hypoglycemia was significantly decreased compared with patients attending the outpatient clinic between 1995 and 2003 (4.8/100 patient years vs. 7.6/100 patient years, p = 0.003). From the beginning to the end of the follow-up period, body mass index dropped significantly in children below 12 yr of age but no effect was observed in adolescents.
Use of insulin detemir allows a safe nocturnal glycemic control in children and adolescents with type 1 diabetes and is associated with significantly improved HbA1c levels and fewer severe hypoglycemic events. This makes insulin detemir a most valuable new tool for the treatment of children and adolescents with type 1 diabetes.
评估胰岛素类似物地特胰岛素对1型糖尿病儿童和青少年血糖控制及严重低血糖的影响。
对2004年至2007年间改用胰岛素地特胰岛素的105例1型糖尿病患者进行回顾性病历分析。12岁以下儿童(n = 53),若未达到治疗目标且血糖水平不可预测或难以控制,则将晚间中效胰岛素(NPH)替换为胰岛素地特胰岛素。12岁以上青少年(n = 52),开始强化胰岛素治疗时启用胰岛素地特胰岛素。
12岁以下儿童,起始糖化血红蛋白(HbA1c)为8.3±0.8%,使用胰岛素地特胰岛素治疗12个月后显著降低(7.6±0.6%,p < 0.001)。在研究开始时12岁以上年龄组,治疗12个月后HbA1c的改善不太明显(8.0±1.2对7.6±1.0%),但仍有显著差异(p < 0.01)。与1995年至2003年门诊患者相比,严重低血糖风险显著降低(4.8/100患者年对7.6/100患者年,p = 0.003)。从随访期开始到结束,12岁以下儿童的体重指数显著下降,但青少年未观察到影响。
使用胰岛素地特胰岛素可使1型糖尿病儿童和青少年实现安全的夜间血糖控制,并与HbA1c水平显著改善及严重低血糖事件减少相关。这使胰岛素地特胰岛素成为治疗1型糖尿病儿童和青少年的极有价值的新工具。