Barbara Davis Center and the Children's Hospital, University of Colorado Denver, Aurora, Colorado, USA.
Diabetes Care. 2010 Sep;33(9):1970-5. doi: 10.2337/dc10-0373. Epub 2010 Jun 2.
To determine the frequency of islet cell autoimmunity in youth clinically diagnosed with type 2 diabetes and describe associated clinical and laboratory findings.
Children (10-17 years) diagnosed with type 2 diabetes were screened for participation in the Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY) study. Measurements included GAD-65 and insulinoma-associated protein 2 autoantibodies using the new National Institute of Diabetes and Digestive and Kidney Diseases/National Institutes of Health (NIDDK/NIH) standardized assays, a physical examination, and fasting lipid, C-peptide, and A1C determinations.
Of the 1,206 subjects screened and considered clinically to have type 2 diabetes, 118 (9.8%) were antibody positive; of these, 71 (5.9%) were positive for a single antibody, and 47 were positive (3.9%) for both antibodies. Diabetes autoantibody (DAA) positivity was significantly associated with race (P < 0.0001), with positive subjects more likely to be white (40.7 vs. 19%) (P < 0.0001) and male (51.7 vs. 35.7%) (P = 0.0007). BMI, BMI z score, C-peptide, A1C, triglycerides, HDL cholesterol, and blood pressure were significantly different by antibody status. The antibody-positive subjects were less likely to display characteristics clinically associated with type 2 diabetes and a metabolic syndrome phenotype, although the range for BMI z score, blood pressure, fasting C-peptide, and serum lipids overlapped between antibody-positive and antibody-negative subjects.
Obese youth with a clinical diagnosis of type 2 diabetes may have evidence of islet autoimmunity contributing to insulin deficiency. As a group, patients with DAA have clinical characteristics significantly different from those without DAA. However, without islet autoantibody analysis, these characteristics cannot reliably distinguish between obese young individuals with type 2 diabetes and those with autoimmune diabetes.
确定临床上被诊断为 2 型糖尿病的青年人群中胰岛自身免疫的发生频率,并描述相关的临床和实验室发现。
对被诊断为 2 型糖尿病的儿童(10-17 岁)进行筛查,以参与青少年和儿童 2 型糖尿病治疗选择(TODAY)研究。测量包括使用新的美国国立糖尿病、消化和肾脏疾病研究所/美国国立卫生研究院(NIDDK/NIH)标准化检测方法的谷氨酸脱羧酶 65 和胰岛相关蛋白 2 自身抗体、体格检查以及空腹血脂、C 肽和 A1C 测定。
在 1206 名经临床考虑患有 2 型糖尿病并进行筛查的患者中,有 118 名(9.8%)抗体阳性;其中,71 名(5.9%)为单一抗体阳性,47 名(3.9%)为两种抗体均阳性。糖尿病自身抗体(DAA)阳性与种族显著相关(P<0.0001),阳性者更有可能为白人(40.7%比 19%)(P<0.0001)和男性(51.7%比 35.7%)(P=0.0007)。根据抗体状态,BMI、BMI z 评分、C 肽、A1C、甘油三酯、高密度脂蛋白胆固醇和血压存在显著差异。抗体阳性者更不可能表现出与 2 型糖尿病和代谢综合征表型相关的临床特征,尽管抗体阳性和抗体阴性者的 BMI z 评分、血压、空腹 C 肽和血清脂质范围存在重叠。
临床诊断为 2 型糖尿病的肥胖青少年可能存在导致胰岛素缺乏的胰岛自身免疫证据。作为一个群体,DAA 患者的临床特征与无 DAA 患者显著不同。然而,如果不进行胰岛自身抗体分析,则这些特征无法可靠地区分肥胖的年轻 2 型糖尿病患者和自身免疫性糖尿病患者。