Department of General Pediatrics, Neonatology, and Pediatric Cardiology, University Children's Hospital, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Department of Pediatric Endocrinology, Diabetes, and Nutrition Medicine, Vestische Hospital for Children and Adolescents Datteln, University of Witten-Herdecke, Datteln, Germany.
Horm Res Paediatr. 2018;89(2):73-81. doi: 10.1159/000484896. Epub 2017 Dec 5.
The hepatokine fetuin A is upregulated in the metabolic syndrome and in type 2 diabetes (T2D), while its role in adolescent type 1 diabetes (T1D) is unclear. We assessed the relationship between circulating fetuin A levels and metabolic control, comorbidities, and complications in adolescent T1D patients.
We studied the relationship between serum fetuin A and clinical diabetes-related data from the DPV registry (Diabetes-Pa-tienten-Verlaufsdokumentation) in 172 adolescent T1D patients with early-onset (<5 years) long-standing (>10 years) T1D. Fetuin A levels were further compared between adolescent T1D and T2D patients.
Serum fetuin A levels in T1D patients (mean 0.267 ± 0.043 g/L) did not correlate with age, diabetes duration, gender, body mass index (BMI), glycated hemoglobin, serum lipid levels, blood pressure, celiac or thyroid disease, nephropathy, or retinopathy. An association of fetuin A levels with insulin requirements was only evident within the subgroup of overweight T1D patients (rs = 0.439, p = 0.028, n = 25, BMI >90th percentile), disappearing after adjustment for multiple testing. Adolescent T1D patients showed distinctly lower fetuin A levels than patients with T2D (p ≤ 0.001).
Overall, we did not observe a clinically relevant association of fetuin A levels with surrogate parameters for insulin sensitivity in our juvenile T1D cohort. A correlation with insulin requirements was detectable in overweight patients only. We hypothesize that multiple factors, such as obesity, puberty, inadequate metabolic control, and hepatic steatosis, have to add up before a clinically relevant effect of fetuin A on insulin sensitivity becomes evident.
在代谢综合征和 2 型糖尿病(T2D)中,肝分泌的胎球蛋白 A 上调,而其在青少年 1 型糖尿病(T1D)中的作用尚不清楚。我们评估了循环胎球蛋白 A 水平与青少年 T1D 患者代谢控制、合并症和并发症之间的关系。
我们研究了来自 DPV 登记处(Diabetes-Pa-tienten-Verlaufsdokumentation)的 172 名青少年 T1D 患者(起病年龄<5 岁,病程>10 年)的血清胎球蛋白 A 与临床相关糖尿病数据之间的关系。进一步比较了青少年 T1D 和 T2D 患者之间的胎球蛋白 A 水平。
T1D 患者的血清胎球蛋白 A 水平(平均值 0.267 ± 0.043 g/L)与年龄、糖尿病病程、性别、体重指数(BMI)、糖化血红蛋白、血脂水平、血压、乳糜泻或甲状腺疾病、肾病或视网膜病变无关。只有在超重的 T1D 患者亚组中(rs = 0.439,p = 0.028,n = 25,BMI>第 90 百分位),胎球蛋白 A 水平与胰岛素需求之间存在关联,在经过多次检验调整后这种关联消失。青少年 T1D 患者的胎球蛋白 A 水平明显低于 T2D 患者(p ≤ 0.001)。
总的来说,我们在青少年 T1D 队列中未观察到胎球蛋白 A 水平与胰岛素敏感性的替代参数之间存在临床相关的关联。仅在超重患者中可以检测到与胰岛素需求的相关性。我们假设,在胎球蛋白 A 对胰岛素敏感性产生临床相关影响之前,必须有多个因素(如肥胖、青春期、代谢控制不佳和肝脂肪变性)共同作用。