Diabetic Clinic, 2nd Department of Pediatrics, 'P. & A. Kyriakou' Children's Hospital, National and Kapodistrian University of Athens, Thivon & Levadeias Str, 115 27, Athens, Greece.
Hormones (Athens). 2024 Sep;23(3):395-405. doi: 10.1007/s42000-023-00518-7. Epub 2023 Dec 27.
We aimed to assess factors associated with the presence and severity of ketoacidosis (DKA) at pediatric type 1 diabetes (T1DM) diagnosis, in relation to pancreatic, associated and familial autoimmunity.
Antibodies against pancreatic beta-cells, organ specific autoantibodies (thyroid, celiac, and parietal) and family history of autoimmunity were retrospectively evaluated in 116 T1DM patients aged 11.9 ± 4.6 (mean ± SD) years, with disease duration 7.62 ± 3.67 years (mean ± SD).
Most patients (67.2%) presented with DKA at diagnosis. Younger children (< 2 years) had tenfold risk of DKA, compared to older children (12.1-15 years) (OR = 10.8, 95% CI: 1.0-116.9, P = 0.05). Fasting c-peptide levels were lower in the DKA group (OR = 0.26, 95% CI = 0.07-0.89, P = 0.033). The number of anti-pancreatic antibodies at disease onset did not show any significant correlations with the presence (p = 0.889) or severity of DKA (p = 0.863). All patients with multiple autoimmunity (> 2 autoimmune diseases plus T1DM) presented with DKA. Familial autoimmunity acted protectively against DKA manifestation (OR = 0.40, 95% CI = 0.16-1.0, P = 0.051).
Among newly diagnosed T1DM patients, 67.2% presented with DKA. Younger age, lower c-peptide and the presence of associated autoimmunity were predictive factors of the presence and severity of DKA at diagnosis. High degree of suspicion, due to family history, may prevent DKA development and severity.
我们旨在评估与胰腺、相关和家族自身免疫相关的因素与儿科 1 型糖尿病(T1DM)诊断时酮症酸中毒(DKA)的存在和严重程度的关系。
回顾性评估了 116 例年龄为 11.9±4.6(均值±标准差)岁、病程为 7.62±3.67 年(均值±标准差)的 T1DM 患者的胰岛β细胞抗体、器官特异性自身抗体(甲状腺、乳糜泻和壁细胞)和家族自身免疫病史。
大多数患者(67.2%)在诊断时出现 DKA。与年龄较大的儿童(12.1-15 岁)相比,年龄较小的儿童(<2 岁)DKA 的风险增加了 10 倍(OR=10.8,95%CI:1.0-116.9,P=0.05)。DKA 组的空腹 C 肽水平较低(OR=0.26,95%CI=0.07-0.89,P=0.033)。疾病发作时抗胰腺抗体的数量与 DKA 的存在(p=0.889)或严重程度(p=0.863)均无显著相关性。所有患有多种自身免疫性疾病(>2 种自身免疫性疾病加 T1DM)的患者均出现 DKA。家族自身免疫对 DKA 的表现具有保护作用(OR=0.40,95%CI=0.16-1.0,P=0.051)。
在新诊断的 T1DM 患者中,67.2%出现 DKA。年龄较小、C 肽较低以及存在相关自身免疫是诊断时 DKA 存在和严重程度的预测因素。由于家族史,高度怀疑可能会预防 DKA 的发生和严重程度。