Department of Endocrinology, Diabetes and Metabolism, Christian Medical College (CMC), Vellore, India.
Department of Endocrinology, Diabetes and Metabolism, Christian Medical College (CMC), Vellore, India.
J Diabetes Complications. 2017 Sep;31(9):1401-1407. doi: 10.1016/j.jdiacomp.2017.06.008. Epub 2017 Jun 23.
Ketosis-prone diabetes (KPD), an atypical form of diabetes, has emerged as a heterogeneous syndrome in multiple ethnic groups. The objectives of this study were to look into the clinical characteristics of adult Asian Indian patients with recently diagnosed, antibody negative diabetes presenting with unprovoked ketoacidosis (A-β+ KPD) and to determine the natural course of recovery of beta-cell functions on serial follow-up over one year.
Newly diagnosed adult diabetes patients (n=11) with suspected KPD (A-β+) were prospectively studied over a period of 1-year with serial evaluations of clinical, biochemical and beta-cell secretion characteristics. These were compared with a control group (n=23) of KPD (A+β-) (classical Type 1A diabetes) with similar presentation. Beta-cell secretion was assessed by fasting and stimulated C-peptide values after a standard mixed meal challenge. Glycaemic control and treatment outcomes were also documented.
In comparison to the A+β- KPD controls, the A-β+ KPD patients had a significantly older age, higher BMI, stronger family history of type 2 diabetes, more severe ketoacidosis and higher fasting and stimulated C-peptide level at presentation. On serial follow-up, the patients with KPD achieved complete recovery of their beta-cell function with remission from insulin-dependence within 3-4months without further recurrences of DKA.
This is the first reported series of A-β+ KPD from India. The phenotype of Indian A-β+ KPD patients differs from their Western counterparts in that they are relatively younger and leaner, though the male preponderance and natural history of recovery of beta-cell dysfunction bears similarity.
酮症倾向糖尿病(KPD)是一种非典型形式的糖尿病,已在多个种族中出现为一种异质综合征。本研究的目的是研究新近诊断的、抗体阴性的、以自发性酮症酸中毒为表现的成年亚裔印度糖尿病患者(A-β+ KPD)的临床特征,并确定在一年的连续随访中β细胞功能恢复的自然病程。
前瞻性研究了 11 例疑诊为 KPD(A-β+)的新诊断成年糖尿病患者,对其进行为期 1 年的临床、生化和β细胞分泌特征的连续评估。将这些患者与具有相似表现的 KPD(A+β-)(经典 1 型糖尿病)对照组(n=23)进行比较。β细胞分泌功能通过标准混合餐刺激前后的空腹和刺激 C 肽值来评估。还记录了血糖控制和治疗结果。
与 A+β- KPD 对照组相比,A-β+ KPD 患者的年龄较大、BMI 较高、2 型糖尿病家族史更强、酮症酸中毒更严重、空腹和刺激 C 肽水平更高。在连续随访中,KPD 患者在 3-4 个月内完全恢复了β细胞功能,胰岛素依赖得到缓解,且没有再次发生 DKA。
这是印度首例 A-β+ KPD 的报告系列。印度 A-β+ KPD 患者的表型与西方患者不同,他们相对较年轻、较瘦,但男性患病率较高和β细胞功能障碍的自然恢复历史相似。