A Case Report of Anti-GAD65 Antibody-Positive Autoimmune Encephalitis Associated with Diabetes.

IF 2
Xiuping Xuan, Liheng Meng, Lulu Chen, Xuemei Xie, Xinghuan Liang, Yingfen Qin
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Abstract

Background: Patients with GAD65 antibody-associated autoimmune encephalitis who also have diabetes are usually considered to have type 1 diabetes mellitus (T1DM). However, previous reports often lacked β-cell function assessments, relying solely on anti-GAD65 positivity for diagnosis, which is insufficient for accurate classification.

Case presentation: We present a 30-year-old Chinese woman diagnosed with GAD65-associated autoimmune encephalitis, hyperthyroidism, and diabetes. Her peak C-peptide level was 3.99 ng/mL, inconsistent with the β-cell dysfunction typical of classic T1DM. The combination of high GAD65 antibody titers and preserved β-cell function made it challenging to determine her diabetes type.

Conclusion: This case suggests that clinicians should pay more attention to assessing and monitoring β-cell function when GAD65-associated autoimmune encephalitis is accompanied by diabetes.

抗gad65抗体阳性的自身免疫性脑炎合并糖尿病1例
背景:GAD65抗体相关自身免疫性脑炎合并糖尿病的患者通常被认为是1型糖尿病(T1DM)。然而,以往的报道往往缺乏β细胞功能评估,仅依靠抗gad65阳性进行诊断,不足以准确分类。病例介绍:我们报告一名30岁的中国女性,诊断为gad65相关的自身免疫性脑炎、甲状腺功能亢进和糖尿病。她的c肽峰值为3.99 ng/mL,与典型T1DM的β细胞功能障碍不一致。GAD65抗体的高滴度和β细胞功能的保存使得确定她的糖尿病类型具有挑战性。结论:本病例提示临床医生在gad65相关自身免疫性脑炎合并糖尿病时应重视β细胞功能的评估和监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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