Quintal-Medina Ismael A, Gómez-Pérez Francisco J, Almeda-Valdes Paloma
Departamento de Endocrinología y Metabolismo, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Unidad de Investigación de Enfermedades Metabólicas, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
AACE Clin Case Rep. 2024 Jul 14;10(5):198-201. doi: 10.1016/j.aace.2024.07.003. eCollection 2024 Sep-Oct.
BACKGROUND/OBJECTIVE: Stiff person syndrome (SPS) and type 1 diabetes (T1D) are heterogeneous disorders characterized by antibodies (Abs) against glutamic acid decarboxylase (GAD).
We describe 2 patients with T1D and autoimmune thyroid disease who presented with muscle rigidity and intermittent spasms that affected gait and with elevated circulating anti-GAD titers. Classic SPS and stiff limb syndrome were diagnosed, respectively. Muscle spasms resolved with immunotherapy and muscle relaxants in both patients, and the ability to ambulate without an assistive device was restored in 1 patient. Patients also had brittle diabetes with high glycemic variability, requiring the use of flash glucose monitoring with an insulin pump and a second-generation basal insulin analog, respectively.
GAD Ab-associated syndromes include SPS, T1D, and other endocrinopathies. The clinical heterogeneity implies variable susceptibility of γ-aminobutyric acid-ergic neurons and pancreatic beta cells to anti-GAD or other autoantibodies.
Our case series represent the heterogeneity in natural history, clinical course, and response to therapy in patients with Abs against GAD-spectrum disorders.
背景/目的:僵人综合征(SPS)和1型糖尿病(T1D)是异质性疾病,其特征为存在针对谷氨酸脱羧酶(GAD)的抗体(Abs)。
我们描述了2例患有T1D和自身免疫性甲状腺疾病的患者,他们出现了影响步态的肌肉僵硬和间歇性痉挛,且循环抗GAD滴度升高。分别诊断为经典SPS和僵肢综合征。两名患者的肌肉痉挛均通过免疫疗法和肌肉松弛剂得到缓解,其中1例患者恢复了无需辅助装置行走的能力。患者还患有脆性糖尿病,血糖变异性高,分别需要使用带有胰岛素泵的动态血糖监测和第二代基础胰岛素类似物。
GAD抗体相关综合征包括SPS、T1D和其他内分泌病。临床异质性意味着γ-氨基丁酸能神经元和胰腺β细胞对抗GAD或其他自身抗体的易感性不同。
我们的病例系列代表了针对GAD谱疾病患者的自然病史、临床过程和治疗反应的异质性。