| Literature DB >> 24147207 |
Eiji Kawasaki1, Jun-Ichi Yasui, Masako Tsurumaru, Haruko Takashima, Toshiyuki Ikeoka, Fumi Mori, Satoru Akazawa, Ikuko Ueki, Masakazu Kobayashi, Hironaga Kuwahara, Norio Abiru, Hironori Yamasaki, Atsushi Kawakami.
Abstract
We have previously reported the high levels of glutamic acid decarboxylase 65 autoantibodies (GAD65A) in patients with type 1 diabetes and autoimmune thyroid disease. Here we describe a 32-year-old Japanese female with a thirteen-year history of type 1 diabetes whose levels of GAD65A were elevated just after the emergence of anti-thyroid autoimmunity. At 19 years of age, she developed diabetic ketoacidosis and was diagnosed with type 1 diabetes. She had GAD65A, insulinoma-associated antigen-2 autoantibodies (IA-2A), and zinc transporter-8 autoantibodies (ZnT8A), but was negative for antibodies to thyroid peroxidase (TPOAb) and thyroglobulin (TGAb) at disease onset. ZnT8A and IA-2A turned negative 2-3 years after the onset, whereas GAD65A were persistently positive at lower level (approximately 40 U/mL). However, just after the emergence of TGAb at disease duration of 12.5 years, GAD65A levels were reelevated up to 5717 U/mL in the absence of ZnT8A and IA-2A. Her thyroid function was normal and TPOAb were consistently negative. She has a HLA-DRB1*03:01/*04:01-DQB1*02:01/*03:02 genotype. Persistent positivity for GAD65A might be associated with increased risk to develop anti-thyroid autoimmunity.Entities:
Keywords: Autoimmune thyroid disease; Case report; Glutamic acid decarboxylase autoantibodies; Type 1 diabetes
Year: 2013 PMID: 24147207 PMCID: PMC3797888 DOI: 10.4239/wjd.v4.i5.227
Source DB: PubMed Journal: World J Diabetes ISSN: 1948-9358