糖尿病和非糖尿病澳大利亚梗和萨摩耶犬1型糖尿病相关自身抗体的评估。

Allison L O'Kell, Clive H Wasserfall, Paula S Henthorn, Mark A Atkinson, Rebecka S Hess
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引用次数: 4

摘要

背景:犬糖尿病的自身免疫性病因的证据是不一致的,并且可能因品种而异。先前的研究表明,一小部分患有糖尿病的狗拥有对人类1型糖尿病重要抗原的自身抗体,但大多数研究都涉及对各种品种的分析。本研究的目的是评估美国糖尿病和非糖尿病澳大利亚梗和萨摩耶犬中谷氨酸脱羧酶65 (GAD65)、胰岛素瘤相关蛋白2 (IA-2)和锌转运蛋白8 (ZnT8)自身抗体的存在。澳大利亚梗和萨摩耶犬是糖尿病患病率相对较高的两个品种。结果:两种犬种中GAD65或ZnT8自身抗体阳性的比例,以及IA-2自身抗体阳性的比例均无显著差异(p > 0.05)。IA-2自身抗体阳性样本比例在糖尿病萨摩耶人中显著高于非糖尿病萨摩耶人(p = 0.003),但在糖尿病和非糖尿病萨摩耶人之间存在大量重叠。结论:目前的研究不支持GAD65、IA-2或ZnT8自身抗体作为萨摩耶犬或澳大利亚梗犬糖尿病自身免疫的标记物,使用人抗原夹心酶联免疫吸附(ELISA)测定。未来的研究需要使用犬类特异性检测,以及对这些犬种和其他犬种自身免疫的替代标记进行调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation for type 1 diabetes associated autoantibodies in diabetic and non-diabetic Australian terriers and Samoyeds.

Evaluation for type 1 diabetes associated autoantibodies in diabetic and non-diabetic Australian terriers and Samoyeds.

Evaluation for type 1 diabetes associated autoantibodies in diabetic and non-diabetic Australian terriers and Samoyeds.

Evaluation for type 1 diabetes associated autoantibodies in diabetic and non-diabetic Australian terriers and Samoyeds.

Background: Evidence for an autoimmune etiology in canine diabetes is inconsistent and could vary based on breed. Previous studies demonstrated that small percentages of diabetic dogs possess autoantibodies to antigens known to be important in human type 1 diabetes, but most efforts involved analysis of a wide variety of breeds. The objective of this study was to evaluate the presence of glutamic acid decarboxylase 65 (GAD65), insulinoma-associated protein 2 (IA-2), and zinc transporter 8 (ZnT8) autoantibodies in diabetic and non-diabetic Australian Terriers and Samoyeds, two breeds with comparatively high prevalence of diabetes, in the United States.

Results: There was no significant difference in the proportion of samples considered positive for GAD65 or ZnT8 autoantibodies in either breed evaluated, or for IA-2 autoantibodies in Australian Terriers (p > 0.05). The proportion of IA-2 autoantibody positive samples was significantly higher in diabetic versus non-diabetic Samoyeds (p = 0.003), but substantial overlap was present between diabetic and non-diabetic groups.

Conclusions: The present study does not support GAD65, IA-2, or ZnT8 autoantibodies as markers of autoimmunity in canine diabetes in Samoyeds or Australian Terriers as measured using human antigen sandwich enzyme-linked immunosorbent (ELISA) assays. Future studies using canine specific assays as well as investigation for alternative markers of autoimmunity in these and other canine breeds are warranted.

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