Objective: This study aimed to investigate the prevalence of the newly-identified islet autoantibody, tetraspanin 7 autoantibody (TSPAN7A) in Chinese type 1 diabetes (T1D) and Latent Autoimmune Diabetes in Adults (LADA), and the correlation between TSPAN7A and islet function in LADA patients.

Research Design and Methods: Patients with newly onset T1D (n=158), long-lasting T1D (n=157), LADA (n=175), type 2 diabetes (T2D; n=204) and healthy control subjects (n=170) were recruited for the cross sectional study. Another cohort including 46 LADA patients with 3-year follow-up was recruited forthe longitudinal study. TSPAN7A was assayed by luciferase immunoprecipitation system assay.

Results: The prevalence of TSPAN7A in newly onset T1D, non-newly onset T1D, T2D, LADA and healthy control subjects were 25.3% (40/158), 10.2% (16/157), 0.5% (1/204), 21.1 (37/175) and 1.2% (2/170), respectively. Out of the 23 patients with newly onset T1D but negative for GADA, IA2 and ZnT8A, 3 patients were positive for TSPAN7A (13.0%) improving the detection of autoantibodies from 81.6% to 83.5% in T1D. In LADA patients, analysis of logistic regression demonstrated that duration (OR=1.77, P=0.026), GADA titer (OR=2.79, P=0.006) and TSPAN7A (OR=2.86, P=0.034) were the risk factors to islet function while BMI was the protection factor (OR=0.35, P=0.001). In the follow-up study, LADA patients with TSPAN7A showed a worse islet function compared those negative for TSPAN7A after 3-year diagnosis.

Conclusion: TSPAN7A is a novel diagnostic tool for T1D and LADA. Combination of TSPAN7A with other autoantibodies can improve the diagnosis of T1D. TSPAN7A is negatively correlated with islet function in LADA.

Disclosure

Z. Zhou: None. X. Shi: None. P. Zheng: None. G. Huang: None. Y. Wang: None. C. Deng: None.

Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://www.diabetesjournals.org/content/license.