Aulanni'am Aulanni'am, Dyah Kinasih Wuragil, Hendra Susanto, Anita Herawati, Yulianto Muji Nugroho, Wahyu Nur Laili Fajri, Perdana Finawati Putri, Susiati Susiati, Jerry Dwi Trijoyo Purnomo, Ahmad Taufiq, Djoko Wahono Soeatmadji
Background: Diabetes mellitus (DM) is a chronic and costly disease that has become a primary concern worldwide. Type 1 diabetes mellitus is categorized as an autoimmune disease, which results in islet cell apoptosis and insulin-dependent. GAD65 is known as a potential marker of impaired pancreatic β cell function that appears in the initial phase of type 1 DM and latent autoimmune diabetes in adults (LADA). This study aimed to develop a novel rapid test of anti-GAD65 autoantibodies in human serum samples. Methods: We have developed a rapid test for anti-GAD65 autoantibodies in this assay based on the reverse-flow immunochromatography method. Human recombinant-protein antigen for GAD65 was attached as the control line over the nitrocellulose membrane. On the other side, the goat anti-mouse immunoglobulin G (IgG) was coated on the same membrane as a control line. The positive result for GAD65 was confirmed by a colloidal gold signal on the strip. Our novel assay analyzed 276 healthy subjects and 51 type 1 diabetes individuals serum samples from several ethnicities in Indonesia for this study. Results: Among the 276 healthy samples, 225 samples were identified as positive for anti-GAD65 autoantibodies, while 51 samples were negative. Interestingly, the positive results for anti-GAD65 autoantibodies were linear to the decreasing of high-density lipoprotein (HDL) levels and inversely associated with triglyceride levels. A significant correlation with age was observed in all groups. The sensitivity and specificity test proved that this kit has higher accuracy (AUC value = 0.960). Conclusion: The significant advantages of our rapid test for anti-GAD65 autoantibodies provide higher sensitivity, specificity, and stability compared to previous commercial kits. Therefore, it could be proposed as the future clinical diagnostic kit for patient management of type 1 DM. © 2021 The Authors
Faculty of Sciences, Brawijaya University, Indonesia; Faculty of Veterinary Medicine, Brawijaya University, Indonesia; Biosains Institute, Brawijaya University, Indonesia; Faculty of Mathematics and Natural Sciences, Universitas Negeri Malang, Indonesia; Faculty of Medicine, Brawijaya University, Indonesia; Faculty of Science and Data Analytics, Institut Teknologi Sepuluh November, Indonesia
