ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Please note that you are viewing an archived section from 2022 and some content may be unavailable. To unlock all content for 2022, please visit the archives.

Abstract: FR-PO813

The Application of Artificial Intelligence in IgA Nephropathy After Kidney Transplantation

Session Information

Category: Transplantation

  • 2002 Transplantation: Clinical

Authors

  • Liu, Xumeng, Nanjing University, Nanjing, Jiangsu, China
  • Lei, Qunjuan, Southern Medical University, Guangzhou, Guangdong, China
  • Hou, Xiaoshuai, Ping An Healthcare Technology, Shanghai, Shanghai, China
  • Liang, Dongmei, Nanjing University, Nanjing, Jiangsu, China
  • Xu, Feng, Nanjing General Hospital of Nanjing Military Command Research Institute of Nephrology, Nanjing, Jiangsu, China
  • Liang, Shaoshan, Nanjing General Hospital of Nanjing Military Command Research Institute of Nephrology, Nanjing, Jiangsu, China
  • Liang, Dandan, Nanjing General Hospital of Nanjing Military Command Research Institute of Nephrology, Nanjing, Jiangsu, China
  • Yang, Fan, Nanjing General Hospital of Nanjing Military Command Research Institute of Nephrology, Nanjing, Jiangsu, China
  • Ni, Yuan, Ping An Healthcare Technology, Shanghai, Shanghai, China
  • Xie, Guotong, Ping An Healthcare Technology, Shanghai, Shanghai, China
  • Zeng, Cai-hong, Nanjing General Hospital of Nanjing Military Command Research Institute of Nephrology, Nanjing, Jiangsu, China
Background

A convolutional neural network named Analytic Renal Pathology System (ARPS) was trained to identify glomerular lesions in immunoglobulin A nephropathy (IgAN). However, whether ARPS can be applied to renal graft biopsy is still unknown. This study aimed to analyze the application of ARPS in transplant patients with IgAN.

Methods

From January 2016 to April 2020, patients diagnosed as IgAN by renal graft biopsy in our center were collected. The performance of ARPS in transplant patients with IgAN was evaluated. The correlation of clinicopathologic data were further analyzed.

Results

A total of 57 patients were enrolled. The median (interquartile range: IQR) age at renal biopsy was 32 (28, 40) years. ARPS could identify the types of glomerular lesions and intrinsic cells in transplant patients with IgAN, achieving F1-scores for different lesions ranged between 72.40% and 96.05%. The ratio of mesangial cells (M), endothelial cells (E), and podocytes (P) was 0.37:0.39:0.25. Compared with autologous IgAN patients (0.41:0.36:0.23), the percentage of E was higher in transplant patients with IgAN. Urine protein level was negatively correlated with the number of P (p<0.05), but positively correlated with mesangial area (p<0.05). Serum creatinine level was negatively correlated with the number of E (p<0.05). The course of disease after transplantation was positively correlated with the glomerular and mesangial area (p<0.05). According to the results of receiver operating characteristic curve, the lower number of E or P, and higher percent segmental sclerosis (SS) or glomerular sclerosis (GS) could indicate poorer prognosis, with all the area under curve of them greater than 0.7 (p<0.05).

Conclusion

ARPS can automatically identify and quantify the types of glomerular lesions and intrinsic cells in transplant patients with IgAN. The ARPS quantified glomerular lesions and intrinsic cells correlated well with key clinical indicators and the prognosis of transplant patients with IgAN.

Funding

  • Government Support – Non-U.S.