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 2023 and some content may be unavailable. To unlock all content for 2023, please visit the archives.

Abstract: TH-PO819

Development of a Predictive Model for Assessing the Risk of Severe Renal Fibrosis in Kidney Biopsy

Session Information

Category: Pathology and Lab Medicine

  • 1800 Pathology and Lab Medicine

Authors

  • Spanuchart, Ittikorn, University of Michigan, Ann Arbor, Michigan, United States
  • Tungphaisal, Veeraphol, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand
  • Thammavaranucupt, Kanin, Chakri Naruebodin Medical Institute, Bang Phli, Samut Prakan, Thailand
Background

Kidney biopsy is an essential diagnostic tool for various kidney diseases, but its clinical utility may be limited in cases of severe fibrosis, coupled with an increased risk of bleeding. Although several clinical parameters are used to predict the extent of renal fibrosis, a validated predictive model has not yet been established. This study aimed to construct a predictive model for assessing the risk of severe renal fibrosis.

Methods

Medical records of patients who underwent native kidney biopsies at Ramathibodi Hospital between January 2017 and December 2021 were reviewed. Severe renal fibrosis was defined as interstitial fibrosis and tubular atrophy (IFTA) greater than 50% or glomerulosclerosis greater than 50% on the pathology report. Clinical data, laboratory results, and ultrasonographic parameters were collected. Multivariable logistic regression analysis was performed to build the predictive model, and its discriminative performance was assessed using the receiver operating characteristic (ROC) curve. The internal validity of the model was evaluated through bootstrapping techniques.

Results

Among 202 patients, 31% exhibited severe renal fibrosis. The predictive model incorporated five significant predictors: nocturia, CKD, anemia, kidney length, and loss of corticomedullary differentiation. The model had an area under the ROC curve of 0.87 (95% CI: 0.818-0.923). The scoring model ranged from 0 to 18, with a score of 10 or higher indicating a positive likelihood ratio of 26 for severe fibrosis prediction. Internal validation using bootstrap resampling yielded an optimism of 0.024, with a shrinkage factor of 0.869.

Conclusion

The developed predictive model, utilizing routine clinical parameters, has demonstrated exceptional discriminative ability and ease of use in predicting renal fibrosis. It holds great potential in assisting clinicians with risk stratification and the planning of kidney biopsies.