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 2020 and some content may be unavailable. To unlock all content for 2020, please visit the archives.

Abstract: PO0961

Assessment of Histopathological Prognosticators in Diabetic Nephropathy: Single-Center Experience

Session Information

Category: Diabetic Kidney Disease

  • 602 Diabetic Kidney Disease: Clinical

Authors

  • Khalaf, Ahmad Mansoor, Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Nauman, Awais, Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Alkadi, Mohamad M., Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Abdelaziz, Adel Ashour, Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Hamdi, Ahmed Farouk, Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Asim, Muhammad, Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Fituri, Omar, Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Al-Malki, Hassan A., Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Akhtar, Mohammed, Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
  • Abuhelaiqa, Essa, Hamad Medical Corporation, Doha, Ad Dawhah, Qatar
Background

Diabetic nephropathy (DN) is the leading cause of end stage kidney disease worldwide. Identification of clinical, laboratory and histopathological predictors of kidney failure in DN may improve outcomes.

Methods

We identified 45 kidney biopsies between 2017 to 2018 that were diagnosed with DN. Clinical, laboratory and histopathological variables were analyzed to prognosticate 1-year kidney failure.

Results

Sixteen of 45 patients with DN had kidney failure within 12 months of kidney biopsy while 29 patients did not. All patients who developed kidney failure had diabetic retinopathy as shown in table 1. Laboratory findings such a serum creatinine (597umol/L vs. 205umol/L, P<0.0001) and presence of hematuria (88% vs. 45%, P=0.01) prognosticated kidney outcome, while neither proteinuria or Hemoglobin A1C did. IFTA score ( 2.4 vs. 1.8, P=0.02) and global glomerular sclerosis (52% vs. 32%, P=0.002) were the only histological findings that prognosticate kidney failure. Patients who have a second kidney diagnosis in addition to DN such as IgA, FSGS and MN had favorable outcomes compared to DN and AIN or DN only [figure 1].

Conclusion

We identified serum creatinine, hematuria, IFTA and glomerular sclerosis as prognosticators of kidney failure at 1-year following DN diagnosis. Identification of patients at risk of kidney failure help individualize therapy and hence improve kidney outcomes.