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

Abstract: SA-PO1083

Angiopoietins and Delayed Graft Function in Kidney Transplant Recipients

Session Information

Category: Transplantation

  • 2102 Transplantation: Clinical

Authors

  • Berry, Shivankshi, Yale School of Medicine, New Haven, Connecticut, United States
  • Turco, David, Yale School of Medicine, New Haven, Connecticut, United States
  • Moore, Kareen, Yale School of Medicine, New Haven, Connecticut, United States
  • Qian, Long, Yale School of Medicine, New Haven, Connecticut, United States
  • Faulkner, Sophia, Yale School of Medicine, New Haven, Connecticut, United States
  • Hall, Isaac E., University of Utah Health, Salt Lake City, Utah, United States
  • Obeid, Wassim, Johns Hopkins University, Baltimore, Maryland, United States
  • Thiessen Philbrook, Heather, Johns Hopkins University, Baltimore, Maryland, United States
  • Parikh, Chirag R., Johns Hopkins University, Baltimore, Maryland, United States
  • Mansour, Sherry, Yale School of Medicine, New Haven, Connecticut, United States
Background

Delayed graft function (DGF) is increasing with greater use of high-risk donors. Early identification of patients at risk and better phenotyping are key for post-transplant management. Vascular biomarkers like angiopoietin-1 (Angpt-1) and angiopoietin-2 (Angpt-2) may aid in risk stratification and post-transplant discharge planning.

Methods

In an ancillary study of a prospectively enrolled cohort of deceased donor kidney transplant recipients, we measured Angpt-1 and Angpt-2 in plasma from 67 patients. Biomarkers were assessed over the first 3 days post-transplant days with the first sample collected soon after
arriving to the ICU after transplant. Day 2 levels—where group differences were most pronounced—were used to evaluate associations with DGF and number of dialysis sessions in the first 7 days. Multivariable logistic and Poisson regression models were adjusted for donor/recipient age, sex, race, donor/recipient hypertension, recipient diabetes, and day 2 creatinine.

Results

A total of 26 recipients experienced DGF, requiring between 1 and 5 inpatient dialysis sessions. While both Angpt-1 and Angpt-2 levels declined after transplant, this decline occurred more gradually in patients with DGF. Angpt-1 was not associated with DGF or number of dialysis sessions. Angpt-2 measurement on the first post-operative day was independently associated with DGF (adjusted OR: 6.34, 95% CI: 1.57–25.65) and dialysis frequency (adjusted RR: 3.77,95% CI: 1.77–8.03). When added to the clinical model, AUC 0.75 (95%CI -.62-0.89), Angpt-2 improved the AUC to 0.81 (95% CI: 0.70–0.92) and yielded a net reclassification index of 0.23 for events and 0.51 for non-events.

Conclusion

Slower Angpt-2 decline in recipients with DGF suggests ongoing vascular injury and impaired repair. Angpt-2 shows promise as a biomarker for DGF risk and severity, improving prediction beyond clinical variables. These findings support further study of Angpt-2 in post-transplant risk stratification and care planning.

Funding

  • NIDDK Support

Digital Object Identifier (DOI)