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-PO099

Postdonation Renal Function Predicts New Onset Antihypertensive Medication Use After Living Kidney Donation

Session Information

Category: Transplantation

  • 1802 Transplantation: Clinical

Authors

  • Lentine, Krista L., Saint Louis University, St. Louis, Missouri, United States
  • Naik, Abhijit S., University Michigan, Ann Arbor, Michigan, United States
  • Lam, Ngan, University of Alberta, Edmonton, Alberta, Canada
  • Garg, Amit X., London Health Sciences Centre, London, Ontario, Canada
  • Segev, Dorry L., Johns Hopkins University, Baltimore, Maryland, United States
  • Axelrod, David A., Lahey Hospital and Clinic, Burlington, Massachusetts, United States
  • Xiao, Huiling, St. Louis University, St. Louis, Missouri, United States
  • Henderson, Macey L., Johns Hopkins, Baltimore, Maryland, United States
  • Massie, Allan, Johns Hopkins School of Medicine, Baltimore, Maryland, United States
  • Hsu, Chi-yuan, University of California San Francisco, San Francisco, California, United States
  • Kasiske, Bertram L., Hennepin County Medical Center, Minneapolis, Minnesota, United States
  • Hess, Gregory P., LDI University of Pennsylvania/Symphony Health, Conshohocken, Pennsylvania, United States
  • Schnitzler, Mark, Saint Louis Univ, St Louis, Missouri, United States
Background

Limited data are available on the outcome implications of renal function after living kidney donation.

Methods

We constructed a novel database linking SRTR registry identifiers, serum creatinine (SCr) values from an electronic medical records warehouse, and pharmacy fill records for 3,593 living kidney donors (1989–2016) without predonation hypertension per the registry. Estimated glomerular filtration rate (eGFR, ml/min/1.73 m2) was computed from SCr by the CKD-EPI equation. Pharmacy enrollment was assessed within ±90 days of each postdonation SCr, followed by identification of antihypertensive medication (AHM) fills in those with pharmacy records eligibility. A mixed effects model was constructed to assess associations of postdonation eGFR (adjusted odds ratio, 95%LCL aOR 95% UCL) and other baseline factors with AHM treatment requirements after donation.

Results

The linked database captured an average of 3 post-donation SCr values per donor (range: 1 to 38). Lower postdonation eGFR bore a graded association with increased AHM use (eGFR 30–44: aOR 0.951.472.26; <30: aOR 1.08 5.902.52). Other significant (P<0.05) correlates of postdonation AHM fills included black race (aOR 2.22), BMI >30 kg/m2 (aOR 2.09), first-degree donor-recipient relationship (aOR 1.79), “pre-hypertension" at donation (SBP 120-139: aOR 1.94; DBP 80-89: aOR 1.99), and longer time since donation. Predonation eGFR was not significantly associated with AHM use in the multi-level model. [Fig.]

Conclusion

Lower eGFR levels after living kidney donation are associated with need for AHM treatment. Further work should define relationships of postdonation renal function with renal and cardiovascular morbidity.

Funding

  • NIDDK Support