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APOL1-Mediated Kidney Disease: Preparing Pharmacists for a New Era of Targeted Therapy

Friday, December 18, 2026 | 1:00 PM & 8:00 PM ETVirtual

Program Description

APOL1-mediated kidney disease (AMKD) is a progressive and highly heterogeneous form of chronic kidney disease (CKD) that may develop in individuals who have inherited 2 high-risk APOL1 gene variants. Although most carriers do not develop kidney disease at all, inflammation or infection signals can trigger APOL1 activity that damages podocytes and contributes to kidney failure. Management strategies have been adapted from supportive therapies associated with general CKD care, such as renin-angiotensin-aldosterone system and sodium-glucose cotransporter 2 inhibitors, but these do not directly target APOL1-mediated disease mechanisms. Genotype-targeted agents are advancing through clinical trials as disease-modifying options for AMKD, and pharmacists must be aware of their potential place in therapy to guide patients through an evolving treatment landscape.

Target audience: Specialty Pharmacists
Type of activity: Application
Release date: December 18, 2026
Expiration date: February 18, 2027
Time to complete activity: 1.0 hour
Learner level: Foundational
Fee: Free

Educational Objectives

At the completion of this activity, pharmacists will be able to:

  • Describe the disease burden and pathophysiology of APOL1-mediated kidney disease (AMKD), including the consequences of delayed recognition and the mechanisms of APOL1-mediated podocyte injury in patients with 2 high-risk variants
  • Explore the limitations associated with the current standard of care and the mechanism of action and clinical evidence for emerging genotype-targeted AMKD therapies
  • Illustrate the pharmacist’s role in AMKD management, including patient counseling on medication adherence and renal risk, genetic testing access, and collaborating with multidisciplinary care teams