Managing Type 2 Diabetes with Dulaglutide in an African American Patient with eGFR of 30
Dulaglutide is an appropriate and safe treatment option for an African American patient with type 2 diabetes and an eGFR of 30 mL/min/1.73m², as it does not require dose adjustment for renal impairment and has demonstrated benefits in slowing eGFR decline in patients with CKD. 1, 2
Understanding Race-Based eGFR Considerations
When evaluating an African American patient with a non-race-adjusted eGFR of 30 mL/min/1.73m², it's important to recognize:
- The NKF-ASN Task Force recommends moving away from race-based eGFR calculations, as they can lead to systematic differences in clinical decisions between racial groups 1
- Using non-race-based eGFR equations (CKD-EPIcr_NB) could increase the number of Black adults meeting eGFR <30 mL/min/1.73m² by up to 52% 1
- This could affect medication dosing decisions, potentially leading to inappropriate drug discontinuation or underdosing in Black patients 1
Treatment Algorithm for This Patient
First-line therapy:
Add GLP-1 receptor agonist (dulaglutide):
- Dulaglutide is recommended for patients with T2D and CKD who don't meet glycemic targets with metformin/SGLT2i or cannot use these medications 1
- No dose adjustment is required for dulaglutide in renal impairment, including end-stage renal disease 2
- Start with 0.75 mg once weekly and titrate to 1.5 mg once weekly as tolerated 4
Additional considerations:
Evidence Supporting Dulaglutide in CKD
Dulaglutide has demonstrated several benefits in patients with CKD:
- In the AWARD-7 trial, dulaglutide produced similar glycemic control to insulin glargine in patients with moderate-to-severe CKD, with significantly reduced decline in eGFR 4
- At 52 weeks, eGFR was significantly higher with dulaglutide 1.5 mg (34.0 mL/min/1.73m²) and 0.75 mg (33.8 mL/min/1.73m²) compared to insulin glargine (31.3 mL/min/1.73m²) 4
- Dulaglutide treatment resulted in lower UACR values compared to placebo, active comparators, and insulin glargine 5
- The REWIND trial showed that long-term use of dulaglutide was associated with reduced composite renal outcomes in people with T2D 6
Safety Considerations
- Dulaglutide has a lower risk of hypoglycemia compared to insulin, with 4.4 events per patient per year with dulaglutide 1.5 mg versus 9.6 with insulin glargine 4
- Common side effects include nausea (14-20%), vomiting, and diarrhea (16-17%) 4
- These gastrointestinal side effects typically improve with continued use and dose titration 1
- Monitor renal function in patients reporting severe adverse gastrointestinal reactions 2
Common Pitfalls to Avoid
Failing to recognize race-based eGFR discrepancies: The non-race-adjusted eGFR of 30 may underestimate actual kidney function in African American patients 1
Inappropriate medication discontinuation: Metformin should be reduced (not stopped) at eGFR 30-44 mL/min/1.73m² 1, 3
Inadequate monitoring: Continue to monitor eGFR every 3-6 months, with more frequent monitoring if on medications affecting kidney function 3
Overlooking cardiovascular benefits: GLP-1 RAs like dulaglutide have demonstrated cardiovascular benefits in addition to glycemic control, which is particularly important in CKD patients who have elevated cardiovascular risk 1, 7
Neglecting comprehensive care: Ensure the patient also receives appropriate blood pressure management, lipid control, and lifestyle modifications as part of a comprehensive approach 1, 3
By following this approach, dulaglutide can be safely and effectively used in an African American patient with type 2 diabetes and an eGFR of 30 mL/min/1.73m², providing benefits for both glycemic control and kidney function preservation.