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-PO162

Anemia Modifies the Associations Between Hemoglobin A1c and Outcomes in CKD

Session Information

Category: Diabetic Kidney Disease

  • 602 Diabetic Kidney Disease: Clinical

Authors

  • Jung, Molly, Johns Hopkins University, Baltimore, California, United States
  • Selvin, Elizabeth, Johns Hopkins University, Baltimore, Maryland, United States
  • Rebholz, Casey, Johns Hopkins University, Baltimore, Maryland, United States
  • Lee, Clare, Johns Hopkins University, Baltimore, Maryland, United States
  • Chen, Jing, Tulane School of Medicine, New Orleans, Louisiana, United States
  • He, Jiang, Tulane School of Public Health and Tropical Medicine, New Orleans, Louisiana, United States
  • Hsu, Chi-yuan, University of California San Francisco, San Francisco, California, United States
  • Lash, James P., University of Illinois at Chicago, Chicago, Illinois, United States
  • Mohanty, Madhumita J., Wayne State University, Detroit, Michigan, United States
  • Navaneethan, Sankar D., Baylor College of Medicine, Sugar Land, Texas, United States
  • Rosas, Sylvia E., Joslin Diabetes Center, Boston, Massachusetts, United States
  • Spanakis, Elias, University of Maryland, Baltimore, Maryland, United States
  • Weir, Matthew R., University of Maryland School of Medicine, Baltimore, Maryland, United States
  • Shafi, Tariq, Johns Hopkins University, Baltimore, Maryland, United States
Background

CKD and diabetes commonly co-occur. However, glycemic control and glycemic targets in these patients remain undefined.

Methods

In 1,833 participants of the Chronic Renal Insufficiency Cohort with diabetes, we assessed the association between baseline hemoglobin A1c (A1c) and death, first cardiovascular disease (CVD) event, and CKD progression using multivariable-adjusted Cox models. We also investigated: a) effect modification by anemia, eGFR, or albuminuria; and b) linearity of the association using spline models.

Results

At baseline, mean age was 59 years, mean eGFR was 41 mL/min/1.73 m2, mean A1c was 7.6%, and mean hemoglobin was 12 g/dL. During a median 6 years of follow-up, higher A1c was associated with worse outcomes (Figure 1); risk per 1% higher A1c was 10% for death, 10% for CVD events, and 5% for CKD progression. Anemia (hemoglobin<11 g/dL) was associated with non-linear associations for all three outcomes (Figure 2). A1c was associated with CKD progression in patients with eGFR≥30 ml/min/1.73m2 but not below that level. There was no effect modification by albuminuria.

Conclusion

In patients with CKD and diabetes, poor glycemic control contributes to a higher risk of death and CVD events. Individualized A1c targets and/or alternative markers of glycemia may be useful in diabetic CKD patients with anemia.

Funding

  • Other NIH Support