Diabetes complications

Poor Glycemic Control Is Associated With More Rapid Kidney Function Decline After the Onset of Diabetic Kidney Disease

J Clin Endocrinol MetabPublished Secondary analysis of the Preventing Early Renal Loss (PERL) and Action to Control Cardiovascular Risk in Diabetes (ACCORD) randomised trials

Authors' conclusion

In both type 1 and type 2 diabetes, poor glycemic control is associated with a more rapid rate of glomerular filtration rate decline after DKD onset, especially in persons with severe albuminuria.

Study context

Population
Individuals with T1D and early-to-moderate diabetic kidney disease (DKD) (PERL trial) and T2D with established DKD (ACCORD trial)
Participants
530 vs 2,378
Comparison
Baseline HbA1c and estimated glomerular filtration rate (eGFR) slope; intensive vs standard glycaemic control
  • PERLn = 530
  • ACCORDn = 2,378
Primary endpoint
Association of baseline HbA1c with rate of eGFR loss during follow-up
Methodological detailsmixed-effects linear regression
  • Mixed-effects linear regression

Primary result

As reported in the abstract

eGFR slope per HbA1c unit increment
GroupValueP
PERL−0.87 mL/min/1.73 m²/year per Hba1c unit incrementP < .0001
ACCORD−0.27 mL/min/1.73 m²/year per Hba1c unit incrementP = .0002

Value

PERL−0.87 mL/min/1.73 m²/year per Hba1c unit increment
ACCORD−0.27 mL/min/1.73 m²/year per Hba1c unit increment

P

PERLP < .0001
ACCORDP = .0002

Further findings

OutcomeP value
Benefit of intensive glycaemic control on eGFR decline (ACCORD), by albuminuriaSevere albuminuria vs Moderate albuminuria · +1.13 vs + 0.26; greater with severe albuminuriaP = 0.01

Effect modification by albuminuria

Strength of association progressively increased with increasing albuminuria in both studies
P for interaction < 0.05

CGM-derived short-term glycaemic variability and eGFR decline (PERL)

No independent associations found

Original publication

Poor Glycemic Control Is Associated With More Rapid Kidney Function Decline After the Onset of Diabetic Kidney Disease. J Clin Endocrinol Metab. Published 23 January 2024. doi:10.1210/clinem/dgae044

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