Diabetes mellitus is a major risk factor for the development of chronic kidney disease (CKD). There is limited data addressing the value of glycated hemoglobin (HbA1c) to predict renal outcomes independent of diabetes status.
This single‐center retrospective observational study presents data of 19,285 subjects, irrespective of initial CKD or diabetes status. The primary endpoint was defined as the time to manifestation of moderate CKD (estimated glomerular filtration rate [eGFR] <60 mL/min/1.73 m 2) in subjects with eGFR ≥60 mL/min/1.73 m 2 at baseline. The secondary endpoint was defined as time to progression of CKD (eGFR <30 mL/min/1.73 m 2) in subjects with eGFR 30–60 mL/min/1.73 m 2. Multivariate time‐to‐event and logistic regression models were applied to estimate the influences of HbA1c, sex, age, eGFR, triglycerides, and cholesterol on both endpoints.
Lowest baseline HbA1c levels were associated with the slowest decline of kidney function (median time to manifestation of moderate CKD for HbA1c <5.7%: 15.9 years [95% confidence interval (CI): 15.2–16.7]; for HbA1c 5.7%–6.5%: 14.5 years [95% CI: 14.0–15.1]; for HbA1c 6.5%–8.5%: 11.1 years [95% CI: 10.4–11.7]; for HbA1c >8.5%: 8.3 years [95% CI: 7.8–9.2]; p < 0.001). Similar results were observed for the secondary endpoint. Covariate‐adjusted time‐to‐event analysis demonstrated an almost linear correlation between continuous baseline HbA1c levels and the probabilities of reaching both endpoints.
See how this article has been cited at scite.ai
scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.