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. 2021 Mar 1;16(3):348–355. doi: 10.2215/CJN.06960520

Table 3.

Temporal associations between AKI and the mean annual change in eGFR by hemoglobin phenotype

Outcomes Normal Hemoglobin Phenotype Sickle Cell Trait Sickle Cell Disease
Median (IQR) number of eGFR values over follow-up 44 (22–120) 65 (25–157) 237 (113–563)
Mean (SD) eGFR at baseline 114.4 (27.4) 103.7 (27.7) 127.9 (35.7)
Adjusted mean annual change in eGFR pre-AKI (including patients who never had AKI) within each group (95% CI)a −0.82 (−0.80 to −0.84) −1.09 (−1.05 to −1.14) −1.68 (−1.60 to −1.76)
Adjusted difference in mean annual change in eGFR pre-AKI (including patients who never had AKI) between groups (95% CI)a 0 (reference) −0.28 (−0.22 to −0.33) −0.86 (−0.79 to −0.94)
Adjusted mean annual change in eGFR post-AKI within each group (95% CI)a −1.63 (−1.56 to −1.69) −2.00 (−1.85 to −2.14) −3.31 (−3.10 to −3.53)
Adjusted difference in mean annual change in eGFR post-AKI between groups (95% CI)a 0 (reference) −0.37 (−0.21 to −0.54) −1.69 (−1.51 to −1.88)
Adjusted difference between mean annual change in eGFR pre-AKI (including patients who never had AKI) and mean annual change in eGFR post-AKI within each group (95% CI)a −0.81 (−0.76 to −0.87) −0.90 (−0.78 to −1.03) −1.63 (−1.44 to −1.82)

IQR, interquartile range; 95% CI, 95% confidence interval.

a

All models were adjusted for baseline age, sex, hypertension, diabetes mellitus, cardiovascular disease, and renin-angiotensin-aldosterone system inhibitors. Hemoglobin electrophoresis indication was included in the sickle cell trait and normal hemoglobin phenotype (reference) models.