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. 2017 Mar 31;2(4):713–720. doi: 10.1016/j.ekir.2017.03.008

Table 3.

Slopes from linear mixed model for estimated glomerular filtration rate (eGFR) over the course of follow-up in African American SPRINT participants by treatment group and APOL1 risk genotype


Group
Time perioda Treatment group APOL1 G1+G2=2
Slope (95% CI)b
APOL1 G1+G2=0/1
Slope (95% CI)b
APOL1 G1+G2: 2 − 0/1
Difference (95% CI)
P value
All Acute (≤6 mo) Standard –0.31 (–2.87, 2.26) 0.80 (–0.46, 2.07) –1.11 (–3.69, 1.47) 0.398
All Acute (≤6 mo) Intensive –4.18 (–6.57, –1.79) –3.53 (–4.82, –2.25) –0.65 (–3.06, 1.77) 0.600
All Chronic (>6 mo) Standard –1.13 (–2.34, 0.08) –0.97 (–1.42, –0.52) –0.16 (–1.45, 1.12) 0.806
All Chronic (>6 mo) Intensive –1.36 (–2.46, –0.26) –1.01 (–1.47, –0.54) –0.35 (–1.54, 0.84) 0.564
CKD (eGFR < 60 ml/min/1.73 m2) Acute (≤6 mo) Standard 0.85 (–2.22, 3.91) 2.07 (0.48, 3.67) –1.23 (–4.46, 2.00) 0.457
CKD (eGFR < 60 ml/min/1.73 m2) Acute (≤6 mo) Intensive 0.06 (–2.93, 3.05) –1.97 (–3.49, –0.45) 2.03 (–1.10, 5.16) 0.204
CKD (eGFR < 60 ml/min/1.73 m2) Chronic (>6 mo) Standard –1.41 (–2.50, –0.32) –0.60 (–1.13, –0.06) –0.81 (–2.03, 0.40) 0.190
CKD (eGFR < 60 ml/min/1.73 m2) Chronic (>6 mo) Intensive –0.82 (–1.91, 0.27) –0.75 (–1.24, –0.26) –0.07 (–1.26, 1.12) 0.908
Non-CKD (eGFR ≥ 60 ml/min/1.73 m2) Acute (≤6 mo) Standard –0.18 (–3.29, 2.93) 0.48 (–0.98, 1.94) –0.66 (–3.77, 2.45) 0.679
Non-CKD (eGFR ≥ 60 ml/min/1.73 m2) Acute (≤6 mo) Intensive –5.44 (–8.27, –2.60) –3.99 (–5.49, –2.48) –1.45 (–4.31, 1.42) 0.322
Non-CKD (eGFR ≥ 60 ml/min/1.73 m2) Chronic (>6 mo) Standard –1.17 (–2.71, 0.36) –1.20 (–1.72, –0.69) 0.03 (–1.59, 1.64) 0.975
Non-CKD (eGFR ≥ 60 ml/min/1.73 m2) Chronic (>6 mo) Intensive –1.83 (–3.18, –0.49) –1.20 (–1.75, –0.64) –0.64 (–2.09, 0.81) 0.388

CI, confidence interval; CKI, chronic kidney disease; SPRINT, Systolic Blood Pressure Intervention Trial.

a

For acute time period (≤6 mo postrandomization), slopes reflect mean change in eGFR (in ml/min/1.73 m2) over 6 mo. For chronic time period (>6 mo postrandomization), slopes reflect mean change in eGFR per 1 yr.

b

Adjusted for baseline eGFR, age, sex, history of cardiovascular disease, proportion of African admixture, and whether or not measurement occurred at a fasting study visit.