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. 2022 Jan 25;7(4):786–796. doi: 10.1016/j.ekir.2022.01.1054

Table 2.

Associations between APOL1 high-risk genotypes and renal outcomes

Participant characteristics N Univariable
Multivariable
OR 95% CI P value OR 95% CI P value
Primary outcome
 End-stage kidney disease 99 10.31 6.81–15.60 <0.001 10.58 6.22–17.99 <0.001a
Secondary outcomes
 Proteinuria (PCR >100 mg/mmol) 67 1.83 0.97–3.46 0.06
 Albuminuria (ACR >30 mg/mmol) 99 2.57 1.59–4.17 <0.001 3.34 2.00–5.56 <0.001b
 eGFR <60 ml/min per 1.73 m2 221 5.65 4.19–7.61 <0.001 5.50 3.81–7.95 <0.001c
 FSGS/HIVAN/hypertensive nephropathy (clinical diagnosis) 19 14.64 5.46–39.27 <0.001 12.77 4.46–36.59 <0.001d
 FSGS (biopsy confirmed) 15 11.81 4.17–33.39 <0.001 12.86 4.04–40.99 <0.001d
 HIVAN (biopsy confirmed) 37 24.49 11.45–52.36 <0.001 30.16 12.48–72.88 <0.001d

ACR, urine albumin-to-creatinine ratio; CVD, cardiovascular disease; DM, diabetes mellitus; eGFR, estimated glomerular filtration rate; FSGS, focal segmental glomerulosclerosis; HCV, hepatitis C virus; HIVAN, HIV-associated nephropathy; OR, odds ratio; PCR, urine protein-to-creatinine ratio.

Models are adjusted for:

a

Demographic (age, sex, and region of ancestry), HIV (AIDS, CD4 cell count), anti-HCV, DM, and CVD.

b

Demographic (age, sex), HIV (Time since HIV diagnosis, AIDS, HIV RNA < 200 copies/ml), DM, and CVD.

c

Demographic (age, sex, and region of ancestry), HIV (Time since HIV diagnosis, AIDS, CD4 cell count), anti-HCV, DM, and CVD.

d

Demographic (age and sex), HIV (AIDS, CD4 cell count), anti-HCV, DM, and CVD.