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. 2019 Nov 8;14(12):1733–1740. doi: 10.2215/CJN.04490419

Table 4.

Hazard ratios and 95% confidence intervals for the association between APOL1 risk genotype group and incident sepsis among blacks stratified by presence or absence of CKD

APOL1 Genotype Modela No. Events (%)b Crude Model 1 Model 2 Model 3
CKD
 Recessive model
  0 or 1 risk allele 141 (6)
  2 risk alleles 24 (6) 0.96 (0.62 to 1.48) 1.01 (0.66 to 1.57) 1.14 (0.73 to 1.79) 1.18 (0.70 to 1.99)
 Dominant model
  0 risk alleles 53 (5)
  1 or 2 risk alleles 112 (7) 1.38 (0.99 to 1.91) 1.41 (1.01 to 1.96) 1.66 (1.16 to 2.37) 1.73 (1.13 to 2.65)
 Additive model
  Per variant allele copy 165 (6) 1.14 (0.92 to 1.42) 1.17 (0.94 to 1.46) 1.31 (1.04 to 1.65) 1.34 (1.02 to 1.76)
No CKD
 Recessive model
  0 or 1 risk allele 118 (2)
  2 risk alleles 23 (3) 1.41 (0.90 to 2.21) 1.46 (0.93 to 2.28) 1.30 (0.77 to 2.18) 0.92 (0.45 to 1.86)
 Dominant model
  0 risk alleles 48 (2)
  1 or 2 risk alleles 93 (2) 1.41 (0.99 to 2.00) 1.41 (1.00 to 2.00) 1.30 (0.89 to 1.90) 1.45 (0.91 to 2.31)
 Additive model
  Per variant allele copy 141 (2) 1.30 (1.02 to 1.65) 1.32 (1.04 to 1.67) 1.23 (0.94 to 1.60) 1.19 (0.86 to 1.65)

Model 1: adjusted for sex, age, income, education. Model 2: Model 1+adjusted for tobacco, deep vein thrombosis, dyslipidemia, peripheral artery disease, eGFR, albumin to creatinine ratio, systolic BP, diastolic BP, prevalent comorbidities (diabetes, coronary heart disease, stroke, dyslipidemia). Model 3: Model 2+adjusted for principal components ancestry. —, reference.

a

Estimated from Cox proportional hazard models.

b

Row percentage, proportion of participants experiencing a sepsis event.