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. Author manuscript; available in PMC: 2022 Jun 1.
Published in final edited form as: Am J Kidney Dis. 2020 Dec 22;77(6):879–888.e1. doi: 10.1053/j.ajkd.2020.10.020

Table 2.

Association of fetal APOL1 risk alleles with risk of preeclampsia

Group APOL1 risk allele Cont., n(%) Cases, n(%) ORa 95%CIa Pa
Total 0 110 (52.9) 91 (43.5) Ref 1.00–1.00
1 79 (38.0) 90 (43.1) 1.17 0.73–1.87 0.5
2b 19 (9.1) 28 (13.4) 1.79 0.87–3.70 0.1
Recessive 19 (9.1) 28 (13.4) 1.67 0.83–3.34 0.2
Dominant 98 (47.1) 118 (56.5) 1.28 0.83–1.99 0.3
Additive - - 1.28 0.93–1.77 0.1
APOL1 × maternal country-of-origin Interaction
APOL1 risk allele in a recessive model 0.04
APOL1 risk allele in an dominant model 0.2
APOL1 risk allele in a additive model 0.05
Stratified by maternal origin of country
African-Americans 0 74 (55.6) 54 (40.3) Ref 1.00–1.00
1 52 (39.1) 59 (44.0) 1.35 0.75–2.44 0.3
2c 7 (5.3) 21 (15.7) 4.06 1.43–11.6 0.009
Recessive 7 (5.3) 21 (15.7) 3.55 1.29–9.74 0.01
Dominant 59 (44.4) 80 (59.7) 1.64 0.94–2.87 0.08
Additive - - 1.72 1.11–2.64 0.01
Haitian 0 36 (48.0) 37 (49.3) Ref 1.00–1.00
1 27 (36.0) 31 (41.3) 0.93 0.42–2.07 0.9
2d 12 (16.0) 7 (9.3) 0.55 0.17–1.78 0.3
Recessive 12 (16.0) 7 (9.3) 0.57 0.18–1.74 0.3
Dominant 39 (52.0) 38 (50.6) 0.81 0.39–1.71 0.6
Additive 0.79 0.46–1.35 0.4

Shown are the association of fetal APOL1 risk alleles with risk of preeclampsia, stratified by maternal country-of-origin.

a

Adjusted for pre-pregnancy BMI category, smoking status during pregnancy, alcohol drinking during pregnancy, chronic hypertension, country-of-origin (for the analyses in the total sample only) and years the mothers stayed in the US;

b,c,d

The 2-degree of freedom test was performed for APOL1 risk allele, with bP=0.3 in the total sample, cP= 0.02 in African Americans, and dP=0.6 in Haitian subset.

In the interaction test, maternal country-of-origin was traited as a binary variable with the “African-American” category as the reference group.