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. 2015 Mar 18;26(11):2882–2890. doi: 10.1681/ASN.2014050469

Table 3.

Association between APOL1 risk alleles and various glomerular diseases

Glomerular Disease HIV-Positive Patients and Controls HIV-Negative Patients and Controls
No. of APOL1 Risk Alleles OR (95% CI) P Value No. of APOL1 Risk Alleles OR (95% CI) P Value
0 1 2 2 versus 1 or 0 risk alleles 0 1 2 2 versus 1 or 0 risk alleles
Controls (n=108) 34 (63) 18 (33) 2 (4) 36 (67) 17 (32) 1 (2)
HIVAN (n=38) 2 (5) 6 (16) 30 (79) 89 (17.7 to 912) 1.2×10−14
Other CKD (n=78) 22 (57) 11 (28) 6 (15) 3.8 (0.6 to 42) 0.13 25 (64) 13 (33) 1(3) 1.4 (0.02 to 11) >0.99
FSGS (n=22) 9 (69) 3 (23) 1 (8) 2.1 (0.03 to 44) 0.48 5 (56) 3 (33) 1 (11) 6 0.3 (0.08 to 527) 0.26
HIVICK (n=12) 4 (33) 5 (42) 3 (25) 5.6 (0.4 to 86) 0.13
Other GN (n=27)a 7 (70) 3 (30) 0 (0) 0.0 (0 to 30) >0.99 10 (59) 7 (41) 0 (0) 0 (0 to 124) >0.99
Other kidney diseases (n=17)b 2 (50) 0 (0) 2 (50) 21 (0.2 to 2029) 0.11 10 (77) 3 (23) 0 (0) 0 (0 to 210) >0.99

Data are given as n (%) unless otherwise indicated. The APOL1 genotype frequencies and associations, tested with the Fisher exact test, are shown for various glomerular diseases among HIV-positive and HIV-negative patients and general population controls. The only glomerular disease that showed a significant association with APOL1 risk alleles was HIVAN. Of note, HIV-positive FSGS, HIV-negative FSGS, and HIVICK were not significantly associated with APOL1 risk alleles, although group sizes were small. Analyses were adjusted for age, sex, and ancestry. P values indicate probability by the Fisher exact test.

a

Other GN is as follows: HIV-positive: membranoproliferative GN (n=1), membranoproliferative GN consistent with C3 glomerulopathy (n=1), and membranous GN (n=8); and HIV-negative: IgA nephropathy (n=1), lupus nephritis (n=3), membranoproliferative GN (n=2), and membranous GN (n=11).

b

Other kidney diseases are as follows: HIV-positive: benign nephrosclerosis (n=1), global glomerulosclerosis (n=1), minimal change disease (n=1), and thrombotic microangiopathy (n=1); and HIV-negative: benign nephrosclerosis (n=1), oxalosis (n=1), global glomerulosclerosis (n=2), minimal change disease (n=5), nodular glomerulosclerosis (n=1), severe arterial nephrosclerosis with secondary FSGS (n=1), and thrombotic microangiopathy (n=2).