Skip to main content
. Author manuscript; available in PMC: 2012 Sep 10.
Published in final edited form as: AIDS. 2011 Sep 10;25(14):1711–1719. doi: 10.1097/QAD.0b013e328349c693

Table 2.

Association of PSIP1 SNPs with HIV-1 acquisition in the CAPRISA AI 002 cohort, dominant model

SNP Risk group n Genotype
22 and 12 versus 11 (reference group)*
Number (Frequency) RH (95% CI) P - value
SNP1 GG AG AA
G→A
SN 183 158 (0.86) 22 (0.12) 3 (0.02)
SP 52 39 (0.75) 12 (0.23) 1 (0.01) 2.21 (0.92 – 5.28) 0.08
SNP2 GG CG CC
G→C
SN 181 66 (0.36) 77 (0.43) 38 (0.21)
SP 52 20 (0.38) 23 (0.44) 9 (0.17) 0.99 (0.44 – 2.24) 0.98
SNP3 TT CT CC
T→C
SN 172 86 (0.49) 64 (0.36) 22 (0.13)
SP 50 29 (0.58) 19 (0.38) 2 (0.04) 0.60 (0.26 – 1.37) 0.23
SNP4 AA AG GG
A→G
SN 172 108 (0.63) 53 (0.31) 11 (0.06)
SP 48 31 (0.65) 16 (0.33) 1 (0.02) 0.85 (0.36 – 2.01) 0.71
SNP5 AA AT TT
A→T
SN 184 162 (0.88) 21 (0.11) 1 (0.005)
SP 51 41 (0.80) 10 (0.20) 0 (0.00) 1.90 (0.71 – 5.09) 0.20

Kaplan-Meier survival statistics and the Cox proportional hazards model (Cox model) were used to assess the effect of each SNP on time to HIV-1 acquisition after enrollment.

P-values uncorrected for multiple comparisons are shown.