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. Author manuscript; available in PMC: 2014 Mar 3.
Published in final edited form as: AIDS. 2012 Oct 23;26(16):2097–2106. doi: 10.1097/QAD.0b013e3283593602

Table 3.

Estimates for the association between the CYP2B6 metabolizer phenotype (using rs3745274 and rs28399499) with virologic response1 to NNRTI-based HAART regimens in women who were naïve to antiretroviral drugs (N=91).

Metabolizer Phenotype2 Responders (%) Non-responders (%) Crude Adjusted for SR Race/Ethnicity3 Adjusted for top three PCs4
OR (95% CI) OR (95% CI) OR (95% CI)
Extensive 28 (40) 12 (57) 1.00 1.00 1.00
Intermediate 33 (47) 9 (43) 1.56 (0.52-4.88) 1.66 (0.47-6.11) 2.90 (0.79-12.28)
Slow 9 (13) 0 5.00 (0.70-inf) 7.69 (1.04-inf) 13.44 (1.66-inf)
 p trend exact 0.09 0.04 0.005
1

Virologic response defined as achievement of undetectable viral load up to 54 weeks after self- reported initiation of NNRTI-based regimen

2

Extensive = no minor alleles at either rs3745274 or rs28399499 Intermediate = one minor allele at either rs3745274 or rs28399499 Slow = two minor alleles at either rs3745274 or rs28399499, or one minor allele at both polymorphisms

3

Adjusted for self-reported race/ethnicity (White, Hispanic, African American, Asian/Other)

4

Adjusted for the top three genetic ancestry principal components (PCs)