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. Author manuscript; available in PMC: 2016 Aug 30.
Published in final edited form as: AIDS. 2014 Aug 24;28(13):1871–1878. doi: 10.1097/QAD.0000000000000371

Table 2.

Mitochondrial haplogroups and virologic and immunological HIV outcomes in 91 HAART-naïve African American adolescents of the REACH study

linear mixed model

setpoint viral load CD4+ T cell count trajectory


Mitochondrial
macrohaplogroup
frequency coefficient (SE) p § frequency coefficient (SE) p §


L1* 17 −0.29 (0.19) 0.143 17 0.007 (0.024) 0.815
L2 6 0.15 (0.30) 0.618 6 −0.150 (0.095) 0.121
L2* 22 −0.02 (0.18) 0.925 22 −0.070 (0.024) 0.002
L3 6 −0.34 (0.30) 0.249 6 0.051 (0.075) 0.499
L3* 30 0.11 (0.16) 0.479 30 0.016 (0.021) 0.450
R0 8 0.44 (0.27) 0.105 6 0.015 (0.042) 0.731
U 4 0.040 (0.034) 0.429
L2 + L2* 28 0.15 (0.30) 0.618 28 −0.081 (0.023) 0.0005

Footnote to Table 2

*

Macro-haplogroups as defined in the histogram of Figure 1. Note that non-L haplogroups H, HV, V and root R0 were grouped as R0, and the U and K haplogroups as U.

Models adjusted for the effects of gender, baseline age and HLA-B.

§

p-values adjusted for multiple comparisons (Tukey-Kramer adjustment). Note that only clades or macrohaplogroups with a frequency greater than 3% are shown. SE=Standard Error of the mean.

Parameter estimates for the covariates in the model with L2 & L2* as predictors were for HLA-B*35 (beta= −1.62; SE=1.81; p= 0.370), HLA-B*57 or HLA-B*27 (beta=3.01; SE=1.44; p=0.037), gender (beta= −1.45; SE=1.30; p =0.265) and for age (beta= 0.066; SE=0.25; p=0.795).