Table 2.
linear mixed model¶ | ||||||||
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setpoint viral load | CD4+ T cell count trajectory | |||||||
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Mitochondrial macrohaplogroup |
frequency | coefficient | (SE) | p § | frequency | coefficient | (SE) | p §† |
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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).