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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: Antivir Ther. 2014 Apr 4;20(1):73–76. doi: 10.3851/IMP2772

Table 2.

Association of HIV-1 sequence synonymous (dS) and non-synonymous (dN) substitution rates with subjects’ baseline characteristics and HIV-1 metrics during low-level viremia.

Pol sequence Non-drm sites
dS dN dS dN
Sex (0.64) (0.99) (0.97) (0.84)
Race (0.44) (0.98) (0.39) (0.44)

Age (years) (0.08) (0.44) (0.11) (0.37)
Pretreatment VL (log10 copies/mL) (0.35) (0.05) (0.43) (0.80)
Pretreatment CD4 (cells/mm3) (0.60) (0.83) (0.78) (0.22)
Length of low-level viremia (weeks) (0.92) (0.22) (0.69) (0.54)
First VL during LLV (copies/mL) 0.46 0.52 0.45 0.38
(<0.01) (<0.001) (<0.0001) (<0.001)
Minimum VL during LLV (copies/mL) 0.29 0.39 0.29 0.29
(<0.05) (<0.05) (<0.01) (<0.05)
Maximum VL during LLV (copies/mL) 0.31 0.35 0.32 0.30
(<0.05) (<0.05) (<0.01) (<0.05)
Time adjusted area under the curve (copies/mL) 0.29 0.40 0.30 0.27
(0.05) (<0.05) (<0.01) (<0.05)

Displayed are Spearman correlations (with significance levels in parentheses). For sex and race and other baseline characteristics, only significance levels are shown (based on Kruskal-Wallis or Wilcoxon rank-sum tests).

DRM, drug resistance mutation; LLV, low-level viremia