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. 2018 Feb 22;67(5):778–784. doi: 10.1093/cid/ciy151

Table 2.

Unadjusted and Adjusted Longitudinal Association between Age and Gait Speed by Mitochondrial DNA Haplogroups

Models Independent Variables Crude Estimation Adjusted Estimationa
Slope (m/s/year) SE P Value Slope (m/s/year) SE P Value
Haplogroup J vs others J*age –0.006 0.003 .026 –0.006 0.003 .012
Gait speed (non-J) –0.012 0.001 <.001 –0.011 0.001 <.001
Gait speed (group J) –0.017 0.003 <.001 –0.018 0.003 <.001
Haplogroup H vs others H*age 0.001 0.002 .48 0.002 0.002 .20
Gait speed (non-H) –0.013 0.001 <.001 –0.012 0.001 <.001
Gait speed (group H) –0.011 0.001 <.001 –0.010 0.001 <.001
Haplogroup T vs others T*age 0.00001 0.002 .996 –0.00007 0.002 .98
Gait speed (non-T) –0.012 0.001 <.001 –0.012 0.001 <.001
Gait speed (group T) –0.012 0.002 <.001 –0.012 0.002 <.001
Haplogroup Uk vs others Uk*age –0.0005 0.002 .78 0.0001 0.002 .94
Gait speed (non-Uk) –0.012 0.001 <.001 –0.012 0.001 <.001
Gait speed (group Uk) –0.013 0.001 <.001 –0.012 0.002 <.001

Gait speed modeled as a continuous variable in meters per second. Boldface indicates statistical significance for the interaction between mitochondrial DNA haplogroup and age.

Abbreviation: SE, standard error.

aModels adjusted for hepatitis C virus infection, AIDS diagnosis, log10 viremia copy-year, college education, cigarette smoking, peripheral neuropathy, weight, height, and time-varying exposure to thymidine analogues (ever vs never). Cigarette smoking was controlled in models by time-varying smoking status (yes vs no), time-varying smoking status (never vs former vs current), or pack-year smoke. All methods returned similar changes of the magnitude of association between haplogroup and gait speed. Time-varying smoking status (never vs former vs current) was selected and used in the final model.