Skip to main content
. 2018 May 14;9:915. doi: 10.3389/fimmu.2018.00915

Table 2.

Results of adjusted mixed multilevel regression analyses of anti-PGL-I, anti-LID-1, and anti-NDO-LID serology overtime in leprosy patients treated with R-MDT and U-MDT.

Coefficient SE z p > z 95% Confidence interval
Anti-PGL-I
Month −0.006871 0.0007285 −9.43 0 −0.0082988 −0.0054431
Group −0.0035163 0.0333417 −0.11 0.916 −0.0688648 0.0618322
_Cons 0.5085021 0.1160942 4.38 0 0.2809617 0.7360426
Anti-LID-1
Month −0.0051023 0.0003361 −15.18 0 −0.005761 −0.0044436
Group −0.0571696 0.0719866 −0.79 0.427 −0.1982608 0.0839216
_Cons 1.618.408 0.2525812 6.41 0 1.123.358 2.113.458
Anti-NDO-LID
Month −0.0164264 0.0012887 −12.75 0 −0.0189521 −0.0139006
Group 0.0016501 0.074866 0.02 0.982 −0.1450847 0.1483848
_Cons 1.379.876 0.2617582 5.27 0 0.866839 1.892.912

The mixed effects multilevel regression analyses evaluated the individual results of anti-PGL-I, anti-LID-1, and anti-ND-O-LID serology during follow-up considering the serological result as the independent variable (constant), the dependent variables were time (month) and treatment group (R-MDT and U-MDT) and the group variable was the patient ID. These analyses showed that the difference in serologic decay to all three antigens was dependent upon time only.

PGL-I, phenollic glycolipid-I antigen; R-MDT, regular multidrug therapy; U-MDT, uniform multidrug therapy.