Skip to main content
. Author manuscript; available in PMC: 2014 Aug 15.
Published in final edited form as: J Neurovirol. 2013 Aug 14;19(4):383–392. doi: 10.1007/s13365-013-0190-x

Table 2.

Neurocognitive tests, baseline and change to month 6

Baseline
Change to month 6
Mean ±1 SD Mean SE P value
QNPZ-5 −0.68* ±0.78 0.17 0.05 <0.001
Test z scoresa
 GPB −0.26* ±1.20 0.25 0.09 <0.001
 CT1 −0.52* ±1.24 0.28 0.10 <0.001
 CT2 −0.00 ±0.99 0.18 0.07 <0.001
 TG −1.64* ±1.75 0.11 0.10 0.15
 FT −0.98* ±1.10 0.03 0.09 0.68
Raw tests scores
 GPB (s) 72.5 ±26.3 −3.8 1.5 <0.001
 CT1 (s) 47.5 ±19.0 −3.8 1.3 <0.001
 CT2 (s) 93.3 ±32.6 −5.1 2.0 <0.001
 TG (s) 11.9 ±2.1 −0.1 0.1 0.19
 FT (taps) 39.3 ±7.9 0.1 0.6 0.90

The QNPZ-5 score, individual test z scores, and raw test scores at baseline, and their change to month 6 are shown for 258 participants, pooled across the intermittent ART and continuous ART treatment groups. At baseline, the mean QNPZ-5 score and mean z scores for four of the five tests were below 0, denoting below-average performance compared with a healthy reference population. The QNPZ-5 score and individual test z scores increased from baseline to month 6; see also Fig. 1. There was no evidence for a treatment difference in mean change in QNPZ-5 or any of the z scores

CT Color Trails test, FT Finger Tapping test (nondominant hand), GPB Grooved Pegboard test (dominant hand), QNPZ-5 quantitative neurocognitive performance z score, TG Timed Gait test

*

P<0.001, mean z scores<0 (two-sided t test)

a

z scores were calculated with reference distributions (matched for education [all tests], age [GPB, CT, and FT], gender [GPB and FT], and race/ethnicity [GPB and FT]). Thirty-five participants (13.6 %) had NCI at baseline, defined as z scores<−2 in at least two cognitive ability domains, and the same number had NCI at month 6. Of those who were impaired at baseline, 16 participants (46 %) were not impaired at month 6, and vice versa