Skip to main content
. 2011 Sep 28;6(9):e25253. doi: 10.1371/journal.pone.0025253

Table 1. Characteristics of study participants.

SCHIZOPHRENIA PATIENTS HEALTHY PARTICIPANTS
MTHFR genotype C/C (n = 14) C/T (n = 13) plus T/T (n = 4) C/C (n = 13) C/T (n = 9) plus T/T (n = 3) P *
DEMOGRAPHICS
Age at fMRI 40±3 45±3 41±3 39±4 n/s
Sex 12 M, 2 F 12 M, 5 F 10 M, 3 F 10 M, 2 F n/s
Race 9 European, 5 Other 14 European, 3 Other 12 European, 1 Other 9 European, 3 Other n/s
Length of illness (yrs) 19±4 19±3 n/s
Edinburgh handedness 64±14 57±13 57±15 67±8 n/s
CLINICAL
PANSS positive 15±5 14±4 n/s
PANSS negative 14±5 15±5 n/s
PANSS general 30±9 31±8 n/s
CPZ equivalents 435±94 465±78 n/s
PERFORMANCE AND MOTION
Estimated verbal IQ 101±3 97±3 106±4 110±4 healthy>patient, p = .01
Antisaccade latency (ms)
• correct trials 300±16 277±14 276±12 272±14 n/s
• error trials 202±13 189±10 185±10 183±15 n/s
Antisaccade % error 26±6 32±5 13±3 18±3 patient>healthy, p = .004
Post-error slowing (ms; positive = slower)** 16±7 −4±7 13±8 7±8 C/C>T, p = .08
Average motion (mm) 2.33±0.28 2.43±0.25 1.98±0.29 2.31±0.30 n/s

Statistical tests were performed using ANOVA or chi-square as appropriate, with alpha (2-tailed) = 0.05. Abbreviations: fMRI, functional magnetic resonance imaging; PANSS, positive and negative syndrome scale; CPZ, chlorpromazine.

*n/s, no significant main effects of genotype or diagnosis, or significant genotype×diagnosis interaction.

**Post-error slowing was calculated as the difference in saccadic latency between correct trials following an error and correct trials immediately prior to errors.