Table 2.
Control | Premanifest | Manifest | P | |
---|---|---|---|---|
LARS-s % clinically relevanta | −9.90 ± 3.1, N = 31 12.9% | −8.65 ± 4.1, N = 17 29.4% | −6.14 ± 5.4, N = 21 52.2% | .009⁎ |
Cognitive apathyb | −4.29 ± 1.8 | −4.24 ± 1.9 | −2.76 ± 3.2 | .050 |
Auto-activation deficitb | −2.36 ± 1.2 | −1.00 ± 2.2 | −0.86 ± 2.3 | .008⁎ |
Emotional apathyb | −3.16 ± 0.90 | −3.12 ± 1.2 | −2.95 ± 1.3 | .279 |
PBA-s, apathyc | - | 4.76 ± 8.6, N = 21 | 8.08 ± 7.6, N = 24 | - |
PBA-s, affectivec | - | 4.91 ± 5.9 | 2.63 ± 3.29 | - |
Data presented as mean ± standard deviation. Greater or more positive numbers indicate more severe behavioral symptoms. P-values refer to one-way ANOVA between controls, premanifest, and manifest groups.
N = number of participants; LARS-s = Lille Apathy Rating Scale, short-from; PBA-s = Problem Behavior Assessment, short-form.
P-values retained significance after false discovery rate correction (q = 0.05).
Cut-off for clinically relevant global apathetic syndromes is defined as a total LARS-s score > −7 (Dujardin et al., 2013).
Subscale computed from the LARS-s.
Measured based on ‘apathy’ and ‘affective behavior’ components of factor analysis in Callaghan et al. (2015).