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. 2020 Sep 1;143(9):2689–2695. doi: 10.1093/brain/awaa221

Table 1.

Summary of demographic, clinical, audiometric and auditory scene analysis task data for all participant groups

Controls PCAa tAD
General
n, male: female 7:8 7:14 9:12
Age, years 63.36 (6.4) 63.02 (9.5) 65.03 (7.9)
Hearing loss, dB 7.9 (7.7) 17.0 (10.5) * 13.6 (6.9)
Symptom duration, years 3.65 (2.3) 5.93 (2.5)
Background neuropsychology
MMSE (/30) 18.48 (4.6) 22.10 (4.2)
RMT Words (z-score)b −2.15 (2.2) −2.65 (1.9)
RMT Faces (z-score)c −1.95 (2.3) −2.28 (2.0)
Digit span forward (/12) 8.40 (1.6) 6.81 (1.9) 7.48 (2.3)
Digit span reverse (/12) 7.27 (1.3) 3.14 (1.3) 5.24 (2.8)
WASI Vocabulary (/72)d 71.36 (4.4) 54.47 (8.8)** 57.00 (14.8)
Graded naming test (/30)d 27.00 (3.3) 13.90 (4.6) 13.95 (9.0)
Graded difficulty arithmetic (/24)d 15.55 (3.7) 1.76 (3.2) 6.33 (4.9)
Single word comprehension (z-score) 0.23 (0.7) −6.41 (7.7)***
ASA tests
ASA segregationb
 ASA segregation test (/20) 19.07 (1.5) 12.14 (3.0)**** 15.45 (4.2)
 Task requirement control test (/10) 10.00 (0.01) 8.95 (1.2) 10.00 (0.0)
 Perceptual cue control test (/10) 9.67 (0.6) 8.71 (1.4) 9.35 (1.0)
ASA grouping
 ASA grouping test (/20)c 18.67 (1.2) 11.05 (3.8) 15.62 (3.8)
 Task requirement control test (/10) 9.93 (0.3) 9.00 (0.8) 10.0 (0.0)
 Perceptual cue control test (/10) 9.87 (0.4) 7.90 (1.9) 9.86 (0.5)

Mean (SD) data are presented unless otherwise indicated; maximum scores for neuropsychological tests are indicated in parentheses. Bold indicates significantly lower than healthy controls, P <0.001 unless otherwise specified (for z-scores, bold indicates average performance outside 95% of the area under normal distribution, i.e. ±1.96); italics indicate significantly lower than the typical Alzheimer’s disease (tAD) group, P 0.01 unless otherwise specified (statistical data including 95% CIs are presented in full in Supplementary Table 3). Certain cognitive functions were assessed using different tests in the PCA and typical Alzheimer’s disease cohorts: the typical Alzheimer’s disease cohort was given the long-form Recognition Memory Test (RMT) for words and faces and the British Picture Vocabulary Scale (BPVS) for single word comprehension; the PCA group were given the short-form RMT for words and faces, and the Concrete Synonyms test for single word comprehension, and to give a comparable indication of how each syndromic group performed in these domains we derived z-scores using age-appropriate normative data (Supplementary Table 3). Administration of the graded naming test differed across groups: control and typical Alzheimer’s disease participants were presented with items visually; participants with PCA were asked to name from verbal description. MMSE = Mini-Mental State Examination score; WASI = Wechsler Abbreviated Scale of Intelligence.

a

CSF profiles of tau and amyloid-β were available for 13 patients with PCA and were consistent with Alzheimer’s pathology in 12 cases, based on local reference ranges (total tau/amyloid-β1-42 ratio > 1). One participant with PCA showed clear response bias on the ASA-grouping task (Supplementary material); this participant was removed from analysis of the ASA-grouping test.

b

Data were not available for one participant with typical Alzheimer’s disease.

c

Data were not available for one participant with PCA.

d

Data were not available for four healthy control participants.

*

P =0.003 versus controls.

**

P =0.002 versus controls.

***

P <0.001 versus PCA.

****

P =0.012 versus typical Alzheimer’s disease.