Skip to main content
. 2010 Jan 21;119(5):579–589. doi: 10.1007/s00401-009-0635-8

Table 1.

Age, gender and disease severity of the groups

Parameter Controls DLB AD VaD
Demographic details
 N 12 31 19 20
 Age (±SD) 75.6 ± 7.8 79.1 ± 5.7 85.5 ± 5.5 81.0 ± 8.5
 Age range (years) 61–92 64–89 75–96 67–93
 Gender (M/F) 6/6 14/17 7/12 10/10
Pathological features
 Mean Braak stage 1.0 ± 1.0 2.3 ± 1.0 4.9 ± 0.8 1.3 ± 0.7
 Neuritic plaque densitya (per mm2) 2 ± 1 21 ± 3 27 ± 4 7 ± 2
 Lewy body pathology (ubiquitin score) <1 7.2 ± 2.6 <1 <1
 Lewy body pathology (α-synuclein score) <1 12.5 ± 5.0 <1 <1
 Number of vascular lesions (range) 0–1 0–3 0–3 3–15
 Degree of CAA (range) 0–1 0–4 1–4 0–4
 Frontal myelin index* 51.1 ± 9.5 41.5 ± 8.5 35.9 ± 11.1 26.5 ± 9.0
 Temporal myelin index 37.3 ± 10.1 32.7 ± 13.4 35.2 ± 11.0 34.4 ± 11.9

Unless otherwise stated numbers show mean values with standard deviation (±SD). AD subjects were significantly older than controls and DLB (P < 0.01). Selected cases stained for amyloid β protein immunoreactivity also showed the severity of neuritic plaque burden in AD and DLB was comparable to the phases 4 and 5 staging described by Thal et al. [46] and the BrainNet Europe Consortium [3]. The presence of Lewy body pathology was determined by ubiquitin and α-synuclein immunostaining [35]. The number of vascular lesions and degree of CAA were recorded according to the Vonsattal grading as previously described [28, 40]

* Significant difference (P < 0.05) between any two groups

aNeuritic plaque densities were comparable to the CERAD ratings in that moderate to severe scores were evident in 95% of AD and 74% of DLB cases