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. Author manuscript; available in PMC: 2024 Apr 4.
Published in final edited form as: J Alzheimers Dis. 2023;94(1):227–246. doi: 10.3233/JAD-221063

Table 4.

Clinical group differences for vesicular glutamate transporter and spinophilin immunoreactivity measures obtained in the frontal cortex

NCI MCI mAD sAD p Groupwise comparison(s)
VGluTl density
Mean ± SD 0.040 ± 0.007 0.044 ± 0.007 0.043 ± 0.008 0.030 ± 0.008 <0.001a NCI, MCI, mAD > sAD
(Median) (0.0401) (0.0451) (0.0417) (0.0305)
VGluTl intensity
Mean ± SD 3071 ± 680.8 3662 ± 786.2 3800 ± 501.0 4031±1083 0.013a MCI, mAD, sAD>NCI
(Median) (3128) (3914) (3951) (3583)
VGluT2 density
Mean ± SD 0.038 ± 0.02 0.05 ± 0.01 0.05 ± 0.02 0.03 ± 0.01 0.013a MCI>sAD
(Median) (0.0331) (0.0473) (0.0471) (0.0284)
VGluT2 intensity
Mean ± SD 422 ± 243 296 ± 94 360±184 463 ± 149 0.13a ANOVA not significant
(Median) (347) (278) (323) (494)
Spinophilin density
Mean ± SD 0.1301 ± 0.06 0.1527 ± 0.03 0.1408 ± 0.06 0.1031 ± 0.05 0.06a ANOVA not significant
(Median) (0.1099) (0.1440) (0.1281) (0.09)
Spinophilin intensity
Mean ± SD 2815 ± 859.7 2323 ± 532.4 3086 ± 704.5 2204 ± 463.8 0.09a ANOVA not significant
(Median) (2604) (2421) (3072) (2247)
a

Kruskal-Wallis one-way analysis of variance.

AD, Alzheimer’s disease; ANOVA, one-way analysis of variance; NCI, no cognitive impairment; MCI, mild cognitive impairment; mAD, mild to moderate AD; sAD, moderate to severe AD; SD, standard deviation; VGluT, vesicular glutamate transporter.