Primary Motor Cortex Involvement in Alzheimer Disease

• Published in: Journal of neuropathology and experimental neurology 1999-11, Vol.58 (11), p.1125-1134
• Main Authors: Suvà, Domizio, Favre, Isabelle, Kraftsik, Rudolf, Esteban, Monica, Lobrinus, Alexander, Miklossy, Jodith
• Format: Article
• Language: English
• Subjects: Adult; Advertising executives; Aged; Aged, 80 and over; Alzheimer Disease - pathology; Alzheimer's disease; Amyloid beta-Peptides - analysis; Analysis; Biological and medical sciences; Brain; Brain Chemistry; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; Entorhinal Cortex - pathology; Humans; Medical sciences; Middle Aged; Motor Cortex - pathology; Neurofibrillary Tangles - pathology; Neurology; Parietal Lobe - pathology; Plaque, Amyloid - pathology; Somatosensory Cortex - pathology
• ISSN: 0022-3069; 1554-6578
• DOI: 10.1097/00005072-199911000-00002

In Alzheimer disease (AD) the involvement of entorhinal cortex, hippocampus, and associative cortical areas is well established. Regarding the involvement of the primary motor cortex the reported data are contradictory. In order to determine whether the primary motor cortex is involved in AD, the brains of 29 autopsy cases were studied, including, 17 cases with severe cortical AD-type changes with definite diagnoses of AD, 7 age-matched cases with discrete to moderate cortical AD-type changes, and 5 control cases without any AD-type cortical changes. Morphometric analysis of the cortical surface occupied by senile plaques (SPs) on β-amyloid-immunostained sections and quantitative analysis of neurofibrillary tangles (NFTs) on Gallyas-stained sections was performed in 5 different cortical areas including the primary motor cortex. The percentage of cortical surface occupied by SPs was similar in all cortical areas, without significant difference and corresponded to 16.7% in entorhinal cortex, 21.3% in frontal associative, 16% in parietal associative, and 15.8% in primary motor cortex. The number of NFTs in the entorhinal cortex was significantly higher (41 per 0.4 mm), compared with those in other cortical areas (20.5 in frontal, 17.9 in parietal and 11.5 in the primary motor cortex). Our findings indicate that the primary motor cortex is significantly involved in AD and suggest the appearance of motor dysfunction in late and terminal stages of the disease.