z-logo
open-access-imgOpen Access
Sensorimotor Cortex Reorganization in Alzheimer's Disease and Metal Dysfunction: A MEG Study
Author(s) -
Carlo Salustri,
Franca Tecchio,
Filippo Zappasodi,
Leo Tomasevic,
Matilde Ercolani,
Filomena Moffa,
Emanuele Cassetta,
Paolo Maria Rossini,
Rosanna Squitti
Publication year - 2013
Publication title -
international journal of alzheimer s disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.657
H-Index - 49
eISSN - 2090-8024
pISSN - 2090-0252
DOI - 10.1155/2013/638312
Subject(s) - medicine , disease , neuroscience , alzheimer's disease , cortex (anatomy) , pathology , psychology
Objective . To verify whether systemic biometals dysfunctions affect neurotransmission in living Alzheimer's disease (AD) patients. Methods . We performed a case-control study using magnetoencephalography to detect sensorimotor fields of AD patients, at rest and during median nerve stimulation. We analyzed position and amount of neurons synchronously activated by the stimulation in both hemispheres to investigate the capability of the primary somatosensory cortex to reorganize its circuitry disrupted by the disease. We also assessed systemic levels of copper, ceruloplasmin, non-Cp copper (i.e., copper not bound to ceruloplasmin), peroxides, transferrin, and total antioxidant capacity. Results . Patients' sensorimotor generators appeared spatially shifted, despite no change of latency and strength, while spontaneous activity sources appeared unchanged. Neuronal reorganization was greater in moderately ill patients, while delta activity increased in severe patients. Non-Cp copper was the only biological variable appearing to be associated with patient sensorimotor transmission. Conclusions . Our data strengthen the notion that non-Cp copper, not copper in general, affects neuronal activity in AD. Significance . High plasticity in the disease early stages in regions controlling more commonly used body parts strengthens the notion that physical and cognitive activities are protective factors against progression of dementia.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom