Evidence map›Paper›PMID 24416615›Full record

ArticleInternational journal of Alzheimer's disease2013

Sensorimotor Cortex Reorganization in Alzheimer's Disease and Metal Dysfunction: A MEG Study.

C Salustri, F Tecchio, F Zappasodi, L Tomasevic, M Ercolani, F Moffa, E Cassetta, P M Rossini, R Squitti

Open access · hybridAbstract read
In one paragraph

Article in International journal of Alzheimer's disease, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. The Role of Zinc in the Treatment of Wilson's Disease.International journal of molecular sciences · 2022
    Review
  4. Article
  5. Unsuspected Involvement of Spinal Cord in Alzheimer Disease.Frontiers in cellular neuroscience · 2020
    Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

C SalustriInstitute of Cognitive Sciences and Technologies (CNR), Unità MEG, Fatebenefratelli Hospital, Isola Tiberina, 00186 Rome, Italy.
F TecchioInstitute of Cognitive Sciences and Technologies (CNR), Unità MEG, Fatebenefratelli Hospital, Isola Tiberina, 00186 Rome, Italy ; Department of Imaging, IRCCS San Raffaele Pisana, 00163 Rome, Italy.
F ZappasodiDepartment of Neuroscience and Imaging, Gabriele d'Annunzio University, 66100 Chieti, Italy.
L TomasevicInstitute of Cognitive Sciences and Technologies (CNR), Unità MEG, Fatebenefratelli Hospital, Isola Tiberina, 00186 Rome, Italy.
M ErcolaniAFaR, Department of Neuroscience, Fatebenefratelli Hospital, Isola Tiberina, 00186 Rome, Italy.
F MoffaAFaR, Department of Neuroscience, Fatebenefratelli Hospital, Isola Tiberina, 00186 Rome, Italy.
E CassettaAFaR, Department of Neuroscience, Fatebenefratelli Hospital, Isola Tiberina, 00186 Rome, Italy.
P M RossiniDepartment of Imaging, IRCCS San Raffaele Pisana, 00163 Rome, Italy ; Institute of Neurology, Department of Neuroscience, Catholic University, A. Gemelli Polyclinic, 00168 Rome, Italy.
R SquittiAFaR, Department of Neuroscience, Fatebenefratelli Hospital, Isola Tiberina, 00186 Rome, Italy ; Laboratory of Neurodegeneration, IRCCS San Raffaele Pisana, 00163 Rome, Italy.
Fatebenefratelli Hospital · ITAgostino Gemelli University Polyclinic · ITUniversity of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Identifiers

PMID24416615
PMCPMC3876721
OpenAlexW2127376721

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.