Lempel-Ziv complexity in schizophrenia: A MEG study

Objective: The neurodevelopmental-neurodegenerative debate is a basic issue in the field of the neuropathological basis of schizophrenia (SCH). Neurophysiological techniques have been scarcely involved in such debate, but nonlinear analysis methods may contribute to it. Methods: Fifteen patients (ag...

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Detalhes bibliográficos
Autores: Fernández Lucas, Alberto Amable, López-Ibor Alcocer, María Inés, Turrero Nogués, Agustín, Santos García, Juan Matías, Morón, María Dolores, Hornero, Roberto, Gómez, Carlos, Méndez, María Andreina, Ortiz Alonso, Tomás, López-Ibor Aliño, Juan José
Tipo de documento: artigo
Data de publicação:2011
País:España
Recursos:Universidad Complutense de Madrid (UCM)
Repositório:Docta Complutense
Idioma:inglês
OAI Identifier:oai:docta.ucm.es:20.500.14352/44635
Acesso em linha:https://hdl.handle.net/20.500.14352/44635
Access Level:Acceso aberto
Palavra-chave:Lempel-Ziv complexity
Magnetoencephalography
Neurodegenerative
Neurodevelopmental
Schizophrenia. EMTREE medical terms: adult
Age
Article
Clinical article
Controlled study
Correlation analysis
Female
Human
Lempel ziv complexity score
Logistic regression analysis
Male
Patient coding
Priority journal
Schizophrenia
Scoring system
Sensitivity and specificity.
MeSH: Adult
Aging
Cerebral Cortex
Cognition Disorders
Disease Progression
Humans
Schizophrenic Psychology
Signal Processing
Computer-Assisted
Young Adult
Descrição
Resumo:Objective: The neurodevelopmental-neurodegenerative debate is a basic issue in the field of the neuropathological basis of schizophrenia (SCH). Neurophysiological techniques have been scarcely involved in such debate, but nonlinear analysis methods may contribute to it. Methods: Fifteen patients (age range 23-42. years) matching DSM IV-TR criteria for SCH, and 15 sex- and age-matched control subjects (age range 23-42. years) underwent a resting-state magnetoencephalographic evaluation and Lempel-Ziv complexity (LZC) scores were calculated. Results: Regression analyses indicated that LZC values were strongly dependent on age. Complexity scores increased as a function of age in controls, while SCH patients exhibited a progressive reduction of LZC values. A logistic model including LZC scores, age and the interaction of both variables allowed the classification of patients and controls with high sensitivity and specificity. Conclusions: Results demonstrated that SCH patients failed to follow the " normal" process of complexity increase as a function of age. In addition, SCH patients exhibited a significant reduction of complexity scores as a function of age, thus paralleling the pattern observed in neurodegenerative diseases. Significance: Our results support the notion of a progressive defect in SCH, which does not contradict the existence of a basic neurodevelopmental alteration.