Predisposición genética y síndrome de distrés respiratorio agudo pediátrico: Nuevas herramientas de estudio genético

Erranz M. Benjamín, Wilhelm B. Jan, Riquelme V. Raquel, Cruces R. Pablo

Resultado de la investigación: Contribución a una revistaArtículorevisión exhaustiva

Resumen

Acute respiratory distress syndrome (ARDS) is the most severe form of respiratory failure. Theoretically, any acute lung condition can lead to ARDS, but only a small percentage of individuals actually develop the disease. On this basis, genetic factors have been implicated in the risk of developing ARDS. Based on the pathophysiology of this disease, many candidate genes have been evaluated as potential modifiers in patient, as well as in animal models, of ARDS. Recent experimental data and clinical studies suggest that variations of genes involved in key processes of tissue, cellular and molecular lung damage may influence susceptibility and prognosis of ARDS. However, the pathogenesis of pediatric ARDS is complex, and therefore, it can be expected that many genes might contribute. Genetic variations such as single nucleotide polymorphisms and copy-number variations are likely associated with susceptibility to ARDS in children with primary lung injury. Genome-wide association (GWA) studies can objectively examine these variations, and help identify important new genes and pathogenetic pathways for future analysis. This approach might also have diagnostic and therapeutic implications, such as predicting patient risk or developing a personalized therapeutic approach to this serious syndrome.

Título traducido de la contribuciónGenetic predisposition and pediatric acute respiratory distress syndrome: New tools for genetic study
Idioma originalEspañol
Páginas (desde-hasta)73-79
Número de páginas7
PublicaciónRevista Chilena de Pediatria
Volumen86
N.º2
DOI
EstadoPublicada - 22 jul 2015

Palabras clave

  • Acute lung injury
  • Acute respiratory distress syndrome
  • Genetics
  • Genome-wide association study
  • Pediatrics
  • Single nucleotide polymorphisms

Áreas temáticas de ASJC Scopus

  • Pediatría, perinaltología y salud infantil

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