Genetic alterations in necrotizing enterocolitis.
An underlying genetic predisposition to necrotizing enterocolitis (NEC) is increasingly being recognized. Candidate gene or pathway approaches as well as genome-wide approaches are beginning to identify potential pathogenic variants for NEC in premature infants. However, a majority of these studies have not yielded definitive results because of limited sample size and lack of validation. Despite these challenges, understanding the contribution of genetic variation to NEC is important for providing new insights into the pathogenesis of NEC as well as allowing for targeted care of infants with inherent susceptibility. In this review we provide a summary of published genetic association studies in NEC along with defining the challenges and possible future approaches.
Seminars in perinatology
Enterocolitis, Necrotizing; Gene Expression Regulation, Developmental; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Humans; Immunity, Innate; Infant, Extremely Premature; Infant, Newborn; Infant, Premature, Diseases; Inflammation; Intestinal Mucosa; Molecular Targeted Therapy; Mutation; Polymorphism, Single Nucleotide
Genetic predisposition; Necrotizing enterocolitis; Preterm newborn; Single nucleotide polymorphism; NEC; Preemies
Cuna, Alain and Sampath, Venkatesh, "Genetic alterations in necrotizing enterocolitis." (2017). Manuscripts, Articles, Book Chapters and Other Papers. 475.