Literature DB >> 32768685

From genetics to epigenetics to unravel the etiology of adolescent idiopathic scoliosis.

Gisselle Pérez-Machado1, Ester Berenguer-Pascual1, Miquel Bovea-Marco2, Pedro Antonio Rubio-Belmar3, Eva García-López1, María José Garzón1, Salvador Mena-Mollá4, Federico V Pallardó5, Teresa Bas3, Juan R Viña6, José Luis García-Giménez7.   

Abstract

Scoliosis is defined as the three-dimensional (3D) structural deformity of the spine with a radiological lateral Cobb angle (a measure of spinal curvature) of ≥10° that can be caused by congenital, developmental or degenerative problems. However, those cases whose etiology is still unknown, and affect healthy children and adolescents during growth, are the commonest form of spinal deformity, known as adolescent idiopathic scoliosis (AIS). In AIS management, early diagnosis and the accurate prediction of curve progression are most important because they can decrease negative long-term effects of AIS treatment, such as unnecessary bracing, frequent exposure to radiation, as well as saving the high costs of AIS treatment. Despite efforts made to identify a method or technique capable of predicting AIS progression, this challenge still remains unresolved. Genetics and epigenetics, and the application of machine learning and artificial intelligence technologies, open up new avenues to not only clarify AIS etiology, but to also identify potential biomarkers that can substantially improve the clinical management of these patients. This review presents the most relevant biomarkers to help explain the etiopathogenesis of AIS and provide new potential biomarkers to be validated in large clinical trials so they can be finally implemented into clinical settings.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Adolescent idiopathic scoliosis; Biomarkers; DNA methylation; Epigenetics; GWAS; Noncoding RNAs

Mesh:

Year:  2020        PMID: 32768685     DOI: 10.1016/j.bone.2020.115563

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  7 in total

1.  The association between idiopathic scoliosis and growth hormone treatment in short children.

Authors:  Mijin Park; Yu Jin Kim; Kyeong Eun Oh; Eungu Kang; Hyo-Kyoung Nam; Young-Jun Rhie; Kee-Hyoung Lee
Journal:  Ann Pediatr Endocrinol Metab       Date:  2022-05-16

2.  Upregulation of microRNA-96-5p is associated with adolescent idiopathic scoliosis and low bone mass phenotype.

Authors:  Huanxiong Chen; Kenneth Guangpu Yang; Jiajun Zhang; Ka-Yee Cheuk; Evguenia Nepotchatykh; Yujia Wang; Alec Lik-Hang Hung; Tsz-Ping Lam; Alain Moreau; Wayne Yuk-Wai Lee
Journal:  Sci Rep       Date:  2022-06-11       Impact factor: 4.996

Review 3.  Epigenetic and Genetic Factors Related to Curve Progression in Adolescent Idiopathic Scoliosis: A Systematic Scoping Review of the Current Literature.

Authors:  Cesare Faldini; Marco Manzetti; Simona Neri; Francesca Barile; Giovanni Viroli; Giuseppe Geraci; Francesco Ursini; Alberto Ruffilli
Journal:  Int J Mol Sci       Date:  2022-05-25       Impact factor: 6.208

4.  Tent5a modulates muscle fiber formation in adolescent idiopathic scoliosis via maintenance of myogenin expression.

Authors:  Ming Luo; Huiliang Yang; Diwei Wu; Xuanhe You; Shishu Huang; Yueming Song
Journal:  Cell Prolif       Date:  2022-02-09       Impact factor: 6.831

5.  Risk Factors, Lifestyle and Prevention among Adolescents with Idiopathic Juvenile Scoliosis: A Cross Sectional Study in Eleven First-Grade Secondary Schools of Palermo Province, Italy.

Authors:  Dalila Scaturro; Claudio Costantino; Pietro Terrana; Fabio Vitagliani; Vincenzo Falco; Daniele Cuntrera; Claudia Emilia Sannasardo; Francesco Vitale; Giulia Letizia Mauro
Journal:  Int J Environ Res Public Health       Date:  2021-11-24       Impact factor: 3.390

6.  Exploring the association between specific genes and the onset of idiopathic scoliosis: a systematic review.

Authors:  Sergio De Salvatore; Laura Ruzzini; Umile Giuseppe Longo; Martina Marino; Alessandra Greco; Ilaria Piergentili; Pier Francesco Costici; Vincenzo Denaro
Journal:  BMC Med Genomics       Date:  2022-05-19       Impact factor: 3.063

7.  A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita.

Authors:  Xenia Latypova; Stefan Giovanni Creadore; Noémi Dahan-Oliel; Anxhela Gjyshi Gustafson; Steven Wei-Hung Hwang; Tanya Bedard; Kamran Shazand; Harold J P van Bosse; Philip F Giampietro; Klaus Dieterich
Journal:  Genes (Basel)       Date:  2021-07-08       Impact factor: 4.096

  7 in total

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