Deleterious fibronectin type III-related gene variants may induce a spinal extradural arachnoid cyst: an exome sequencing study of identical twin cases

• Published in: Child's nervous system Vol. 37; no. 7; pp. 2329 - 2334
• Main Authors: Hana, Taijun, Ogiwara, Hideki, Migita, Ohsuke, Nakabayashi, Kazuhiko, Hata, Kenichiro, Morota, Nobuhito
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.07.2021
• Subjects: Arachnoid Cysts - diagnostic imaging; Arachnoid Cysts - genetics; Exome - genetics; Fibronectins - genetics; Humans; Medicine; Medicine & Public Health; Neurosciences; Neurosurgery; Original Article; Pedigree; Twins, Monozygotic; Whole Exome Sequencing; Genetic etiology; Tarlov cyst; Exome sequencing analysis; Spinal extradural arachnoid cyst
• ISSN: 0256-7040; 1433-0350; 1433-0350
• DOI: 10.1007/s00381-021-05137-4

Purpose Despite numerous studies, the etiology of spinal extradural arachnoid cyst (SEDAC), a lesion associated with neurological symptoms, remains unknown. In this genomic twin study, we investigated the genetic etiology of SEDACs. Methods The subjects were identical twins who developed notably similar SEDACs at the same vertebral level. Accordingly, we performed whole-exome sequencing analyses of genomic material from the twins and their parents using a next-generation sequencer. Additionally, we determined their detailed family history and analyzed the family pedigree. Results The pedigree analysis suggested the potential presence of SEDACs in certain family members, indicating a genetic disease. Sequenced data were analyzed and filtered using a purpose-built algorithm, leading to the identification of 155 novel single-nucleotide polymorphisms (SNPs), of which 118 encoded missense or nonsense variants. A functional analysis of the proteins encoded by these SNP alleles revealed strong enrichment for the fibronectin type III (FN3) protein domain ( q  = 0.00576). Specifically, the data indicated that a missense variant affecting the FN3 protein domain of fibronectin 1 ( FN1, p.P969S) can be the causal mutation underlying the SEDACs. Conclusion The data suggest that deleterious mutations in fibronectin-related genes may cause SEDACs. In particular, it was suspected that a variant of FN1 may be the cause of the SEDACs in the twin cases studied herein. Detailed studies with a larger number of cases are needed.