Molecular and Genetic Mechanisms of Spinal Stenosis Formation: Systematic Review

• Published in: International journal of molecular sciences Vol. 23; no. 21; p. 13479
• Main Authors: Byvaltsev, Vadim A., Kalinin, Andrei A., Hernandez, Phillip A., Shepelev, Valerii V., Pestryakov, Yurii Y., Aliyev, Marat A., Giers, Morgan B.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-11-2022; MDPI
• Subjects: Achondroplasia; Asian Americans; Bone morphogenetic protein 2; Collagen (type I); congenital disease; Congenital diseases; degenerative disease; Epidemiology; Etiology; Fibroblast growth factor receptor 3; Genes; Genetics; Growth factors; Hypertrophy; Intervertebral discs; Kinases; Ligaments; molecular mechanisms; Mutation; Ossification; Osteoarthritis; Pathology; Phosphorylation; Proteins; Regulation; Review; Spinal cord; Spinal stenosis; Stem cells; Systematic review; Transforming growth factor-b; Wnt protein; β-Catenin; North America
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms232113479

Spinal stenosis (SS) is a multifactorial polyetiological condition characterized by the narrowing of the spinal canal. This condition is a common source of pain among people over 50 years old. We perform a systematic review of molecular and genetic mechanisms that cause SS. The five main mechanisms of SS were found to be ossification of the posterior longitudinal ligament (OPLL), hypertrophy and ossification of the ligamentum flavum (HLF/OLF), facet joint (FJ) osteoarthritis, herniation of the intervertebral disc (IVD), and achondroplasia. FJ osteoarthritis, OPLL, and HLF/OLFLF/OLF have all been associated with an over-abundance of transforming growth factor beta and genes related to this phenomenon. OPLL has also been associated with increased bone morphogenetic protein 2. FJ osteoarthritis is additionally associated with Wnt/β-catenin signaling and genes. IVD herniation is associated with collagen type I alpha 1 and 2 gene mutations and subsequent protein dysregulation. Finally, achondroplasia is associated with fibroblast growth factor receptor 3 gene mutations and fibroblast growth factor signaling. Although most publications lack data on a direct relationship between the mutation and SS formation, it is clear that genetics has a direct impact on the formation of any pathology, including SS. Further studies are necessary to understand the genetic and molecular changes associated with SS.