Proprioception‐related gene mutations in relation to the aetiopathogenesis of idiopathic scoliosis: A scoping review
Since idiopathic scoliosis is a multifactorial disorder, the proprioceptive defect is considered one of its etiological factors. Genetic studies have separately revealed this relationship, yet it remains indeterminate which specific genes that related to proprioception contributed to the initiation,...
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Published in | Journal of orthopaedic research Vol. 41; no. 12; pp. 2694 - 2702 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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United States
01.12.2023
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ISSN | 0736-0266 1554-527X 1554-527X |
DOI | 10.1002/jor.25626 |
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Abstract | Since idiopathic scoliosis is a multifactorial disorder, the proprioceptive defect is considered one of its etiological factors. Genetic studies have separately revealed this relationship, yet it remains indeterminate which specific genes that related to proprioception contributed to the initiation, progression, pathology, and treatment outcomes of the curvature. A systematic search was conducted on four online databases, including PubMed, Web of Science, Embase, and Academic search complete. Studies were included if they involved human or animal subjects with idiopathic scoliosis and evaluated with proprioceptive genes. The search period was the inception of the database to February 21, 2023. Four genes (i.e., Ladybird homeobox 1 [LBX1], Piezo type mechanosensitive ion channel component 2 [PIEZO2], Runx family transcription factor 3 [RUNX3], and neurotrophin 3 [NTF3]) investigated in 19 studies were included. LBX1 has confirmed the correlation with the development of idiopathic scoliosis in 10 ethnicities, whereas PIEZO2 has shown a connection with clinical proprioceptive tests in subjects with idiopathic scoliosis. However, curve severity was less likely to be related to the proprioceptive genes. The potential pathology took place at the proprioceptive neurons. Evidence of proprioception‐related gene mutations in association with idiopathic scoliosis was established. Nevertheless, the causation between the initiation, progression, and treatment outcomes with proprioceptive defect requires further investigation. |
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AbstractList | Since idiopathic scoliosis is a multifactorial disorder, the proprioceptive defect is considered one of its etiological factors. Genetic studies have separately revealed this relationship, yet it remains indeterminate which specific genes that related to proprioception contributed to the initiation, progression, pathology, and treatment outcomes of the curvature. A systematic search was conducted on four online databases, including PubMed, Web of Science, Embase, and Academic search complete. Studies were included if they involved human or animal subjects with idiopathic scoliosis and evaluated with proprioceptive genes. The search period was the inception of the database to February 21, 2023. Four genes (i.e., Ladybird homeobox 1 [LBX1], Piezo type mechanosensitive ion channel component 2 [PIEZO2], Runx family transcription factor 3 [RUNX3], and neurotrophin 3 [NTF3]) investigated in 19 studies were included. LBX1 has confirmed the correlation with the development of idiopathic scoliosis in 10 ethnicities, whereas PIEZO2 has shown a connection with clinical proprioceptive tests in subjects with idiopathic scoliosis. However, curve severity was less likely to be related to the proprioceptive genes. The potential pathology took place at the proprioceptive neurons. Evidence of proprioception-related gene mutations in association with idiopathic scoliosis was established. Nevertheless, the causation between the initiation, progression, and treatment outcomes with proprioceptive defect requires further investigation.Since idiopathic scoliosis is a multifactorial disorder, the proprioceptive defect is considered one of its etiological factors. Genetic studies have separately revealed this relationship, yet it remains indeterminate which specific genes that related to proprioception contributed to the initiation, progression, pathology, and treatment outcomes of the curvature. A systematic search was conducted on four online databases, including PubMed, Web of Science, Embase, and Academic search complete. Studies were included if they involved human or animal subjects with idiopathic scoliosis and evaluated with proprioceptive genes. The search period was the inception of the database to February 21, 2023. Four genes (i.e., Ladybird homeobox 1 [LBX1], Piezo type mechanosensitive ion channel component 2 [PIEZO2], Runx family transcription factor 3 [RUNX3], and neurotrophin 3 [NTF3]) investigated in 19 studies were included. LBX1 has confirmed the correlation with the development of idiopathic scoliosis in 10 ethnicities, whereas PIEZO2 has shown a connection with clinical proprioceptive tests in subjects with idiopathic scoliosis. However, curve severity was less likely to be related to the proprioceptive genes. The potential pathology took place at the proprioceptive neurons. Evidence of proprioception-related gene mutations in association with idiopathic scoliosis was established. Nevertheless, the causation between the initiation, progression, and treatment outcomes with proprioceptive defect requires further investigation. Since idiopathic scoliosis is a multifactorial disorder, the proprioceptive defect is considered one of its etiological factors. Genetic studies have separately revealed this relationship, yet it remains indeterminate which specific genes that related to proprioception contributed to the initiation, progression, pathology, and treatment outcomes of the curvature. A systematic search was conducted on four online databases, including PubMed, Web of Science, Embase, and Academic search complete. Studies were included if they involved human or animal subjects with idiopathic scoliosis and evaluated with proprioceptive genes. The search period was the inception of the database to February 21, 2023. Four genes (i.e., Ladybird homeobox 1 [LBX1], Piezo type mechanosensitive ion channel component 2 [PIEZO2], Runx family transcription factor 3 [RUNX3], and neurotrophin 3 [NTF3]) investigated in 19 studies were included. LBX1 has confirmed the correlation with the development of idiopathic scoliosis in 10 ethnicities, whereas PIEZO2 has shown a connection with clinical proprioceptive tests in subjects with idiopathic scoliosis. However, curve severity was less likely to be related to the proprioceptive genes. The potential pathology took place at the proprioceptive neurons. Evidence of proprioception‐related gene mutations in association with idiopathic scoliosis was established. Nevertheless, the causation between the initiation, progression, and treatment outcomes with proprioceptive defect requires further investigation. |
Author | Lau, Kenney K. L. Kwan, Kenny Y. H. Cheung, Kenneth M. C. Cheung, Jason P. Y. Law, Karlen K. P. |
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Cites_doi | 10.1016/j.spinee.2015.05.013 10.1371/journal.pgen.1005802 10.3389/fcell.2021.777890 10.1146/annurev-biochem-081720-023244 10.1097/BRS.0b013e31823e5890 10.1038/nrdp.2015.30 10.1097/BRS.0000000000002111 10.1126/science.1193270 10.1038/jhg.2012.11 10.1097/BRS.0000000000003224 10.1371/journal.pone.0053234 10.1007/s00586-012-2532-4 10.2106/JBJS.18.01370 10.1016/j.spinee.2015.01.019 10.1242/jcs.011668 10.1016/j.spinee.2018.10.009 10.1038/s41467-021-21173-9 10.1371/journal.pone.0117708 10.1016/j.devcel.2017.07.022 10.1097/BRS.0000000000002866 10.32725/jab.2019.011 10.1038/1757 10.1056/NEJMoa1307337 10.1177/21925682211066824 10.1038/s41467-020-16971-6 10.3390/genes13091556 10.1097/BRS.0b013e3181bcc835 10.1016/S0896-6273(02)00689-X 10.1038/ncomms9355 10.1302/0301-620X.104B8.BJJ-2021-1638.R1 10.1016/j.spinee.2019.06.014 10.1038/nn.4162 10.1097/BPO.0000000000001808 10.2174/138920208783884874 10.1177/1545968315573055 10.1016/S0896-6273(02)00690-6 10.1038/ng.974 10.1186/1749-8104-3-20 10.1097/BRS.0000000000002280 10.1007/s00586-022-07338-0 10.1016/j.conb.2022.102572 10.1152/physrev.00048.2011 |
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Keywords | aetiology idiopathic scoliosis genetics pathology proprioceptive defect proprioceptive deficit |
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Title | Proprioception‐related gene mutations in relation to the aetiopathogenesis of idiopathic scoliosis: A scoping review |
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