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Scoliosis

, 7:O71 | Cite as

Genetic aspects of idiopathic scoliosis – literature review

  • P Janusz
  • T Kotwicki
  • K Małgorzata
  • A Szulc
Open Access
Oral presentation

Keywords

Estrogen Receptor Tryptophan Melatonin Genetic Background Gene Polymorphism 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Purpose of the study

The purpose of this study was to review relevant literature describing polymorphisms of genes associated to idiopathic scoliosis. Etiology of idiopathic scoliosis (IS) remains unrevealed, however genetic background is strongly advocated. Loci on chromosomes and genes polymorphisms associated to occurrence and progression of IS were the subject of research.

Materials and methods

Medline, Embase and Cochrane Library electronic databases were searched from 1990 till 2010. The search was limited to English language. The following key words were used: idiopathic scoliosis, gene, genetics, chromosome. Based on the abstract, the relevance of each article was assessed, then full-text articles were obtained [1, 2, 3, 4, 5].

Results

558 abstracts were identified, 51 full texts were obtained and 18 were analyzed. The genes polymorphisms with the evidence of association to occurrence or progression of IS were identified. Both the papers confirming or denying genetic background of IS were found. The genes presenting polymorphisms susceptible to be related to IS were as follows: estrogen receptors (ER), melatonin receptors (MTNR), matrilin (MATNI), chromodomain helicase DNA-binding protein (CHD7), interleukin-6 (IL-6), metalloproteinases (MMP-3), γ1-syntrophin (SNTG1), aggrecan, tryptophan hydroxylase 1 (TPH1), arylalkylamine N-acetyltransferase (AANAT), growth hormone receptor (GHR), collagen and elastic fibers genes. Up to now seven of the above mentioned could be excluded while others are subject of further investigation.

Conclusion

There is still insufficient data about the genetic origin and development of IS. The amount and quality of the existing publications increases, suggesting possible discovery of genetic background and understanding of molecular course of IS.

References

  1. 1.
    Ward K, Ogilvie JW, Singleton MV, Chettier R, Engler G, Nelson LM: Validation of DNA-based prognostic testing to predict spinal curve progression in adolescent idiopathic scoliosis. Spine. 2010, 35 (25): E1455-64. 10.1097/BRS.0b013e3181ed2de1.CrossRefPubMedGoogle Scholar
  2. 2.
    Takahashi Y, Matsumoto M, Karasugi T, Watanabe K, Chiba K, Kawakami N, Tsuji T, Uno K, Suzuki T, Ito M, Sudo H, Minami S, Kotani T, Kono K, Yanagida H, Taneichi H, Takahashi A, Toyama Y, Ikegawa S: Replication study of the association between adolescent idiopathic scoliosis and two estrogen receptor genes. J Orthop Res. 2011, 29 (6): 834-7. 10.1002/jor.21322.CrossRefPubMedGoogle Scholar
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    Gao X, Gordon D, Zhang D, Browne R, Helms C, Gillum J, Weber S, Devroy S, Swaney S, Dobbs M, Morcuende J, Sheffield V, Lovett M, Bowcock A, Herring J, Wise C: CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. Am J Hum Genet. 2007, 80 (5): 957-65. 10.1086/513571.PubMedCentralCrossRefPubMedGoogle Scholar
  4. 4.
    Takahashi Y, Matsumoto M, Karasugi T, Watanabe K, Chiba K, Kawakami N, Tsuji T, Uno K, Suzuki T, Ito M, Sudo H, Minami S, Kotani T, Kono K, Yanagida H, Taneichi H, Takahashi A, Toyama Y, Ikegawa S: Lack of association between adolescent idiopathic scoliosis and previously reported single nucleotide polymorphisms in MATN1, MTNR1B, TPH1, and IGF1 in a Japanese population. J Orthop Res. 2011, 29 (7): 1055-8. 10.1002/jor.21347.CrossRefPubMedGoogle Scholar
  5. 5.
    Mórocz M, Czibula A, Grózer ZB, Szécsényi A, Almos PZ, Raskó I, Illés T: Association study of BMP4, IL6, Leptin, MMP3, and MTNR1B gene promoter polymorphisms and adolescent idiopathic scoliosis. Spine. 2011, 36 (2): E123-30. 10.1097/BRS.0b013e318a511b0e.CrossRefPubMedGoogle Scholar

Copyright information

© Janusz et al; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Authors and Affiliations

  • P Janusz
    • 1
  • T Kotwicki
    • 1
  • K Małgorzata
    • 2
  • A Szulc
    • 1
  1. 1.Spine Disorders Unit Department of Pediatric Orthopedics and Traumatology University of Medical SciencesPoznanPoland
  2. 2.Department of Cell Biology University of Medical SciencesPoznanPoland

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