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BioMed Research International
Volume 2017 (2017), Article ID 3681645, 7 pages
https://doi.org/10.1155/2017/3681645
Research Article

A Study of IL-1β, MMP-3, TGF-β1, and GDF5 Polymorphisms and Their Association with Primary Frozen Shoulder in a Chinese Han Population

Department of Orthopedics, Jinling Hospital, Southern Medical University, 305 Zhongshan East Road, Nanjing, Jiangsu 210002, China

Correspondence should be addressed to Nirong Bao; moc.anis@rnbrnb

Received 15 March 2017; Revised 22 April 2017; Accepted 8 May 2017; Published 6 June 2017

Academic Editor: Sae H. Kim

Copyright © 2017 Wenxiang Chen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. T. D. Bunker, “Frozen shoulder: Unravelling the enigma,” Annals of the Royal College of Surgeons of England, vol. 79, no. 3, pp. 210–213, 1997. View at Google Scholar · View at Scopus
  2. G. C. R. Hand, N. A. Athanasou, T. Matthews, and A. J. Carr, “The pathology of frozen shoulder,” Journal of Bone and Joint Surgery B, vol. 89, no. 7, pp. 928–932, 2007. View at Publisher · View at Google Scholar · View at Scopus
  3. J. D. Zuckerman and A. Rokito, “Frozen shoulder: A consensus definition,” Journal of Shoulder and Elbow Surgery, vol. 20, no. 2, pp. 322–325, 2011. View at Publisher · View at Google Scholar · View at Scopus
  4. K. Tamai, M. Akutsu, and Y. Yano, “Primary frozen shoulder: brief review of pathology and imaging abnormalities,” Journal of Orthopaedic Science, vol. 19, no. 1, pp. 1–5, 2014. View at Publisher · View at Google Scholar · View at Scopus
  5. J. P. Yoon, S. W. Chung, J.-E. Kim et al., “Intra-articular injection, subacromial injection, and hydrodilatation for primary frozen shoulder: A randomized clinical trial,” Journal of Shoulder and Elbow Surgery, vol. 25, no. 3, pp. 376–383, 2016. View at Publisher · View at Google Scholar · View at Scopus
  6. C. Hand, K. Clipsham, J. L. Rees, and A. J. Carr, “Long-term outcome of frozen shoulder,” Journal of Shoulder and Elbow Surgery, vol. 17, no. 2, pp. 231–236, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. T. D. Bunker, J. Reilly, K. S. Baird, D. L. Hamblen et al., “Expression of growth factors, cytokines and matrix metalloproteinases in frozen shoulder,” Journal of Bone and Joint Surgery - Series B, vol. 82, no. 5, pp. 768–773, 2000. View at Publisher · View at Google Scholar · View at Scopus
  8. T. A. Blaine, Y.-S. Kim, I. Voloshin et al., “The molecular pathophysiology of subacromial bursitis in rotator cuff disease,” Journal of Shoulder and Elbow Surgery, vol. 14, no. 1, pp. S84–S89, 2005. View at Publisher · View at Google Scholar · View at Scopus
  9. S. A. Rodeo, J. A. Hannafin, J. Tom, R. F. Warren, and T. L. Wickiewicz, “Immunolocalization of cytokines and their receptors in adhesive capsulitis of the shoulder,” Journal of Orthopaedic Research, vol. 15, no. 3, pp. 427–436, 1997. View at Publisher · View at Google Scholar · View at Scopus
  10. Y.-M. Lho, E. Ha, C.-H. Cho et al., “Inflammatory cytokines are overexpressed in the subacromial bursa of frozen shoulder,” Journal of Shoulder and Elbow Surgery, vol. 22, no. 5, pp. 666–672, 2013. View at Publisher · View at Google Scholar · View at Scopus
  11. B. Kabbabe, S. Ramkumar, and M. Richardson, “Cytogenetic analysis of the pathology of frozen shoulder,” International Journal of Shoulder Surgery, vol. 4, no. 3, pp. 75–78, 2010. View at Publisher · View at Google Scholar · View at Scopus
  12. B. Saccomanni, “Inflammation and shoulder pain - A perspective on rotator cuff disease, adhesive capsulitis, and osteoarthritis: Conservative treatment,” Clinical Rheumatology, vol. 28, no. 5, pp. 495–500, 2009. View at Publisher · View at Google Scholar · View at Scopus
  13. K. Cajanus, E. J. Holmström, M. Wessman, V. Anttila, M. A. Kaunisto, and E. Kalso, “Effect of endocannabinoid degradation on pain: Role of FAAH polymorphisms in experimental and postoperative pain in women treated for breast cancer,” Pain, vol. 157, no. 2, pp. 361–369, 2016. View at Publisher · View at Google Scholar · View at Scopus
  14. H. Hou, K. Zheng, G. Wang et al., “Influence of intra-articular administration of trichostatin a on autologous osteochondral transplantation in a rabbit model,” BioMed Research International, vol. 2015, Article ID 470934, 2015. View at Publisher · View at Google Scholar · View at Scopus
  15. M. Hanabayashi, N. Takahashi, Y. Sobue et al., “Hyaluronan oligosaccharides induce MMP-1 and -3 via transcriptional activation of NF-κB and p38 MAPK in rheumatoid synovial fibroblasts,” PloS One, vol. 11, no. 8, p. e0161875, 2016. View at Publisher · View at Google Scholar
  16. S. M. Raleigh, L. Van Der Merwe, W. J. Ribbans, R. K. W. Smith, M. P. Schwellnus, and M. Collins, “Variants within the MMP3 gene are associated with Achilles tendinopathy: Possible interaction with the COL5A1 gene,” British Journal of Sports Medicine, vol. 43, no. 7, pp. 514–520, 2009. View at Publisher · View at Google Scholar · View at Scopus
  17. R. Menezes-Silva, S. Khaliq, K. Deeley, A. Letra, and A. R. Vieira, “Genetic susceptibility to periapical disease: Conditional contribution of MMP2 and MMP3 genes to the development of periapical lesions and healing response,” Journal of Endodontics, vol. 38, no. 5, pp. 604–607, 2012. View at Publisher · View at Google Scholar · View at Scopus
  18. T. D. Bunker and P. P. Anthony, “The pathology of frozen shoulder. A dupuytren-like disease,” Journal of Bone and Joint Surgery - Series B, vol. 77, no. 5, pp. 677–683, 1995. View at Google Scholar · View at Scopus
  19. A. M. T. Lubis and V. K. Lubis, “Matrix metalloproteinase, tissue inhibitor of metalloproteinase and transforming growth factor-beta 1 in frozen shoulder, and their changes as response to intensive stretching and supervised neglect exercise,” Journal of Orthopaedic Science, vol. 18, no. 4, pp. 519–527, 2013. View at Publisher · View at Google Scholar · View at Scopus
  20. J. W. Hutchinson, G. M. Tierney, S. L. Parsons, and T. R. C. Davis, “Dupuytren's disease and frozen shoulder induced by treatment with a matrix metalloproteinase inhibitor,” Journal of Bone and Joint Surgery - Series B, vol. 80, no. 5, pp. 907-908, 1998. View at Publisher · View at Google Scholar · View at Scopus
  21. B. Li, A. Khanna, V. Sharma, T. Singh, M. Suthanthiran, and P. August, “TGF-β1 DNA polymorphisms, protein levels, and blood pressure,” Hypertension, vol. 33, no. 1, pp. 271–275, 1999. View at Publisher · View at Google Scholar · View at Scopus
  22. J.-Y. Chen, J.-H. Liu, H.-D. I. Wu, K.-H. Lin, K.-C. Chang, and Y.-M. Liou, “Transforming growth factor-β1 T869C gene polymorphism is associated with acquired sick sinus syndrome via linking a higher serum protein level,” PLoS ONE, vol. 11, no. 7, Article ID e0158676, 2016. View at Publisher · View at Google Scholar · View at Scopus
  23. G. M. Risinger Jr., D. L. Updike, E. C. Bullen, J. J. Tomasek, and E. W. Howard, “TGF-β suppresses the upregulation of MMP-2 by vascular smooth muscle cells in response to PDGF-BB,” American Journal of Physiology - Cell Physiology, vol. 298, no. 1, pp. C191–C201, 2010. View at Publisher · View at Google Scholar · View at Scopus
  24. R. J. Egli, L. Southam, J. M. Wilkins et al., “Functional analysis of the osteoarthritis susceptibility-associated GDF5 regulatory polymorphism,” Arthritis and Rheumatism, vol. 60, no. 7, pp. 2055–2064, 2009. View at Publisher · View at Google Scholar · View at Scopus
  25. Y.-C. Lee, S.-Y. Hung, H.-H. Liou et al., “Vitamin D Can Ameliorate Chlorhexidine Gluconate-Induced Peritoneal Fibrosis and Functional Deterioration through the Inhibition of Epithelial-to-Mesenchymal Transition of Mesothelial Cells,” BioMed Research International, vol. 2015, Article ID 595030, 2015. View at Publisher · View at Google Scholar · View at Scopus
  26. H. Date, T. Furumatsu, Y. Sakoma et al., “GDF-5/7 and bFGF activate integrin α2-mediated cellular migration in rabbit ligament fibroblasts,” Journal of Orthopaedic Research, vol. 28, no. 2, pp. 225–231, 2010. View at Publisher · View at Google Scholar · View at Scopus
  27. T. Mikami, A. Meguro, and T. Teshigawara, “Interleukin 1 beta promoter polymorphism is associated with keratoconus in a japanese population,” Molecular Vision, vol. 19, no. 4, pp. 845–851, 2013. View at Google Scholar
  28. A. Letra, R. M. Silva, R. J. Rylands et al., “MMP3 and TIMP1 variants contribute to chronic periodontitis and may be implicated in disease progression,” Journal of Clinical Periodontology, vol. 39, no. 8, pp. 707–716, 2012. View at Publisher · View at Google Scholar · View at Scopus
  29. F. M. K. Williams, M. Popham, D. J. Hart et al., “GDF5 single-nucleotide polymorphism rs143383 is associated with lumbar disc degeneration in Northern European women,” Arthritis and Rheumatism, vol. 63, no. 3, pp. 708–712, 2011. View at Publisher · View at Google Scholar · View at Scopus
  30. G. Gokalp, O. Algin, N. Yildirim, and Z. Yazici, “Adhesive capsulitis: Contrast-enhanced shoulder MRI findings,” Journal of Medical Imaging and Radiation Oncology, vol. 55, no. 2, pp. 119–125, 2011. View at Publisher · View at Google Scholar · View at Scopus
  31. Z. Wang, Z. Qu, C. Fu et al., “Interleukin 1 polymorphisms contribute to intervertebral disc degeneration risk: A meta-analysis,” PLoS ONE, vol. 11, no. 6, Article ID e0156412, 2016. View at Publisher · View at Google Scholar · View at Scopus
  32. R. Patel, M. Dwivedi, M. S. Mansuri et al., “Association of Neuropeptide-Y (NPY) and Interleukin-1beta (IL1B), Genotype-Phenotype Correlation and Plasma Lipids with Type-II Diabetes,” PloS One, vol. 11, no. 10, p. e0164437, 2016. View at Publisher · View at Google Scholar
  33. J. Loughlin, B. Dowling, Z. Mustafa, and K. Chapman, “Association of the interleukin-1 gene cluster on chromosome 2q13 with knee osteoarthritis,” Arthritis and Rheumatism, vol. 46, no. 6, pp. 1519–1527, 2002. View at Publisher · View at Google Scholar · View at Scopus
  34. X. Wang, F. Jiang, Y. Liang et al., “Interleukin-1β-31C/T and -511T/C polymorphisms were associated with preeclampsia in chinese Han population,” PLoS ONE, vol. 9, no. 9, Article ID e106919, 2014. View at Publisher · View at Google Scholar · View at Scopus
  35. J. Y. Ban, M. K. Kim, S. W. Park, and K. H. Kwon, “Interleukin-1 beta polymorphisms are associated with lymph node metastasis in korean patients with papillary thyroid carcinoma,” Immunological Investigations, vol. 41, no. 8, pp. 888–905, 2012. View at Publisher · View at Google Scholar · View at Scopus
  36. J. H. Cho, J. S. Choi, S. W. Chun, S. Lee, K. J. Han, and H. M. Kim, “The IL-1B genetic polymorphism is associated with aspirin-induced peptic ulcers in a Korean ethnic group,” Gut and Liver, vol. 10, no. 3, pp. 362–368, 2016. View at Publisher · View at Google Scholar · View at Scopus
  37. Q. Xu, P. Y. Gai, H. L. Lv, G. R. Li, and X. Y. Liu, “Association of MMP3 genotype with susceptibility to frozen shoulder: A case-control study in a Chinese Han population,” Genetics and Molecular Research, vol. 15, no. 1, 2016. View at Publisher · View at Google Scholar · View at Scopus
  38. M. P. S. Sie, A. G. Uitterlinden, M. J. Bos et al., “TGF-β1 polymorphisms and risk of myocardial infarction and stroke: The Rotterdam study,” Stroke, vol. 37, no. 11, pp. 2667–2671, 2006. View at Publisher · View at Google Scholar · View at Scopus
  39. P. Raina, R. Sikka, R. Kaur et al., “Association of transforming growth factor beta-1 (TGF-β1) genetic variation with type 2 diabetes and end stage renal disease in two large population samples from North India,” OMICS A Journal of Integrative Biology, vol. 19, no. 5, pp. 306–317, 2015. View at Publisher · View at Google Scholar · View at Scopus