The effect of genetical factors on the risk of carpal tunnel syndrome occurrence: a review

1 Puchalski P, Żyluk P, Szlosser Z, Żyluk A. Factors involved in the clinical profile of carpal tunnel syndrome. Handchir Mikrochir Plast Chir 2018;50(1):8-13. Search in Google Scholar

2 Gossett JG, Chance PF. Is there a familial carpal tunnel syndrome? An evaluation and literature review. Muscle Nerve 1998;21(11):1533-6. Search in Google Scholar

3 Żyluk A. The role of genetic factors in the carpal tunnel syndrome etiology: a review. Adv Clin Exp Med 2020;29(5):623-8. doi: 10.17219/acem/118846. Search in Google Scholar

4 Hakim AJ, Cherkas L, El Zayat S, MacGregor AJ, Spector TD. The genetic contribution to carpal tunnel syndrome in women: a twin study. Arthritis Rheum 2002;47(3):275-9. Search in Google Scholar

5 Wiberg A, Ng M, Schmid AB, Smillie RW, Baskozos G, Holmes MV, et al. A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome. Nat Commun 2019;10(1):1030. doi: 10.1038/s41467-019-08993-6. Search in Google Scholar

6 Pasternak B, Aspenberg P. Metalloproteinases and their inhibitors – diagnostic and therapeutic opportunities in orthopaedics. Acta Orthop 2009;80(6):693-703. Search in Google Scholar

7 Burger MC, De Wet H, Collins M. Matrix metalloproteinase genes on chromosome 11q22 and risk of carpal tunnel syndrome. Rheumatol Int 2016;36(3):413-9. doi: 10.1007/s00296-015-3385-z. Search in Google Scholar

8 Raleigh SM, van der Merwe L, Ribbans WJ, Smith RKW, Schwellnus MP, Collins M. Variants within the MMP3 gene are associated with Achilles tendinopathy: possible interaction with the COL5A1 gene. Br J Sports Med 2009;43(7):514-20. Search in Google Scholar

9 Posthumus M, Collins M, van der Merwe L, O’Cuinneagain D, van der Merwe W, Ribbans WJ, et al. Matrix metalloproteinase genes on chromosome 11q22 and the risk of anterior cruciate ligament (ACL) rupture. Scand J Med Sci Sports 2012;22(4):523-33. Search in Google Scholar

10 Somerville RPT, Oblader SA, Apte SS. Matrix metalloproteinases: old dogs with new tricks. Genome Biol 2003;4(6):216. doi: 10.1186/gb-2003-4-6-216. Search in Google Scholar

11 Shah MH, Bhat V, Shetty JS, Kumar A. Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome. Mol Vis 2014;20:790-6. Search in Google Scholar

12 Eldridge CF, Bunge MB, Bunge RP. Differentiation of axon-related Schwann cells in vitro: II. Control of myelin formation by basal lamina. J Neurosci 1989;9(2):625-38. Search in Google Scholar

13 Lin YJ, Liao WL, Wang CH, Tsai LP, Tang CH, Chen CH, et al. Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan. Sci Rep 2017;7(1):6372. Search in Google Scholar

14 Hay M, Patricios J, Collins R, Branfield A, Cook J, Handley CJ, et al. Association of type XI collagen genes with chronic Achilles tendinopathy in independent populations form South Africa and Australia. Br J Sports Med 2013;47(9):569-74. Search in Google Scholar

15 Mio F, Chiba K, Hirose Y, Kawaguchi Y, Mikami Y, Oya T, et al. A functional polymorphism in COL11A1, which encodes the alpha 1 chain of type XI collagen, is associated with susceptibility to lumbar disc herniation. Am J Hum Genet 2007:81(6):1271-7. Search in Google Scholar

16 Dada S, Burger MC, Massij F, de Wet H, Collins M. Carpal tunnel syndrome: The role of collagen gene variants. Gene 2016;578(1):53-8. doi: 10.1016/j. gene.2016.04.030. Search in Google Scholar

17 Ficek K, Cieszyk P, Kaczmarczyk M, Maciejewska-Karłowska A, Sawczuk M, Cholewinski J, et al. Gene variants within the COL1A1 gene are associated with reduced anterior cruciate ligament injury in professional soccer players. J Sci Med Sport 2013;16(5):396-400. Search in Google Scholar

18 Li C, Wang N, Schäffer AA, Liu X, Zhao Z, Elliott G, et al. Mutations in COMP cause familial carpal tunnel syndrome. Nat Commun 2020;11(1):3642. doi: 10.1038/s41467-020-17378-z. Search in Google Scholar