Association of a single nucleotide polymorphism in Tbx4 with developmental dysplasia of the hip: A case-control study

Osteoarthritis and Cartilage

Volumn 18, Issue 12, 2010, Pages 1592-1595

  Wang, K ^a,b   Shi, D ^b   Zhu, P ^c   Dai, J ^b   Zhu, L ^b   Zhu, H ^c   Lv, Y ^a,b   Zhao, B ^c   Jiang, Q ^a,b  

^a NANJING MEDICAL UNIVERSITY   (China)

^b NANJING UNIVERSITY   (China)

^c Kang'ai Hospital   (China)

Author keywords

Developmental dysplasia of the hip; Polymorphism; Tbx4

Indexed keywords

CYSTEINE; GLYCINE; T BOX TRANSCRIPTION FACTOR; T BOX TRANSCRIPTION FACTOR TBX4; UNCLASSIFIED DRUG;

ADULT; AGED; ALLELE; ARTICLE; CASE CONTROL STUDY; CHILD; CHINESE; CONTROLLED STUDY; DEVELOPMENTAL DYSPLASIA OF THE HIP; DISEASE SEVERITY; GENDER; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC MODEL; GENOTYPE; HIP DISLOCATION; HIP DYSPLASIA; HUMAN; INFANT; JOINT INSTABILITY; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SUBLUXATION;

CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HIP DISLOCATION, CONGENITAL; HUMANS; INFANT; JOINT INSTABILITY; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEX FACTORS; T-BOX DOMAIN PROTEINS;

EID: 78649692441     PISSN: 10634584     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.joca.2010.09.008     Document Type: Article

References (28)

1. Weinstein S.L. Natural history of congenital hip dislocation (CDH) and hip dysplasia. Clin Orthop Relat Res 1987, 62-76.
2. Sollazzo V., Bertolani G., Calzolari E., Atti G., Scapoli C. A two-locus model for non-syndromic congenital dysplasia of the hip (CDH). Ann Hum Genet 2000, 64:51-59.
3. Carter C., Wilkinson J. Persistent joint laxity and congenital dislocation of the hip. J Bone Joint Surg Br 1964, 46:40-45.
4. Bialik V., Bialik G.M., Blazer S., Sujov P., Wiener F., Berant M. Developmental dysplasia of the hip: a new approach to incidence. Pediatrics 1999, 103:93-99.
5. Laurence M., Harper P.S., Harris R., Nevin N.C., Roberts D.F. Report of the delegation of clinical geneticists to China, Spring 1986. Biol Soc 1987, 4:61-77.
6. Jacobsen S., Sonne-Holm S. Hip dysplasia: a significant risk factor for the development of hip osteoarthritis. A cross-sectional survey. Rheumatology (Oxford) 2005, 44:211-218.
7. Lane N.E., Lin P., Christiansen L., Gore L.R., Williams E.N., Hochberg M.C., et al. Association of mild acetabular dysplasia with an increased risk of incident hip osteoarthritis in elderly white women: the study of osteoporotic fractures. Arthritis Rheum 2000, 43:400-404.
8. Reijman M., Hazes J.M., Pols H.A., Koes B.W., Bierma-Zeinstra S.M. Acetabular dysplasia predicts incident osteoarthritis of the hip: the Rotterdam study. Arthritis Rheum 2005, 52:787-793.
9. Stevenson D.A., Mineau G., Kerber R.A., Viskochil D.H., Schaefer C., Roach J.W. Familial predisposition to developmental dysplasia of the hip. J Pediatr Orthop 2009, 29:463-466.
10. Chan A., McCaul K.A., Cundy P.J., Haan E.A., Byron-Scott R. Perinatal risk factors for developmental dysplasia of the hip. Arch Dis Child Fetal Neonatal Ed 1997, 76:F94-F100.
11. Stein-Zamir C., Volovik I., Rishpon S., Sabi R. Developmental dysplasia of the hip: risk markers, clinical screening and outcome. Pediatr Int 2008, 50:341-345.
12. Mabuchi A., Nakamura S., Takatori Y., Ikegawa S. Familial osteoarthritis of the hip joint associated with acetabular dysplasia maps to chromosome 13q. Am J Hum Genet 2006, 79:163-168.
13. Dai J., Shi D., Zhu P., Qin J., Ni H., Xu Y., et al. Association of a single nucleotide polymorphism in growth differentiate factor 5 with congenital dysplasia of the hip: a case-control study. Arthritis Res Ther 2008, 10:R126.
14. Schulte-Merker S., van Eeden F.J., Halpern M.E., Kimmel C.B., Nusslein-Volhard C. no tail (ntl) is the zebrafish homologue of the mouse T (Brachyury) gene. Development 1994, 120:1009-1015.
15. Naiche L.A., Papaioannou V.E. Loss of Tbx4 blocks hindlimb development and affects vascularization and fusion of the allantois. Development 2003, 130:2681-2693.
16. Isaac A., Rodriguez-Esteban C., Ryan A., Altabef M., Tsukui T., Patel K., et al. Tbx genes and limb identity in chick embryo development. Development 1998, 125:1867-1875.
17. Bongers E.M., Duijf P.H., van Beersum S.E., Schoots J., Van Kampen A., Burckhardt A., et al. Mutations in the human TBX4 gene cause small patella syndrome. Am J Hum Genet 2004, 74:1239-1248.
18. Naiche L.A., Papaioannou V.E. Tbx4 is not required for hindlimb identity or post-bud hindlimb outgrowth. Development 2007, 134:93-103.
19. Sherk H.H., Pasquariello P.S., Watters W.C. Congenital dislocation of the hip. a review. Clin Pediatr (Phila) 1981, 20:513-520.
20. Walsh P.S., Metzger D.A., Higuchi R. Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material. Biotechniques 1991, 10:506-513.
21. Ceylaner G., Ceylaner S., Ustunkan F., Inan M. Autosomal dominant inheritance of congenital dislocation of the hip in 16 members of a family. Acta Orthop Traumatol Turc 2008, 42:289-291.
22. Kapoor B., Dunlop C., Wynn-Jones C., Fryer A.A., Strange R.C., Maffulli N. Vitamin D and oestrogen receptor polymorphisms in developmental dysplasia of the hip and primary protrusio acetabuli - a preliminary study. J Negat Results Biomed 2007, 6:7.
23. Jiang J., Ma H.W., Li Q.W., Lu J.F., Niu G.H., Zhang L.J., et al. Association analysis on the polymorphisms of PCOL2 and Sp1 binding sites of COL1A1 gene and the congenital dislocation of the hip in Chinese population. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2005, 22:327-329.
24. Krause A., Zacharias W., Camarata T., Linkhart B., Law E., Lischke A., et al. Tbx5 and Tbx4 transcription factors interact with a new chicken PDZ-LIM protein in limb and heart development. Dev Biol 2004, 273:106-120.
25. Cebra-Thomas J.A., Bromer J., Gardner R., Lam G.K., Sheipe H., Gilbert S.F. T-box gene products are required for mesenchymal induction of epithelial branching in the embryonic mouse lung. Dev Dyn 2003, 226:82-90.
26. Kelemen L.E., Wang X., Fredericksen Z.S., Pankratz V.S., Pharoah P.D., Ahmed S., et al. Genetic variation in the chromosome 17q23 amplicon and breast cancer risk. Cancer Epidemiol Biomarkers Prev 2009, 18:1864-1868.
27. Qi T., Han J., Cui Y., Zong M., Liu X., Zhu B. Comparative proteomic analysis for the detection of biomarkers in pancreatic ductal adenocarcinomas. J Clin Pathol 2008, 61:49-58.
28. Wacholder S., Chanock S., Garcia-Closas M., El Ghormli L., Rothman N. Assessing the probability that a positive report is false: an approach for molecular epidemiology studies. J Natl Cancer Inst 2004, 96:434-442.