Transforming Growth Factor-Beta3 Gene Polymorphisms and Nonsyndromic Cleft Lip and Palate Risk: A Meta-Analysis

被引:13
作者
Tang, Mingrui [1 ]
Wang, Yuxin [1 ]
Han, Siyuan [1 ]
Guo, Shu [1 ]
Wang, Di [1 ]
机构
[1] China Med Univ, Hosp 1, Dept Plast Surg, Shenyang 110001, Liaoning Provin, Peoples R China
关键词
EXTRACELLULAR-MATRIX; AND/OR PALATE; FACTOR-BETA; ASSOCIATION; POPULATION; SUSCEPTIBILITY; HETEROGENEITY; PATHOGENESIS; JAPANESE; TGFB3;
D O I
10.1089/gtmb.2013.0334
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aims: To investigate the association between transforming growth factor-beta3 (TGF-3) genetic polymorphisms and nonsyndromic cleft lip and palate (NSCLP) risk. Methods: An extensive literature search for relevant studies was conducted on PubMed, Embase, Web of Science, Cochrane Library, and CBM databases from their inception through June 1st, 2013. Case-control studies addressing the correlation between TGF-3 gene polymorphisms and NSCLP risk. The genotype distribution of the controls should conform to Hardy-Weinberg equilibrium. The quality of the included studies was assessed independently by two authors based on the Newcastle-Ottawa scale. All analyses were calculated using the STATA 12.0 software. Results: The association between TGF-3 gene polymorphisms and NSCLP risk was assessed. Eleven case-control studies were included with a total of 1601 NSCLP cases and 1463 healthy controls. Our meta-analysis results indicated that mutant variants of the TGF-3 gene may be associated with an increased risk of NSCLP, especially among Asian populations. Further subgroup analyses also revealed significant associations between mutant variants of the TGF-3 gene and an increased risk of NSCLP in the population-based and polymerase chain reaction-restriction fragment length polymorphism studies. Meta-regression analyses showed that ethnicity may be a major source of heterogeneity. Conclusion: Our meta-analysis suggests that TGF-3 gene polymorphisms may contribute to NSCLP susceptibility, especially among Asian populations.
引用
收藏
页码:881 / 889
页数:9
相关论文
共 49 条
[1]  
Britto JA, 2002, CLEFT PALATE-CRAN J, V39, P332, DOI 10.1597/1545-1569(2002)039<0332:TPOACP>2.0.CO
[2]  
2
[3]  
Carinci P, 2007, EUR J HISTOCHEM, V51, P105
[4]   Genetic analysis of the mammalian transforming growth factor-β superfamily [J].
Chang, H ;
Brown, CW ;
Matzuk, MM .
ENDOCRINE REVIEWS, 2002, 23 (06) :787-823
[5]  
Ciminello Frank S., 2009, Comprehensive Therapy, V35, P37
[6]   The complex genetics of cleft lip and palate [J].
Cobourne, MT .
EUROPEAN JOURNAL OF ORTHODONTICS, 2004, 26 (01) :7-16
[7]   Overexpression of Smad2 in Tgf-β3-null mutant mice rescues cleft palate [J].
Cui, XM ;
Shiomi, N ;
Chen, JC ;
Saito, T ;
Yamamoto, T ;
Ito, Y ;
Bringas, P ;
Chat, Y ;
Shuler, CF .
DEVELOPMENTAL BIOLOGY, 2005, 278 (01) :193-202
[8]   Uses and misuses of the STROBE statement: bibliographic study [J].
da Costa, Bruno R. ;
Cevallos, Myriam ;
Altman, Douglas G. ;
Rutjes, Anne W. S. ;
Egger, Matthias .
BMJ OPEN, 2011, 1 (01)
[9]   Cleft lip and palate: understanding genetic and environmental influences [J].
Dixon, Michael J. ;
Marazita, Mary L. ;
Beaty, Terri H. ;
Murray, Jeffrey C. .
NATURE REVIEWS GENETICS, 2011, 12 (03) :167-178
[10]   Common variation in the CETP gene and the implications for cardiovascular disease and its treatment:: an updated analysis [J].
Dullaart, Robin P. F. ;
Sluiter, Wim J. .
PHARMACOGENOMICS, 2008, 9 (06) :747-763