Analytical and Quantitative Cytopathology and Histopathology
2018, Volume 40, Issue 4
Research Article
Association of 2 polymorphisms in transforming growth factor beta 1 and their effect on the risk of acute liver graft rejection
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1
Department of Gastroenterology, Southern Medical University, Guangzhou, Guangdong, China
2
Department of Gastroenterology and Hepatology, Guangdong Provincial People’s Hospital of Southern Medical University, Guangzhou, Guangdong, China
3
Department of Gastroenterology and Hepatology, Jiujiang No. 1 People's Hospital, Jiujiang, Jiangxi, China
4
Department of Anesthesiology, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei, China
5
Department of Otorhinolaryngology, Hubei Provincial Hospital of Integrated Chinese and Western Medicine, Wuhan, Hubei, China
6
Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, United States
Abstract
OBJECTIVE: To investigate the association of the transforming growth factor beta 1 (TGF-β1) polymorphism with acute liver graft rejection (AR) and to conduct a comprehensive analysis encompassing all relevant studies, which have shown conflicting results over the past years. STUDY DESIGN: A systematic literature was done for articles assessing the association between TGF-β1 polymorphism and AR. The OR and 95% CI were applied to investigate the strength of the associations. RESULTS: Overall, the pooled analysis showed a null association between TGF-T869C and AR, with ORs (95% CIs) of 1.13 (0.60-2.12) for TT versus CC. G915C was negatively associated with AR, and the ORs (95% CIs) were 0.91 (0.29-2.86) for G carrier versus CC. For subgroup analyses according to ethnicity, results indicated that TGF-T869C was not associated with risk of AR for either Asians (1.21 [0.64-2.31] for T carrier versus CC) or Caucasians (1.27 [0.76-2.10] for T carrier versus CC). G915C was also not associated with risk of AR for Caucasians (0.91 [0.29-2.186] for G carrier versus CC). CONCLUSION: Our study suggests that TGF β-T869C and G915C may have a null association with AR risk. The above findings reinforce the need for further and more rigorous association studies. © Science Printers and Publishers, Inc.
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Volume 40, Issue 4
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