BMC Infectious Diseases Volume 8
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Research articleRoles of TNF-α gene polymorphisms in the occurrence and progress of SARS-Cov infection: A case-control studyShixin Wang* 1 , Maoti Wei* 2 , Yi Han1 , Keju Zhang1 , Li He1 , Zhen Yang1 , Bing Su3 , Zhilun Zhang4 , Yilan Hu2 and Wuli Hui2  1Proteomics Laboratory, Medical College of Chinese People's Armed Police Force, Tianjin, China 2Department of Epidemiology, Medical College of Chinese People's Armed Police Force, Tianjin, China 3Department of Respiratory, Pingjin Hospital, Medical College of Chinese People's Armed Police Force, Tianjin, China 4Department for Emergency Diseases, Center for Disease Control and Prevention, Tianjin, China author email corresponding author email* Contributed equally
BMC Infectious Diseases 2008,
8:27doi:10.1186/1471-2334-8-27
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| Published: |
29 February 2008 |
Abstract
Background
Host genetic factors may play a role in the occurrence and progress of SARS-Cov infection. This study was to investigate the relationship between tumor necrosis factor (TNF)-α gene polymorphisms with the occurrence of SARS-CoV infection and its role in prognosis of patients with lung interstitial fibrosis and femoral head osteonecrosis.
Methods
The association between genetic polymorphisms of TNF-α gene and susceptibility to severe acute respiratory syndromes (SARS) was conducted in a hospital-based case-control study including 75 SARS patients, 41 health care workers and 92 healthy controls. Relationships of TNF-α gene polymorphisms with interstitial lung fibrosis and femoral head osteonecrosis were carried out in two case-case studies in discharged SARS patients. PCR sequencing based typing (PCR-SBT) method was used to determine the polymorphisms of TNF-α gene in locus of the promoter region and univariate logistic analysis was conducted in analyzing the collected data.
Results
Compared to TT genotype, the CT genotype at the -204 locus was found associated with a protective effect on SARS with OR(95%CI) of 0.95(0.90–0.99). Also, TT genotype, CT and CC were found associated with a risk effect on femoral head necrosis with ORs(95%CI) of 5.33(1.39–20.45) and 5.67(2.74–11.71), respectively and the glucocorticoid adjusted OR of CT was 5.25(95%CI 1.18–23.46) and the combined (CT and CC) genotype OR was 6.0 (95%CI 1.60–22.55) at -1031 site of TNF-α gene. At the same time, the -863 AC genotype was manifested as another risk effect associated with femoral head necrosis with OR(95%CI) of 6.42(1.53–26.88) and the adjusted OR was 8.40(95%CI 1.76–40.02) in cured SARS patients compared to CC genotype.
Conclusion
SNPs of TNF-α gene of promoter region may not associate with SARS-CoV infection. And these SNPs may not affect interstitial lung fibrosis in cured SARS patients. However, the -1031CT/CC and -863 AC genotypes may be risk factors of femoral head necrosis in discharged SARS patients. |