Sixth Hospital of Shaoxing

Shaoxing, China

Sixth Hospital of Shaoxing

Shaoxing, China
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Wei L.-L.,Sixth Hospital of Shaoxing | Meng C.-P.,Sixth Hospital of Shaoxing | Li X.,Zhejiang Province Peoples Hospital | Zhang W.-J.,Shihezi University | And 4 more authors.
Acta Anatomica Sinica | Year: 2012

Objective: The present study is aimed to investigate potential association of SNPs in exon 7 of the MRC1 gene with pulmonary tuberculosis (TB) in Chinese Han and Kazak populations. Methods: Six SNPs (G1186A, G1195A, T1212C, C1221G, C1303T and C1323T) of the MRC1 gene were genotyped using the PCR and DNA sequencing methods in 454 Chinese Han and 595 Uygur subjects. Linkage disequilibrium analysis was performed to determine anylinkage between the polymorphic sites. Results: In a Chinese Han population, we found that the allele frequency of 186A had a significant difference in frequency distribution between the two groups (P = 0.037; OR = 0.76; 95% CI, 0.58 - 0.98). The AG genotypes were significantly correlated with pulmonary TB (P < 0.01; OR = 0.57; 95% CI, 0.37 - 0.87). After adjustment for age and gender, G1186A site was found to be dominant (P < 0.01; OR = 0.59; 95% CI, 0.40-0.87), over-dominant (P = 0.045; OR= 0.69; 95% CI, 0.47 - 0.99) and additive models (P = 0.041; OR = 0.76; 95% CI, 0.59 - 0.99) in association with pulmonary TB. In the Chinese Uygur population, we found that the allele frequency of G1186A was a significant difference between the two groups (P = 0.031; OR = 1.29; 95% CI = 1.02 - 1.62). The AA genotype was significantly correlated with pulmonary TB (P = 0.033; OR = 1.64; 95% CI = 1.04 - 2.60). After adjustment for age and gender, G1186A site was found to be additive models (P = 0.033; OR = 1.28; 95% CI = 1.02 - 1.61) in association with pulmonary TB. By calculating the pairwise LD between 6 SNPs in the Chinese Uygur population, we found that the frequency of the haplotype GGTCCT (P = 0.032; OR = 0.75; 95% CI = 0.57 - 0.97) and GGTCCC (P = 0.044; OR = 0.57; 95% CI = 0.33 - 0.99) was significantly associated with pulmonary TB. No association was found between the other 5 SNPs and TB (P > 0.05) in the Chinese population. Conclusion: This study reports that genetic variants in the MRC1 gene may be associated with pulmonary TB in a Chinese population.


Xue Y.,Zhejiang University | Jin L.,Zhejiang University | Wang H.-J.,Sixth Hospital of Shaoxing | Li M.,Zhejiang University | And 3 more authors.
Clinical Chemistry and Laboratory Medicine | Year: 2010

Background: Toll-like receptor 2 (TLR2) is essential for the immune response to tuberculosis (TB). The goal of the present study was to investigate whether the guanine-thymine (GT) repeat microsatellite polymorphism in intron 2 of the TLR2 gene might be correlated with susceptibility to TB in Han Chinese. Methods: The number of (GT)n repeats was determined by gene scanning from 244 patients with TB and 233 control subjects. The expression of TLR2 on CD14+ peripheral blood mononuclear cells was determined using flow cytometry. Results: No association in allelic polymorphism between control subjects and patients with TB was found. However, the S/M genotype of the microsatellite polymorphism was more frequent in TB patients than in healthy controls (p=0.01). The S/L genotype was more popular in controls than in patients with TB (p=0.007). TLR2 expression was higher in subjects with the S/L genotype than in those with the S/M genotype (p<0.05). Conclusions: Our data suggest that the S/M genotype of the microsatellite (GT)n polymorphisms in intron 2 of the TLR2 gene may increase susceptibility to TB in Chinese, and the S/L genotype may act as a negative risk factor. Clin Chem Lab Med 2010;48:785-9. © 2010 by Walter de Gruyter Berlin New York.


Liu J.-Y.,Zhejiang University | Jin L.,Zhejiang University | Zhao M.-Y.,Zhejiang University | Zhang X.,Zhejiang University | And 6 more authors.
Clinical Chemistry and Laboratory Medicine | Year: 2011

Background: New technologies for the early detection of tuberculosis (TB) are urgently needed. Pathological changes within an organ might be reflected in proteomic patterns in serum. The aim of the present study was to screen for the potential protein biomarkers in serum for the diagnosis of TB using proteomic fingerprint technology. Methods: Proteomic fingerprint technology combining protein chips with surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF MS) was used to profile the serum proteins from 50 patients with TB, 25 patients with lung disease other than TB, and 25 healthy volunteers. The protein fingerprint expression of all the serum samples and the resulting profiles between TB and control groups were analyzed with the Biomarker Wizard system. Results: A total of 30 discriminating m/z peaks were detected that were related to TB (p<0.01). The model of biomarkers constructed by the Biomarker Patterns Software based on the three biomarkers (2024, 8007, and 8598 Da) generated excellent separation between the TB and control groups. The sensitivity was 84.0% and the specificity was 86.0%. Blind test data indicated a sensitivity of 80.0% and a specificity of 84.2%. Conclusions: The data suggested a potential application of SELDI-TOF MS as an effective technology to profile serum proteome, and with pattern analysis, a diagnostic model comprising three potential biomarkers was indicated to differentiate people with TB and healthy controls rapidly and precisely. © 2011 by Walter de Gruyter Berlin Boston.


Zhang X.,Zhejiang University | Li X.,Zhejiang Province Peoples Hospital | Zhang W.,Shihezi University | Wei L.,Sixth Hospital of Shaoxing | And 10 more authors.
Molecular Biology Reports | Year: 2013

The MRC1 gene, encoding the human mannose receptor (MR), is a member of the C-type lectin receptors family. MR can recognize and bind to Mycobacterium tuberculosis by the extracellular structure, and play a role in antigen-presenting and maintaining a stable internal environment. This study aimed to investigate potential associations of SNPs in exon 7 of the MRC1 gene with pulmonary tuberculosis (TB). G1186A, G1195A, T1212C, C1221G, C1303T and C1323T were genotyped using PCR and DNA sequencing in 595 Chinese Uygur and 513 Kazak subjects. In the Uygur, the frequency of allele G (P = 0.031, OR = 1.29, 95 % CI = 1.02-1.62) and AA genotype (P = 0.033, OR = 1.64, 95 % CI = 1.04-2.60) for G1186A was lower in the pulmonary TB than healthy control and were significantly correlated with pulmonary TB. After adjustment for age and gender, G1186A was found to be additive models in association with pulmonary TB (P = 0.04, OR = 1.27, 95 % CI = 1.01-1.60). By calculating linkage disequilibrium, the frequency of haplotype GGTCCT (P = 0.032, OR = 0.75, 95 % CI = 0.57-0.97) and GGTCCC (P = 0.044, OR = 0.57, 95 % CI = 0.33-0.99) was significantly associated with pulmonary TB. No association was found between other SNPs and pulmonary TB. In the Kazak, all SNPs were not associated with pulmonary TB. Our results suggest that genetic factors play an important role in susceptibility to pulmonary TB at the individual level, and provide an experimental basis to clarify the pathogenesis of pulmonary TB. © 2013 Springer Science+Business Media Dordrecht.


Li J.C.,Zhejiang University | Zhang Y.C,Zhejiang University | Zhang X.,Zhejiang University | Zhao M.Y,Zhejiang University | And 7 more authors.
Genetics and Molecular Research | Year: 2012

Although the role of CD14 in mediating signals from Toll-like receptors to recognize Mycobacterium tuberculosis is known, how polymorphisms in this gene affect the susceptibility to develop tuberculosis are still not clear. We examined whether single nucleotide polymorphisms at positions -1145 and -159 in the promoter region of the CD14 gene are associated with tuberculosis in a Chinese Han population in a case-control study of 432 Chinese patients with tuberculosis and 404 ethnically matched healthy controls. Genotyping was performed to identify polymorphisms of the CD14 gene by PCR-DNA sequencing. Both the frequency of allele T in the C(-159)T polymorphism (odds ratio (OR) = 1.4; 95% confdence interval (95%CI) = 1.148-1.708) and allele G in the G(-1145)A polymorphism (OR = 1.512; 95%CI = 1.236- 1.849) were signifcantly more frequent in cases than in controls. The frequencies of genotypes CC and CT in the C(-159)T polymorphism, as well as the frequencies of genotypes AA and AG, were lower in cases than in controls. Based on our results, we conclude that G(-1145)A and C(-159)T polymorphisms of CD14 are associated with decreased risk for the development of tuberculosis in the Chinese Han population. ©FUNPEC-RP.


Xu D.-D.,Zhejiang University | Wang C.,Zhejiang University | Jiang F.,Beijing University of Chinese Medicine | Wei L.-L.,Sixth Hospital of Shaoxing | And 10 more authors.
PLoS ONE | Year: 2015

Ficolin-2 (FCN2) is an innate immune pattern recognition molecule that can activate the complement pathway, opsonophagocytosis, and elimination of the pathogens. The present study aimed to investigate the association of the FCN2 gene single nucleotide polymorphisms (SNPs) with susceptibility to pulmonary tuberculosis (TB). A total of seven SNPs in exon 8 (+6359 C>T and +6424 G>T) and in the promoter region (-986 G>A, -602 G>A, -557 A>G, -64 A>C and -4 A>G) of the FCN2 gene were genotyped using the PCR amplification and DNA sequencing methods in the healthy controls group (n = 254) and the pulmonary TB group (n = 282). The correlation between SNPs and pulmonary TB was analyzed using the logistic regression method. The results showed that there were no significant differences in the distribution of allelic frequencies of seven SNPs between the pulmonary TB group and the healthy controls group. However, the frequency of the variant homozygous genotype (P = 0.037, -557 A>G; P = 0.038, -64 A>C; P = 0.024, +6424 G>T) in the TB group was significantly lower than the control group. After adjustment for age and gender, these variant homozygous genotypes were found to be recessive models in association with pulmonary TB. In addition, -64 A>C (P = 0.047) and +6424 G>T (P = 0.03) were found to be codominant models in association with pulmonary TB. There was strong linkage disequilibrium (r2 > 0.80, P < 0.0001) between 7 SNPs except the -602 G>A site. Therefore, -557 A>G, -64 A>C and +6424 G>T SNPs of the FCN2 gene were correlated with pulmonary TB, and may be protective factors for TB. This study provides a novel idea for the prevention and control of TB transmission from a genetics perspective. Copyright: © 2015 Xu et al.


Liu J.,Zhejiang University | Liu J.,Hangzhou Normal University | Li Y.,Zhejiang University | Wei L.,Sixth Hospital of Shaoxing | And 9 more authors.
Journal of Ethnopharmacology | Year: 2014

Ethnopharmacological relevance Chemotherapy is the mainstay of modern tuberculosis (TB) control. Traditional Chinese Medicine (TCM) can enhance the effect of anti-TB drug, promote the absorption of the foci in the lung and reduce drug toxicity. In TCM, the determination of treatment is based on ZHENG (also called TCM syndrome). To establish a diagnostic model by using proteomics technology in order to identify potential biomarkers for TCM syndromes of TB. Materials and methods The surface-enhanced laser desorption ionization time of flight mass spectrometer (SELDI-TOF MS) combined with weak cation exchange (WCX) magnetic beads was used to screen serum samples from 71 cases of deficiency of lung yin syndrome (DLYS), 64 cases of fire (yang) excess yin deficiency syndrome (FEYDS) and 45 cases of deficiency of both qi and yin syndrome (DQYS). A classification model was established by Biomarker Pattern Software (BPS). Candidate protein biomarkers were purified by reverse phase-high performance liquid chromatograph (RP-HPLC), identified by MALDI-TOF MS, LC-MS/MS and validated by ProteinChip Immunoassays. Results A total of 74 discriminating m/z peaks (P<0.001) among three TCM syndromes of TB were detected. A diagnostic model for the TCM syndrome of TB based on the five biomarkers (3961.7, 4679.7, 5646.4, 8891.2 and 9416.7 m/z) was established which could discriminate DLYS, FEYDS and DQYS patients with an accuracy of 74.0%, 72.5%, and 96.7%, respectively. The candidate biomarker with m/z of 9416.7 was identified as a fragment of apolipoprotein C-III (apoC-III) by MALDI-TOF-MS and LC-MS/MS. Conclusion The TCM syndrome diagnostic model of TB could successfully distinguish the three TCM syndromes of TB patients. This provided a biological basis for the determination of treatment based on different TCM syndromes of TB. ApoC-III was identified as a potential biomarker for TCM syndromes of TB and revealed the biochemical basis and pathogenesis of TCM syndromes in TB. © 2014 Elsevier Ireland Ltd.


Xue Y.,Zhejiang University | Zhao Z.Q.,Henan University of Science and Technology | Wang H.J.,Sixth Hospital of Shaoxing | Jin L.,Zhejiang University | And 3 more authors.
International Journal of Immunogenetics | Year: 2010

Polymorphisms of the toll-like receptor 2 (TLR2) gene (Arg677Trp, Arg753Gln) and the TLR4 gene (As-p299Gly, Thr399Ile) were investigated in 205 tuberculosis (TB) patients and 203 controls. Genetic variations were analysed by DNA sequencing. We revealed that these polymorphisms were rare in the southeastern Chinese population and were not associated with susceptibility to TB. © 2009 Blackwell Publishing Ltd.

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