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1.
Zhonghua Gan Zang Bing Za Zhi ; 29(6): 527-532, 2021 Jun 20.
Artigo em Chinês | MEDLINE | ID: mdl-34225426

RESUMO

Objective: To investigate the expressional condition of interleukin-16 (IL-16) in the liver and serum of patients with primary biliary cholangitis (PBC). Methods: Liver biopsies samples were collected from 70 cases and 10 healthy controls, and serum samples were collected from 62 cases and 87 healthy controls. The expression of IL-16 in liver was detected by immunohistochemistry, and the serum level of IL-16 was determined by enzyme-linked immunosorbent assay. The correlation between the expression level of IL-16 and the severity of disease was determined by correlation analysis with clinical biomarker. The t-test was used for normally distributed data. Wilcoxon signed rank sum test was used for non-normally distributed data. Results: The expression level of IL-16 in the liver of PBC patients was significantly higher than that in the healthy control group (P = 0.002 5), and it was mainly expressed in infiltrating lymphocytes in the portal area. Correlation analysis showed that the level of IL-16 in liver tissue was positively correlated with the degree of liver inflammation (r = 0.36, P = 0.002). In addition, the serum IL-16 level of PBC patients were significantly higher than that of healthy people (P = 0.000 5), and serum IL-16 level was correlated with the level of cholestasis biomarker γ-glutamyltransferase (r = 0.31, P = 0.03). Conclusion: The expression level of IL-16 is significantly increased in liver and serum of PBC patients, and it is positively correlated with the severity of the disease, suggesting that IL-16 may be used as a biomarker to assess the severity of the disease.


Assuntos
Colangite , Colestase , Interleucina-16 , Cirrose Hepática Biliar , Humanos , gama-Glutamiltransferase
2.
Ann Oncol ; 23(12): 3163-3170, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22855553

RESUMO

BACKGROUND: A number of epidemiological studies have reported inconsistent findings on the association between meat consumption and lung cancer. DESIGN: We therefore conducted a systematic review and meta-analysis to investigate the relationship between meat consumption and lung cancer risk in epidemiological studies. RESULTS: Twenty-three case-control and 11 cohort studies were included. All studies adjusted for smoking or conducted in never smokers. The summary relative risks (RRs) of lung cancer for the highest versus lowest intake categories were 1.35 (95% confidence interval (CI) 1.08-1.69) for total meat, 1.34 (95% CI 1.18-1.52) for red meat, and 1.06 (95% CI 0.90-1.25) for processed meat. An inverse association was found between poultry intake and lung cancer (RR = 0.91, 95% CI 0.85-0.97), but not for total white meat (RR = 1.06, 95% CI 0.82-1.37) or fish (RR = 1.01, 95% CI 0.96-1.07). CONCLUSIONS: The relationship between meat intake and lung cancer risk appears to depend on the types of meat consumed. A high intake of red meat may increase the risk of lung cancer by about 35%, while a high intake of poultry decreases the risk by about 10%. More well-designed cohort studies on meat mutagens or heme iron, meat cooking preferences, and doneness level are needed to fully characterize this meat-lung cancer association.


Assuntos
Comportamento Alimentar , Neoplasias Pulmonares/epidemiologia , Carne , Animais , Estudos de Casos e Controles , Estudos de Coortes , Culinária , Peixes , Humanos , Aves Domésticas , Risco , Fatores de Risco , Fumar
3.
Prog Neuropsychopharmacol Biol Psychiatry ; 32(5): 1210-3, 2008 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-18430503

RESUMO

Although there is evidence pointing to CAPON as a susceptible gene for schizophrenia, the results of independent association studies have so far been inconsistent. A recent case-control study by Zheng et al. supported CAPON as a susceptible site for the disease in the Chinese Han population. In their study both the single polymorphism (rs348624) and individual haplotypes showed significant association with schizophrenia. Our study further investigates this relationship this time using a family-based association. We selected 5 SNPs including rs348624 and performed a Transmission Disequilibrium Test (TDT) in 319 Chinese Han trios. Our results identified no single marker nor haplotype associated with schizophrenia, which did not suggest that CAPON was a susceptible site in the Chinese Han population, or it appeared unlikely that the CAPON played a major role in the aetiology of schizophrenia. Since there is consistent evidence pointing to 1q21-22 as a positional candidate region for schizophrenia, we suggest that further research should focus on other genes located in this region.


Assuntos
Proteínas Adaptadoras de Transdução de Sinal/genética , Saúde da Família , Predisposição Genética para Doença , Polimorfismo de Nucleotídeo Único/genética , Esquizofrenia/genética , Adolescente , Adulto , Povo Asiático/etnologia , Análise Mutacional de DNA , Feminino , Frequência do Gene , Genótipo , Humanos , Desequilíbrio de Ligação , Masculino
4.
Mol Psychiatry ; 11(4): 395-9, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16402136

RESUMO

Recently, Pimm et al. identified Epsin 4 on chromosome 5q33 as a susceptibility gene for schizophrenia in the British population, based on linkage and association evidence. In Pimm's case-control study, both the single polymorphisms and the individual haplotypes at the 5' end of the gene showed genetic association with schizophrenia. Here, we report the first study evaluating the relevance of Epsin 4 and schizophrenia outside the British population. Markers showing positive results in the original work as well as two additional polymorphisms were genotyped in 308 Han Chinese family trios. Transmission disequilibrium analysis was used to test for association of single-locus markers and multi-locus haplotypes with schizophrenia. Although no individual marker was significant at the P=0.05 level, the haplotypes detected in our samples, different from those previously reported, showed strong evidence of association (most significant global P=0.0021). Our results indicate the presence of a locus near the 5' end of Epsin 4 conferring susceptibility to the disease and provide further support for Epsin 4 as an important potential contributor to genetic risk in schizophrenia.


Assuntos
Proteínas Adaptadoras de Transporte Vesicular/genética , Povo Asiático/genética , Cromossomos Humanos Par 5/genética , Predisposição Genética para Doença , Esquizofrenia/genética , Adulto , DNA/análise , Feminino , Humanos , Desequilíbrio de Ligação , Masculino , Linhagem , Polimorfismo de Nucleotídeo Único/genética
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