课题基金 / 基金详情

A COHORT STUDY ON THE CANCER INCIDENCE IN AN AREA WHERE HTLV I, HCV AND HBV ARE ENDEMIC

A COHORT STUDY ON THE CANCER INCIDENCE IN AN AREA WHERE HTLV I, HCV AND HBV ARE ENDEMIC
HTLV I、HCV 和 HBV 流行地区癌症发病率的队列研究
批准号:
14570342
负责人:
ARISAWA Kokichi
金额:
$1.6万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2003

项目摘要

项目成果

ARISAWA Kokichi的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
(1) Interleukin-10 promoter polymorphism and liver fibrosis progression in patients with chronic hepatitis C in Japan.We examined the inheritance of three biallelic polymorphisms in the IL-10 gene promoter, at positions -1082, -819, and -592 from the transcription start site, which produce three different haplotypes, in 52 healthy subjects and 114 patients with post-transfusion hepatitis C. Patients were classified into slow or no-progression group (34 patients), intermediate progression group (33 patients) and rapid progression group (47 patients), based on the degree of fibrosis of liver biopsy specimens : The slow progression group had the putative high IL-10 producing GCC haplotype more often than, the intermediate and rapid progression groups (p<0.01). Individuals with the GCC haplotype were more likely to have less hepatic fibrosis than individuals with the ATA or ACC haplotypes (odds ratio 0.1, 95% confidence interval 0.01-0.9). These results indicate that, in chronic hepatitis … More C, the putative high IL-10 production haplotype GCC is associated with inhibition of the progression of liver fibrosis.(2)The des-gamma-carboxy prothrombin index is a new prognostic indicator for hepatocellular carcinoma.Background : Des-gamma-carboxy prothrombin (DCP) has been reported to be an important prognostic factor in patients with hepatocellular carcinoma (HCC). Recently, a monoclonal antibody, 19B7, which recognizes the Gla domain of. DCP, has been identified. The 19B7 antibody recognizes an epitope different from that recognized by MU-3, which is another antibody against DCP. In this study, the authors investigated the measurement of DCP using the antibodies MU-3 and 19B7, respectively, as a prognostic factor for patients with HCC who had solitary, small tumors and or Child Stage AHCC.Methods : One hundred four patients with HCC who had solitary, small tumors or Child Stage A tumors were enrolled in the study between 1991 and 2001. All patients were treated and were followed for a mean of 3.2 years. The authors analyzed the correlation between the DCP Index (DCP measured by MU-3 and DCP measured by 19B7) and patient prognosis. The patients were classified into 3 groups based on their DCP Index :1) DCP negative (DCP<40 milli arbitrary unit (mAU)/mL)), 2)low DCP Index (DCP> or = 40mAU/mL ; MU-3:19B7 ratio, <3.0, and-3) high DCP Index (DCP> or 40mAU/mL ; MU-3:19B7 ratio, > or= 3.0).Results : The survival rate for patients in the high DCP Index group was lower compared with the survival rate for patients in the DCP-negative group and was significantly lower compared with the survival rate for patients in the low DCP Index group. In a univariate Cox proportional hazards model, the positive factors were high DCP Index and low DCP Index. Among the positive predictive factors that were analyzed using a multivariate Cox proportional hazards model were age (hazard ratio, 3.27; P=0.006), low DCP Index (hazard ratio, 2.87; P=0.012), and high DCP Index (hazard ratio, 12.3, P<0.0001).Conclusions : The prognosis of patients who had a high DCP Index score was poorer compared with patients who had a low DCP Index score and patients who were classified as DCP negative. The authors concluded that the DP Index is a prognostic indicator for patients with HCC. Copyright 2003 American Cancer Society.(3)Human T lymphotropic virus type-I infection, survival and cancer risk in southwestern Japan : A prospective cohort study.Objectives : This study prospectively evaluated the associations of HTLV I infection with survival and cancer incidence.Methods : The study base comprised 4,297 adults (aged 40-69 years in 1993) who had either visited the outpatient clinic or who had received annual health check-ups at the A Hospital, Nagasaki, Japan, between 1985 and 1992 (HTLV I seropositivity=24.7%). During the follow-up period (1993-1999 or 2000), 290 deaths and 261 cases of malignant neoplasms occurred, including 10 deaths and six incident cases of adult T -cell leukemia/lymphoma (ATL).Results : After adjustment for gender, age and other covariates, HTLV-I seropositivity was associatedd with an increased mortality from all-causes excluding ATL (rate ratio [RR] 1.3, 95% confidence interval [CI] 1.0-1.7), all non-neoplastic diseases (RR 1.6, 95% CI 1.1-2.3) and heart diseases. HTLV I infection was not found to be associated with an increased risk of developing total cancers other than ATL (RR 0.97, 95% CI 0.73-1.3), colorectal cancers, liver cancer or lung cancer, but was associated with a reduced risk of gastric cancer, (RR=0.42, 95% CI 0.18-0.99).Conclusions : HTLV I infection is associated with increased mortality from all-causes excluding ATL and all non-neoplastic diseases. HTLV I carriers may not be at increased general cancer risk, but at reduced risk of gastric cancer. Less
期刊论文(49)
专著(0)
科研奖励(0)
会议论文
Hamada H, Yatsuhashi H, Hamasaki K, Yano K, Arisawa K, Daikoku M, Koga M, Miyazoe S, Nakao K, Eguchi K, Yano M.: "Interleukin-10 promoter polymorphism and liver fibrosis progression in patients with chronic hepatitis C in Japan."Journal of Hepatology. 39(
Hamada H、Yatsuhashi H、Hamasaki K、Yano K、Arisawa K、Daikoku M、Koga M、Miyazoe S、Nakao K、Eguchi K、Yano M.:“慢性丙型肝炎患者的白细胞介素 10 启动子多态性与肝纤维化进展
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Arisawa K, Sobue T, Yoshimi I, Soda M, Shirahama S, Doi H, Katamine S, SaitoH, Urata M.: "Human T-lymphotropic virus type-I infection, survival and cancer risk in southwestern Japan : A prospective cohort study."Cancer Causes and Control. 14(9). 889-896 (
Arisawa K、Sobue T、Yoshimi I、Soda M、Shirahama S、Doi H、Katamine S、SaitoH、Urata M.:“日本西南部人类 T 淋巴细胞病毒 I 型感染、生存和癌症风险:一项前瞻性队列研究
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Arisawa K, Matsumura T, Tohyama C, Saito H, Satoh H, Nagai M, Morita M, Suzuki T: "Fish intake, plasma omega-3 polyunsaturated fatty acids, and polychlorinated dibenzo p-dioxins (PCDDs)/polychlorinated dibenzo-furans (PCDFs) and coplanar polychlorinated b
Arisawa K、Matsumura T、Tohyama C、Saito H、Satoh H、Nagai M、Morita M、Suzuki T:“鱼类摄入量、血浆 omega-3 多不饱和脂肪酸和多氯二苯并对二恶英 (PCDD)/多氯二苯并呋喃
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
20
    Analysis of associations between dietary pattern, nutient pattern, and metabolic syndrome, mortality and cancer incidence
    • 批准号:
      18K10086
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $1.0万
    • 财政年份:
      2018
    • 负责人:
      ARISAWA Kokichi
    • 依托单位:
    Molecular epidemiologic study on the health effects of exposure to environmental cadmium
    • 批准号:
      20590603
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.08万
    • 财政年份:
      2008
    • 负责人:
      ARISAWA Kokichi
    • 依托单位:
    Exploration of new biological marker of the health effects caused by environmental pollutants using genomic and proteomic analyses
    • 批准号:
      18590559
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.37万
    • 财政年份:
      2006
    • 负责人:
      ARISAWA Kokichi
    • 依托单位:
    A Nation-wide estimation of the cumulative incidence and disease burden of the rotavirus gastroenteritis
    • 批准号:
      16590504
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.24万
    • 财政年份:
      2004
    • 负责人:
      ARISAWA Kokichi
    • 依托单位:
    国内基金
    海外基金
    三种凤尾蕨属植物中吡咯生物碱及其抗菌和抗HCV病毒功能研究
    • 批准号:
      82360689
    • 项目类别:
      地区科学基金项目
    • 资助金额:
      32.00万元
    • 批准年份:
      2023
    • 负责人:
      邹娟
    • 依托单位:
    KIR/HLAI基因遗传变异及HCV逃逸突变与感染免疫应答相关性的分子流行病学及机制研究
    • 批准号:
      82273691
    • 项目类别:
      面上项目
    • 资助金额:
      52万元
    • 批准年份:
      2022
    • 负责人:
      岳明
    • 依托单位:
    基于“逆向免疫学”理论筛选具有交叉保护作用的抗HCV抗原表位的研究
    • 批准号:
      --
    • 项目类别:
      面上项目
    • 资助金额:
      52万元
    • 批准年份:
      2022
    • 负责人:
      边中启
    • 依托单位:
    云南省HCV感染人群C19orf66基因遗传易感性分析及其机制研究
    • 批准号:
      32160148
    • 项目类别:
      地区科学基金项目
    • 资助金额:
      34万元
    • 批准年份:
      2021
    • 负责人:
      张阿梅
    • 依托单位: