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    Bioregulation of Helicobacter pylori Infection with Red Ginseng; Double Blinded Randomized Controlled Trial (DB-RCT)

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    https://www.riss.kr/link?id=A104775311

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    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    The fact that mass eradication of Helicobacter pylori (H. pylori) can not be recommended as a cost-effective means to prevent the development of gastric cancer, although H. pylori was defined as class I carcinogen and cohort study confirmed H. pylori as causative bacteria responsible for gastric carcinogenesis drives us to search for the way either to kill bacteria or lessen gastric inflammations. Since our previous study suggested red ginseng capsule could be candidate, randomized controlled trial was done to document the efficacy of 10-week supplementation of red ginseng capsules (2.7 g/day) after triple therapy for eradication compared to that of the placebo supplementation. Total 84 patients were enrolled and 70 patients completed the trial (83.3% PP). The eradication rates were statistically significantly augmented in red ginseng group compared to placebo group (79.4% in placebo group and 91.7% in red ginseng group, p<0.05). In respective analysis of gastritis, red ginseng group showed statistically significant improvement in neutrophil infiltrations, mononuclear cell infiltrations, gastric atrophy, and even intestinal metaplasia than placebo group (p<0.05). H. pylori infection was associated with significant generation and nuclear translocation of 8-OHdG, but red ginseng group was excellent in lessening 8-OHdG generations in parallel with attenuated apoptosis and single cell nuclear damages than placebo group (p<0.05). Conclusively, red ginseng supplementary treatment after H. pylori eradication was beneficial in either quantitative or qualitative aspect for H. pylori infection and the considerable cytoprotective properties and anti-inflammatory activities of red ginseng might contribute to the treatment of H. pylori-associated chronic gastritis. (Cancer Prev Res 10, 102-110, 2005)
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    The fact that mass eradication of Helicobacter pylori (H. pylori) can not be recommended as a cost-effective means to prevent the development of gastric cancer, although H. pylori was defined as class I carcinogen and cohort study confirmed H. pylori ...

    The fact that mass eradication of Helicobacter pylori (H. pylori) can not be recommended as a cost-effective means to prevent the development of gastric cancer, although H. pylori was defined as class I carcinogen and cohort study confirmed H. pylori as causative bacteria responsible for gastric carcinogenesis drives us to search for the way either to kill bacteria or lessen gastric inflammations. Since our previous study suggested red ginseng capsule could be candidate, randomized controlled trial was done to document the efficacy of 10-week supplementation of red ginseng capsules (2.7 g/day) after triple therapy for eradication compared to that of the placebo supplementation. Total 84 patients were enrolled and 70 patients completed the trial (83.3% PP). The eradication rates were statistically significantly augmented in red ginseng group compared to placebo group (79.4% in placebo group and 91.7% in red ginseng group, p<0.05). In respective analysis of gastritis, red ginseng group showed statistically significant improvement in neutrophil infiltrations, mononuclear cell infiltrations, gastric atrophy, and even intestinal metaplasia than placebo group (p<0.05). H. pylori infection was associated with significant generation and nuclear translocation of 8-OHdG, but red ginseng group was excellent in lessening 8-OHdG generations in parallel with attenuated apoptosis and single cell nuclear damages than placebo group (p<0.05). Conclusively, red ginseng supplementary treatment after H. pylori eradication was beneficial in either quantitative or qualitative aspect for H. pylori infection and the considerable cytoprotective properties and anti-inflammatory activities of red ginseng might contribute to the treatment of H. pylori-associated chronic gastritis. (Cancer Prev Res 10, 102-110, 2005)

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    참고문헌 (Reference)

    1 "Quantitative and qualitative usefulnessof rebamipide in eradication regimen of Helicobacter pylori" 43 : 1998

    2 "Protective mechanism of epigallocatechin-3-gallate against Helicobacter pylori-induced gastric epithelial cytotoxicity via the blockage of TLR-4 signaling" 9 : 632-642, 2004

    3 "Possibility of chemoprevention by the eradication of Helicobacter pylori oxidative DNA damage and apoptosis in H" 1853-18571997

    4 "Possibility of chemoprevention by the eradication of Helicobacter pylori oxidative DNA damage and apoptosis in H" 1853-18571997

    5 "Phenotypinc and genotypic events in gastric carcinogenesis" 54 : 1994

    6 "Microsome-mediated 8-hydroxydeoxyguanosine of guanine bases of DNA by steroid estrogens:Cor-relation of DNA damage by free radicals with metabolic activation to quinones" 16 : 2571-2574, 1995

    7 "Increased oxidative DNA damage in Helicobacter pylori-infected human gastric mucosa" 56 : 1279-1282, 1996

    8 "Immune and inflammatory responses to Helicobacter pylori infection" 215 : 3-10, 1996

    9 "Helicobacter pylori^gastric cancer^an overrated risk" 1041-1046, 1996

    10 "Helicobacter pylori,free radicals and gastroduodenal disease" 6 : 1-10, 1994

    1 "Quantitative and qualitative usefulnessof rebamipide in eradication regimen of Helicobacter pylori" 43 : 1998

    2 "Protective mechanism of epigallocatechin-3-gallate against Helicobacter pylori-induced gastric epithelial cytotoxicity via the blockage of TLR-4 signaling" 9 : 632-642, 2004

    3 "Possibility of chemoprevention by the eradication of Helicobacter pylori oxidative DNA damage and apoptosis in H" 1853-18571997

    4 "Possibility of chemoprevention by the eradication of Helicobacter pylori oxidative DNA damage and apoptosis in H" 1853-18571997

    5 "Phenotypinc and genotypic events in gastric carcinogenesis" 54 : 1994

    6 "Microsome-mediated 8-hydroxydeoxyguanosine of guanine bases of DNA by steroid estrogens:Cor-relation of DNA damage by free radicals with metabolic activation to quinones" 16 : 2571-2574, 1995

    7 "Increased oxidative DNA damage in Helicobacter pylori-infected human gastric mucosa" 56 : 1279-1282, 1996

    8 "Immune and inflammatory responses to Helicobacter pylori infection" 215 : 3-10, 1996

    9 "Helicobacter pylori^gastric cancer^an overrated risk" 1041-1046, 1996

    10 "Helicobacter pylori,free radicals and gastroduodenal disease" 6 : 1-10, 1994

    11 "Helicobacter pylori infection and the risk of gastric carcinoma" 325 : 1127-1131, 1991

    12 "Helicobacter pylori infection and the development of gastric cancer" 784-789, 2001

    13 "Exposure of mammalian cell cultures to benzopyrene and light results in oxidative DNA damage as measured by 8-hydroxydeoxyguanosine formation" carci (carci): 133-137, 1995

    14 "Classification and grading of gastritis International Workshop on the Histopathology of Gastritis" 1161-1181, 1996

    15 "A human model of gastric carcinogenesis" 48 : 3554-3560, 1988

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    학술지 이력

    학술지 이력
    연월일 이력구분 이력상세 등재구분
    2022 평가 재인증평가 신청대상 (재인증)
    2019-01-01 등재 등재학술지 선정 (계속평가) KCI등재
    2018-12-01 등재 등재후보로 하락 (계속평가) KCI등재후보
    2015-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2013-10-14 학술지명변경 외국어명 : Cancer Prevention Research -> Journal of Cancer Prevention KCI등재
    2012-10-15 학회명변경 영문명 : Korean Association of Cancer Prevention -> Korean Society of Cancer Preveniton KCI등재
    2011-04-04 학술지명변경 외국어명 : Journal of Korean Association of Cancer Prevention -> Cancer Prevention Research KCI등재
    2011-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2008-01-01 등재 등재학술지 선정 (등재후보2차) KCI등재
    2007-01-01 등재 등재후보 1차 PASS (등재후보1차) KCI등재후보
    2005-01-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
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    학술지 인용정보

    학술지 인용정보
    기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
    2016 0.22 0.22 0.18
    KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
    0.15 0.12 0.405 0.13
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