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Eight‐year nationwide survival analysis in relatives of patients with hepatocellular carcinoma: Role of viral infection

Identifieur interne : 003242 ( Istex/Corpus ); précédent : 003241; suivant : 003243

Eight‐year nationwide survival analysis in relatives of patients with hepatocellular carcinoma: Role of viral infection

Auteurs : Dar-In Tai ; Chien-Hung Chen ; Ting-Tsung Chang ; Shinn-Cherng Chen ; Li-Ying Liao ; Chung-Huang Kuo ; Yangyuan Chen ; Gran-Hum Chen ; Sien-Sing Yang ; Huang-Shang Tang ; Hsien Hong Lin ; Deng-Yn Lin ; Sing Kai Lo ; Jeng-Ming Du ; Kwo-Chuan Lin ; Chi-Sin Changchien ; Wen-Yu Chang ; Jin-Chuan Sheu ; Yun-Fan Liaw ; Ding-Shinn Chen ; Juei-Low Sung

Source :

RBID : ISTEX:C3664FE0E4E3F5661A504A36E6BEC38739E74E53

English descriptors

Abstract

Abstract Background: Families of patients with hepatocellular carcinoma (HCC) carry a high risk of developing HCC. We determine the number of fatalities in relatives of HCC patients during an 8‐year period to understand the risk and cause of HCC in relatives of patients with HCC.
Methods: From 1992 to 1997, 15 410 relatives of HCC patients in three generations were screened prospectively for HCC by ultrasonography, α‐fetoprotein, liver biochemistry and viral markers. By using national citizen identification numbers, we searched the total fatalities in relatives of HCC patients between 1992 and 1999 from the national mortality data bank. The results were compared among different viral infection groups.
Results: Of the relatives studied, 37.8% were hepatitis B s antigen (HBsAg) positive (+), 4.3% were anti‐hepatitis C virus (HCV) (+) and 1.7% were both HBsAg (+) and anti‐HCV (+). A total of 399 fatalities, including 139 because of HCC (34.8%), 37 because of liver diseases (9.3%), 88 because of other cancers (22.1%) and 135 because of other diseases (33.8%), were found. Relatives who were HBsAg (+) or anti‐HCV (+)showed a lower cumulative survival than did relatives who were negative for both HBsAg and anti‐HCV. Relatives with dual infection of hepatitis B and C virus showed the highest mortality due to HCC or terminal liver diseases.
Conclusions: Chronic viral infection rather than a hereditary factor is the main cause of a familial tendency for HCC. Dual infection of hepatitis B and C virus increases the risk of HCC or decompensated liver diseases.

Url:
DOI: 10.1046/j.1440-1746.2002.02747.x

Links to Exploration step

ISTEX:C3664FE0E4E3F5661A504A36E6BEC38739E74E53

Le document en format XML

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<name sortKey="Lo, Sing Kai" sort="Lo, Sing Kai" uniqKey="Lo S" first="Sing Kai" last="Lo">Sing Kai Lo</name>
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<name sortKey="Changchien, Chi In" sort="Changchien, Chi In" uniqKey="Changchien C" first="Chi-Sin" last="Changchien">Chi-Sin Changchien</name>
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<name sortKey="Chen, Yangyuan" sort="Chen, Yangyuan" uniqKey="Chen Y" first="Yangyuan" last="Chen">Yangyuan Chen</name>
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<name sortKey="Chen, Gran Um" sort="Chen, Gran Um" uniqKey="Chen G" first="Gran-Hum" last="Chen">Gran-Hum Chen</name>
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<name sortKey="Yang, Sien Ing" sort="Yang, Sien Ing" uniqKey="Yang S" first="Sien-Sing" last="Yang">Sien-Sing Yang</name>
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<name sortKey="Tang, Huang Hang" sort="Tang, Huang Hang" uniqKey="Tang H" first="Huang-Shang" last="Tang">Huang-Shang Tang</name>
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<mods:affiliation>Department of Internal Medicine, Tri‐service General Hospital, National Defence Medical Center,</mods:affiliation>
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<name sortKey="Lin, Hsien Hong" sort="Lin, Hsien Hong" uniqKey="Lin H" first="Hsien Hong" last="Lin">Hsien Hong Lin</name>
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<name sortKey="Lo, Sing Kai" sort="Lo, Sing Kai" uniqKey="Lo S" first="Sing Kai" last="Lo">Sing Kai Lo</name>
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</affiliation>
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<name sortKey="Du, Jeng Ing" sort="Du, Jeng Ing" uniqKey="Du J" first="Jeng-Ming" last="Du">Jeng-Ming Du</name>
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<mods:affiliation>Department of Medical Information Management, Chang Gung Memorial Hospital,</mods:affiliation>
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<name sortKey="Lin, Kwo Huan" sort="Lin, Kwo Huan" uniqKey="Lin K" first="Kwo-Chuan" last="Lin">Kwo-Chuan Lin</name>
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<mods:affiliation>Department of Internal Medicine, National Taiwan University Hospital,</mods:affiliation>
</affiliation>
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<name sortKey="Sung, Juei Ow" sort="Sung, Juei Ow" uniqKey="Sung J" first="Juei-Low" last="Sung">Juei-Low Sung</name>
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</affiliation>
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<title level="j" type="main">Journal of Gastroenterology and Hepatology</title>
<title level="j" type="alt">JOURNAL OF GASTROENTEROLOGY HEPATOLOGY</title>
<idno type="ISSN">0815-9319</idno>
<idno type="eISSN">1440-1746</idno>
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<term>Carcinoma</term>
<term>Chang</term>
<term>Chen</term>
<term>Chronic hepatitis</term>
<term>Cumulative mortality</term>
<term>Decompensated liver diseases</term>
<term>Dual infection</term>
<term>Familial tendency</term>
<term>Fatality</term>
<term>Gastroenterol</term>
<term>General population</term>
<term>Hbcv</term>
<term>Hbcv group</term>
<term>Hbcv groups</term>
<term>Hbsag</term>
<term>Hbsag carriers</term>
<term>Hepatitis</term>
<term>Hepatocellular</term>
<term>Hepatocellular carcinoma</term>
<term>Hepatology</term>
<term>Higher mortality</term>
<term>Higher prevalence</term>
<term>Infection</term>
<term>Infection groups</term>
<term>Internal medicine</term>
<term>Liaw</term>
<term>Liver disease</term>
<term>Liver diseases</term>
<term>Maternal transmission</term>
<term>None group</term>
<term>Present study</term>
<term>Prevalence</term>
<term>Risk factors</term>
<term>Surface antigen</term>
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<div type="abstract">Abstract Background: Families of patients with hepatocellular carcinoma (HCC) carry a high risk of developing HCC. We determine the number of fatalities in relatives of HCC patients during an 8‐year period to understand the risk and cause of HCC in relatives of patients with HCC.</div>
<div type="abstract">Methods: From 1992 to 1997, 15 410 relatives of HCC patients in three generations were screened prospectively for HCC by ultrasonography, α‐fetoprotein, liver biochemistry and viral markers. By using national citizen identification numbers, we searched the total fatalities in relatives of HCC patients between 1992 and 1999 from the national mortality data bank. The results were compared among different viral infection groups.</div>
<div type="abstract">Results: Of the relatives studied, 37.8% were hepatitis B s antigen (HBsAg) positive (+), 4.3% were anti‐hepatitis C virus (HCV) (+) and 1.7% were both HBsAg (+) and anti‐HCV (+). A total of 399 fatalities, including 139 because of HCC (34.8%), 37 because of liver diseases (9.3%), 88 because of other cancers (22.1%) and 135 because of other diseases (33.8%), were found. Relatives who were HBsAg (+) or anti‐HCV (+)showed a lower cumulative survival than did relatives who were negative for both HBsAg and anti‐HCV. Relatives with dual infection of hepatitis B and C virus showed the highest mortality due to HCC or terminal liver diseases.</div>
<div type="abstract">Conclusions: Chronic viral infection rather than a hereditary factor is the main cause of a familial tendency for HCC. Dual infection of hepatitis B and C virus increases the risk of HCC or decompensated liver diseases.</div>
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<name>Chien‐Hung Chen</name>
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<name>YangYuan Chen</name>
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<json:string>Department of Internal Medicine,Changhua Christian Hospital, Changhua,</json:string>
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<name>Gran‐Hum Chen</name>
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<json:string>Department of Internal Medicine, Taichung Veterans General Hospital, Taichung,</json:string>
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<name>Sien‐Sing Yang</name>
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<json:string>Liver Unit, Clinical Research Center, Cathay General Hospital,</json:string>
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<json:item>
<name>Huang‐Shang Tang</name>
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<json:string>Department of Internal Medicine, Tri‐service General Hospital, National Defence Medical Center,</json:string>
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<json:item>
<name>Hsien Hong Lin</name>
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<json:string>Department of Internal Medicine, Buddhist Tzu Chi General Hospital, Hualien, Taiwan and</json:string>
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<name>Deng‐Yn Lin</name>
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<hi rend="italic">Abstract</hi>
<hi rend="italic"> Background:</hi>
Families of patients with hepatocellular carcinoma (HCC) carry a high risk of developing HCC. We determine the number of fatalities in relatives of HCC patients during an 8‐year period to understand the risk and cause of HCC in relatives of patients with HCC.</p>
<p>
<hi rend="italic">Methods:</hi>
From 1992 to 1997, 15 410 relatives of HCC patients in three generations were screened prospectively for HCC by ultrasonography, α‐fetoprotein, liver biochemistry and viral markers. By using national citizen identification numbers, we searched the total fatalities in relatives of HCC patients between 1992 and 1999 from the national mortality data bank. The results were compared among different viral infection groups.</p>
<p>
<hi rend="italic">Results:</hi>
Of the relatives studied, 37.8% were hepatitis B s antigen (HBsAg) positive (+), 4.3% were anti‐hepatitis C virus (HCV) (+) and 1.7% were both HBsAg (+) and anti‐HCV (+). A total of 399 fatalities, including 139 because of HCC (34.8%), 37 because of liver diseases (9.3%), 88 because of other cancers (22.1%) and 135 because of other diseases (33.8%), were found. Relatives who were HBsAg (+) or anti‐HCV (+)showed a lower cumulative survival than did relatives who were negative for both HBsAg and anti‐HCV. Relatives with dual infection of hepatitis B and C virus showed the highest mortality due to HCC or terminal liver diseases.</p>
<p>
<hi rend="italic">Conclusions:</hi>
Chronic viral infection rather than a hereditary factor is the main cause of a familial tendency for HCC. Dual infection of hepatitis B and C virus increases the risk of HCC or decompensated liver diseases.</p>
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<correspondenceTo> Juei‐Low Sung, President Emeritus, Sun Yat‐Sen Cancer Center Hospital, No. 125 Lih‐Der Road, Pei‐Tou District, Taipei, Taiwan 112. Email:
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<personName>
<givenNames>Deng‐Yn </givenNames>
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<personName>
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<familyName>Changchien</familyName>
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<personName>
<givenNames>Wen‐Yu</givenNames>
<familyName>Chang</familyName>
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<personName>
<givenNames>Jin‐Chuan</givenNames>
<familyName>Sheu</familyName>
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<familyName>Chen</familyName>
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<personName>
<givenNames>Juei‐Low</givenNames>
<familyName>Sung</familyName>
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<unparsedAffiliation>Liver Research Unit and</unparsedAffiliation>
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<unparsedAffiliation>Department of Medical Information Management, Chang Gung Memorial Hospital,</unparsedAffiliation>
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<affiliation xml:id="a3">
<unparsedAffiliation>Department of Internal Medicine, National Taiwan University Hospital,</unparsedAffiliation>
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<unparsedAffiliation>Department of Gastroenterology, Taipei Municipal Jen‐Ai Hospital,</unparsedAffiliation>
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<unparsedAffiliation>Liver Unit, Clinical Research Center, Cathay General Hospital,</unparsedAffiliation>
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<unparsedAffiliation>Liver Unit, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung,</unparsedAffiliation>
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<keyword xml:id="k1">familial tendency</keyword>
<keyword xml:id="k2">hepatitis B</keyword>
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<keyword xml:id="k4">hepatocellular carcinoma</keyword>
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<b>Abstract</b>
<b> Background:</b>
Families of patients with hepatocellular carcinoma (HCC) carry a high risk of developing HCC. We determine the number of fatalities in relatives of HCC patients during an 8‐year period to understand the risk and cause of HCC in relatives of patients with HCC.</p>
<p>
<b>Methods:</b>
From 1992 to 1997, 15 410 relatives of HCC patients in three generations were screened prospectively for HCC by ultrasonography, α‐fetoprotein, liver biochemistry and viral markers. By using national citizen identification numbers, we searched the total fatalities in relatives of HCC patients between 1992 and 1999 from the national mortality data bank. The results were compared among different viral infection groups.</p>
<p>
<b>Results:</b>
Of the relatives studied, 37.8% were hepatitis B s antigen (HBsAg) positive (+), 4.3% were anti‐hepatitis C virus (HCV) (+) and 1.7% were both HBsAg (+) and anti‐HCV (+). A total of 399 fatalities, including 139 because of HCC (34.8%), 37 because of liver diseases (9.3%), 88 because of other cancers (22.1%) and 135 because of other diseases (33.8%), were found. Relatives who were HBsAg (+) or anti‐HCV (+)showed a lower cumulative survival than did relatives who were negative for both HBsAg and anti‐HCV. Relatives with dual infection of hepatitis B and C virus showed the highest mortality due to HCC or terminal liver diseases.</p>
<p>
<b>Conclusions:</b>
Chronic viral infection rather than a hereditary factor is the main cause of a familial tendency for HCC. Dual infection of hepatitis B and C virus increases the risk of HCC or decompensated liver diseases.</p>
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<title>Eight‐year nationwide survival analysis in relatives of patients with hepatocellular carcinoma: Role of viral infection</title>
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<title>Mortality in HCC families</title>
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<title>Eight‐year nationwide survival analysis in relatives of patients with hepatocellular carcinoma: Role of viral infection</title>
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<namePart type="given">Dar‐In</namePart>
<namePart type="family">Tai</namePart>
<affiliation>Liver Research Unit and</affiliation>
<affiliation>Liver Unit, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung,</affiliation>
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<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Chien‐Hung</namePart>
<namePart type="family">Chen</namePart>
<affiliation>Department of Internal Medicine, National Taiwan University Hospital,</affiliation>
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<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Ting‐Tsung</namePart>
<namePart type="family">Chang</namePart>
<affiliation>Department of Internal Medicine, National Cheng Kung University Hospital, Tainan,</affiliation>
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<namePart type="given">Shinn‐Cherng</namePart>
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<name type="personal">
<namePart type="given">Li‐Ying</namePart>
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<namePart type="given">YangYuan</namePart>
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<namePart type="given">Huang‐Shang</namePart>
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<abstract>Abstract Background: Families of patients with hepatocellular carcinoma (HCC) carry a high risk of developing HCC. We determine the number of fatalities in relatives of HCC patients during an 8‐year period to understand the risk and cause of HCC in relatives of patients with HCC.</abstract>
<abstract>Methods: From 1992 to 1997, 15 410 relatives of HCC patients in three generations were screened prospectively for HCC by ultrasonography, α‐fetoprotein, liver biochemistry and viral markers. By using national citizen identification numbers, we searched the total fatalities in relatives of HCC patients between 1992 and 1999 from the national mortality data bank. The results were compared among different viral infection groups.</abstract>
<abstract>Results: Of the relatives studied, 37.8% were hepatitis B s antigen (HBsAg) positive (+), 4.3% were anti‐hepatitis C virus (HCV) (+) and 1.7% were both HBsAg (+) and anti‐HCV (+). A total of 399 fatalities, including 139 because of HCC (34.8%), 37 because of liver diseases (9.3%), 88 because of other cancers (22.1%) and 135 because of other diseases (33.8%), were found. Relatives who were HBsAg (+) or anti‐HCV (+)showed a lower cumulative survival than did relatives who were negative for both HBsAg and anti‐HCV. Relatives with dual infection of hepatitis B and C virus showed the highest mortality due to HCC or terminal liver diseases.</abstract>
<abstract>Conclusions: Chronic viral infection rather than a hereditary factor is the main cause of a familial tendency for HCC. Dual infection of hepatitis B and C virus increases the risk of HCC or decompensated liver diseases.</abstract>
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