Hepatitis C virus infection in patients with chronic liver disease or chronic renal failure and blood donors in Thailand
Hepatitis C virus (HCV) RNA and genotypes, as well as markers of hepatitis B virus infection, were surveyed in 171 patients with chronic liver disease, 276 patients with chronic renal failure, and 961 blood donors in Thailand. HCV RNA was detected in 30 (23%) of 128 patients with nonalcoholic chroni...
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Veröffentlicht in: | Journal of medical virology 1994-11, Vol.44 (3), p.287-292 |
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creator | Luengrojanakul, Pairoj Vareesangthip, Kriengsak Chainuvati, Termchai Murata, Kazumoto Tsuda, Fumio Tokita, Hajime Okamoto, Hiroaki Miyakawa, Yuzo Mayumi, Makoto |
description | Hepatitis C virus (HCV) RNA and genotypes, as well as markers of hepatitis B virus infection, were surveyed in 171 patients with chronic liver disease, 276 patients with chronic renal failure, and 961 blood donors in Thailand. HCV RNA was detected in 30 (23%) of 128 patients with nonalcoholic chronic liver disease and hepatitis B surface antigen (HBsAg) in 60 (47%), and both HCV RNA and HBsAg in 3; the cause of liver disease was not established in 41 (32%) patients. HCV RNA was detected in 44 (20%) of 221 patients on maintenance hemodialysis or with kidney transplantation, but in none of 55 patients on peritoneal dialysis. Antibodies to synthetic HCV core peptides were detected in 39 (4.1%) of sera from 961 blood donors, and HCV RNA was detected in 8 (0.8%). Of the 90 HCV RNA samples from patients and donors, genotype V prevailed (46%) followed by II (22%), I (14%), III (3%), and VI (2%); genotypes were not classifiable into any of I‐VI in the remaining 10%. There were six sera which contained HCV RNA, but were without antibody to HCV detectable by the second‐generation enzyme immunoassay. HCV RNA titers were high in four patients with kidney transplantation, but low in one patient with chronic liver disease and one patient on maintenance hemodialysis. HCV RNA at high titer (≥104/ml) was not classifiable in one patient. These results indicate HCV of novel genotypes in Thailand, seronegative HCV infection in patients with kidney transplantation, and a low risk of HCV infection in patients treated by peritoneal dialysis. © 1994 wiiey‐Liss, Inc. |
doi_str_mv | 10.1002/jmv.1890440313 |
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HCV RNA was detected in 30 (23%) of 128 patients with nonalcoholic chronic liver disease and hepatitis B surface antigen (HBsAg) in 60 (47%), and both HCV RNA and HBsAg in 3; the cause of liver disease was not established in 41 (32%) patients. HCV RNA was detected in 44 (20%) of 221 patients on maintenance hemodialysis or with kidney transplantation, but in none of 55 patients on peritoneal dialysis. Antibodies to synthetic HCV core peptides were detected in 39 (4.1%) of sera from 961 blood donors, and HCV RNA was detected in 8 (0.8%). Of the 90 HCV RNA samples from patients and donors, genotype V prevailed (46%) followed by II (22%), I (14%), III (3%), and VI (2%); genotypes were not classifiable into any of I‐VI in the remaining 10%. There were six sera which contained HCV RNA, but were without antibody to HCV detectable by the second‐generation enzyme immunoassay. HCV RNA titers were high in four patients with kidney transplantation, but low in one patient with chronic liver disease and one patient on maintenance hemodialysis. HCV RNA at high titer (≥104/ml) was not classifiable in one patient. These results indicate HCV of novel genotypes in Thailand, seronegative HCV infection in patients with kidney transplantation, and a low risk of HCV infection in patients treated by peritoneal dialysis. © 1994 wiiey‐Liss, Inc.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.1890440313</identifier><identifier>PMID: 7531758</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Base Sequence ; Biological and medical sciences ; Blood Donors ; chronic hepatitis ; Female ; Genotype ; HBV subtypes ; HCV genotypes ; hemodialysis ; Hepacivirus - classification ; Hepacivirus - genetics ; Hepatitis Antibodies - blood ; Hepatitis B - complications ; Hepatitis B - epidemiology ; Hepatitis B Surface Antigens - blood ; hepatitis B virus (HBV) ; Hepatitis C - complications ; Hepatitis C - epidemiology ; Hepatitis C Antibodies ; hepatitis C virus ; hepatitis C virus (HCV) ; Human viral diseases ; Humans ; Immunoenzyme Techniques ; Infectious diseases ; Kidney Failure, Chronic - complications ; kidney transplantation ; Kidney Transplantation - adverse effects ; Liver Diseases - complications ; Male ; Medical sciences ; Middle Aged ; Molecular Sequence Data ; peritoneal dialysis ; Renal Dialysis - adverse effects ; RNA, Viral - blood ; Thailand - epidemiology ; Tropical medicine ; Viral diseases ; Viral hepatitis</subject><ispartof>Journal of medical virology, 1994-11, Vol.44 (3), p.287-292</ispartof><rights>Copyright © 1994 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4383-14860d7cc4cf1841a15b371499c6bbc28d47d826d6b81f4fd98a45c2d334ad193</citedby><cites>FETCH-LOGICAL-c4383-14860d7cc4cf1841a15b371499c6bbc28d47d826d6b81f4fd98a45c2d334ad193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.1890440313$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.1890440313$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3326105$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7531758$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luengrojanakul, Pairoj</creatorcontrib><creatorcontrib>Vareesangthip, Kriengsak</creatorcontrib><creatorcontrib>Chainuvati, Termchai</creatorcontrib><creatorcontrib>Murata, Kazumoto</creatorcontrib><creatorcontrib>Tsuda, Fumio</creatorcontrib><creatorcontrib>Tokita, Hajime</creatorcontrib><creatorcontrib>Okamoto, Hiroaki</creatorcontrib><creatorcontrib>Miyakawa, Yuzo</creatorcontrib><creatorcontrib>Mayumi, Makoto</creatorcontrib><title>Hepatitis C virus infection in patients with chronic liver disease or chronic renal failure and blood donors in Thailand</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>Hepatitis C virus (HCV) RNA and genotypes, as well as markers of hepatitis B virus infection, were surveyed in 171 patients with chronic liver disease, 276 patients with chronic renal failure, and 961 blood donors in Thailand. HCV RNA was detected in 30 (23%) of 128 patients with nonalcoholic chronic liver disease and hepatitis B surface antigen (HBsAg) in 60 (47%), and both HCV RNA and HBsAg in 3; the cause of liver disease was not established in 41 (32%) patients. HCV RNA was detected in 44 (20%) of 221 patients on maintenance hemodialysis or with kidney transplantation, but in none of 55 patients on peritoneal dialysis. Antibodies to synthetic HCV core peptides were detected in 39 (4.1%) of sera from 961 blood donors, and HCV RNA was detected in 8 (0.8%). Of the 90 HCV RNA samples from patients and donors, genotype V prevailed (46%) followed by II (22%), I (14%), III (3%), and VI (2%); genotypes were not classifiable into any of I‐VI in the remaining 10%. There were six sera which contained HCV RNA, but were without antibody to HCV detectable by the second‐generation enzyme immunoassay. HCV RNA titers were high in four patients with kidney transplantation, but low in one patient with chronic liver disease and one patient on maintenance hemodialysis. HCV RNA at high titer (≥104/ml) was not classifiable in one patient. These results indicate HCV of novel genotypes in Thailand, seronegative HCV infection in patients with kidney transplantation, and a low risk of HCV infection in patients treated by peritoneal dialysis. © 1994 wiiey‐Liss, Inc.</description><subject>Adult</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Blood Donors</subject><subject>chronic hepatitis</subject><subject>Female</subject><subject>Genotype</subject><subject>HBV subtypes</subject><subject>HCV genotypes</subject><subject>hemodialysis</subject><subject>Hepacivirus - classification</subject><subject>Hepacivirus - genetics</subject><subject>Hepatitis Antibodies - blood</subject><subject>Hepatitis B - complications</subject><subject>Hepatitis B - epidemiology</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>hepatitis B virus (HBV)</subject><subject>Hepatitis C - complications</subject><subject>Hepatitis C - epidemiology</subject><subject>Hepatitis C Antibodies</subject><subject>hepatitis C virus</subject><subject>hepatitis C virus (HCV)</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Infectious diseases</subject><subject>Kidney Failure, Chronic - complications</subject><subject>kidney transplantation</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Liver Diseases - complications</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>peritoneal dialysis</subject><subject>Renal Dialysis - adverse effects</subject><subject>RNA, Viral - blood</subject><subject>Thailand - epidemiology</subject><subject>Tropical medicine</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTtv2zAURomgReqmWbMF4FB0k8srvsfCyKNB0i5pMhIUScFMZdElJSf595Vhw0WnTLzAOffjBT6EzoDMgZD669NqMwelCWOEAj1CMyBaVJpIeIdmBJiohAD-AX0s5YkQonRdH6NjySlIrmbo5Tqs7RCHWPACb2IeC459G9wQUz9NeAtDPxT8HIcldsuc-uhwFzchYx9LsCXglA8gh952uLWxG3PAtve46VLy2Kc-5W00vl9OcAKf0PvWdiWc7t8T9Ovy4n5xXd3-vPq--HZbOUYVrYApQbx0jrkWFAMLvKESmNZONI2rlWfSq1p40ShoWeu1soy72lPKrAdNT9CXXe46pz9jKINZxeJCN90Q0liMlJIzBvRNEQSXCvg2cb4TXU6l5NCadY4rm18NELPtxEydmH-dTAvn--SxWQV_0PclTPzzntvibNdm27tYDhqltQDCJ03vtOfYhdc3PjU3dw__nVDtdmMZwsth1-bfRkgquXn8cWXuFKPw-HBpbuhfiAq0zw</recordid><startdate>199411</startdate><enddate>199411</enddate><creator>Luengrojanakul, Pairoj</creator><creator>Vareesangthip, Kriengsak</creator><creator>Chainuvati, Termchai</creator><creator>Murata, Kazumoto</creator><creator>Tsuda, Fumio</creator><creator>Tokita, Hajime</creator><creator>Okamoto, Hiroaki</creator><creator>Miyakawa, Yuzo</creator><creator>Mayumi, Makoto</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199411</creationdate><title>Hepatitis C virus infection in patients with chronic liver disease or chronic renal failure and blood donors in Thailand</title><author>Luengrojanakul, Pairoj ; Vareesangthip, Kriengsak ; Chainuvati, Termchai ; Murata, Kazumoto ; Tsuda, Fumio ; Tokita, Hajime ; Okamoto, Hiroaki ; Miyakawa, Yuzo ; Mayumi, Makoto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4383-14860d7cc4cf1841a15b371499c6bbc28d47d826d6b81f4fd98a45c2d334ad193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Adult</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Blood Donors</topic><topic>chronic hepatitis</topic><topic>Female</topic><topic>Genotype</topic><topic>HBV subtypes</topic><topic>HCV genotypes</topic><topic>hemodialysis</topic><topic>Hepacivirus - classification</topic><topic>Hepacivirus - genetics</topic><topic>Hepatitis Antibodies - blood</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis B - epidemiology</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>hepatitis B virus (HBV)</topic><topic>Hepatitis C - complications</topic><topic>Hepatitis C - epidemiology</topic><topic>Hepatitis C Antibodies</topic><topic>hepatitis C virus</topic><topic>hepatitis C virus (HCV)</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Infectious diseases</topic><topic>Kidney Failure, Chronic - complications</topic><topic>kidney transplantation</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Liver Diseases - complications</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Sequence Data</topic><topic>peritoneal dialysis</topic><topic>Renal Dialysis - adverse effects</topic><topic>RNA, Viral - blood</topic><topic>Thailand - epidemiology</topic><topic>Tropical medicine</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luengrojanakul, Pairoj</creatorcontrib><creatorcontrib>Vareesangthip, Kriengsak</creatorcontrib><creatorcontrib>Chainuvati, Termchai</creatorcontrib><creatorcontrib>Murata, Kazumoto</creatorcontrib><creatorcontrib>Tsuda, Fumio</creatorcontrib><creatorcontrib>Tokita, Hajime</creatorcontrib><creatorcontrib>Okamoto, Hiroaki</creatorcontrib><creatorcontrib>Miyakawa, Yuzo</creatorcontrib><creatorcontrib>Mayumi, Makoto</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luengrojanakul, Pairoj</au><au>Vareesangthip, Kriengsak</au><au>Chainuvati, Termchai</au><au>Murata, Kazumoto</au><au>Tsuda, Fumio</au><au>Tokita, Hajime</au><au>Okamoto, Hiroaki</au><au>Miyakawa, Yuzo</au><au>Mayumi, Makoto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis C virus infection in patients with chronic liver disease or chronic renal failure and blood donors in Thailand</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. Med. Virol</addtitle><date>1994-11</date><risdate>1994</risdate><volume>44</volume><issue>3</issue><spage>287</spage><epage>292</epage><pages>287-292</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><coden>JMVIDB</coden><abstract>Hepatitis C virus (HCV) RNA and genotypes, as well as markers of hepatitis B virus infection, were surveyed in 171 patients with chronic liver disease, 276 patients with chronic renal failure, and 961 blood donors in Thailand. HCV RNA was detected in 30 (23%) of 128 patients with nonalcoholic chronic liver disease and hepatitis B surface antigen (HBsAg) in 60 (47%), and both HCV RNA and HBsAg in 3; the cause of liver disease was not established in 41 (32%) patients. HCV RNA was detected in 44 (20%) of 221 patients on maintenance hemodialysis or with kidney transplantation, but in none of 55 patients on peritoneal dialysis. Antibodies to synthetic HCV core peptides were detected in 39 (4.1%) of sera from 961 blood donors, and HCV RNA was detected in 8 (0.8%). Of the 90 HCV RNA samples from patients and donors, genotype V prevailed (46%) followed by II (22%), I (14%), III (3%), and VI (2%); genotypes were not classifiable into any of I‐VI in the remaining 10%. There were six sera which contained HCV RNA, but were without antibody to HCV detectable by the second‐generation enzyme immunoassay. HCV RNA titers were high in four patients with kidney transplantation, but low in one patient with chronic liver disease and one patient on maintenance hemodialysis. HCV RNA at high titer (≥104/ml) was not classifiable in one patient. These results indicate HCV of novel genotypes in Thailand, seronegative HCV infection in patients with kidney transplantation, and a low risk of HCV infection in patients treated by peritoneal dialysis. © 1994 wiiey‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7531758</pmid><doi>10.1002/jmv.1890440313</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Base Sequence Biological and medical sciences Blood Donors chronic hepatitis Female Genotype HBV subtypes HCV genotypes hemodialysis Hepacivirus - classification Hepacivirus - genetics Hepatitis Antibodies - blood Hepatitis B - complications Hepatitis B - epidemiology Hepatitis B Surface Antigens - blood hepatitis B virus (HBV) Hepatitis C - complications Hepatitis C - epidemiology Hepatitis C Antibodies hepatitis C virus hepatitis C virus (HCV) Human viral diseases Humans Immunoenzyme Techniques Infectious diseases Kidney Failure, Chronic - complications kidney transplantation Kidney Transplantation - adverse effects Liver Diseases - complications Male Medical sciences Middle Aged Molecular Sequence Data peritoneal dialysis Renal Dialysis - adverse effects RNA, Viral - blood Thailand - epidemiology Tropical medicine Viral diseases Viral hepatitis |
title | Hepatitis C virus infection in patients with chronic liver disease or chronic renal failure and blood donors in Thailand |
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