Chronic HDV/HBV co-infection: Predictors of disease stage – a case series of HDV-3 patients
Background & Aims Chronic HDV/HBV co-infection is perhaps the most intriguing amongst all viral hepatitis. Only few studies focus deeply on this topic, particularly with patients infected with HDV-3. This study aimed to identify predictors of advanced disease, examining a cross-sectional data of...
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Veröffentlicht in: | Journal of hepatology 2014-12, Vol.61 (6), p.1205-1211 |
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creator | Braga, Wornei Silva Miranda de Oliveira, Cintia Mara Costa de Araújo, José Ribamar Castilho, Marcia da Costa Rocha, Joelma Martins Gimaque, Joao Bosco de Lima Silva, Maria Luana Cristiny Rodrigues Vasconcelos, Heline Lira Ramasawmy, Rajendranath Paraná, Raymundo |
description | Background & Aims Chronic HDV/HBV co-infection is perhaps the most intriguing amongst all viral hepatitis. Only few studies focus deeply on this topic, particularly with patients infected with HDV-3. This study aimed to identify predictors of advanced disease, examining a cross-sectional data of 64 patients. Methods Histological grading was used to characterize the disease stages and viral loads were tested as predictors of necroinflammatory activity and fibrosis. Results We identified three HDV/HBV co-infection patterns: patients with predominant HDV replication (56.3%), patients with similar viral loads of both viruses (40.6%), and patients with predominant HBV replication (3.1%). Mean HDV-RNA showed a positive trend regarding inflammatory activity and grade of fibrosis. HDV viral load correlated positively with serum levels of liver enzymes and inversely with platelets count. HBV viral load showed no correlation with any of the above parameters. Advanced fibrosis was associated with age, splenomegaly, and HDV viral load of more than 2 log10 . Multiple logistic regression confirmed the independent effect of HDV viral predominance. Advanced necroinflammatory activity was independently associated with HDV viral load and splenomegaly. Conclusions HDV may possibly play an important and direct role in the establishment of necroinflammatory activity and fibrosis. Data show an indigenous HDV genotype, HDV-3, similar to those described in the Amazon region. |
doi_str_mv | 10.1016/j.jhep.2014.05.041 |
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Only few studies focus deeply on this topic, particularly with patients infected with HDV-3. This study aimed to identify predictors of advanced disease, examining a cross-sectional data of 64 patients. Methods Histological grading was used to characterize the disease stages and viral loads were tested as predictors of necroinflammatory activity and fibrosis. Results We identified three HDV/HBV co-infection patterns: patients with predominant HDV replication (56.3%), patients with similar viral loads of both viruses (40.6%), and patients with predominant HBV replication (3.1%). Mean HDV-RNA showed a positive trend regarding inflammatory activity and grade of fibrosis. HDV viral load correlated positively with serum levels of liver enzymes and inversely with platelets count. HBV viral load showed no correlation with any of the above parameters. Advanced fibrosis was associated with age, splenomegaly, and HDV viral load of more than 2 log10 . Multiple logistic regression confirmed the independent effect of HDV viral predominance. Advanced necroinflammatory activity was independently associated with HDV viral load and splenomegaly. Conclusions HDV may possibly play an important and direct role in the establishment of necroinflammatory activity and fibrosis. Data show an indigenous HDV genotype, HDV-3, similar to those described in the Amazon region.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2014.05.041</identifier><identifier>PMID: 24905491</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adolescent ; Adult ; Amino Acid Sequence ; Brazil - epidemiology ; Comorbidity ; Cross-Sectional Studies ; Disease Progression ; Female ; Fibrosis ; Gastroenterology and Hepatology ; Genotype ; Hepatitis B and D coinfection ; Hepatitis B virus - genetics ; Hepatitis B virus - physiology ; Hepatitis B, Chronic - diagnosis ; Hepatitis B, Chronic - epidemiology ; Hepatitis B, Chronic - genetics ; Hepatitis D virus ; Hepatitis D, Chronic - diagnosis ; Hepatitis D, Chronic - epidemiology ; Hepatitis D, Chronic - genetics ; Hepatitis Delta Virus - genetics ; Hepatitis Delta Virus - physiology ; Humans ; Liver - enzymology ; Logistic Models ; Male ; METAVIR ; Middle Aged ; Molecular Sequence Data ; Severity of Illness Index ; Viral Load ; Virus Replication - physiology ; Young Adult</subject><ispartof>Journal of hepatology, 2014-12, Vol.61 (6), p.1205-1211</ispartof><rights>European Association for the Study of the Liver</rights><rights>2014 European Association for the Study of the Liver</rights><rights>Copyright © 2014 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c547t-b8aa75184a54602a32ec8a9a4a2e19718a523aa132af4648142a9599236d13d33</citedby><cites>FETCH-LOGICAL-c547t-b8aa75184a54602a32ec8a9a4a2e19718a523aa132af4648142a9599236d13d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168827814003894$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24905491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Braga, Wornei Silva Miranda</creatorcontrib><creatorcontrib>de Oliveira, Cintia Mara Costa</creatorcontrib><creatorcontrib>de Araújo, José Ribamar</creatorcontrib><creatorcontrib>Castilho, Marcia da Costa</creatorcontrib><creatorcontrib>Rocha, Joelma Martins</creatorcontrib><creatorcontrib>Gimaque, Joao Bosco de Lima</creatorcontrib><creatorcontrib>Silva, Maria Luana Cristiny Rodrigues</creatorcontrib><creatorcontrib>Vasconcelos, Heline Lira</creatorcontrib><creatorcontrib>Ramasawmy, Rajendranath</creatorcontrib><creatorcontrib>Paraná, Raymundo</creatorcontrib><title>Chronic HDV/HBV co-infection: Predictors of disease stage – a case series of HDV-3 patients</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>Background & Aims Chronic HDV/HBV co-infection is perhaps the most intriguing amongst all viral hepatitis. Only few studies focus deeply on this topic, particularly with patients infected with HDV-3. This study aimed to identify predictors of advanced disease, examining a cross-sectional data of 64 patients. Methods Histological grading was used to characterize the disease stages and viral loads were tested as predictors of necroinflammatory activity and fibrosis. Results We identified three HDV/HBV co-infection patterns: patients with predominant HDV replication (56.3%), patients with similar viral loads of both viruses (40.6%), and patients with predominant HBV replication (3.1%). Mean HDV-RNA showed a positive trend regarding inflammatory activity and grade of fibrosis. HDV viral load correlated positively with serum levels of liver enzymes and inversely with platelets count. HBV viral load showed no correlation with any of the above parameters. Advanced fibrosis was associated with age, splenomegaly, and HDV viral load of more than 2 log10 . Multiple logistic regression confirmed the independent effect of HDV viral predominance. Advanced necroinflammatory activity was independently associated with HDV viral load and splenomegaly. Conclusions HDV may possibly play an important and direct role in the establishment of necroinflammatory activity and fibrosis. Data show an indigenous HDV genotype, HDV-3, similar to those described in the Amazon region.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Amino Acid Sequence</subject><subject>Brazil - epidemiology</subject><subject>Comorbidity</subject><subject>Cross-Sectional Studies</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Gastroenterology and Hepatology</subject><subject>Genotype</subject><subject>Hepatitis B and D coinfection</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B virus - physiology</subject><subject>Hepatitis B, Chronic - diagnosis</subject><subject>Hepatitis B, Chronic - epidemiology</subject><subject>Hepatitis B, Chronic - genetics</subject><subject>Hepatitis D virus</subject><subject>Hepatitis D, Chronic - diagnosis</subject><subject>Hepatitis D, Chronic - epidemiology</subject><subject>Hepatitis D, Chronic - genetics</subject><subject>Hepatitis Delta Virus - genetics</subject><subject>Hepatitis Delta Virus - physiology</subject><subject>Humans</subject><subject>Liver - enzymology</subject><subject>Logistic Models</subject><subject>Male</subject><subject>METAVIR</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>Severity of Illness Index</subject><subject>Viral Load</subject><subject>Virus Replication - physiology</subject><subject>Young Adult</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1DAUhS0EokPhBVggL9kk9V8cGyEkGAqDVAkkoDtk3To31CETD3YGqTvegTfsk-B0CgsWrCxdfedI_g4hjzmrOeP6ZKiHS9zVgnFVs6Zmit8hK64Zq5hW_C5ZFchURrTmiDzIeWCMSWbVfXIklGWNsnxFvqwvU5yCp5vX5yebV-fUxypMPfo5xOkZ_ZCwC36OKdPY0y5khIw0z_AV6fXPXxSovzlgCniDlJpK0h3MAac5PyT3ehgzPrp9j8nnN6ef1pvq7P3bd-uXZ5VvVDtXFwagbbhR0CjNBEiB3oAFBQK5bbmBRkgALgX0SivDlQDbWCuk7rjspDwmTw-9uxS_7zHPbhuyx3GECeM-O66FtVq12hRUHFCfYs4Je7dLYQvpynHmFq1ucItWt2h1rHFFawk9ue3fX2yx-xv547EAzw8All_-CJhc9sWAL_ZScem6GP7f_-KfuB9DWQXGb3iFeYj7NBV_jrssHHMfl2GXXbkqkxqr5G-Sapuh</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Braga, Wornei Silva Miranda</creator><creator>de Oliveira, Cintia Mara Costa</creator><creator>de Araújo, José Ribamar</creator><creator>Castilho, Marcia da Costa</creator><creator>Rocha, Joelma Martins</creator><creator>Gimaque, Joao Bosco de Lima</creator><creator>Silva, Maria Luana Cristiny Rodrigues</creator><creator>Vasconcelos, Heline Lira</creator><creator>Ramasawmy, Rajendranath</creator><creator>Paraná, Raymundo</creator><general>Elsevier B.V</general><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>7X8</scope></search><sort><creationdate>20141201</creationdate><title>Chronic HDV/HBV co-infection: Predictors of disease stage – a case series of HDV-3 patients</title><author>Braga, Wornei Silva Miranda ; de Oliveira, Cintia Mara Costa ; de Araújo, José Ribamar ; Castilho, Marcia da Costa ; Rocha, Joelma Martins ; Gimaque, Joao Bosco de Lima ; Silva, Maria Luana Cristiny Rodrigues ; Vasconcelos, Heline Lira ; Ramasawmy, Rajendranath ; Paraná, Raymundo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c547t-b8aa75184a54602a32ec8a9a4a2e19718a523aa132af4648142a9599236d13d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Amino Acid Sequence</topic><topic>Brazil - epidemiology</topic><topic>Comorbidity</topic><topic>Cross-Sectional Studies</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Gastroenterology and Hepatology</topic><topic>Genotype</topic><topic>Hepatitis B and D coinfection</topic><topic>Hepatitis B virus - genetics</topic><topic>Hepatitis B virus - physiology</topic><topic>Hepatitis B, Chronic - diagnosis</topic><topic>Hepatitis B, Chronic - epidemiology</topic><topic>Hepatitis B, Chronic - genetics</topic><topic>Hepatitis D virus</topic><topic>Hepatitis D, Chronic - diagnosis</topic><topic>Hepatitis D, Chronic - epidemiology</topic><topic>Hepatitis D, Chronic - genetics</topic><topic>Hepatitis Delta Virus - genetics</topic><topic>Hepatitis Delta Virus - physiology</topic><topic>Humans</topic><topic>Liver - enzymology</topic><topic>Logistic Models</topic><topic>Male</topic><topic>METAVIR</topic><topic>Middle Aged</topic><topic>Molecular Sequence Data</topic><topic>Severity of Illness Index</topic><topic>Viral Load</topic><topic>Virus Replication - physiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Braga, Wornei Silva Miranda</creatorcontrib><creatorcontrib>de Oliveira, Cintia Mara Costa</creatorcontrib><creatorcontrib>de Araújo, José Ribamar</creatorcontrib><creatorcontrib>Castilho, Marcia da Costa</creatorcontrib><creatorcontrib>Rocha, Joelma Martins</creatorcontrib><creatorcontrib>Gimaque, Joao Bosco de Lima</creatorcontrib><creatorcontrib>Silva, Maria Luana Cristiny Rodrigues</creatorcontrib><creatorcontrib>Vasconcelos, Heline Lira</creatorcontrib><creatorcontrib>Ramasawmy, Rajendranath</creatorcontrib><creatorcontrib>Paraná, Raymundo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Braga, Wornei Silva Miranda</au><au>de Oliveira, Cintia Mara Costa</au><au>de Araújo, José Ribamar</au><au>Castilho, Marcia da Costa</au><au>Rocha, Joelma Martins</au><au>Gimaque, Joao Bosco de Lima</au><au>Silva, Maria Luana Cristiny Rodrigues</au><au>Vasconcelos, Heline Lira</au><au>Ramasawmy, Rajendranath</au><au>Paraná, Raymundo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic HDV/HBV co-infection: Predictors of disease stage – a case series of HDV-3 patients</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>61</volume><issue>6</issue><spage>1205</spage><epage>1211</epage><pages>1205-1211</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><abstract>Background & Aims Chronic HDV/HBV co-infection is perhaps the most intriguing amongst all viral hepatitis. Only few studies focus deeply on this topic, particularly with patients infected with HDV-3. This study aimed to identify predictors of advanced disease, examining a cross-sectional data of 64 patients. Methods Histological grading was used to characterize the disease stages and viral loads were tested as predictors of necroinflammatory activity and fibrosis. Results We identified three HDV/HBV co-infection patterns: patients with predominant HDV replication (56.3%), patients with similar viral loads of both viruses (40.6%), and patients with predominant HBV replication (3.1%). Mean HDV-RNA showed a positive trend regarding inflammatory activity and grade of fibrosis. HDV viral load correlated positively with serum levels of liver enzymes and inversely with platelets count. HBV viral load showed no correlation with any of the above parameters. Advanced fibrosis was associated with age, splenomegaly, and HDV viral load of more than 2 log10 . Multiple logistic regression confirmed the independent effect of HDV viral predominance. Advanced necroinflammatory activity was independently associated with HDV viral load and splenomegaly. Conclusions HDV may possibly play an important and direct role in the establishment of necroinflammatory activity and fibrosis. Data show an indigenous HDV genotype, HDV-3, similar to those described in the Amazon region.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>24905491</pmid><doi>10.1016/j.jhep.2014.05.041</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Amino Acid Sequence Brazil - epidemiology Comorbidity Cross-Sectional Studies Disease Progression Female Fibrosis Gastroenterology and Hepatology Genotype Hepatitis B and D coinfection Hepatitis B virus - genetics Hepatitis B virus - physiology Hepatitis B, Chronic - diagnosis Hepatitis B, Chronic - epidemiology Hepatitis B, Chronic - genetics Hepatitis D virus Hepatitis D, Chronic - diagnosis Hepatitis D, Chronic - epidemiology Hepatitis D, Chronic - genetics Hepatitis Delta Virus - genetics Hepatitis Delta Virus - physiology Humans Liver - enzymology Logistic Models Male METAVIR Middle Aged Molecular Sequence Data Severity of Illness Index Viral Load Virus Replication - physiology Young Adult |
title | Chronic HDV/HBV co-infection: Predictors of disease stage – a case series of HDV-3 patients |
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