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
Hauptverfasser: 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
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container_end_page 1211
container_issue 6
container_start_page 1205
container_title Journal of hepatology
container_volume 61
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. 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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. 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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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