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1.
Transplantation ; 104(3): 476-481, 2020 03.
Article in English | MEDLINE | ID: mdl-31634329

ABSTRACT

The development of multiple highly effective and safe direct-acting antivirals to treat hepatitis C virus (HCV) has resulted in greater ease and confidence in managing HCV infection in transplant recipients that in turn has impacted the solid organ transplant community as well. In the United States, the opioid epidemic has increased the number of overdose deaths with a concomitant increase in younger HCV viremic donors after brain death being identified. At the same time, a decrease in HCV viremic transplant candidates has led to a growing interest in exploring the use of HCV viremic liver and kidney donor allografts in HCV-negative recipients. To date, experience with the use of HCV viremic liver and kidney allografts in HCV-negative recipients is limited to a few small prospective research trials, case series, and case reports. There are also limited data on recipient and donor selection for HCV viremic liver and kidney allografts. In response to this rapidly changing landscape in the United States, experts in the field of viral hepatitis and liver and kidney transplantation convened a meeting to review current data on liver and kidney recipient selection and developed consensus opinions related specifically to recipient and donor selection of HCV viremic liver and kidney allografts.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C, Chronic/transmission , Kidney Transplantation/adverse effects , Liver Transplantation/adverse effects , Patient Selection , Postoperative Complications/prevention & control , Allografts/pathology , Allografts/virology , Antibiotic Prophylaxis/standards , Biopsy , Consensus , Consensus Development Conferences as Topic , Donor Selection/standards , Hepacivirus/isolation & purification , Hepatitis C, Chronic/virology , Humans , Kidney/virology , Kidney Transplantation/standards , Liver/pathology , Liver/virology , Liver Transplantation/standards , Postoperative Complications/virology , Transplant Recipients , United States , Viremia/transmission , Viremia/virology
2.
Gac Med Mex ; 155(1): 80-89, 2019.
Article in Spanish | MEDLINE | ID: mdl-30799461

ABSTRACT

La infección por el virus de hepatitis C es un problema global de salud pública; en México aproximadamente 2 % de la población se encuentra infectada. En niños, los datos de prevalencia son variables según la edad, pero se estima que 0.1 a 2 % de los niños presenta infección crónica por virus de hepatitis C, cuya principal vía de transmisión es la perinatal. Actualmente existen antivirales de acción directa aprobados en adultos con una tasa de respuesta viral sostenida superior a 95 %; sin embargo, en niños aún son pocos los estudios que confirman su seguridad y efectividad. Aunque todavía estamos lejos de la meta, avanzamos rápidamente hacia un tratamiento óptimo de curación también para pacientes pediátricos.


Infection with hepatitis C virus is a global health problem; in Mexico, approximately 2% of the population is infected. In children, data on prevalence are variable according to the age group, but 0.1-2% of children are estimated to have chronic infection with hepatitis C virus, the main way of transmission of which is perinatal. Currently, there are direct-acting antiviral agents approved in adults that offer a sustained viral response rate higher than 95%; however, in children there are still only few studies confirming their safety and effectiveness. Although we are still far from the goal, we are rapidly advancing towards an optimal curative treatment also for pediatric patients.


Subject(s)
Antiviral Agents/administration & dosage , Hepatitis C, Chronic/epidemiology , Age Factors , Antiviral Agents/adverse effects , Child , Female , Hepatitis C, Chronic/drug therapy , Hepatitis C, Chronic/transmission , Humans , Infectious Disease Transmission, Vertical/statistics & numerical data , Mexico/epidemiology , Pregnancy , Pregnancy Complications, Infectious/virology , Prevalence
3.
Gac. méd. Méx ; Gac. méd. Méx;155(1): 80-89, Jan.-Feb. 2019. tab
Article in English, Spanish | LILACS | ID: biblio-1286463

ABSTRACT

Resumen La infección por el virus de hepatitis C es un problema global de salud pública; en México aproximadamente 2 % de la población se encuentra infectada. En niños, los datos de prevalencia son variables según la edad, pero se estima que 0.1 a 2 % de los niños presenta infección crónica por virus de hepatitis C, cuya principal vía de transmisión es la perinatal. Actualmente existen antivirales de acción directa aprobados en adultos con una tasa de respuesta viral sostenida superior a 95 %; sin embargo, en niños aún son pocos los estudios que confirman su seguridad y efectividad. Aunque todavía estamos lejos de la meta, avanzamos rápidamente hacia un tratamiento óptimo de curación también para pacientes pediátricos.


Abstract Infection with hepatitis C virus is a global health problem; in Mexico, approximately 2% of the population is infected. In children, data on prevalence are variable according to the age group, but 0.1-2% of children are estimated to have chronic infection with hepatitis C virus, the main way of transmission of which is perinatal. Currently, there are direct-acting antiviral agents approved in adults that offer a sustained viral response rate higher than 95%; however, in children there are still only few studies confirming their safety and effectiveness. Although we are still far from the goal, we are rapidly advancing towards an optimal curative treatment also for pediatric patients.


Subject(s)
Humans , Female , Pregnancy , Child , Antiviral Agents/administration & dosage , Hepatitis C, Chronic/epidemiology , Antiviral Agents/adverse effects , Pregnancy Complications, Infectious/virology , Prevalence , Age Factors , Infectious Disease Transmission, Vertical/statistics & numerical data , Hepatitis C, Chronic/drug therapy , Hepatitis C, Chronic/transmission , Mexico/epidemiology
4.
Rev. medica electron ; 40(2): 383-393, mar.-abr. 2018. ilus
Article in Spanish | LILACS, CUMED | ID: biblio-902306

ABSTRACT

RESUMEN El virus de la hepatitis C es la principal infección trasmitida por los derivados de la sangre en los Estados Unidos, con 3.2 millones de individuos infectados. El alfa interferón inyectable ha sido históricamente la piedra angular en la terapia del virus de hepatitis C. Se revisaron las publicaciones los trabajos publicados en Medline, Scielo, PubMed, e Hinari, hasta comienzos del año 2016. Las principales palabras clave utilizadas fueron virus de la hepatitis C, hepatitis C crónica, Interferón, antivirales. Recientes adelantos han llevado a la disponibilidad de nuevos medicamentos antivirales, que con el desarrollo de nuevas terapias orales libres de interferón han convertido la terapia del virus de la hepatitis C más eficaz además de simplificar los regímenes del tratamiento. Aunque estos regímenes de tratamiento aún permanecen complicados, las nuevas recomendaciones y guías evolucionan rápidamente. El rápido desarrollo de nuevas terapias para la hepatitis C, han logrado métodos más eficaces con menos reacciones adversas que optimizan el tratamiento de estos enfermos (AU).


ABSTRACT The hepatitis C virus is the main infection transmitted by blood products in the United States, with 3.2 million of infected individuals. The injected alpha interferon has historically been the key stone in the therapy of the hepatitis C virus. The works published in Medline, Scielo, PubMed and Hinary until the beginning of 2016 were reviewed. The main used key words were HVC, cronic hepatitis C, interferon, antivirals. Recent advances have led to the availability on new antiviral drugs, developing new interferon-free oral therapies that make the therapy of hepatitis C virus more efficacious and make easier the treatment regimens. Although these treatment regimens are still complicated, the new recommendations and guidelines evolve quickly. The fast development of new therapies against hepatitis C has led to more efficacious methods with less adverse reactions, optimizing the treatment of these patients (AU).


Subject(s)
Humans , Antiviral Agents , Virology/methods , Risk Factors , Interferon-alpha/therapeutic use , Hepacivirus/pathogenicity , Hepatitis C, Chronic/epidemiology , Epidemiological Monitoring , United States/epidemiology , Hepacivirus/drug effects , Clinical Laboratory Techniques/methods , Hepatitis C, Chronic/complications , Hepatitis C, Chronic/prevention & control , Hepatitis C, Chronic/drug therapy , Hepatitis C, Chronic/transmission , Cuba/epidemiology , Kidney Function Tests/methods , Liver Function Tests
5.
São Paulo med. j ; São Paulo med. j;136(2): 109-115, Mar.-Apr. 2018. tab, graf
Article in English | LILACS | ID: biblio-904153

ABSTRACT

ABSTRACT BACKGROUND: Hepatitis C virus infection is one of the main causes of chronic liver disease, with high death rates. The aim here was to analyze case outcomes, sociodemographic and clinical characteristics and spatial distribution among patients diagnosed with hepatitis C in the city of Santa Cruz do Sul (RS), Brazil. DESIGN AND SETTING: Cross-sectional study on 200 cases of hepatitis C in Santa Cruz do Sul that were notified between 2002 and 2015. METHODS: Secondary data including sociodemographic and clinical variables and type of outcome (death, follow-up, abandonment or clinical cure) were gathered. The spatial distribution analysis on hepatitis C virus cases according to outcome was based on information regarding residential address. RESULTS: 58.5% of the patients were 41 years of age and over, 67% were males and 92.5% had the chronic form of the disease. The most frequent transmission route was illicit drug injection (29%); 15.1% of the patients presented coinfection with the human immunodeficiency virus (HIV). Regarding outcomes, 31% achieved clinical cure, 10% died and 20% abandoned follow-up. The cases studied were mainly located in regions of the city characterized by lower socioeconomic status, with high frequency of places used for drug trafficking. CONCLUSION: The population consisted of adults aged 41 years and over, mostly with chronic hepatitis C. The most common transmission routes were illicit drug injection and blood transfusions. There were high rates of HIV coinfection and abandonment of disease monitoring and predominance of cases in neighborhoods with low socioeconomic status.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged , Young Adult , Hepatitis C, Chronic/mortality , Socioeconomic Factors , Brazil/epidemiology , Prevalence , Cross-Sectional Studies , Hepatitis C, Chronic/transmission , Geographic Mapping
6.
Sao Paulo Med J ; 136(2): 109-115, 2018.
Article in English | MEDLINE | ID: mdl-29267536

ABSTRACT

BACKGROUND: Hepatitis C virus infection is one of the main causes of chronic liver disease, with high death rates. The aim here was to analyze case outcomes, sociodemographic and clinical characteristics and spatial distribution among patients diagnosed with hepatitis C in the city of Santa Cruz do Sul (RS), Brazil. DESIGN AND SETTING: Cross-sectional study on 200 cases of hepatitis C in Santa Cruz do Sul that were notified between 2002 and 2015. METHODS: Secondary data including sociodemographic and clinical variables and type of outcome (death, follow-up, abandonment or clinical cure) were gathered. The spatial distribution analysis on hepatitis C virus cases according to outcome was based on information regarding residential address. RESULTS: 58.5% of the patients were 41 years of age and over, 67% were males and 92.5% had the chronic form of the disease. The most frequent transmission route was illicit drug injection (29%); 15.1% of the patients presented coinfection with the human immunodeficiency virus (HIV). Regarding outcomes, 31% achieved clinical cure, 10% died and 20% abandoned follow-up. The cases studied were mainly located in regions of the city characterized by lower socioeconomic status, with high frequency of places used for drug trafficking. CONCLUSION: The population consisted of adults aged 41 years and over, mostly with chronic hepatitis C. The most common transmission routes were illicit drug injection and blood transfusions. There were high rates of HIV coinfection and abandonment of disease monitoring and predominance of cases in neighborhoods with low socioeconomic status.


Subject(s)
Hepatitis C, Chronic/mortality , Adult , Aged , Brazil/epidemiology , Cross-Sectional Studies , Female , Geographic Mapping , Hepatitis C, Chronic/transmission , Humans , Male , Middle Aged , Prevalence , Socioeconomic Factors , Young Adult
7.
Ann Hepatol ; 14(5): 642-51, 2015.
Article in English | MEDLINE | ID: mdl-26256892

ABSTRACT

BACKGROUND: The evolving pattern of HCV genotypes (GTs) and risk factors (RFs) in HCV-infected patients in Mexico is poorly understood. This study aimed to access the temporal trend of HCV GTs and RFs in HCV patients from two care centers. MATERIAL AND METHODS: Chronic HCV patients [177 and 153 patients from the Northeast (NE) and Central West (CW) regions, respectively] were selected. Baseline features were demographics, date of birth (DOB), blood transfusion before 1992 (BTb1992), RFs, sexual promiscuity (SP), dental procedure (DP), injection drug use (IDU), viral load (VL), GTs, cirrhosis status and antiviral therapy (AT). Data were analyzed by Chi-square test for trends, unpaired T-test, and logistic regression. RESULTS: HCV GT distribution was: GT1, 67%; GT2, 16%; GT3, 12% and GT4, 1%. RFs were BTb1992, 56%; surgeries, 56%; tattooing, 18% and IDU, 16%. GT1a mostly prevailed in CW than NE patients. GT1b, surgeries, BTb1992 and cirrhosis were more prevalent in older patients (p < 0.05); GT3, male gender IDU, SP, and tattooing showed an upward trend as younger were the patients in both regions (p < 0.05), contrariwise to the prevalence of GT1b. BTb1992 and surgeries were seen in elder women; BTb1992 was an independent RF for GT1. Age ≥ 50 years old, GT1 and exposure to AT (p < 0.05) were associated with cirrhosis. CONCLUSION: GT1a prevalence in CW Mexico remained stable, whereas GT3 increased and GT1b decreased in younger patients in both regions, along with associated RFs. Further regional molecular epidemiology and RF analyses are required in order to avoid the dissemination of new cases of HCV infection.


Subject(s)
Hepacivirus/genetics , Hepatitis C, Chronic/epidemiology , Hepatitis C, Chronic/virology , Substance-Related Disorders/epidemiology , Adult , Age Factors , Antiviral Agents/therapeutic use , Chi-Square Distribution , Cross-Sectional Studies , Female , Genotype , Hepacivirus/drug effects , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/drug therapy , Hepatitis C, Chronic/transmission , Humans , Liver Cirrhosis/epidemiology , Liver Cirrhosis/virology , Logistic Models , Male , Mexico/epidemiology , Middle Aged , Molecular Epidemiology , Odds Ratio , Phenotype , Prevalence , Residence Characteristics , Retrospective Studies , Risk Factors , Sex Factors , Substance-Related Disorders/diagnosis , Tattooing/adverse effects , Time Factors , Transfusion Reaction , Unsafe Sex , Viral Load
8.
World J Gastroenterol ; 21(2): 408-22, 2015 Jan 14.
Article in English | MEDLINE | ID: mdl-25593456

ABSTRACT

Hepatitis C virus (HCV) infection is highly prevalent among chronic kidney disease (CKD) subjects under hemodialysis and in kidney transplantation (KT) recipients, being an important cause of morbidity and mortality in these patients. The vast majority of HCV chronic infections in the hemodialysis setting are currently attributable to nosocomial transmission. Acute and chronic hepatitis C exhibits distinct clinical and laboratorial features, which can impact on management and treatment decisions. In hemodialysis subjects, acute infections are usually asymptomatic and anicteric; since spontaneous viral clearance is very uncommon in this context, acute infections should be treated as soon as possible. In KT recipients, the occurrence of acute hepatitis C can have a more severe course, with a rapid progression of liver fibrosis. In these patients, it is recommended to use pegylated interferon (PEG-IFN) in combination with ribavirin, with doses adjusted according to estimated glomerular filtration rate. There is no evidence suggesting that chronic hepatitis C exhibits a more aggressive course in CKD subjects under conservative management. In these subjects, indication of treatment with PEG-IFN plus ribavirin relies on the CKD stage, rate of progression of renal dysfunction and the possibility of a preemptive transplant. HCV infection has been associated with both liver disease-related deaths and cardiovascular mortality in hemodialysis patients. Among those individuals, low HCV viral loads and the phenomenon of intermittent HCV viremia are often observed, and sequential HCV RNA monitoring is needed. Despite the poor tolerability and suboptimal efficacy of antiviral therapy in CKD patients, many patients can achieve sustained virological response, which improve patient and graft outcomes. Hepatitis C eradication before KT theoretically improves survival and reduces the occurrence of chronic graft nephropathy, de novo glomerulonephritis and post-transplant diabetes mellitus.


Subject(s)
Antiviral Agents/therapeutic use , Cross Infection/drug therapy , Hepatitis C, Chronic/drug therapy , Kidney Transplantation , Renal Dialysis , Renal Insufficiency, Chronic/therapy , Antiviral Agents/adverse effects , Cross Infection/diagnosis , Cross Infection/mortality , Cross Infection/transmission , Drug Therapy, Combination , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/mortality , Hepatitis C, Chronic/transmission , Humans , Kidney Transplantation/adverse effects , Kidney Transplantation/mortality , Renal Dialysis/adverse effects , Renal Dialysis/mortality , Renal Insufficiency, Chronic/diagnosis , Renal Insufficiency, Chronic/mortality , Risk Factors , Treatment Outcome
9.
Rev Soc Bras Med Trop ; 47(3): 295-301, 2014.
Article in English | MEDLINE | ID: mdl-25075479

ABSTRACT

INTRODUCTION: Hepatitis C virus (HCV) is primarily transmitted via contact with the blood of infected patients, although the form of contact has not been identified for a significant percentage of carriers. The present study evaluated possible risk factors for HCV transmission in a medium-sized town located in the northwest region of the State of São Paulo. METHODS: This was a case-control study, with the case group consisting of 190 chronic HCV carriers older than 18 years residing in the municipality of Catanduva. The control group also consisted of 190 individuals with HCV-negative serology. The groups were paired (1:1) for gender, age range (± five years), and place of residence. The same structured questionnaire was applied to all subjects, who gave written informed consent to participate in the study. The data were statistically analyzed using crude and adjusted logistic regression, and the results were expressed as odds ratios with a 95% confidence interval. RESULTS: The demographic profiles of the groups indicated a predominance of males (68.9%) and mean ages of 47.1 years (case group) and 47.3 years (control group). After adjusting for conditional regression, the following factors were found to represent risks for HCV: history of sexually transmitted disease (STD) and blood transfusion; accidents with syringes and/or needles; tattoos; and the use of non-injectable drugs and injectable medications. CONCLUSIONS: The transmission of HCV via the blood route has been well characterized. Other forms of contact with human blood and/or secretions are likely to transmit the virus, although with a lower frequency of occurrence.


Subject(s)
Hepacivirus/immunology , Hepatitis C, Chronic/transmission , Brazil/epidemiology , Case-Control Studies , Female , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/epidemiology , Humans , Male , Middle Aged , Risk Factors
10.
Rev. Soc. Bras. Med. Trop ; Rev. Soc. Bras. Med. Trop;47(3): 295-301, May-Jun/2014. tab
Article in English | LILACS | ID: lil-716408

ABSTRACT

Introduction Hepatitis C virus (HCV) is primarily transmitted via contact with the blood of infected patients, although the form of contact has not been identified for a significant percentage of carriers. The present study evaluated possible risk factors for HCV transmission in a medium-sized town located in the northwest region of the State of São Paulo. Methods This was a case-control study, with the case group consisting of 190 chronic HCV carriers older than 18 years residing in the municipality of Catanduva. The control group also consisted of 190 individuals with HCV-negative serology. The groups were paired (1:1) for gender, age range (± five years), and place of residence. The same structured questionnaire was applied to all subjects, who gave written informed consent to participate in the study. The data were statistically analyzed using crude and adjusted logistic regression, and the results were expressed as odds ratios with a 95% confidence interval. Results The demographic profiles of the groups indicated a predominance of males (68.9%) and mean ages of 47.1 years (case group) and 47.3 years (control group). After adjusting for conditional regression, the following factors were found to represent risks for HCV: history of sexually transmitted disease (STD) and blood transfusion; accidents with syringes and/or needles; tattoos; and the use of non-injectable drugs and injectable medications. Conclusions The transmission of HCV via the blood route has been well characterized. Other forms of contact with human blood and/or secretions are likely to transmit the virus, although with a lower frequency of occurrence. .


Subject(s)
Female , Humans , Male , Middle Aged , Hepacivirus/immunology , Hepatitis C, Chronic/transmission , Brazil/epidemiology , Case-Control Studies , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/epidemiology , Risk Factors
11.
Rio de Janeiro; s.n; 2014. 145f p. ilus, tab, mapas.
Thesis in Portuguese | LILACS | ID: lil-750998

ABSTRACT

Introdução e objetivos: Polimorfismos naturais de resistência aos agentes antivirais de atuação direta (DAAs) no vírus da hepatite C (HCV) podem representar um fator limitante para a eficácia dessa terapia. A análise de sequências virais de regiões geográficas distintas pode apresentar diferenças significativas nas frequências de mutações de resistência aos DAAs. Neste contexto, o objetivo deste estudo foi investigar as mutações associadas à resistência aos DAAs nos genes nãoestruturais (NS) do HCV em isolados virais que circulam no Brasil. Métodos: Foram estudados um total de 390 sequências do genótipo 1 do HCV de pacientes brasileiros virgens de tratamento cronicamente infectados. O RNA viral foi extraído, e as regiões abrangendo os genes NS3, NS4 e NS5 foram amplificadas por RT-PCR e sequenciadas. Resultados: No domínio NS3/4A protease, a variação V36L foi encontrada em 5,60 porcento dos isolados do subtipo 1b, e a substituição T54S em 4,16 porcento das sequências do subtipo 1a; na posição 55, 4,16 porcento dos isolados continham a variação V55A, responsável por causar constrição no sítio de ligação do inibidor de protease boceprevir. Em relação à proteína NS4B, um isolado do subtipo 1b apresentou a substituição F98L, responsável por conferir resistência aos inibidores AP80978, PTC725 e silibina. Na proteína NS5A, 3,84 porcento das sequências do subtipo 1a mostraram as mutações de resistência M28T ou Y93H, e 13,46 porcento, as mutações secundárias H58P e E62D. Dentre os isolados do subtipo 1b, 3,70 porcento continham a mutação Y93H, e 14,8 porcento, as mutações secundárias R30Q, L31M, P58S e I280VEm NS5B, 25 porcento das sequências do subtipo 1b brasileiras apresentaram a variação L159F na população viral dominante, mas nenhuma sequência do subtipo 1a exibiu tal substituição...


Background and aims: Natural resistance polymorphisms to direct antiviral agents (DAAs)in hepatitis C virus (HCV) may represent a limiting factor for therapy efficacy. Analysis of viralsequences from distinct geographical regions may show significant differences in the frequencies ofresistance mutations to DAAs. In this context, the aim of this study was to investigate mutationsassociated with resistance to DAAs of HCV non-structural genes (NS) in viral isolates circulating inBrazil. Methods: A total of 390 HCV genotype 1 sequences from therapy-naive Brazilian patientschronically infected. Viral RNA was extracted, and the region encompassing the non-structuralgenes NS3, NS4, and NS5 was RT-PCR amplified and sequenced. Results: In the NS3/4A proteasedomain, a V36L variation was found in 5,60 percent of subtype 1b isolates and a T54S substitution in4,16 percent of subtype 1a sequences; at position 55, 4,16 percent of strains contained the V55A variationwhich is responsible to cause constriction in the binding site of the protease inhibitor boceprevir.Concerning the NS4B protein, one subtype 1b isolate showed the F98L substitution, responsible forconferring resistance to inhibitors AP80978, PTC725 and Silybin. In the NS5A protein, 3,84 percent ofsubtype 1a sequences showed the resistance mutations M28T and Y93H, while 13,46 percent , thesecondary mutations H58P and E62D. Among subtype 1b isolates, 3,70 percent of patients showed theY93H mutation, while 14,8 percent the secondary mutations R30Q, L31M, P58S and I280V. For NS5B,25 percent of Brazilian subtype 1b sequences presented the L159F variation in the dominant viralpopulation, but none of subtype 1a sequence showed such substitution. Moreover, 15 subtype 1bisolates (29 percent ), were observed the C316N variant, responsible to confer resistance to non-nucleosideinhibitors, while only 2,12 percent of subtype 1a isolates showed the C316Y substitution...


Subject(s)
Humans , Antiviral Agents/antagonists & inhibitors , Hepacivirus/chemistry , Hepatitis C, Chronic/transmission , RNA, Viral
12.
Infect Genet Evol ; 20: 465-70, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24140559

ABSTRACT

Globally, hepatitis C virus (HCV) infection affects approximately 130 million people and 3 million new infections occur annually. HCV is also recognized as an important cause of chronic liver disease in children. The absence of proofreading properties of the HCV RNA polymerase leads to a highly error prone replication process, allowing HCV to escape host immune response. The adaptive nature of HCV evolution dictates the outcome of the disease in many ways. Here, we investigated the molecular evolution of HCV in three unrelated children who acquired chronic HCV infection as a result of mother-to-child transmission, two of whom were also coinfected with HIV-1. The persistence of discrete HCV variants and their population structure were assessed using median joining network and Bayesian approaches. While patterns of viral evolution clearly differed between subjects, immune system dysfunction related to HIV coinfection or persistent HCV seronegativity stand as potential mechanisms to explain the lack of molecular evolution observed in these three cases. In contrast, treatment of HCV infection with PegIFN, which did not lead to sustained virologic responses in all 3 cases, was not associated with commensurate variations in the complexity of the variant spectrum. Finally, the differences in the degree of divergence suggest that the mode of transmission of the virus was not the main factor driving viral evolution.


Subject(s)
Hepacivirus/drug effects , Hepatitis C, Chronic/transmission , Infectious Disease Transmission, Vertical , Pregnancy Complications, Infectious/drug therapy , Antiviral Agents/therapeutic use , Child , Coinfection/virology , Evolution, Molecular , Female , Genetic Variation , HIV Infections/drug therapy , HIV Infections/transmission , HIV Infections/virology , HIV Seropositivity/drug therapy , HIV Seropositivity/transmission , HIV-1 , Hepacivirus/genetics , Hepatitis C, Chronic/drug therapy , Hepatitis C, Chronic/virology , Humans , Interferon alpha-2 , Interferon-alpha/therapeutic use , Male , Polyethylene Glycols/therapeutic use , Pregnancy , Pregnancy Complications, Infectious/virology , RNA, Viral , Recombinant Proteins/therapeutic use , Ribavirin/therapeutic use , Treatment Outcome
13.
Ann Hepatol ; 12(3): 399-407, 2013.
Article in English | MEDLINE | ID: mdl-23619256

ABSTRACT

INTRODUCTION: It is known that patients with chronic hepatitis C have a lower health-related quality of life (HRQOL) than the general population and evidence suggests that the hepatitis C virus (HCV) could exert direct neuropathic action on HRQOL. From this perspective, the virus clearance should be accompanied by improvement in HRQOL. Thus, we sought to review systematically the evidence in the literature and perform a meta-analysis of HRQOL changes caused by sustained virologic response (SVR). MATERIAL AND METHODS: The PubMed was searched using the keywords Hepatitis C, Quality of Life and Therapy. The reviewers came to a consensus on articles that were selected to full reading and those that should be included in the study and a meta-analysis was performed of mean change difference between responders and non-responders. RESULTS: Eleven studies were included in the systematic review and four in the metaanalysis. Of these, nine studies showed more favorable outcome for responders, and they had a better outcome even in studies that evaluated only cirrhotic patients, previous non-responders, relapsers, patients in first treatment and patients unaware of treatment response. Moreover, the meta-analysis showed that the general health and vitality domains had statistically significant mean change difference between responders and non-responders, presenting a summary effect of 6.3 (CI 95% 2.5-10.0) and 7.8 (CI 95% 3.4- 12.1) respectively. CONCLUSION: There is evidence indicating that SVR is accompanied by an improvement in HRQOL and patients reaching SVR have clinically relevant improvement in domains of general health and vitality.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C, Chronic/drug therapy , Quality of Life , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/psychology , Hepatitis C, Chronic/transmission , Humans , Surveys and Questionnaires , Treatment Outcome , Viral Load
14.
Actual. SIDA. infectol ; 21(79): 3-21, apr.2013. tab, graf
Article in Spanish | LILACS | ID: lil-776936

ABSTRACT

Aproximadamente 175 millones de personas están infectadas por el virus de la hepatitis C (VHC), lo que representa un 3% de la población mundial. En ausencia de tratamiento eficaz, un 25% de los pacientes desarrollan complicaciones hepáticas tras 25 años de hepatitis crónica C. Hasta hace poco, la única opción terapéutica en estos pacientes era la combinación de interferón pegilado (peg-IFN) y ribavirina (RBV). Alcanzaban la erradicación del VHC un 30-40% de los pacientes infectados con el genotipo 1 del VHC. Recientes avances han permitido desarrollar replicones y sistemas de cultivo tisulares para el VHC. Esto ha facilitado el diseño de fármacos antivirales directos (DAA) que inhiben específicamente la replicación del VHC. Los dos primeros inhibidores de la proteasa del VHC fueron aprobados en mayo de 2011. Permiten obtener tasas de curación en el 70% de los pacientes infectados con el genotipo 1 sin experiencia previa a interferón. La respuesta es menor en pacientes con fracasos previos, excepto en los recidivantes, en los que tasa de curación es del 90%...


Approximately 175 million people worldwide are chronically infected with the hepatitis C virus (HCV), representing 3% of the total world population. In the absence of successful therapy nearly 25% of these patients will develop hepatic complications within 25 years. Until recently, the only available therapeutic option for these patients was the combination of peginterferon-a plus ribavirin. Overall it allowed achievement of eradication in only 30-40% of patients infected by HCV genotype 1. The development of HCV replicons and the chance of producing infectious viral particles in culture systems have both enabled the rational design of direct-acting antivirals (DAA) that specifically inhibit HCV replication. The first two HCV protease inhibitors were marketed in May 2011. Triple therapy has increased the response rate to 70% in HCV genotype 1 carrier naïve to interferon. Although response rates are lower in prior failures, 90% sustained virological response rates are achieved in prior relapsers...


Subject(s)
Humans , Antiviral Agents/immunology , Clinical Trials, Phase III as Topic , Hepacivirus , HIV , Hepatitis C, Chronic/immunology , Hepatitis C, Chronic/therapy , Hepatitis C, Chronic/transmission , Protease Inhibitors/pharmacokinetics , Protease Inhibitors , Ribavirin/pharmacokinetics
15.
Arch. argent. pediatr ; 109(3): 245-250, jun. 2011. tab
Article in Spanish | LILACS | ID: lil-602395

ABSTRACT

La hepatitis C se adquiere por las vías parenteral, materno-fetal y sexual. Afecta al 3 por ciento de la población mundial. La transmisión vertical constituye la principal forma de diseminación del virus actualmente. La mayoría de los niños desarrolla enfermedad crónica asintomática; sin embargo, puede observarse progresión de la enfermedad en la edad pediátrica. Los anticuerpos contra el virus de la hepatitis C no permiten discriminar entre infección activa y resuelta. Se requiere la determinación por PCR del HCV-ARN. La combinación de peginterferón y ribavirina parece ser el tratamiento más eficaz. El desarrollo de nuevos fármacos, así como el de una vacuna, constituyen los próximos desafíos.


The modes of transmission of hepatitis C virus are parenteral, sexual and maternal-fetal. It affects 3 percent of the population worldwide. Currently, vertical infection is the main way of virus spreading. Most children are clinically asymptomatic, but progression of liver disease has been described. The positivity of antibodies against hepatitis C virus does not discriminate between active and resolved infection, so determination of serum HCV-RNA is necessary. The combination of peginterferon and ribavirin appears to be the most effective treatment. Future challenges are the development of new drugs and a vaccine.


Subject(s)
Humans , Male , Female , Child , Hepatitis C, Chronic/epidemiology , Hepatitis C, Chronic/therapy , Hepatitis C, Chronic/transmission , Infectious Disease Transmission, Vertical , Ribavirin/therapeutic use , Virus Diseases
16.
Ann Hepatol ; 9 Suppl: 34-8, 2010.
Article in English | MEDLINE | ID: mdl-20713993

ABSTRACT

The current optimal approach to detecting hepatitis C virus (HCV) infection involves screening people for risk factors and only testing selected individuals at risk. Blood transfusion from infectious donors, unsafe therapeutic injection practices, and illegal intravenous drug use have been the predominant modes of transmission of HCV infection. Virological markers that are currently used for the clinical management of patients with hepatitis C include serologic assays (ELISA or immunoblot assays), which detect specific antibodies (IgG) to HCV, and virological assays, which detect serum HCV RNA, by highly sensitive qualitative and quantitative techniques. The applicability of these tests is for the diagnoses and monitoring of the treatment but they have no role in the assessment of disease severity or prognosis. Patients diagnosed with HCV infection must be educated in order to avoid the spread of the disease to other people.


Subject(s)
Hepacivirus , Hepatitis C, Chronic/diagnosis , Mass Screening , Biomarkers/blood , Hepacivirus/genetics , Hepacivirus/immunology , Hepatitis C Antibodies/blood , Hepatitis C Antigens/blood , Hepatitis C, Chronic/epidemiology , Hepatitis C, Chronic/transmission , Humans , Mass Screening/methods , Practice Guidelines as Topic , Predictive Value of Tests , RNA, Viral/blood , Risk Assessment , Risk Factors
17.
Ann Hepatol ; 9 Suppl: 98-102, 2010.
Article in English | MEDLINE | ID: mdl-20714004

ABSTRACT

Infection with hepatitis C virus (HCV) is a worldwide health problem with more than 170 million infected individuals. In children, since 1992 almost all infections occurred through vertical transmission from an infected mother to her newborn infant. Natural history of HCV infection in children is not yet well defined, most children are asymptomatic and may remain so for decades. Most infected individuals (60-80%), regardless of their age at infection, become chronically infected with HCV. Spontaneous resolution in children appears to be infrequent. Positive HCV antibody implicate that patient has been exposed to the virus (EIA test). To discriminate between active or resolved HCV viral infection it is necessary to perform HCV RNA (PCR). Liver biopsy assess degree of liver injury and exclude concurrent diseases. HCV chronic infection is slow progressive in childhood. Progression of fibrosis seems to be a function of infection duration. Treatment objective is clearance of HCVRNA. IFNa is recognized as the drug approved for hepatitis C treatment in pediatric population. Combination therapy with IFNa or pegylated IFNa plus ribavirin is recently approved by US FDA and EMEA and clinical trials are in progress.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C, Chronic/drug therapy , Asymptomatic Infections , Biopsy , Child , Child, Preschool , Drug Therapy, Combination , Genotype , Hepacivirus/genetics , Hepacivirus/immunology , Hepatitis C Antibodies/blood , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/epidemiology , Hepatitis C, Chronic/transmission , Humans , Infant , Infant, Newborn , Infectious Disease Transmission, Vertical , Interferon-alpha/therapeutic use , RNA, Viral/blood , Ribavirin/therapeutic use , Risk Factors , Treatment Outcome , Viral Load
18.
Addiction ; 105(2): 311-8, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19922515

ABSTRACT

BACKGROUND: Human immunodeficiency virus (HIV) outbreaks occur among injecting drug users (IDUs), but where HIV is low insight is required into the future risk of increased transmission. The relationship between hepatitis C virus (HCV) and HIV prevalence among IDUs is explored to determine whether HCV prevalence could indicate HIV risk. METHODS: Systematic review of IDU HIV/HCV prevalence data and regression analysis using weighted prevalence estimates and time-series data. RESULTS: HIV/HCV prevalence estimates were obtained for 343 regions. In regions other than South America/sub-Saharan Africa (SAm/SSA), mean IDU HIV prevalence is likely to be negligible if HCV prevalence is <30% (95% confidence interval 22-38%) but increases progressively with HCV prevalence thereafter [linearly (beta = 0.39 and R(2) = 0.67) or in proportion to cubed HCV prevalence (beta = 0.40 and R(2) = 0.67)]. In SAm/SSA, limited data suggest that mean HIV prevalence is proportional to HCV prevalence (beta = 0.84, R(2) = 0.99), but will be much greater than in non-SAm/SSA settings with no threshold HCV prevalence that corresponds to low HIV risk. At low HCV prevalences (<50%), time-series data suggest that any change in HIV prevalence over time is likely to be much smaller (<25%) than the change in HCV prevalence over the same time-period, but that this difference diminishes at higher HCV prevalences. CONCLUSIONS: HCV prevalence could be an indicator of HIV risk among IDUs. In most settings, reducing HCV prevalence below a threshold (30%) would reduce substantially any HIV risk, and could provide a target for HIV prevention.


Subject(s)
HIV Infections/epidemiology , HIV-1 , Hepacivirus , Hepatitis C, Chronic/epidemiology , Substance Abuse, Intravenous/epidemiology , Africa South of the Sahara/epidemiology , Confidence Intervals , Disease Outbreaks , HIV Infections/transmission , Hepacivirus/isolation & purification , Hepatitis C, Chronic/transmission , Humans , Prevalence , Risk Factors , South America/epidemiology , Substance Abuse, Intravenous/virology
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