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  1. Article ; Online: Introducing Norah Terrault, MD, MPH, Our 2023 AASLD President.

    Peters, Marion G / Lai, Jennifer C

    Hepatology (Baltimore, Md.)

    2023  Volume 77, Issue 5, Page(s) 1482–1485

    MeSH term(s) Gastroenterology ; Societies, Medical
    Language English
    Publishing date 2023-01-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 604603-4
    ISSN 1527-3350 ; 0270-9139
    ISSN (online) 1527-3350
    ISSN 0270-9139
    DOI 10.1097/HEP.0000000000000288
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Long-Term Use of Azathioprine in the Management of Autoimmune Hepatitis.

    Peters, Marion G

    Gastroenterology & hepatology

    2019  Volume 15, Issue 5, Page(s) 277–279

    Language English
    Publishing date 2019-06-30
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2386402-3
    ISSN 1554-7914
    ISSN 1554-7914
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Hepatitis B Virus Infection: What Is Current and New.

    Peters, Marion G

    Topics in antiviral medicine

    2019  Volume 26, Issue 4, Page(s) 112–116

    Abstract: ... with the aim of achieving HBV eradication. This article summarizes an IAS-USA webinar given by Marion G. Peters ...

    Abstract Hepatitis B virus (HBV) infection is a lifelong dynamic disease that can be controlled with treatment but cannot yet be cured. Risk of end-stage liver disease and hepatocellular carcinoma (HCC) increases with ongoing inflammation and HBV viremia. Initial treatments consist of tenofovir or entecavir. Patients who require treatment include those with chronic hepatitis, cirrhosis, HCC, or HIV coinfection; patients receiving immunosuppressive treatments; and women in the third trimester of pregnancy who have elevated HBV DNA level. A number of virologic and host immune approaches are being investigated with the aim of achieving HBV eradication. This article summarizes an IAS-USA webinar given by Marion G. Peters, MD, on June 14, 2018.
    MeSH term(s) Carcinoma, Hepatocellular/complications ; Carcinoma, Hepatocellular/drug therapy ; Coinfection/drug therapy ; Female ; Hepatitis B, Chronic/complications ; Hepatitis B, Chronic/drug therapy ; Humans ; Liver Cirrhosis/complications ; Liver Cirrhosis/drug therapy ; Male ; Pregnancy ; Pregnancy Complications, Infectious/drug therapy ; United States
    Language English
    Publishing date 2019-01-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2656632-1
    ISSN 2161-5853 ; 2161-5861
    ISSN (online) 2161-5853
    ISSN 2161-5861
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Management of Autoimmune Hepatitis in Pregnant Women.

    Peters, Marion G

    Gastroenterology & hepatology

    2017  Volume 13, Issue 8, Page(s) 504–506

    Language English
    Publishing date 2017-03-09
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2386402-3
    ISSN 1554-7914
    ISSN 1554-7914
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Design and analysis considerations for early phase clinical trials in hepatitis B (HBV) cure research: the ACTG A5394 study in persons with both HIV and HBV.

    Kang, Minhee / Price, Jennifer C / Peters, Marion G / Lewin, Sharon R / Sulkowski, Mark

    Journal of virus eradication

    2023  Volume 9, Issue 3, Page(s) 100344

    Abstract: With growing interest and efforts to achieve a hepatitis B (HBV) cure, HBV therapeutics have increasingly entered the clinical testing phase. In designing an early phase clinical trial aimed at HBV cure, the heterogeneity in participants and the choice ... ...

    Abstract With growing interest and efforts to achieve a hepatitis B (HBV) cure, HBV therapeutics have increasingly entered the clinical testing phase. In designing an early phase clinical trial aimed at HBV cure, the heterogeneity in participants and the choice of a biomarker endpoint that signals a cure requires careful consideration. We describe the key elements to consider during the development of HBV clinical trials aimed at a functional cure, and how we have addressed them in the design of a phase II AIDS Clinical Trials Group (ACTG) study, A5394 (NCT05551273). The trial we present is for persons with both HIV and HBV, a unique population that has much to gain from an HBV cure. Our decisions on the design elements are specific to the study agent and the targeted population, but our deliberations may be informative in the emerging field of early phase HBV trials aimed at cure.
    Language English
    Publishing date 2023-08-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 2868549-0
    ISSN 2055-6659 ; 2055-6640
    ISSN (online) 2055-6659
    ISSN 2055-6640
    DOI 10.1016/j.jve.2023.100344
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Adverse Impact of HIV-1 on Long-term Outcomes Following HCV DAA Treatment: Final Results of ACTG A5320, the Viral Hepatitis C Infection Long-term Cohort Study (VHICS).

    Wyles, David L / Kang, Minhee / Matining, Roy M / Murphy, Robert L / Peters, Marion G

    Open forum infectious diseases

    2023  Volume 10, Issue 3, Page(s) ofad115

    Abstract: Background: Long-term outcome data after hepatitis C virus (HCV) treatment are limited, particularly for comparisons between persons with and without HIV.: Methods: A5320 was a prospective cohort study that enrolled participants within 12 months of ... ...

    Abstract Background: Long-term outcome data after hepatitis C virus (HCV) treatment are limited, particularly for comparisons between persons with and without HIV.
    Methods: A5320 was a prospective cohort study that enrolled participants within 12 months of completing HCV DAA therapy, with or without sustained virologic response (SVR). The primary end point was composite: time to death or development of a targeted diagnosis. Component outcomes (death and targeted diagnosis) and liver-related events were also analyzed. The effects of HIV serostatus, HIV RNA and CD4, and liver disease stage on the outcomes were assessed. Follow-up was designated for 5 years.
    Results: Three hundred thirty-two participants enrolled: 184 with HIV/HCV (130 SVR) and 148 with HCV (125 SVR). The primary analysis was dominated by targeted diagnoses. Increased rates of targeted diagnoses were seen in HCV-HIV/SVR compared with HCV/SVR (
    Conclusions: HCV cure following therapy reduces subsequent development of new clinical events, supporting the use of SVR as a predictor for clinical outcomes. Despite HIV control, a significant decrease in incident events or mortality was not demonstrated for people with HIV who achieved SVR, suggesting that coinfection attenuates the beneficial impact of SVR. Research is needed to better define mechanisms accounting for the long-term negative impact of controlled HIV infection.
    Language English
    Publishing date 2023-03-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2757767-3
    ISSN 2328-8957
    ISSN 2328-8957
    DOI 10.1093/ofid/ofad115
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: The Pathogenesis of Liver Disease in People Living With Human Immunodeficiency Virus: The Emerging Role of the Microbiome.

    Kardashian, Ani / Peters, Marion G / Tien, Phyllis C / Price, Jennifer C

    Clinical liver disease

    2020  Volume 15, Issue 1, Page(s) 46–51

    Language English
    Publishing date 2020-02-25
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2657644-2
    ISSN 2046-2484
    ISSN 2046-2484
    DOI 10.1002/cld.880
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: New Direct-Acting Antiviral Agents and Immunomodulators for Hepatitis B Virus Infection.

    Peters, Marion G / Locarnini, Stephen

    Gastroenterology & hepatology

    2017  Volume 13, Issue 6, Page(s) 348–356

    Abstract: Chronic hepatitis B (CHB) affects over 350 million individuals worldwide and is the most common cause of liver cancer. In the United States, CHB affects at least 2 to 3 million individuals, and current therapies can control the disease but not cure it. ... ...

    Abstract Chronic hepatitis B (CHB) affects over 350 million individuals worldwide and is the most common cause of liver cancer. In the United States, CHB affects at least 2 to 3 million individuals, and current therapies can control the disease but not cure it. There are over 30 new molecules being studied in CHB in preclinical to phase 2 studies, targeting specific parts of the hepatitis B virus (HBV) life cycle and the host immune response. When discussing new therapies for CHB, it is critical to understand both the various phases of CHB and the life cycle of HBV. This article will discuss both of these issues, as well as mechanisms of action of potential therapies and possible ways to combine such therapies in the various phases of CHB.
    Language English
    Publishing date 2017-07-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2386402-3
    ISSN 1554-7914
    ISSN 1554-7914
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Continued Low Rates of Hepatitis C Virus (HCV) Recurrence in HCV/HIV- and HCV-Infected Participants Who Achieved Sustained Virologic Response After Direct-Acting Antiviral Treatment: Final Results From the AIDS Clinical Trials Group A5320 Viral Hepatitis C Infection Long-term Cohort Study (V-HICS).

    Wyles, David L / Kang, Minhee / Matining, Roy M / Murphy, Robert L / Peters, Marion G

    Open forum infectious diseases

    2021  Volume 8, Issue 12, Page(s) ofab511

    Abstract: Final results from the long-term Viral Hepatitis C Infection Long-term Cohort Study (V-HICS) found low rates of hepatitis C virus (HCV) recurrence after direct-acting antiviral therapy in both HCV/human immunodeficiency virus (HIV)-coinfected (0.67/100 ... ...

    Abstract Final results from the long-term Viral Hepatitis C Infection Long-term Cohort Study (V-HICS) found low rates of hepatitis C virus (HCV) recurrence after direct-acting antiviral therapy in both HCV/human immunodeficiency virus (HIV)-coinfected (0.67/100 person-years) and HCV-infected (0.2/100 person-years) groups with >500 person-years of follow-up. Confirmed reinfections were in participants with HIV who reported high-risk behaviors.
    Language English
    Publishing date 2021-10-14
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2757767-3
    ISSN 2328-8957
    ISSN 2328-8957
    DOI 10.1093/ofid/ofab511
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: HIV and the liver.

    Sherman, Kenneth E / Peters, Marion G / Thomas, David L

    Topics in antiviral medicine

    2019  Volume 27, Issue 3, Page(s) 101–110

    Abstract: Among individuals with HIV infection, liver disease remains an important cause of morbidity and mortality, even with the availability of agents that cure hepatitis C infection and suppress hepatitis B replication. The causes of liver disease are ... ...

    Abstract Among individuals with HIV infection, liver disease remains an important cause of morbidity and mortality, even with the availability of agents that cure hepatitis C infection and suppress hepatitis B replication. The causes of liver disease are multifaceted and continue to evolve as the population ages and new etiologies arise. Nonalcoholic fatty liver disease and nonalcoholic steatohepatitis and hepatitis viruses such as A, D, and E have emerged even as hepatitis C has receded. Newer antiretroviral agents may increase risk of weight gain and subsequent fatty infiltration, and prior use of nucleotide-based therapies may continue to impact liver health. Several barriers including economics, social stigma, and psychiatric disease impact identification of liver disease, as well as management and treatment interventions. Hepatocellular carcinoma is emerging as a more common and late-diagnosed complication in those with HIV infection and liver disease.
    MeSH term(s) Antirheumatic Agents/therapeutic use ; Carcinoma, Hepatocellular/epidemiology ; Carcinoma, Hepatocellular/etiology ; Fatty Liver/complications ; Fatty Liver/epidemiology ; Fatty Liver, Alcoholic/complications ; Fatty Liver, Alcoholic/epidemiology ; HIV Infections/complications ; HIV Infections/epidemiology ; Hepatitis A/complications ; Hepatitis A/epidemiology ; Hepatitis B/complications ; Hepatitis B/epidemiology ; Hepatitis C/complications ; Hepatitis C/epidemiology ; Hepatitis D/complications ; Hepatitis D/epidemiology ; Hepatitis E/complications ; Hepatitis E/epidemiology ; Hepatitis Viruses ; Hepatitis, Viral, Human/complications ; Hepatitis, Viral, Human/epidemiology ; Humans ; Liver/injuries ; Liver/virology ; Liver Diseases/etiology ; Non-alcoholic Fatty Liver Disease
    Chemical Substances Antirheumatic Agents
    Language English
    Publishing date 2019-10-18
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2656632-1
    ISSN 2161-5853 ; 2161-5853
    ISSN (online) 2161-5853
    ISSN 2161-5853
    Database MEDical Literature Analysis and Retrieval System OnLINE

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