Residual low HDV viraemia is associated HDV RNA relapse after PEG-IFNa-based antiviral treatment of hepatitis delta: Results from the HIDIT-II study.
Birgit BremerOlympia Evdoxia AnastasiouSvenja HardtkeFlorin Alexandru CaruntuManuela G CurescuKendal YalcinUlus S AkarcaSelim GürelStefan ZeuzemAndreas ErhardtStefan LüthGeorgios PapatheodoridisMonica RaduRamazan IdilmanMichael P MannsMarkus CornbergCihan YurdaydinHeiner WedemeyerPublished in: Liver international : official journal of the International Association for the Study of the Liver (2020)
The role of low levels of HDV-RNA during and after interferon therapy of hepatitis D is unknown. We re-analysed HDV RNA in 372 samples collected in the HIDIT-2 trial (Wedemeyer et al, Lancet Infectious Diseases 2019) with the Robogene assay (RA; Jena Analytics). Data were compared with the previously reported in-house assay (IA). We detected HDV-RNA in one-third of samples previously classified as undetectable using the highly sensitive RA. Low HDV viraemia detectable at week 48 or week 96 was associated with a high risk for post-treatment relapse, defined as HDV RNA positivity in both assays at week 120. HDV RNA relapses occurred in 10/15 (67%) patients with detectable low HDV RNA at week 48 and in 10/13 (77%) patients with low viraemia samples at week 96. In contrast, the post-treatment relapse rate was lower in patients with undetectable HDV RNA in both assays during treatment.
Keyphrases
- high throughput
- nucleic acid
- infectious diseases
- clinical trial
- rheumatoid arthritis
- magnetic resonance imaging
- magnetic resonance
- stem cells
- systemic lupus erythematosus
- study protocol
- mesenchymal stem cells
- computed tomography
- big data
- electronic health record
- cell therapy
- dendritic cells
- artificial intelligence
- ankylosing spondylitis
- high resolution
- contrast enhanced
- bone marrow
- systemic sclerosis
- smoking cessation
- molecularly imprinted
- phase iii
- double blind
- replacement therapy
- label free