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Longitudinal assessment of HCV core antigen kinetics to monitor therapeutic response in the age of DAAs.
Ponnuvel, Suresh; Prakash, Arul; Steve, Runal John; Doss, George Priya; Goel, Ashish; Zachariah, Uday George; Eapen, Chundamannil Eapen; Rebekah, Grace; Kannangai, Rajesh; Fletcher, Gnanadurai John; Abraham, Priya.
Afiliação
  • Ponnuvel S; Department of Clinical Virology, Christian Medical College, Vellore, India.
  • Prakash A; Department of Clinical Virology, Christian Medical College, Vellore, India.
  • Steve RJ; Department of Clinical Virology, Christian Medical College, Vellore, India.
  • Doss GP; Department of Integrative Biology, Vellore Institute of Technology, Vellore, India.
  • Goel A; Department of Hepatology, Christian Medical College, Vellore, India.
  • Zachariah UG; Department of Hepatology, Christian Medical College, Vellore, India.
  • Eapen CE; Department of Hepatology, Christian Medical College, Vellore, India.
  • Rebekah G; Department of Biostatistics, Christian Medical College, Vellore, India.
  • Kannangai R; Department of Clinical Virology, Christian Medical College, Vellore, India.
  • Fletcher GJ; Department of Clinical Virology, Christian Medical College, Vellore, India.
  • Abraham P; Department of Clinical Virology, Christian Medical College, Vellore, India.
PLoS One ; 18(2): e0282013, 2023.
Article em En | MEDLINE | ID: mdl-36800372
ABSTRACT

BACKGROUND:

In the economy of therapeutic monitoring, an affordable viral marker is essential in the era of direct-acting antivirals (DAAs). We elucidated the kinetics of HCVcAg to delineate its precise role in monitoring therapeutic response.

METHODS:

In this longitudinal study, 3208 patients were tested for HCV RNA. A total of 423 patients were started on DAAs. Treatment response and kinetics of HCVcAg/RNA were assessed in treatment-naïve (n = 383) and previously treated (n = 40) patients with follow-up for 2 years.

RESULTS:

After the initiation of DAAs, the rate of relapse was significantly higher in the previously treated group than naive group [12.5% (5/40) Vs 2% (7/383), p<0.0001]. The response rate at RVR was significantly higher with HCVcAg than RNA in both groups (p<0.02). The kinetics of HCVcAg and RNA were significantly different at ETR and SVR12 in the naïve (p<0.04), but similar at all therapeutic points in the previously treated group. The correlation between HCVcAg and RNA was good at baseline, ETR and SVR, except RVR in both groups (r>0.6; p<0.0001). Furthermore, HCV genotypes, treatment regimen, CTP (<7/≥7) and MELD (<15/≥15) did not influence the therapeutic response and the viral replication kinetics (p>0.05).

CONCLUSIONS:

It is the first longitudinal study from India shows that the response rate and kinetics of HCVcAg are comparable to HCV RNA for an extended duration, except at RVR, irrespective of the HCV genotypes, treatment regimen, and liver disease severity. Hence, HCVcAg can be considered as a pragmatic marker to monitor therapeutic response and predict relapse in the era of DAAs.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Hepatite C Crônica Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Hepatite C Crônica Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article