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      Vibration-Controlled Transient Elastography for the Detection of Cirrhosis in Chronic Hepatitis D Infection

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          Abstract

          Non-invasive detection of cirrhosis via vibration-controlled transient elastography (VCTE) has revolutionized the management of chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infection. However, VCTE has not been studied in chronic hepatitis D virus (HDV) infection and accuracy remains in question due to the significant hepatic inflammation associated with this infection. Consecutive HBV, HCV, and HDV patients who underwent VCTE (2006–2019) were evaluated. Diagnosis of cirrhosis was made via liver biopsy or clinical findings. VCTE was compared to other non-invasive serum fibrosis tests using AUROC curves. The performance of VCTE in HBV/HCV/HDV was also compared. We evaluated 319 patients (HBV-112; HCV-132; HDV-75), 278(87%) patients had histology for evaluation. HDV patients had evidence of higher hepatic inflammation as evidence by aspartate aminotransferase, alanine aminotransferase, and histology activity index. Cirrhotic HDV patients had higher mean liver stiffness measurements compared to non-cirrhotic patients (29.0 vs 8.3 kPa, P<0.0001). VCTE demonstrated excellent diagnostic accuracy for the detection of cirrhosis with an AUROC of 0.90 compared to APRI (0.83), FIB-4 (0.88), AAR (0.73), and RPR (0.85). Performance of VCTE in HDV was comparable to HBV (0.93) and HCV (0.94). At the optimized cut-off value of ≥14.0 kPa for determining cirrhosis in HDV, VCTE had a sensitivity of 0.78, specificity of 0.86, NPV of 0.93, and PPV of 0.64. Hence VCTE is a useful non-invasive test in HDV for determining cirrhosis despite the presence of significant hepatic inflammation.

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          Author and article information

          Journal
          9435672
          8796
          J Viral Hepat
          J. Viral Hepat.
          Journal of viral hepatitis
          1352-0504
          1365-2893
          5 December 2019
          09 December 2019
          April 2020
          01 April 2021
          : 27
          : 4
          : 428-436
          Affiliations
          [1 ]Digestive Diseases Branch, National Institute of Diabetes & Digestive & Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA
          [2 ]Liver Diseases Branch, National Institute of Diabetes & Digestive & Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA
          [3 ]Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA
          Author notes

          Author Statement:

          Guarantor of article: CK

          Concept and Design: BD, PS, TH, CK

          Acquisition of Data: BD, PS, VT, DEK, TH, CK

          Statistical Analysis and Interpretation of Data: BD, PS, VT, DEK, TH, CK

          Drafting and Revision of Manuscript: BD, PS, DEK, TH, CK

          All authors approve the final version of the article.

          Address for reprint and correspondence:Christopher Koh, MD MHSc, Liver Diseases Branch, National Institute of Diabetes & Digestive & Kidney Diseases, National Institutes of Health, 10 Center Drive, Bldg. 10, Room 5-2740, Bethesda, MD 20892, Telephone: 301-451-1721, Fax: 301-402-0491, Christopher.koh@ 123456nih.gov
          Author information
          http://orcid.org/0000-0002-7750-240X
          http://orcid.org/0000-0002-4755-5607
          Article
          PMC7080586 PMC7080586 7080586 nihpa1060498
          10.1111/jvh.13235
          7080586
          31742822
          73dda38e-8c1f-49fe-b3dc-12edafd92809
          History
          Categories
          Article

          transient elastography,cirrhosis,hepatitis B,non-invasive marker,hepatitis D

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