Syed Bilal Shah
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Syed Bilal Shah has a total of 25 co-authors. Here are the top co-authors by number of shared publications:
- Daryl Tan-Yeung Lau
Liver Center, Division of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA
2 shared publications - Naeem Ahmed Khan
Department of Internal Medicine, NYC Health + Hospitals/Woodhull, Brooklyn, NY 11206, USA
2 shared publications - Sadia Paracha
Liver Center, Division of Gastroenterology and Hepatology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States, USA
2 shared publications - Saeed Ahmad
Beth Israel Deaconess Medical Center Harvard Medical School Boston Massachusetts USA
2 shared publications A. Ullah
Beth Israel Deaconess Medical Center, Harvard Medical School Boston Massachusetts USA
1 shared publication- Ashraf Ullah
Department of Internal Medicine, Guthrie Robert Packer Hospital, Sayre, PA 18840, USA
1 shared publication
Latest Publications
- Open Access
- 11 February 2026
- Published by MDPI AG in Preprints.org
Prevalence of Hepatitis D Virus Infection in a Tertiary Liver Center in the United States
Background/Aim: Hepatitis D virus (HDV) infection is the most severe form of viral hepatitis but is under-recognized. We evaluated HDV screening frequency and clinical characteristics of HDV-positive patients in our liver center in the United States. Method: Patients with chronic hepatitis B (CHB) evaluated between January 2021 and December 2023 were included. For those tested anti-HDV(+), HDV RNA was performed and clinical data were recorded. Results: Among 1,337 (M=716, F=621) CHB patients, 93.3% were foreign-born. The cohort included 74.9% Asians, 12.3% Blacks, 9.1% Whites and 1.3% Hispanics. HDV screening significantly increased after 2011 reflecting an increase in HDV awareness. Patients aged 18-40 years had the highest screening rate of 58%. Overall, 13 (1.95%) were tested HDV positive and 11 were repeatedly HDV RNA(+). PWID was noted in 5 of 11. Despite low HBV DNA levels, all had ≥stage 2 fibrosis, and 7 had advanced stage 3-4 disease. After a median follow-up of 8.75 years, 8 (73%) developed hepatic decompensation and 4 had hepatocellular carcinoma. Conclusion: HDV screening reached 51.3% among our predominantly foreign-born CHB patients. The high prevalence of advanced fibrosis at diagnosis underscores the importance of HDV screening. Early diagnosis and effective therapy are urgently needed for this challenging disease.
- 11 February 2026
- Published by MDPI AG in Preprints.org
Open AccessPrevalence of Hepatitis D Virus Infection in a Tertiary Liver Center in the United States
Background/Aim: Hepatitis D virus (HDV) infection is the most severe form of viral hepatitis but is under-recognized. We evaluated HDV screening frequency and clinical characteristics of HDV-positive patients in our liver center in the United States. Method: Patients with chronic hepatitis B (CHB) evaluated between January 2021 and December 2023 were included. For those tested anti-HDV(+), HDV RNA was performed and clinical data were recorded. Results: Among 1,337 (M=716, F=621) CHB patients, 93.3% were foreign-born. The cohort included 74.9% Asians, 12.3% Blacks, 9.1% Whites and 1.3% Hispanics. HDV screening significantly increased after 2011 reflecting an increase in HDV awareness. Patients aged 18-40 years had the highest screening rate of 58%. Overall, 13 (1.95%) were tested HDV positive and 11 were repeatedly HDV RNA(+). PWID was noted in 5 of 11. Despite low HBV DNA levels, all had ≥stage 2 fibrosis, and 7 had advanced stage 3-4 disease. After a median follow-up of 8.75 years, 8 (73%) developed hepatic decompensation and 4 had hepatocellular carcinoma. Conclusion: HDV screening reached 51.3% among our predominantly foreign-born CHB patients. The high prevalence of advanced fibrosis at diagnosis underscores the importance of HDV screening. Early diagnosis and effective therapy are urgently needed for this challenging disease.
- Open Access
- 1 February 2026
- Published by Wolters Kluwer Health in ACG Case Reports Journal
- Vol. 13 (2)
Nonadherence to Antiviral Therapy Leading to Severe Hepatic Decompensation in a Patient With Chronic Hepatitis B
Patients with chronic hepatitis B often require prolonged nucleos(t)ide analogue since functional cure is rarely achieved. Medication nonadherence can trigger life-threatening hepatitis B virus (HBV) reactivation. We report a 58-year-old Asian man with HBeAg-negative chronic hepatitis B and cirrhosis. After 10 years of entecavir therapy, he achieved undetectable HBV DNA and fibrosis regression, but quantitative hepatitis B surface antigen remained >1200 IU/mL. He self-discontinued medication and presented with severe hepatitis reactivation. Liver condition gradually improved on restarting nucleos(t)ide analogue. This case highlights that medication cessation with a high hepatitis B surface antigen titer can precipitate severe hepatitis and liver failure, even after long-term HBV DNA suppression.
- 1 February 2026
- Published by Wolters Kluwer Health in ACG Case Reports Journal
- Vol. 13 (2)
Open AccessNonadherence to Antiviral Therapy Leading to Severe Hepatic Decompensation in a Patient With Chronic Hepatitis B
Patients with chronic hepatitis B often require prolonged nucleos(t)ide analogue since functional cure is rarely achieved. Medication nonadherence can trigger life-threatening hepatitis B virus (HBV) reactivation. We report a 58-year-old Asian man with HBeAg-negative chronic hepatitis B and cirrhosis. After 10 years of entecavir therapy, he achieved undetectable HBV DNA and fibrosis regression, but quantitative hepatitis B surface antigen remained >1200 IU/mL. He self-discontinued medication and presented with severe hepatitis reactivation. Liver condition gradually improved on restarting nucleos(t)ide analogue. This case highlights that medication cessation with a high hepatitis B surface antigen titer can precipitate severe hepatitis and liver failure, even after long-term HBV DNA suppression.
- 9 December 2024
- Published by Wiley in Alimentary Pharmacology & Therapeutics
Letter: Should HBV Therapy Be Stopped Based on HBsAg Level Alone?
- 9 December 2024
- Published by Wiley in Alimentary Pharmacology & Therapeutics
Letter: Should HBV Therapy Be Stopped Based on HBsAg Level Alone?
- Open Access
- 30 October 2024
- Published by Wolters Kluwer Health in Hepatology Communications
- Vol. 8 (11)
Baveno VII for HCC: Are we there yet?
- 30 October 2024
- Published by Wolters Kluwer Health in Hepatology Communications
- Vol. 8 (11)
Open AccessBaveno VII for HCC: Are we there yet?