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Serum GSDMD as a New Biomarker for Assessing Clinical Progression Of  Chronic HBV Infection

39 Pages Posted: 28 Jul 2020

See all articles by Lijing Zhou

Lijing Zhou

Chongqing Medical University - Department of Laboratory Medicine

Jing Shi

Chongqing Medical University - Department of Laboratory Medicine

Qin Hu

Chongqing Medical University - Department of Laboratory Medicine

Xiaolan Zhou

Chongqing Medical University - Department of Medical Record Management

Yuan Yuan

Chongqing Medical University - College of Laboratory Medicine

Li Jun Zhang

Chongqing Medical University - Department of Laboratory Medicine

Bo Wang

Chongqing Medical University - Department of Laboratory Medicine

Liang Duan

Chongqing Medical University - Department of Laboratory Medicine

Dandan Li

Chongqing Medical University - Department of Laboratory Medicine

Yane Du

Chongqing Medical University - Department of Laboratory Medicine

Lifang Wu

Chongqing Medical University - Department of Laboratory Medicine

Ling Yan

Chongqing Medical University - Department of Laboratory Medicine

Xuemei Peng

Chongqing People's Hospital - Department of Neurology

Weixian Chen

Chongqing Medical University - Department of Laboratory Medicine

Pu Li

Chongqing Medical University - Department of Laboratory Medicine

More...

Abstract

Background: Distinguishing the natural course of chronic HBV infection (CHB) development is extremely desired. The pore-forming protein Gasdermin D (GSDMD) contributes to the development of HBV infection and might be used to distinguish different phases of CHB. We aim to investigate the serum expression of GSDMD in the natural course of CHB development and to evaluate its diagnostic efficacy.

Methods: Levels of GSDMD were measured with ELISA kits that we developed. We evaluated the ability of serum GSDMD to differentiate clinical stages in 73 CHB patients. Besides, The HepG2-NTCP cells infected by virus from HepAD38-cell and CHB patients’ serum were applied to evaluate the GSDMD expression in vitro.

Findings: The GSDMD elevated gradually with the development of HBV infection (P < 0.05) and the same phenomenon was observed in vitro. A cutoff value as ≤ 3·0 ng/mL identified healthy individuals from liver diseases patients with 96·479 % sensitivity (AUC, 0·954; P < 0.01). When the cutoff value as 3·0-104·5 ng/mL, the AUC and sensitivity of asymptomatic carriers patients were 0·694 and 91·603 %. In CHB patients, with the cutoff value as 104·5-160·0 ng/mL, the AUC and sensitivity were 0·701 and 56·897 %. When the cutoff value as 160-178 ng/mL, the active chronic hepatitis B patients, the AUC and sensitivity were 0·662 and 52·174 %. Additionally, HBV-related cirrhosis patients, GSDMD positive defined as > 178 ng/mL, the sensitivity was 52·174 %.

Interpretation: Serum GSDMD, varied along with the development of HBV-related diseases, making it an early and efficacious serum biomarker for auxiliary definitions of the natural course of CHB.

Funding Statement: This work was supported by the Outstanding Young Talents Plan of the Second Hospital of Chongqing Medical University (Pu Li).

Declaration of Interests: There are no conflicts of interest.

Ethics Approval Statement: The study was carried out based on the principles of the Declaration of Helsinki and was approved by the medical ethics committee of the Second Affiliated Hospital of Chongqing Medical University.

Keywords: Hepatitis B virus; GSDMD; Chronic hepatitis B; Biomarker; Pyroptosis

Suggested Citation

Zhou, Lijing and Shi, Jing and Hu, Qin and Zhou, Xiaolan and Yuan, Yuan and Zhang, Li Jun and Wang, Bo and Duan, Liang and Li, Dandan and Du, Yane and Wu, Lifang and Yan, Ling and Peng, Xuemei and Chen, Weixian and Li, Pu, Serum GSDMD as a New Biomarker for Assessing Clinical Progression Of  Chronic HBV Infection (4/21/2020). Available at SSRN: https://ssrn.com/abstract=3582731 or http://dx.doi.org/10.2139/ssrn.3582731

Lijing Zhou

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Jing Shi

Chongqing Medical University - Department of Laboratory Medicine

Chongqing
China

Qin Hu

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Xiaolan Zhou

Chongqing Medical University - Department of Medical Record Management

Chongqing
China

Yuan Yuan

Chongqing Medical University - College of Laboratory Medicine

China

Li Jun Zhang

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Bo Wang

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Liang Duan

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Dandan Li

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Yane Du

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Lifang Wu

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Ling Yan

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Xuemei Peng

Chongqing People's Hospital - Department of Neurology

China

Weixian Chen

Chongqing Medical University - Department of Laboratory Medicine

Chongqing, 400014
China

Pu Li (Contact Author)

Chongqing Medical University - Department of Laboratory Medicine ( email )

Chongqing, 400014
China

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