Clinical Validity of a Machine Learning Decision Support System for Early Detection of Hepatitis B Virus: A Binational External Validation Study

Author:

Ajuwon Busayo I.12ORCID,Richardson Alice3ORCID,Roper Katrina1,Lidbury Brett A.1ORCID

Affiliation:

1. National Centre for Epidemiology and Population Health, ANU College of Health and Medicine, The Australian National University, Acton, Canberra, ACT 2601, Australia

2. Department of Biosciences and Biotechnology, Faculty of Pure and Applied Sciences, Kwara State University, Malete 241103, Nigeria

3. Statistical Support Network, The Australian National University, Acton, Canberra, ACT 2601, Australia

Abstract

HepB LiveTest is a machine learning decision support system developed for the early detection of hepatitis B virus (HBV). However, there is a lack of evidence on its generalisability. In this study, we aimed to externally assess the clinical validity and portability of HepB LiveTest in predicting HBV infection among independent patient cohorts from Nigeria and Australia. The performance of HepB LiveTest was evaluated by constructing receiver operating characteristic curves and estimating the area under the curve. Delong’s method was used to estimate the 95% confidence interval (CI) of the area under the receiver-operating characteristic curve (AUROC). Compared to the Australian cohort, patients in the derivation cohort of HepB LiveTest and the hospital-based Nigerian cohort were younger (mean age, 45.5 years vs. 38.8 years vs. 40.8 years, respectively; p < 0.001) and had a higher incidence of HBV infection (1.9% vs. 69.4% vs. 57.3%). In the hospital-based Nigerian cohort, HepB LiveTest performed optimally with an AUROC of 0.94 (95% CI, 0.91–0.97). The model provided tailored predictions that ensured most cases of HBV infection did not go undetected. However, its discriminatory measure dropped to 0.60 (95% CI, 0.56–0.64) in the Australian cohort. These findings indicate that HepB LiveTest exhibits adequate cross-site transportability and clinical validity in the hospital-based Nigerian patient cohort but shows limited performance in the Australian cohort. Whilst HepB LiveTest holds promise for reducing HBV prevalence in underserved populations, caution is warranted when implementing the model in older populations, particularly in regions with low incidence of HBV infection.

Funder

National Centre for Epidemiology and Population Health, Australian National University.

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference43 articles.

1. World Health Organization (2022, September 29). Hepatitis B Key Facts. Available online: https://www.who.int/newsroom/factsheets/detail/hepatitis-b.

2. Hepatitis B in sub-Saharan Africa: Strategies to achieve the 2030 elimination targets;Spearman;Lancet Gastroenterol. Hepatol.,2017

3. Ajuwon, B.I., Yujuico, I., Roper, K., Richardson, A., Sheel, M., and Lidbury, B.A. (2021). Hepatitis B virus infection in Nigeria: A systematic review and meta-analysis of data published between 2010 and 2019. BMC Infect. Dis., 21.

4. Time for universal hepatitis B screening for Australian adults;Allard;Med. J. Aust.,2021

5. World Health Organization (2022, December 15). Global Health Sector Strategy on Viral Hepatitis 2016–2021. Towards Ending Viral Hepatitis. Available online: https://apps.who.int/iris/handle/10665/246177.

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