Mitigating Machine Learning Bias Between High Income and Low-Middle Income Countries for Enhanced Model Fairness and Generalizability

Jenny Yang,Lei Clifton, Nguyen Thanh Dung, Nguyen Thanh Phong,Lam Minh Yen, Doan Bui Xuan Thy,Andrew A. S. Soltan,Louise Thwaites,David A. Clifton

medrxiv(2024)

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摘要
Collaborative efforts in artificial intelligence (AI) are increasingly common between high-income countries (HICs) and low-to middle-income countries (LMICs). Given the resource limitations often encountered by LMICs, collaboration becomes crucial for pooling resources, expertise, and knowledge. Despite the apparent advantages, ensuring the fairness and equity of these collaborative models is essential, especially considering the distinct differences between LMIC and HIC hospitals. In this study, we show that collaborative AI approaches can lead to divergent performance outcomes across HIC and LMIC settings, particularly in the presence of data imbalances. Through a real-world COVID-19 screening case study, we demonstrate that implementing algorithmic-level bias mitigation methods significantly improves outcome fairness between HIC and LMIC sites while maintaining high diagnostic sensitivity. We compare our results against previous benchmarks, utilizing datasets from four independent United Kingdom Hospitals and one Vietnamese hospital, representing HIC and LMIC settings, respectively. ### Competing Interest Statement DAC reports personal fees from Oxford University Innovation, personal fees from BioBeats, personal fees from Sensyne Health, outside the submitted work. ### Funding Statement This work was supported by the Wellcome Trust/University of Oxford Medical & Life Sciences Translational Fund (Award: 0009350), and the Oxford National Institute for Health and Care Research (NIHR) Biomedical Research Centre (BRC). This work was also supported by the Wellcome Trust (Awards: WT 214906/Z/18/Z and WT217650/Z/19/Z). JY is a Marie Sklodowska-Curie Fellow, under the European Union Horizon 2020 research and innovation programme (Grant agreement: 955681, MOIRA). AAS is an NIHR Academic Clinical Fellow (Award: ACF-2020-13-015). DAC was supported by a Royal Academy of Engineering Research Chair, an NIHR Research Professorship, the InnoHK Hong Kong Centre for Cerebro-cardiovascular Health Engineering (COCHE), and the Pandemic Sciences Institute at the University of Oxford. The funders of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the manuscript. The views expressed in this publication are those of the authors and not necessarily those of the funders. ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: United Kingdom National Health Service (NHS) approval via the national oversight/regulatory body, the Health Research Authority (HRA), has been granted for use of routinely collected clinical data to develop and validate artificial intelligence models to detect Covid-19 (CURIAL; NHS HRA IRAS ID: 281832). The ethics committee at the Hospital for Tropical Diseases (HTD) approved use of the HTD dataset for COVID-19 diagnosis. I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable. Yes
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