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Automating biomedical literature review for rapid drug discovery: Leveraging GPT-4 to expedite pandemic response.
Yang, Jingmei; Walker, Kenji C; Bekar-Cesaretli, Ayse A; Hao, Boran; Bhadelia, Nahid; Joseph-McCarthy, Diane; Paschalidis, Ioannis Ch.
Affiliation
  • Yang J; Department of Electrical & Computer Engineering and Division of Systems Engineering, Boston University, Boston, MA, United States of America.
  • Walker KC; Department of Biomedical Engineering, Boston University, Boston, MA, United States of America.
  • Bekar-Cesaretli AA; Department of Chemistry, Boston University, Boston, MA, United States of America.
  • Hao B; Department of Electrical & Computer Engineering and Division of Systems Engineering, Boston University, Boston, MA, United States of America.
  • Bhadelia N; Chobanian & Avedisian School of Medicine and Center for Emerging Infectious Diseases Policy and Research, Boston University, Boston, MA, United States of America.
  • Joseph-McCarthy D; Department of Biomedical Engineering, Boston University, Boston, MA, United States of America.
  • Paschalidis IC; Department of Electrical & Computer Engineering and Division of Systems Engineering, Boston University, Boston, MA, United States of America; Department of Biomedical Engineering, Boston University, Boston, MA, United States of America; Faculty of Computing & Data Sciences, Boston University
Int J Med Inform ; 189: 105500, 2024 Sep.
Article in En | MEDLINE | ID: mdl-38815316
ABSTRACT

OBJECTIVE:

The rapid expansion of the biomedical literature challenges traditional review methods, especially during outbreaks of emerging infectious diseases when quick action is critical. Our study aims to explore the potential of ChatGPT to automate the biomedical literature review for rapid drug discovery. MATERIALS AND

METHODS:

We introduce a novel automated pipeline helping to identify drugs for a given virus in response to a potential future global health threat. Our approach can be used to select PubMed articles identifying a drug target for the given virus. We tested our approach on two known pathogens SARS-CoV-2, where the literature is vast, and Nipah, where the literature is sparse. Specifically, a panel of three experts reviewed a set of PubMed articles and labeled them as either describing a drug target for the given virus or not. The same task was given to the automated pipeline and its performance was based on whether it labeled the articles similarly to the human experts. We applied a number of prompt engineering techniques to improve the performance of ChatGPT.

RESULTS:

Our best configuration used GPT-4 by OpenAI and achieved an out-of-sample validation performance with accuracy/F1-score/sensitivity/specificity of 92.87%/88.43%/83.38%/97.82% for SARS-CoV-2 and 87.40%/73.90%/74.72%/91.36% for Nipah.

CONCLUSION:

These results highlight the utility of ChatGPT in drug discovery and development and reveal their potential to enable rapid drug target identification during a pandemic-level health emergency.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Discovery / Pandemics / SARS-CoV-2 / COVID-19 Limits: Humans Language: En Journal: Int J Med Inform Journal subject: INFORMATICA MEDICA Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Irlanda

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Discovery / Pandemics / SARS-CoV-2 / COVID-19 Limits: Humans Language: En Journal: Int J Med Inform Journal subject: INFORMATICA MEDICA Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Irlanda