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Empowering personalized pharmacogenomics with generative AI solutions.
Murugan, Mullai; Yuan, Bo; Venner, Eric; Ballantyne, Christie M; Robinson, Katherine M; Coons, James C; Wang, Liwen; Empey, Philip E; Gibbs, Richard A.
Afiliação
  • Murugan M; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, United States.
  • Yuan B; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, United States.
  • Venner E; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.
  • Ballantyne CM; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, United States.
  • Robinson KM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.
  • Coons JC; Sections of Cardiology and Cardiovascular Research, Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
  • Wang L; School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, United States.
  • Empey PE; School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, United States.
  • Gibbs RA; Department of Pharmacy, UPMC Presbyterian-Shadyside Hospital, Pittsburgh, PA, United States.
J Am Med Inform Assoc ; 31(6): 1356-1366, 2024 May 20.
Article em En | MEDLINE | ID: mdl-38447590
ABSTRACT

OBJECTIVE:

This study evaluates an AI assistant developed using OpenAI's GPT-4 for interpreting pharmacogenomic (PGx) testing results, aiming to improve decision-making and knowledge sharing in clinical genetics and to enhance patient care with equitable access. MATERIALS AND

METHODS:

The AI assistant employs retrieval-augmented generation (RAG), which combines retrieval and generative techniques, by harnessing a knowledge base (KB) that comprises data from the Clinical Pharmacogenetics Implementation Consortium (CPIC). It uses context-aware GPT-4 to generate tailored responses to user queries from this KB, further refined through prompt engineering and guardrails.

RESULTS:

Evaluated against a specialized PGx question catalog, the AI assistant showed high efficacy in addressing user queries. Compared with OpenAI's ChatGPT 3.5, it demonstrated better performance, especially in provider-specific queries requiring specialized data and citations. Key areas for improvement include enhancing accuracy, relevancy, and representative language in responses.

DISCUSSION:

The integration of context-aware GPT-4 with RAG significantly enhanced the AI assistant's utility. RAG's ability to incorporate domain-specific CPIC data, including recent literature, proved beneficial. Challenges persist, such as the need for specialized genetic/PGx models to improve accuracy and relevancy and addressing ethical, regulatory, and safety concerns.

CONCLUSION:

This study underscores generative AI's potential for transforming healthcare provider support and patient accessibility to complex pharmacogenomic information. While careful implementation of large language models like GPT-4 is necessary, it is clear that they can substantially improve understanding of pharmacogenomic data. With further development, these tools could augment healthcare expertise, provider productivity, and the delivery of equitable, patient-centered healthcare services.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Farmacogenética / Medicina de Precisão Limite: Humans Idioma: En Revista: J Am Med Inform Assoc Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Farmacogenética / Medicina de Precisão Limite: Humans Idioma: En Revista: J Am Med Inform Assoc Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos