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Large language models streamline automated machine learning for clinical studies
Open accessAbstract
A knowledge gap persists between machine learning (ML) developers (e.g., data scientists) and practitioners (e.g., clinicians), hampering the full utilization of ML for clinical data analysis. We investigated the potential of the ChatGPT Advanced Data Analysis (ADA), an extension of GPT-4, to bridge this gap and perform ML analyses efficiently. Real-world clinical datasets and study details from large trials across various medical specialties were presented to ChatGPT ADA without specific guidance. ChatGPT ADA autonomously developed state-of-the-art ML models based on the original study’s training data to predict clinical outcomes such as cancer development, cancer progression, disease complications, or biomarkers such as pathogenic gene sequences. Following the re-implementation and optimization of the published models, the head-to-head comparison of the ChatGPT ADA-crafted ML models and their respective manually crafted counterparts revealed no significant differences in traditional performance metrics ( p ≥ 0.072). Strikingly, the ChatGPT ADA-crafted ML models often outperformed their counterparts. In conclusion, ChatGPT ADA offers a promising avenue to democratize ML in medicine by simplifying complex data analyses, yet should enhance, not replace, specialized training and resources, to promote broader applications in medical research and practice.
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![Fig. 4 Model explainability through the top 10 predictive features for the ChatGPT ADA-selected machine-learning models. An explainability analysis was performed for each clinical trial including (a) Metastatic Disease [Endocrinologic Oncology], b Oesophageal Cancer [Gastrointestinal Oncology], c Hereditary Hearing Loss [Otolaryngology], and d Cardiac Amyloidosis [Cardiology], and ChatGPT ADA-selected machine-learning model. Indicated are SHapley Additive exPlanations (SHAP) values of each predictive feature that measure the feature’s influence on model predictions. High absolute SHAP values signify substantial influence. The features are ranked from top to bottom based on the mean absolute SHAP values (color-coded on the right). In c, specific gene locations are indicated. Please refer to the Methods for more details on abbreviations. Box plots indicate the ranges (x-axes) of each feature (y-axes). Crosses indicate (arithmetic) means, boxes the ranges (first [Q1] to third [Q3] quartile), with the central line representing the (arithmetic) median (second quartile [Q2]). Whiskers extend to 1.5 times the interquartile range above Q3 and below Q1. Any data point outside this range is considered an outlier (dots). Mind the different scales for the color codes and SHAP values. Source data are provided as a Source Data file. ChatGPT ADA performed the SHAP analysis on the training sets (number of independent samples: Endocrinologic Oncology dataset, n = 493, Gastrointestinal Oncology dataset, n = 7899, Otolaryngology dataset, n = 1209, and Cardiology dataset, n = 1712). Plasma MN plasma concentrations of metanephrine, plasma NMN plasma concentrations of normetanephrine, SDHB succinate dehydrogenase complex iron-sulfur subunit B, Plasma MTY plasma concentrations of methoxytyramine, AGC atypical glandular cells, DNA deoxyribonucleic acid, Chron. chronic, Cong. congenital, Dias. diastolic, Sys. systolic. Note: The feature “Hyp. heart w/ HF & Stg 1–4 Unsp. CKD” refers to “Hypertensive heart with heart failure coexisting with unspecified stage 1–4 chronic kidney disease”, while “Prev. hist. PGGLs” refers to “Previous history of Pheochromocytomas and Paragangliomas”.](/paper-figures/d8b79dad53304c489d40defea4efac1a/large-language-models-streamline-automated-machine-learning-for-clinical-studies-figure-4.jpg)
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“Arasteh et al. used the integrated data analysis tools of an LLM to analyze scientific data, achieving results on par with human researchers19.”
From Development and validation of an autonomous artificial intelligence agent for clinical decision-making in oncology (2025) · cites this paper as [19]
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Metadata
- Authors
- Tayebi Arasteh, S., Han, T., Lotfinia, M., Kuhl, C., Kather, J. N., Truhn, D., & Nebelung, S.
- Affiliations
- Universitätsklinikum Aachen (DE)
- University Hospital Heidelberg (DE)
- Corresponding author
- Han, Tianyu
- ORCID
- Venue
- Nature Communications
- Published
- 2024-02-21
- Volume
- 15
- Issue
- 1
- Pages
- 1603-1603
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC10881983
- OpenAlex
- W4392016947
- Cited by
- 114
- References
- 53
- Citations by year
- 2026: 34 · 2025: 53 · 2024: 27
- FWCI
- 10.45
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- arXiv (Cornell University) (submittedVersion, cc-by-sa)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- RWTH Publications (RWTH Aachen) (submittedVersion, other-oa)
- arXiv (Cornell University)
- RWTH Publications (RWTH Aachen)
- Funders
- European Commission (101057091)
- Deutsche Forschungsgemeinschaft (TR 1700/7‐1, NE2136/3-1, 2136/3-1)
- Bundesministerium für Bildung und Forschung (01KD2215B, 031L0312A, 01KX2021)
- HORIZON EUROPE Framework Programme (101057091)
- Topics
- Health Sciences › Medicine › Health Informatics › Artificial Intelligence in Healthcare and Education
- Physical Sciences › Computer Science › Artificial Intelligence › Machine Learning in Healthcare
- Health Sciences › Health Professions › Health Information Management › Artificial Intelligence in Healthcare
- Keywords
- large language models, ChatGPT, automated machine learning, clinical trials, medical data analysis, GPT-4, clinical outcome prediction, biomarker prediction, tumor progression, model performance comparison
- MeSH terms
- Machine Learning, Algorithms, Humans, Language, Neoplasms, Benchmarking
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