Unsupervised machine learning highlights the challenges of subtyping disorders of gut‐brain interaction

Author:

Dowrick Jarrah M.12ORCID,Roy Nicole C.234,Bayer Simone25,Frampton Chris M. A.256,Talley Nicholas J.27ORCID,Gearry Richard B.25,Angeli‐Gordon Timothy R.1248

Affiliation:

1. Auckland Bioengineering Institute University of Auckland Auckland New Zealand

2. High‐Value Nutrition National Science Challenge Auckland New Zealand

3. Department of Human Nutrition University of Otago Dunedin New Zealand

4. Riddet Institute Massey University Palmerston North New Zealand

5. Department of Medicine University of Otago Christchurch New Zealand

6. Department of Psychological Medicine University of Otago Christchurch New Zealand

7. School of Medicine and Public Health University of Newcastle Callaghan New South Wales Australia

8. Department of Surgery University of Auckland Auckland New Zealand

Abstract

AbstractBackgroundUnsupervised machine learning describes a collection of powerful techniques that seek to identify hidden patterns in unlabeled data. These techniques can be broadly categorized into dimension reduction, which transforms and combines the original set of measurements to simplify data, and cluster analysis, which seeks to group subjects based on some measure of similarity. Unsupervised machine learning can be used to explore alternative subtyping of disorders of gut‐brain interaction (DGBI) compared to the existing gastrointestinal symptom‐based definitions of Rome IV.PurposeThis present review aims to familiarize the reader with fundamental concepts of unsupervised machine learning using accessible definitions and provide a critical summary of their application to the evaluation of DGBI subtyping. By considering the overlap between Rome IV clinical definitions and identified clusters, along with clinical and physiological insights, this paper speculates on the possible implications for DGBI. Also considered are algorithmic developments in the unsupervised machine learning community that may help leverage increasingly available omics data to explore biologically informed definitions. Unsupervised machine learning challenges the modern subtyping of DGBI and, with the necessary clinical validation, has the potential to enhance future iterations of the Rome criteria to identify more homogeneous, diagnosable, and treatable patient populations.

Funder

National Health and Medical Research Council

Ministry of Business, Innovation and Employment

Royal Society Te Apārangi

Publisher

Wiley

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