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Machine learning estimation of human body time using metabolomic profiling.
Woelders, Tom; Revell, Victoria L; Middleton, Benita; Ackermann, Katrin; Kayser, Manfred; Raynaud, Florence I; Skene, Debra J; Hut, Roelof A.
Affiliation
  • Woelders T; Chronobiology unit, Groningen Institute of Evolutionary Life Sciences, University of Groningen, 9700 CC Groningen, the Netherlands.
  • Revell VL; Chronobiology, Faculty of Health and Medical Sciences, University of Surrey, Guildford GU2 7XH, United Kingdom.
  • Middleton B; Chronobiology, Faculty of Health and Medical Sciences, University of Surrey, Guildford GU2 7XH, United Kingdom.
  • Ackermann K; Department of Genetic Identification, Erasmus University Medical Center, 3000 CA Rotterdam, the Netherlands.
  • Kayser M; Department of Genetic Identification, Erasmus University Medical Center, 3000 CA Rotterdam, the Netherlands.
  • Raynaud FI; Cancer Research UK Cancer Therapeutics Unit, Division of Cancer Therapeutics, The Institute of Cancer Research, London SM2 5NG, United Kingdom.
  • Skene DJ; Chronobiology, Faculty of Health and Medical Sciences, University of Surrey, Guildford GU2 7XH, United Kingdom.
  • Hut RA; Chronobiology unit, Groningen Institute of Evolutionary Life Sciences, University of Groningen, 9700 CC Groningen, the Netherlands.
Proc Natl Acad Sci U S A ; 120(18): e2212685120, 2023 05 02.
Article in En | MEDLINE | ID: mdl-37094145
ABSTRACT
Circadian rhythms influence physiology, metabolism, and molecular processes in the human body. Estimation of individual body time (circadian phase) is therefore highly relevant for individual optimization of behavior (sleep, meals, sports), diagnostic sampling, medical treatment, and for treatment of circadian rhythm disorders. Here, we provide a partial least squares regression (PLSR) machine learning approach that uses plasma-derived metabolomics data in one or more samples to estimate dim light melatonin onset (DLMO) as a proxy for circadian phase of the human body. For this purpose, our protocol was aimed to stay close to real-life conditions. We found that a metabolomics approach optimized for either women or men under entrained conditions performed equally well or better than existing approaches using more labor-intensive RNA sequencing-based methods. Although estimation of circadian body time using blood-targeted metabolomics requires further validation in shift work and other real-world conditions, it currently may offer a robust, feasible technique with relatively high accuracy to aid personalized optimization of behavior and clinical treatment after appropriate validation in patient populations.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Human Body / Melatonin Type of study: Guideline Limits: Female / Humans / Male Language: En Journal: Proc Natl Acad Sci U S A Year: 2023 Type: Article Affiliation country: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Human Body / Melatonin Type of study: Guideline Limits: Female / Humans / Male Language: En Journal: Proc Natl Acad Sci U S A Year: 2023 Type: Article Affiliation country: Netherlands