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PubMed Publications| Keyword search (4,163 papers available) |  |
"Chen J" Authored Publications:
| Title | Authors | PubMed ID | |
|---|---|---|---|
| 1 | Integrated metabolomics and metagenomics analysis identifies a unique signature characterizing metabolic syndrome | Wannaiampikul S; Lee B; Chen J; Prentice KJ; Ayansola R; Xu A; Santosa S; Pantopoulos K; Sweeney G; | 41794383 HKAP |
| 2 | Personalized biomarkers of multiscale functional alterations in temporal lobe epilepsy | Xie K; Sahlas E; Ngo A; Chen J; Arafat T; Royer J; Zhou Y; RodrÃguez-Cruces R; Dascal A; Caldairou B; Fadaie F; Barnett A; Audrain S; Larivière S; Caciagli L; Pana R; Weil AG; Grova C; Frauscher B; Schrader DV; Zhang Z; Concha L; Bernasconi A; Bernasconi N; Bernhardt BC; | 41258102 SOH |
| 3 | An active bifunctional natural dye for stable all-solid-state organic batteries | Yu Q; Hu Y; Deng S; Shakouri M; Chen J; Martins V; Nie HY; Huang Y; Zhao Y; Zaghib K; Sham TK; Li X; | 40993135 PHYSICS |
| 4 | Upconversion Lanthanide-Based 2D Metal-Organic Frameworks for Multimode Information Encryption | Chen J; Xie Y; Yang W; Sun R; Xing F; Mandl GA; Capobianco JA; Sun L; | 40557752 CNSR |
| 5 | Upconversion Luminescence through Cooperative and Energy-Transfer Mechanisms in Yb3+ -Metal-Organic Frameworks | Xie Y; Sun G; Mandl GA; Maurizio SL; Chen J; Capobianco JA; Sun L; | 36437239 CNSR |
| 6 | Practical fixed-time trajectory tracking control of constrained wheeled mobile robots with kinematic disturbances | Lu Q; Chen J; Wang Q; Zhang D; Sun M; Su CY; | 35039151 ENCS |
| 7 | Energy migration control of multi-modal emissions in an Er3+ doped nanostructure toward information encryption and deep learning decoding | Song Y; Lu M; Mandl GA; Xie Y; Sun G; Chen J; Liu X; Capobianco JA; Sun L; | 34476872 ENCS |
| 8 | Wastewater treatment in amine-based carbon capture. | Dong C, Huang G, Cheng G, An C, Yao Y, Chen X, Chen J | 30738317 ENCS |
| 9 | On the Conflicting Estimations of Pigment Site Energies in Photosynthetic Complexes: A Case Study of the CP47 Complex. | Reinot T, Chen J, Kell A, Jassas M, Robben KC, Zazubovich V, Jankowiak R | 27279733 PHYSICS |
| Title: | Integrated metabolomics and metagenomics analysis identifies a unique signature characterizing metabolic syndrome | ||||
| Authors: | Wannaiampikul S, Lee B, Chen J, Prentice KJ, Ayansola R, Xu A, Santosa S, Pantopoulos K, Sweeney G | ||||
| Link: | https://pubmed.ncbi.nlm.nih.gov/41794383/ | ||||
| DOI: | 10.1016/j.jnutbio.2026.110327 | ||||
| Publication: | The Journal of nutritional biochemistry | ||||
| Keywords: | Host-Microbiome Interaction; Metabolic Syndrome; Metagenomics; Obesity; Serum Metabolomics; Thai Population; | ||||
| PMID: | 41794383 | Category: | Date Added: | 2026-03-08 | |
| Dept Affiliation: |
HKAP
1 Thai Canada Research Centre, Faculty of Medicine, Srinakharinwirot University, Ongkharak, Thailand.; Division of Internal Medicine, HRH Princess Maha Chakri Sirindhorn Medical Center, Srinakharinwirot University, Ongkharak, Thailand. 2 Division of Internal Medicine, HRH Princess Maha Chakri Sirindhorn Medical Center, Srinakharinwirot University, Ongkharak, Thailand. 3 State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong SAR, China; Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong SAR, China; Guangdong Provincial Key Laboratory of Food, Nutrition and Health, and Department of Nutrition, School of Public Health, Sun Yat-sen University, Guangzhou, P.R. China. 4 Department of Physiology, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada; Banting and Best Diabetes Centre, Toronto, Canada. 5 Department of Biology, York University, Toronto, Canada. 6 State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong SAR, China; Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong SAR, China; Guangdong-Hong Kong Joint Institute for Metabolic Medicine, The University of Hong Kong, Hong Kong SAR, China. 7 Department of Health, Kinesiology, and Applied Physiology, Concordia University, Montreal, Quebec, Canada. 8 Lady Davis Institute for Medical Research, Jewish General Hospital and Department of Medicine, McGill University, Montreal, Quebec, Canada. 9 Thai Canada Research Centre, Faculty of Medicine, Srinakharinwirot University, Ongkharak, Thailand.; Department of Biology, York University, Toronto, Canada.. Electronic address: gsweeney@yorku.ca. |
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Description: |
Background: Metabolic Syndrome (MetS) presents a global health challenge, characterized by obesity, hypertension, dyslipidemia, and insulin resistance. Despite recognition of the gut microbiome's role in metabolic health, there remains scope for defining association of unique microbes with clinical status. Unique genetic, dietary, and lifestyle factors may influence gut microbial composition and circulating metabolites, and consequently susceptibility to MetS. By identifying specific microbial and metabolomic signatures associated with MetS, we aim to uncover potential targets for reducing the disease burden. Methods: We correlate comprehensive clinical parameters with fecal metagenomics and untargeted serum metabolomics to delineate population-specific characteristics from 142 individuals with MetS (N=97) or control (CTRL; N=45). Results: Microbiome species-level alpha diversity was reduced in MetS compared to CTRL. After adjustment for sex, age, BMI, and intensity of statin usage, we identified 20 MetS-related species. A co-abundant network analysis revealed Eubacterium eligens, enriched in the CTRL population, with the highest node degree. Serum metabolomics identified 106 significantly differentially regulated metabolites. N-arachidonoyl dopamine (NADA), an endocannabinoid implicated in GABAergic signaling, was the most significantly altered, enriched in CTRL and correlated with E. Eligens. sPLS-DA modeling revealed that E. eligens and D. formicigenerans species cluster together with metabolites NADA and tetrahydrocorticosterone (THB), representing defining characteristics distinguishing MetS in this population. Conclusions: Our data reveal a distinct multi-omic signature of MetS, characterized by a significant reduction in E. eligens and D. formicigenerans abundance, and in circulating NADA and THB levels. |
