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  • 标题:Metabolomic Salivary Signature of Pediatric Obesity Related Liver Disease and Metabolic Syndrome
  • 本地全文:下载
  • 作者:Jacopo Troisi ; Federica Belmonte ; Antonella Bisogno
  • 期刊名称:Nutrients
  • 电子版ISSN:2072-6643
  • 出版年度:2019
  • 卷号:11
  • 期号:2
  • 页码:274-290
  • DOI:10.3390/nu11020274
  • 出版社:MDPI Publishing
  • 摘要:Pediatric obesity-related metabolic syndrome (MetS) and nonalcoholic fatty liver disease (NAFLD) are increasingly frequent conditions with a still-elusive diagnosis and low-efficacy treatment and monitoring options. In this study, we investigated the salivary metabolomic signature, which has been uncharacterized to date. In this pilot-nested case-control study over a transversal design, 41 subjects (23 obese patients and 18 normal weight (NW) healthy controls), characterized based on medical history, clinical, anthropometric, and laboratory data, were recruited. Liver involvement, defined according to ultrasonographic liver brightness, allowed for the allocation of the patients into four groups: obese with hepatic steatosis ([St ], n = 15) and without hepatic steatosis ([St–], n = 8), and with (n = 10) and without (n = 13) MetS. A partial least squares discriminant analysis (PLS-DA) model was devised to classify the patients’ classes based on their salivary metabolomic signature. Pediatric obesity and its related liver disease and metabolic syndrome appear to have distinct salivary metabolomic signatures. The difference is notable in metabolites involved in energy, amino and organic acid metabolism, as well as in intestinal bacteria metabolism, possibly reflecting diet, fatty acid synthase pathways, and the strict interaction between microbiota and intestinal mucins. This information expands the current understanding of NAFLD pathogenesis, potentially translating into better targeted monitoring and/or treatment strategies in the future.
  • 关键词:pediatric obesity; nonalcoholic fatty liver disease; metabolic syndrome; saliva; metabolomics; gas-chromatography mass spectrometry pediatric obesity ; nonalcoholic fatty liver disease ; metabolic syndrome ; saliva ; metabolomics ; gas-chromatography mass spectrometry
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