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                  <mods:namePart>Costa, Andrea</mods:namePart>
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                  <mods:namePart>van der Stelt, Inge</mods:namePart>
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                  <mods:namePart>Reynés, Bárbara</mods:namePart>
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                  <mods:namePart>Konieczna, Jadwiga</mods:namePart>
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                  <mods:namePart>Fiol Sala, Miquel</mods:namePart>
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                  <mods:namePart>Keijer, Jaap</mods:namePart>
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                  <mods:namePart>Palou, Andreu</mods:namePart>
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                  <mods:namePart>Romaguera, Dora</mods:namePart>
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                  <mods:namePart>van Schothorst, Evert M</mods:namePart>
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                  <mods:namePart>Oliver, Paula</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-10-09T06:36:35Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2023-02</mods:dateIssued>
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               <mods:identifier type="citation">Costa A, van der Stelt I, Reynés B, Konieczna J, Fiol M, Keijer J, et al. Whole-Genome Transcriptomics of PBMC to Identify Biomarkers of Early Metabolic Risk in Apparently Healthy People with Overweight-Obesity and in Normal-Weight Subjects. Mol Nutr Food Res. 2022 Dec;e2200503.</mods:identifier>
               <mods:identifier type="doi">10.1002/mnfr.202200503</mods:identifier>
               <mods:identifier type="e-issn">1613-4133</mods:identifier>
               <mods:identifier type="journal">Molecular nutrition &amp; food research</mods:identifier>
               <mods:identifier type="other">https://hdl.handle.net/20.500.13003/18827</mods:identifier>
               <mods:identifier type="pubmedID">36564895</mods:identifier>
               <mods:identifier type="pui">L639858010</mods:identifier>
               <mods:identifier type="scopus">2-s2.0-85147267084</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/20.500.12105/23805</mods:identifier>
               <mods:identifier type="wos">921501800001</mods:identifier>
               <mods:abstract>Scope: Peripheral blood mononuclear cells (PBMC) provide a useful and minimally invasive source of biomarkers. Here to identify PBMC transcriptomic biomarkers predictive of metabolic impairment related to increased adiposity is aimed. Methods and results: The study analyzed the global PBMC transcriptome in metabolically healthy (normoglycemic) volunteers with overweight-obesity (OW-OB, n = 12), and in subjects with metabolically obese normal-weight (MONW, n = 5) phenotype, in comparison to normal-weight (NW, n = 12) controls. The study identifies 1072 differentially expressed genes (DEGs) in OW-OB versus NW and 992 in MONW versus NW. Hierarchical clustering of the top 100 DEGs clearly distinguishes OW-OB and MONW from NW. Remarkably, the OW-OB and MONW phenotypes share 257 DEGs regulated in the same direction. The top up-regulated gene CXCL8, coding for interleukin 8, with a role in obesity-related pathologies, is of special interest as a potential marker for predicting increased metabolic risk. CXCL8 expression is increased mainly in the MONW group and correlated directly with C-reactive protein levels. Conclusions: PBMC gene expression analysis of CXCL8 or a pool of DEGs may be used to identify early metabolic risk in an apparently healthy population regardless of their BMI, i.e., subjects with OW-OB or MONW phenotype and to apply adequate and personalized nutritional preventive strategies.</mods:abstract>
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                  <mods:title>Whole-Genome Transcriptomics of PBMC to Identify Biomarkers of Early Metabolic Risk in Apparently Healthy People with Overweight-Obesity and in Normal-Weight Subjects</mods:title>
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