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    Metabolically Healthy Obesity Is Characterized by a Distinct Proteome Signature

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    ijms-26-02262.pdf (1.980Mb)
    Date
    2025
    Author
    Mir, Fayaz Ahmad
    Abdesselem, Houari B.
    Cyprian, Farhan
    Iskandarani, Ahmad
    Doudin, Asmma
    Shraim, Mutasem AbdelRahim
    Alkhalaf, Bader M.
    Alkasem, Meis
    Abdalhakam, Ibrahem
    Bensmail, Ilham
    Al Halabi, Hamza A.
    Taheri, Shahrad
    Abou-Samra, Abdul-Badi
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    Abstract
    Obesity is commonly associated with metabolic diseases including type 2 diabetes, hypertension, and dyslipidemia. Moreover, individuals with obesity are at increased risk of cardiovascular disease. However, a subgroup of individuals within the obese population presents without concurrent metabolic disorders. Even though this group has a stable metabolic status and does not exhibit overt metabolic disease, this status may be transient; these individuals may have subclinical metabolic derangements. To investigate the latter hypothesis, an analysis of the proteome signature was conducted. Plasma samples from 27 subjects with obesity but without an associated metabolic disorder (obesity only (OBO)) and 15 lean healthy control (LHC) subjects were examined. Fasting samples were subjected to Olink proteomics analysis targeting 184 proteins enriched in cardiometabolic and inflammation pathways. Our results distinctly delineated two groups with distinct plasma protein expression profiles. Specifically, a total of 24 proteins were differentially expressed in individuals with obesity compared to LHC. Among these, 13 proteins were downregulated, whereas 11 proteins were upregulated. The pathways that were upregulated in the OBO group were related to chemoattractant activity, growth factor activity, G protein-coupled receptor binding, chemokine activity, and cytokine activity, whereas the pathways that were downregulated include regulation of T cell differentiation, leukocyte differentiation, reproductive system development, inflammatory response, neutrophil, lymphocyte, monocyte and leukocyte chemotaxis, and neutrophil migration. The study identifies several pathways that are altered in individuals with obesity compared to healthy control subjects. These findings provide valuable insights into the underlying mechanisms, potentially paving the way for the identification of therapeutic targets aimed at improving metabolic health in individuals with obesity.
    DOI/handle
    http://dx.doi.org/10.3390/ijms26052262
    http://hdl.handle.net/10576/64143
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