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المؤلفMir, Fayaz Ahmad
المؤلفAbdesselem, Houari B.
المؤلفCyprian, Farhan
المؤلفIskandarani, Ahmad
المؤلفDoudin, Asmma
المؤلفShraim, Mutasem AbdelRahim
المؤلفAlkhalaf, Bader M.
المؤلفAlkasem, Meis
المؤلفAbdalhakam, Ibrahem
المؤلفBensmail, Ilham
المؤلفAl Halabi, Hamza A.
المؤلفTaheri, Shahrad
المؤلفAbou-Samra, Abdul-Badi
تاريخ الإتاحة2025-04-13T04:46:16Z
تاريخ النشر2025
اسم المنشورInternational Journal of Molecular Sciences
المصدرScopus
المعرّفhttp://dx.doi.org/10.3390/ijms26052262
الرقم المعياري الدولي للكتاب16616596
معرّف المصادر الموحدhttp://hdl.handle.net/10576/64143
الملخصObesity 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.
راعي المشروعThis publication was made possible by MRC grant #16245/16 from the Medical Research Centre, Hamad Medical Corporation, Doha, Qatar.
اللغةen
الناشرMultidisciplinary Digital Publishing Institute (MDPI)
الموضوعcomorbidities
obesity
Olink
proteomics
العنوانMetabolically Healthy Obesity Is Characterized by a Distinct Proteome Signature
النوعArticle
رقم العدد5
رقم المجلد26
dc.accessType Open Access


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