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Associations between plasma metabolism-associated proteins and future development of giant cell arteritis: results from a prospective study

Wadstrom, Karin (författare)
Rheumatology, Department of Clinical Sciences, Lund University, Malmö, Sweden; Center for Rheumatology, Academic Specialist Center, Region Stockholm, Stockholm, Sweden
Jacobsson, Lennart T. H., 1954 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research,Rheumatology, Department of Clinical Sciences, Lund University, Malmö, Sweden; Department of Rheumatology & Inflammation Research, Institute of Medicine, The Sahlgrenska Academy, University of Gotherburg, Gothenburg, Sweden
Mohammad, Aladdin J. (författare)
Department of Rheumatology, Skåne University Hospital, Malmö, Sweden; Department of Medicine, University of Cambridge, Cambridge, UK
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Warrington, Kenneth J. (författare)
Division of Rheumatology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota, USA
Matteson, Eric L. (författare)
Division of Rheumatology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota, USA
Jakobsson, Magnus E (författare)
Malmö universitet,Institutionen för biomedicinsk vetenskap (BMV),Biofilms Research Center for Biointerfaces
Turesson, Carl (författare)
Rheumatology, Department of Clinical Sciences, Lund University, Malmö, Sweden; Department of Rheumatology, Skåne University Hospital, Malmö, Sweden
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 (creator_code:org_t)
Oxford University Press, 2024
2024
Engelska.
Ingår i: RHEUMATOLOGY. - : Oxford University Press. - 1462-0324 .- 1462-0332.
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Objective: The aim of this study was to investigate the relationship between biomarkers associated with metabolism and subsequent development of GCA. Method Participants in the population-based Malmo Diet Cancer Study (MDCS; N = 30 447) who were subsequently diagnosed with GCA were identified in a structured process. Matched: GCA-free controls were selected from the study cohort. Baseline plasma samples were analysed using the antibody-based OLINK proteomics metabolism panel (92 metabolic proteins). Analyses were pre-designated as hypothesis-driven or hypothesis-generating. In the latter, principal component analysis was used to identify groups of proteins that explained the variance in the proteome. Results: There were 95 cases with a confirmed incident diagnosis of GCA (median 12.0 years after inclusion). Among biomarkers with a priori hypotheses, adhesion G protein-coupled receptor E2 (ADGRE2) was positively associated [odds ratio (OR) per S.D. 1.67; 95% CI 1.08-2.57], and fructose-1,6-bisphosphatase 1 (FBP1) was negatively associated (OR per S.D. 0.59; 95% CI 0.35-0.99) with GCA. In particular, ADGRE2 levels were associated with subsequent GCA in the subset sampled <8.5 years before diagnosis. For meteorin-like protein (Metrnl), the highest impact on the risk of GCA was observed in those patients sampled closest to diagnosis, with a decreasing trend with longer time to GCA (P = 0.03). In the hypothesis-generating analyses, elevated levels of receptor tyrosine-like orphan receptor 1 (ROR1) were associated with subsequent GCA. Conclusion: Biomarkers identified years before clinical diagnosis indicated a protective role of gluconeogenesis (FBP1) and an association with macrophage activation (ADGRE2 and Metrnl) and proinflammatory signals (ROR1) for development of GCA.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Nyckelord

giant cell arteritis
biomarkers
metabolism
macrophage activation
pathogenesis
Giant cell arteritis

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