Serum amyloid A and metabolic disease: evidence for a critical role in chronic inflammatory conditions.

SAA adipocytes, macrophages cardiovascular disease diabetes intestine liver obesity

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2023
Historique:
received: 31 03 2023
accepted: 15 05 2023
medline: 3 7 2023
pubmed: 3 7 2023
entrez: 3 7 2023
Statut: epublish

Résumé

Serum amyloid A (SAA) subtypes 1-3 are well-described acute phase reactants that are elevated in acute inflammatory conditions such as infection, tissue injury, and trauma, while SAA4 is constitutively expressed. SAA subtypes also have been implicated as playing roles in chronic metabolic diseases including obesity, diabetes, and cardiovascular disease, and possibly in autoimmune diseases such as systemic lupus erythematosis, rheumatoid arthritis, and inflammatory bowel disease. Distinctions between the expression kinetics of SAA in acute inflammatory responses and chronic disease states suggest the potential for differentiating SAA functions. Although circulating SAA levels can rise up to 1,000-fold during an acute inflammatory event, elevations are more modest (∼5-fold) in chronic metabolic conditions. The majority of acute-phase SAA derives from the liver, while in chronic inflammatory conditions SAA also derives from adipose tissue, the intestine, and elsewhere. In this review, roles for SAA subtypes in chronic metabolic disease states are contrasted to current knowledge about acute phase SAA. Investigations show distinct differences between SAA expression and function in human and animal models of metabolic disease, as well as sexual dimorphism of SAA subtype responses.

Identifiants

pubmed: 37396595
doi: 10.3389/fcvm.2023.1197432
pmc: PMC10311072
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1197432

Informations de copyright

© 2023 den Hartigh, May, Zhang, Chait and Blaser.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Laura J den Hartigh (LJ)

Department of Medicine, Division of Metabolism, Endocrinology, and Nutrition, University of Washington, Seattle, WA, United States.
Diabetes Institute, University of Washington, Seattle, WA, United States.

Karolline S May (KS)

Department of Medicine, Division of Metabolism, Endocrinology, and Nutrition, University of Washington, Seattle, WA, United States.
Diabetes Institute, University of Washington, Seattle, WA, United States.

Xue-Song Zhang (XS)

Center for Advanced Biotechnology and Medicine, Rutgers University, Piscataway, NJ, United States.

Alan Chait (A)

Department of Medicine, Division of Metabolism, Endocrinology, and Nutrition, University of Washington, Seattle, WA, United States.
Diabetes Institute, University of Washington, Seattle, WA, United States.

Martin J Blaser (MJ)

Center for Advanced Biotechnology and Medicine, Rutgers University, Piscataway, NJ, United States.

Classifications MeSH