Circulating Adipokines and Associations With Incident Cardiovascular Disease in Rheumatoid Arthritis

Objective To assess whether circulating levels of adiponectin, leptin, and fibroblast growth factor 21 (FGF‐21) are associated with incident cardiovascular disease (CVD) in rheumatoid arthritis (RA). Methods Adipokines were measured using banked enrollment serum from patients with RA and dichotomize...

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Published inArthritis care & research (2010) Vol. 75; no. 4; pp. 768 - 777
Main Authors Federico, Lydia E., Johnson, Tate M., England, Bryant R., Wysham, Katherine D., George, Michael D., Sauer, Brian, Hamilton, Bartlett C., Hunter, Carlos D., Duryee, Michael J., Thiele, Geoffrey M., Mikuls, Ted R., Baker, Joshua F.
Format Journal Article
LanguageEnglish
Published Boston, USA Wiley Periodicals, Inc 01.04.2023
Wiley Subscription Services, Inc
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Summary:Objective To assess whether circulating levels of adiponectin, leptin, and fibroblast growth factor 21 (FGF‐21) are associated with incident cardiovascular disease (CVD) in rheumatoid arthritis (RA). Methods Adipokines were measured using banked enrollment serum from patients with RA and dichotomized above/below the median value. Incident CVD events (coronary artery disease [CAD], stroke, heart failure [HF] hospitalization, venous thromboembolism, CVD‐related deaths) were identified using administrative data and the National Death Index. Covariates were derived from medical record, biorepository, and registry databases. Multivariable Cox models were generated to quantify associations between adipokine concentrations and CVD incidence. Five‐year incidence rates were predicted. Results Among 2,598 participants, 639 (25%) had at least 1 CVD event over 19,585 patient‐years of follow‐up. High adiponectin levels were independently associated with HF hospitalization (hazard ratio [HR] 1.39 [95% confidence interval (95% CI) 1.07–1.79], P = 0.01) and CVD‐related death (HR 1.49 [95% CI 1.16–1.92], P = 0.002) but not with other CVD events. High leptin was independently associated with CVD‐related death (HR 1.44 [95% CI 1.05–1.97], P = 0.02). High FGF‐21 levels were independently associated with lower rates of CAD (HR 0.75 [95% CI 0.58–0.97], P = 0.03). In subgroup analyses, associations between high adiponectin and leptin levels with CVD‐related death were driven by strong associations in nonobese patients. Conclusion Adipokines are associated with HF hospitalization and CVD‐related death in patients with RA, with stronger associations in nonobese participants. These findings suggest that adipokines effectively predict clinically important outcomes in RA perhaps through an association with body composition and metabolic health. Further study is needed to determine whether adipokine measures might augment existing tools to identify RA patients at increased risk of CVD.
Bibliography:Supported by the Center of Excellence for Suicide Prevention, Joint Department of Veterans Affairs and Department of Defense Mortality Data Repository, National Death Index. Dr. England's work was supported by the Veterans Affairs Career Development Award (grant IK2CX002203). Dr. Wysham's work was supported by the Department of Veterans Affairs and the Rheumatology Research Foundation. Dr. George's work was supported by the NIH (National Institute of Arthritis and Musculoskeletal and Skin Diseases grant K23‐AR‐073931). Dr. Mikuls' work was supported by the Department of Veterans Affairs (Merit Award grant I01BX0046000), the Department of Defense (grant PR200793), and the NIH (National Institute on Alcohol Abuse and Alcoholism grant R25‐AA‐020818, National Institute of General Medical Sciences grant U54‐GM‐115458, and National Institute of Arthritis and Musculoskeletal and Skin Diseases grant P50‐AR‐60772). Dr. Baker's work was supported by the Department of Veterans Affairs (Clinical Science Research and Development Career Merit Award grant I01CX001703 and Rehabilitation Research and Development grants I21CX003157 and I01CX003644).
https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Facr.24885&file=acr24885‐sup‐0001‐Disclosureform.pdf
The contents herein do not represent the views of the Department of Veterans Affairs or the US government.
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All authors were involved in drafting the article or revising it critically for important intellectual content, and all authors approved the final version to be submitted for publication. Dr. Baker had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Acquisition of data. England, Mikuls, Baker.
AUTHOR CONTRIBUTIONS
Study conception and design. Federico, Mikuls, Baker.
Analysis and interpretation of data. Federico, Johnson, England, Wysham, George, Sauer, Hamilton, Hunter, Duryee, Thiele, Mikuls, Baker.
ISSN:2151-464X
2151-4658
DOI:10.1002/acr.24885