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Research ArticleArticle

Circulating Fibroblast Growth Factor-21 Levels in Rheumatoid Arthritis: Associations With Disease Characteristics, Body Composition, and Physical Functioning

Patrick W. Gould, Babette S. Zemel, Elena G. Taratuta and Joshua F. Baker
The Journal of Rheumatology November 2020, jrheum.200673; DOI: https://doi.org/10.3899/jrheum.200673
Patrick W. Gould
JFB was supported by a Veterans Affairs Clinical Science Research and Development Career Development Award and VA Merit Award (IK2 CX000955, I01 CX001703), and by the University of Pennsylvania Clinical and Translational Research Center (UL1 RR024134). Research reported in this publication was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under award number UL1TR001878. The contents of this work do not represent the views of the Department of Veterans Affairs or the US Government. P.W. Gould, BA, E.G. Taratuta, MD, Perelman School of Medicine, University of Pennsylvania; B.S. Zemel, PhD, Perelman School of Medicine, University of Pennsylvania, and Children’s Hospital of Philadelphia; J.F. Baker, MD, MSCE, Perelman School of Medicine, University of Pennsylvania, Philadelphia VA Medical Center, Division of Rheumatology, University of Pennsylvania, and Department of Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. The authors declare no conflicts of interest. Address correspondence to Dr. J.F. Baker, 5th Floor White Building, 3400 Spruce Street, Philadelphia, PA 19104, USA. Email: Joshua.Baker@pennmedicine.upenn.edu. Accepted October 21, 2020.
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Babette S. Zemel
JFB was supported by a Veterans Affairs Clinical Science Research and Development Career Development Award and VA Merit Award (IK2 CX000955, I01 CX001703), and by the University of Pennsylvania Clinical and Translational Research Center (UL1 RR024134). Research reported in this publication was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under award number UL1TR001878. The contents of this work do not represent the views of the Department of Veterans Affairs or the US Government. P.W. Gould, BA, E.G. Taratuta, MD, Perelman School of Medicine, University of Pennsylvania; B.S. Zemel, PhD, Perelman School of Medicine, University of Pennsylvania, and Children’s Hospital of Philadelphia; J.F. Baker, MD, MSCE, Perelman School of Medicine, University of Pennsylvania, Philadelphia VA Medical Center, Division of Rheumatology, University of Pennsylvania, and Department of Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. The authors declare no conflicts of interest. Address correspondence to Dr. J.F. Baker, 5th Floor White Building, 3400 Spruce Street, Philadelphia, PA 19104, USA. Email: Joshua.Baker@pennmedicine.upenn.edu. Accepted October 21, 2020.
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Elena G. Taratuta
JFB was supported by a Veterans Affairs Clinical Science Research and Development Career Development Award and VA Merit Award (IK2 CX000955, I01 CX001703), and by the University of Pennsylvania Clinical and Translational Research Center (UL1 RR024134). Research reported in this publication was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under award number UL1TR001878. The contents of this work do not represent the views of the Department of Veterans Affairs or the US Government. P.W. Gould, BA, E.G. Taratuta, MD, Perelman School of Medicine, University of Pennsylvania; B.S. Zemel, PhD, Perelman School of Medicine, University of Pennsylvania, and Children’s Hospital of Philadelphia; J.F. Baker, MD, MSCE, Perelman School of Medicine, University of Pennsylvania, Philadelphia VA Medical Center, Division of Rheumatology, University of Pennsylvania, and Department of Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. The authors declare no conflicts of interest. Address correspondence to Dr. J.F. Baker, 5th Floor White Building, 3400 Spruce Street, Philadelphia, PA 19104, USA. Email: Joshua.Baker@pennmedicine.upenn.edu. Accepted October 21, 2020.
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Joshua F. Baker
JFB was supported by a Veterans Affairs Clinical Science Research and Development Career Development Award and VA Merit Award (IK2 CX000955, I01 CX001703), and by the University of Pennsylvania Clinical and Translational Research Center (UL1 RR024134). Research reported in this publication was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under award number UL1TR001878. The contents of this work do not represent the views of the Department of Veterans Affairs or the US Government. P.W. Gould, BA, E.G. Taratuta, MD, Perelman School of Medicine, University of Pennsylvania; B.S. Zemel, PhD, Perelman School of Medicine, University of Pennsylvania, and Children’s Hospital of Philadelphia; J.F. Baker, MD, MSCE, Perelman School of Medicine, University of Pennsylvania, Philadelphia VA Medical Center, Division of Rheumatology, University of Pennsylvania, and Department of Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. The authors declare no conflicts of interest. Address correspondence to Dr. J.F. Baker, 5th Floor White Building, 3400 Spruce Street, Philadelphia, PA 19104, USA. Email: Joshua.Baker@pennmedicine.upenn.edu. Accepted October 21, 2020.
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Abstract

Objective This study evaluated associations between fibroblast growth factor (FGF)-21, an adipokine associated with metabolic stress, and adverse longitudinal changes in body composition and physical functioning in patients with rheumatoid arthritis (RA).

Methods At baseline and follow-up, patients with RA aged 18–70 years completed whole-body dual-energy X-ray absorptiometry and peripheral quantitative computed tomography to quantify lean mass, fat mass, and muscle density. Dynamometry assessed muscle strength at the hand and knee, and physical functioning was measured with the Health Assessment Questionnaire (HAQ) and the Short Physical Performance Battery (SPPB). FGF-21 and inflammatory cytokines were measured at baseline. Linear and logistic regression analyses assessed associations between FGF-21 levels and both body composition and physical functioning over time.

Results There were 113 patients with RA enrolled, and 84 (74%) returned for follow-up at a median of 2.68 years. At baseline, FGF-21 was associated with age, smoking, methotrexate use, adiposity, and inflammatory cytokines: tumor necrosis factor receptor type I, YKL-40, vascular endothelial growth factor (VEGF), and resistin. The highest FGF-21 quartile was associated with worse SPPB and HAQ. Higher baseline FGF-21 levels (per 1 SD) were associated with worsening in muscle density and area Z-scores (β –0.06, 95% CI –0.12 to 0.008, P = 0.08; and β –0.05, 95% CI –0.10 to 0.006, P = 0.08, respectively) and a greater probability of a clinically meaningful worsening of HAQ (OR 2.37, 95% CI 1.21–4.64, P= 0.01). The fourth FGF-21 quartile was associated with worsening of SPPB (β –0.57, 95% CI –1.04 to –0.09, P = 0.02).

Conclusion FGF-21 levels are associated with obesity and inflammatory cytokines, and with worsening in physical functioning in RA. These data support the hypothesis that FGF-21 can identify patients at risk of functional decline.

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Circulating Fibroblast Growth Factor-21 Levels in Rheumatoid Arthritis: Associations With Disease Characteristics, Body Composition, and Physical Functioning
Patrick W. Gould, Babette S. Zemel, Elena G. Taratuta, Joshua F. Baker
The Journal of Rheumatology Nov 2020, jrheum.200673; DOI: 10.3899/jrheum.200673

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Circulating Fibroblast Growth Factor-21 Levels in Rheumatoid Arthritis: Associations With Disease Characteristics, Body Composition, and Physical Functioning
Patrick W. Gould, Babette S. Zemel, Elena G. Taratuta, Joshua F. Baker
The Journal of Rheumatology Nov 2020, jrheum.200673; DOI: 10.3899/jrheum.200673
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