TY - JOUR
T1 - Fibroblast Growth Factor 23 and Exercise Capacity in Heart Failure with Preserved Ejection Fraction
T2 - FGF23 and Exercise Capacity in HFpEF
AU - Ghuman, Jasleen
AU - Cai, Xuan
AU - Patel, Ravi B.
AU - Khan, Sadiya S.
AU - Hecktman, Jonathan
AU - Redfield, Margaret M.
AU - Lewis, Gregory
AU - Shah, Sanjiv J.
AU - Wolf, Myles
AU - Isakova, Tamara
AU - Mehta, Rupal
N1 - Funding Information:
Supported by grants P30DK114857, R01DK102438 (TI) R01 HL107577 (SJS), R01 HL127028 (SJS), R01 HL140731 (SJS), and R01 HL149423 (SJS), American Heart Association #16SFRN28780016 (SJS) and #19TPA34890060 (SSK), and a National Kidney Foundation of Illinois Young Investigator Grant (RM). Research reported in this publication was also supported, in part, by the National Institutes of Health's National Center for Advancing Translational Sciences, Grant Number KL2TR001424 and by the National Institutes of Health's National Center for Advancing Translational Sciences, Grant Number UL1TR001422. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The views expressed in this article are those of the authors and do not necessarily reflect the position or policy of the Department of Veterans Affairs or the United States government. The Heart Failure Clinical Research Network is supported by the NHLBI, National Institutes of Health Funding/Support: U10 HL084904 (awarded to the coordinating center) and U10 HL110312, U10 HL110337, U10 HL110342, U10 HL110262, U10 HL110297, U10 HL110302, U10 HL110309, U10 HL110336, and U10 HL110338 (awarded to the regional clinical centers).
Funding Information:
RM has interest in Abbott Laboratories, AbbVie, Inc., and Teva Pharmaceuticals Industries Ltd, and has received honoraria from Akebia/Otsuka. TI has received honoraria from Kyowa Hakko Kirin Co., Ltd and grant support from Shire. MW has received research support, honoraria or consultant fees from Amgen, Ardelyx, DiaSorin, Keryx, Lilly, Pfizer, Shire and Ultragenyx. GDL has received research support from Abbott, Actelion, Amgen, AstraZeneca, Cytokinetics, Corvia, Cyclerion, and Novartis; and has served as a consultant, scientific advisory board member, and/or executive committee/steering committee member for American Regent, Amgen, AstraZeneca, Cytokinetics, Cyclerion, Novartis, Pfizer and Sonivie. SJS has received research grants from Actelion, AstraZeneca, Corvia, Novartis, and Pfizer; and has served as a consultant, scientific advisory board member, and/or executive committee/steering committee member for Abbott, Actelion, AstraZeneca, Amgen, Axon Therapeutics, Bayer, Boehringer-Ingelheim, Bristol-Myers Squibb, Cardiora, CVRx, Cytokinetics, Eisai, GSK, Ionis, Ironwood, Merck, MyoKardia, Novartis, Pfizer, Sanofi, Shifamed, Tenax, and United Therapeutics.
Publisher Copyright:
© 2020
PY - 2021/3
Y1 - 2021/3
N2 - Background: Heart failure with preserved ejection fraction (HFpEF) is characterized by left ventricular hypertrophy and decreased exercise capacity. Fibroblast growth factor 23 (FGF23), a hormone involved in phosphate, vitamin D, and iron homeostasis, is linked to left ventricular hypertrophy and HF. We measured c-terminal FGF23 (cFGF23) and intact FGF23 (iFGF23) levels and examined their associations with exercise capacity in patients with HFpEF. Methods and Results: Using multivariable linear regression and linear mixed models, we studied the associations of cFGF23 and iFGF23 with baseline and mean weekly change over 24 weeks in peak oxygen consumption and 6-minute walk distance in individuals enrolled in the Phosphodiesterase-5 Inhibition to Improve Clinical Status and Exercise Capacity in HFpEF trial. Our study population included 172 individuals with available plasma for cFGF23 and iFGF23 measurements. Median (25th–75th percentile) baseline cFGF23 and iFGF23 levels were 208.7 RU/mL (132.1–379.5 RU/mL) and 90.3 pg/mL (68.6–128.5 pg/mL), respectively. After adjustment for cardiovascular disease and hematologic and kidney parameters, higher cFGF23 was independently associated with a lower peak oxygen consumption at baseline. Higher iFGF23 was independently associated with shorter 6-minute walk distance at baseline. No significant associations were appreciated with the longitudinal outcomes. Conclusions: In patients with HFpEF, higher FGF23 levels are independently associated with decreased exercise capacity at baseline.
AB - Background: Heart failure with preserved ejection fraction (HFpEF) is characterized by left ventricular hypertrophy and decreased exercise capacity. Fibroblast growth factor 23 (FGF23), a hormone involved in phosphate, vitamin D, and iron homeostasis, is linked to left ventricular hypertrophy and HF. We measured c-terminal FGF23 (cFGF23) and intact FGF23 (iFGF23) levels and examined their associations with exercise capacity in patients with HFpEF. Methods and Results: Using multivariable linear regression and linear mixed models, we studied the associations of cFGF23 and iFGF23 with baseline and mean weekly change over 24 weeks in peak oxygen consumption and 6-minute walk distance in individuals enrolled in the Phosphodiesterase-5 Inhibition to Improve Clinical Status and Exercise Capacity in HFpEF trial. Our study population included 172 individuals with available plasma for cFGF23 and iFGF23 measurements. Median (25th–75th percentile) baseline cFGF23 and iFGF23 levels were 208.7 RU/mL (132.1–379.5 RU/mL) and 90.3 pg/mL (68.6–128.5 pg/mL), respectively. After adjustment for cardiovascular disease and hematologic and kidney parameters, higher cFGF23 was independently associated with a lower peak oxygen consumption at baseline. Higher iFGF23 was independently associated with shorter 6-minute walk distance at baseline. No significant associations were appreciated with the longitudinal outcomes. Conclusions: In patients with HFpEF, higher FGF23 levels are independently associated with decreased exercise capacity at baseline.
KW - Heart failure with preserved ejection fraction
KW - chronic kidney disease
KW - exercise capacity
KW - fibroblast growth factor 23
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U2 - 10.1016/j.cardfail.2020.09.477
DO - 10.1016/j.cardfail.2020.09.477
M3 - Article
C2 - 33035687
AN - SCOPUS:85095806517
SN - 1071-9164
VL - 27
SP - 309
EP - 317
JO - Journal of Cardiac Failure
JF - Journal of Cardiac Failure
IS - 3
ER -