FGF23 levels as a marker of physical performance and falls in community-dwelling very old individuals.

Fibroblast growth factor 23 aging body balance falls muscle strength physical performance very old

Journal

Archives of endocrinology and metabolism
ISSN: 2359-4292
Titre abrégé: Arch Endocrinol Metab
Pays: Brazil
ID NLM: 101652058

Informations de publication

Date de publication:
25 May 2022
Historique:
entrez: 25 5 2022
pubmed: 26 5 2022
medline: 26 5 2022
Statut: aheadofprint

Résumé

The fibroblast growth factor 23 (FGF23) has been related to biological aging, but data in elderly individuals are scant. We determined the profile of serum FGF23 levels in a population of very-old individuals and studied their correlations with parameters of bone metabolism and health markers, as functional performance. This cross-sectional study was performed on 182 community dwellers aged ≥ 80 years. Serum levels of FGF23, PTH, calcium, albumin, phosphorus, creatinine, bone markers, and bone mineral density data were analyzed. Physical performance was evaluated with the stationary march (Step), Flamingo, and functional reach tests, along with questionnaires to assess falls and fractures in the previous year, energy expenditure (MET), and the Charlson index (CI). Physical activity was evaluated with the International Physical Activity Questionnaire (IPAQ). Most participants (75%) had FGF23 levels between 30-120 RU/mL (range: 6.0-3,170.0 RU/mL). FGF23 levels correlated with estimated glomerular filtration rate (eGFR; r = -0.335; p = 0.001) and PTH (r = 0.318; p < 0.0001). Individuals with FGF23 in the highest tertile had more falls in the previous year (p = 0.032), worse performance in the Flamingo (p = 0.009) and Step (p < 0.001) tests, worse CI (p = 0.009) and a trend toward sedentary lifestyle (p = 0.056). On multiple regression, FGF23 tertiles remained significant, independently of eGFR, for falls in the previous year, performance in the Flamingo and stationary march tests, lean mass index, and IPAQ classification. In a population of very elderly individuals, FGF23 levels were inversely associated with neuromuscular and functional performances. Higher concentrations were related to more falls, lower muscle strength and aerobic capacity, and poorer balance, regardless of renal function, suggesting a potentially deleterious role of high FGF23 concentrations in musculoskeletal health.

Identifiants

pubmed: 35612845
pii: 2359-3997000000488
doi: 10.20945/2359-3997000000488
pmc: PMC9832858
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Références

J Bone Miner Res. 2003 Jul;18(7):1227-34
pubmed: 12854832
Metabolism. 2016 May;65(5):747-756
pubmed: 27085781
Sci Rep. 2018 Feb 23;8(1):3573
pubmed: 29476104
Med Sci Sports Exerc. 2000 Sep;32(9 Suppl):S498-504
pubmed: 10993420
Neuroscience. 2007 Nov 30;150(1):202-11
pubmed: 17905520
J Clin Endocrinol Metab. 2016 Oct;101(10):3779-3786
pubmed: 27501282
Clin Chem Lab Med. 2013 Oct;51(10):1971-81
pubmed: 23729624
J Gerontol A Biol Sci Med Sci. 2014 May;69(5):584-90
pubmed: 24737561
Curr Opin Endocrinol Diabetes Obes. 2016 Dec;23(6):423-429
pubmed: 27652999
Am J Epidemiol. 1998 Apr 15;147(8):755-63
pubmed: 9554417
N Engl J Med. 2008 Aug 7;359(6):584-92
pubmed: 18687639
Age Ageing. 2010 Jul;39(4):412-23
pubmed: 20392703
Ann Intern Med. 2009 May 5;150(9):604-12
pubmed: 19414839
J Bone Miner Res. 2011 Apr;26(4):857-64
pubmed: 20928885
Aging Dis. 2018 Oct 1;9(5):769-784
pubmed: 30271655
Calcif Tissue Int. 2017 Nov;101(5):510-518
pubmed: 28761972
Br Med J. 1973 Dec 15;4(5893):643-6
pubmed: 4758544
Med Sci Sports Exerc. 2003 Aug;35(8):1381-95
pubmed: 12900694
J Chronic Dis. 1987;40(5):373-83
pubmed: 3558716
Pediatr Nephrol. 2010 Apr;25(4):583-90
pubmed: 19626341
Spine (Phila Pa 1976). 2016 Feb;41(3):E108-15
pubmed: 26583471
J Am Geriatr Soc. 2016 Feb;64(2):270-6
pubmed: 26889836
BMC Nephrol. 2012 Sep 26;13:122
pubmed: 23013306
Nephrology (Carlton). 2014 Dec;19(12):784-90
pubmed: 25185859
J Bone Miner Res. 1994 Aug;9(8):1137-41
pubmed: 7976495
Biochem Biophys Res Commun. 2016 Feb 12;470(3):657-662
pubmed: 26797283
Toxins (Basel). 2019 Mar 22;11(3):
pubmed: 30909513
J Am Geriatr Soc. 2021 Feb;69(2):467-473
pubmed: 33289072
J Atheroscler Thromb. 2021 Mar 1;28(3):203-213
pubmed: 33028781
J Bone Miner Res. 2000 Aug;15(8):1526-36
pubmed: 10934651
Prim Care. 1994 Mar;21(1):55-67
pubmed: 8197257
J Gerontol. 1990 Nov;45(6):M192-7
pubmed: 2229941

Auteurs

Mariana Zuccolotto Foroni (MZ)

Divisão de Endocrinologia, Escola Paulista de Medicina - Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil, marianazforoni@gmail.com.

Maysa Seabra Cendoroglo (MS)

Divisão de Geriatria, Escola Paulista de Medicina - Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil.

Aline Granja Costa (AG)

Divisão de Endocrinologia, Escola Paulista de Medicina - Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil.

Rosangela Villa Marin-Mio (RV)

Divisão de Endocrinologia, Escola Paulista de Medicina - Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil.

Patricia Ferreira do Prado Moreira (PF)

Divisão de Geriatria, Escola Paulista de Medicina - Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil.

Sergio Setsuo Maeda (SS)

Divisão de Endocrinologia, Escola Paulista de Medicina - Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil.

John P Bilezikian (JP)

Department of Medicine, Division of Endocrinology, College of Physicians and Surgeons, Columbia University, New York, New York, USA.

Marise Lazaretti-Castro (M)

Divisão de Endocrinologia, Escola Paulista de Medicina - Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brasil.

Classifications MeSH