Association Between Insulin-Like Growth Factor-1 and Frailty Among Older Adults

Frailty is a course experienced in advanced aging. Identification of a biological factor associated with frailty is required. Although serum insulin-like growth factor-1 (IGF-1) is a potential factor related with frailty, consensus has not been reached regarding this relationship. This study aimed t...

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Published inThe Journal of nutrition, health & aging Vol. 22; no. 1; pp. 68 - 72
Main Authors Doi, Takehiko, Makizako, H., Tsutsumimoto, K., Hotta, R., Nakakubo, S., Makino, K., Suzuki, T., Shimada, H.
Format Journal Article
LanguageEnglish
Published Paris Elsevier Masson SAS 01.01.2018
Springer Paris
Springer Nature B.V
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Summary:Frailty is a course experienced in advanced aging. Identification of a biological factor associated with frailty is required. Although serum insulin-like growth factor-1 (IGF-1) is a potential factor related with frailty, consensus has not been reached regarding this relationship. This study aimed to investigate the association between IGF-1 and frailty in older adults. Cross-sectional study. Cohort study that was part of the “National Center for Geriatrics and Gerontology–Study of Geriatric Syndromes. The study participants were 4133 older adults (mean age, 71.8 ± 5.4 years). We assessed serum IGF-1 levels and frailty status and collected demographic variables, including cognitive function, as covariates. Frailty and pre-frailty were present in 274 subjects (7%) and 1930 subjects (47%), respectively. Subjects were divided into four groups based on quartiles of IGF-1 levels. Multinomial logistic analysis showed that the lowest group had significant odds of pre-frailty (crude model: odds ratio [OR] 1.58, 95% confidence interval [CI] 1.30–1.90, p <.001; adjusted model: OR 1.38, 95% CI 1.13–1.68, p =.002) and frailty (crude model: OR 3.42, 95% CI 2.38-4.92, p <.001; adjusted model: OR 1.54, 95% CI 1.02–2.32, p =.039), compared with the highest group. Lower serum IGF-1 levels were independently related with frailty in older adults.
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ISSN:1279-7707
1760-4788
1760-4788
DOI:10.1007/s12603-017-0916-1