Lamin A expression in circulating osteoprogenitors as a potential biomarker for frailty: The Nepean Osteoporosis and Frailty (NOF) Study

被引:14
作者
Al Saedi, Ahmed [1 ,2 ]
Gunawardene, Piumali [3 ,4 ]
Bermeo, Sandra [3 ,5 ]
Vogrin, Sara [1 ,2 ]
Boersma, Derek [4 ]
Phu, Steven [1 ,2 ]
Singh, Lakshman [1 ,2 ]
Suriyaarachchi, Pushpa [3 ]
Duque, Gustavo [1 ,2 ,3 ]
机构
[1] Univ Melbourne & Western Hlth, Australian Inst Musculoskeletal Sci AIMSS, Melbourne, Vic, Australia
[2] Univ Melbourne, Melbourne Med Sch, Dept Med Western Hlth, Melbourne, Vic, Australia
[3] Univ Sydney, Sydney Med Sch Nepean, Penrith, NSW, Australia
[4] Nepean Hosp, Dept Geriatr Med, Penrith, NSW, Australia
[5] Univ Simon Bolivar, Fac Ciencias Basicas & Biomed, Barranquilla, Colombia
关键词
Lamin A; Aging; Frailty; COP cells; Circulating osteoprogenitors; Flow cytometry; GILFORD-PROGERIA-SYNDROME; MESENCHYMAL STEM-CELLS; NUCLEAR LAMINA; OLDER-ADULTS; AGE; DIFFERENTIATION; DEFINITION; SARCOPENIA; DISEASE; SYSTEM;
D O I
10.1016/j.exger.2017.11.015
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Lamin A is a protein of the nuclear lamina. Low levels of lamin A expression are associated with osteosarcopenia in mice. In this study, we hypothesized that low lamin A expression is also associated with frailty in humans. We aimed to develop a non-invasive method to quantify lamin A expression in epithelial and circulating osteo-progenitor (COP) cells, and to determine the relationship between lamin A expression and frailty in older individuals. COP cells and buccal swabs were obtained from 66 subjects (median age 74; 60% female; 26 non-frail, 23 pre-frail, and 17 frail) participating at the Nepean Osteoporosis and Frailty (NOF) Study. We quantified physical performance and disability, and stratified frailty in this population. Lamin A expression in epithelial and COP cells was quantified by flow cytometry. Linear regression models estimated the relationship between lamin A expression in buccal and COP cells, and prevalent disability and frailty. Lamin A expression in buccal cells showed no association with either disability or frailty. Low lamin A expression values in COP cells were associated with frailty. Frail individuals showed 60% lower levels of lamin A compared to non-frail (95% CI - 36 to - 74%, p < 0.001) and 62% lower levels compared to pre-frail (95% CI - 40 to - 76%, p < 0.001). In summary, we have identified lamin A expression in COP cells as a strong indicator of frailty. Further work is needed to understand lamin A expression as a risk stratifier, biomarker, or therapeutic target in frail older persons.
引用
收藏
页码:69 / 75
页数:7
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