血清肌酐/胱抑素 C 比值对识别低 MRI 肌肉体积和低握力的诊断能力:来自 9,731 至 149,707 名英国生物库老年人的数据。

Ben Kirk, Chia-Ling Kuo, Peiran Liu, Meiruo Xiang, Jesse Zanker, Konstantinos Prokopidis, Marc Sim, Richard H Fortinsky, George A Kuchel, Gustavo Duque
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引用次数: 0

摘要

背景:肌肉疏松症缺乏生物标志物。在一项针对英国生物库老年人的大型观察研究中,我们研究了血清肌酐与胱抑素 C(Cr:Cyc)比值对识别核磁共振成像肌肉体积低和握力低的诊断能力:在基线访问(2008-2010 年)时,通过免疫测定法(贝克曼库尔特 AU5800 和西门子 Advia 1800)测量血清肌酐和胱抑素 C,并通过液压手部测力计测量握力。核磁共振成像-大腿无脂肌肉体积(FFMV)和DXA衍生的附肢瘦体重在成像访问(2014-2018年)时进行测量。剔除了极端离群值,并在统计模型中调整了协变量(人口统计学、生活方式和临床因素,以及基线-成像访问之间的时间间隔):12,873 名老年人(平均年龄:63.5 ± 2.7 岁,44.2% 为女性)被纳入 FFMV 和 ALM/BMI 的研究;149,707 名老年人(平均年龄:64.0 ± 2.9 岁,50.5% 为女性)被纳入握力的研究。尽管存在明显关联(p结论:Cr:Cyc可能不是识别老年人肌肉量低或力量低的合适生物标志物。这一发现是通过大量样本和使用先进的医学成像技术得出的,是对肌肉疏松症领域的重要贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic power of serum creatinine/cystatin C ratio for identifying low MRI-muscle volume and low grip strength: Data from 9,731 to 149,707 UK Biobank older adults.

Background: Biomarkers for sarcopenia are lacking. We examined the diagnostic power of serum creatinine to cystatin C (Cr:Cyc) ratio for identifying low MRI-muscle volume and low grip strength in a large observational study of UK Biobank older adults.

Methods: Serum creatinine and cystatin C were measured via immunoassays (Beckman Coulter AU5800 and Siemens Advia 1800, respectively) and grip strength by hydraulic hand dynamometer at baseline visit (2008-2010). MRI-thigh fat-free muscle volume (FFMV) and DXA-derived appendicular lean mass were measured at imaging visit (2014-2018). Extreme outliers were removed, and covariates (demographic, lifestyle, and clinical factors, as well as time elapsed between baseline-imaging visit) were adjusted for in statistical models.

Results: 12,873 older adults (mean age: 63.5 ± 2.7 years, 44.2% women) were included for FFMV and ALM/BMI; 149,707 older adults (mean age: 64.0 ± 2.9 years, 50.5% women) for grip strength. Despite significant associations (p<0.05), in fully-adjusted models, Cr:Cyc showed poor to acceptable diagnostic power for identifying low FFMV when using cutpoints of 20th percentile (AUC: 0.577 men; 0.622 women) and T scores of -2 (AUC: 0.596 men; 0.659 women) and -2.5 (AUC: 0.609 men; 0.722 women). In fully-adjusted model, Cr:Cyc showed poor diagnostic power (AUCs: <0.70) for identifying low ALM/BMI or low grip strength irrespective of the cutpoint used.

Conclusions: Cr:Cyc may not be a suitable biomarker for identifying low muscle volume or low strength in older adults. This finding, drawn from a large sample size and the use of advanced medical imaging, marks an important contribution to the sarcopenia field.

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