Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome 00168, Italy.
Università Cattolica del Sacro Cuore, Rome 00168, Italy.
Nutrients. 2018 Nov 6;10(11):1691. doi: 10.3390/nu10111691.
Physical frailty and sarcopenia (PF&S) are hallmarks of aging that share a common pathogenic background. Perturbations in protein/amino acid metabolism may play a role in the development of PF&S. In this initial report, 68 community-dwellers aged 70 years and older, 38 with PF&S and 30 non-sarcopenic, non-frail controls (nonPF&S), were enrolled as part as the "BIOmarkers associated with Sarcopenia and Physical frailty in EldeRly pErsons" (BIOSPHERE) study. A panel of 37 serum amino acids and derivatives was assayed by UPLC-MS. Partial Least Squares⁻Discriminant Analysis (PLS-DA) was used to characterize the amino acid profile of PF&S. The optimal complexity of the PLS-DA model was found to be three latent variables. The proportion of correct classification was 76.6 ± 3.9% (75.1 ± 4.6% for enrollees with PF&S; 78.5 ± 6.0% for nonPF&S). Older adults with PF&S were characterized by higher levels of asparagine, aspartic acid, citrulline, ethanolamine, glutamic acid, sarcosine, and taurine. The profile of nonPF&S participants was defined by higher concentrations of α-aminobutyric acid and methionine. Distinct profiles of circulating amino acids and derivatives characterize older people with PF&S. The dissection of these patterns may provide novel insights into the role played by protein/amino acid perturbations in the disabling cascade and possible new targets for interventions.
身体虚弱和肌少症(PF&S)是衰老的标志,它们具有共同的发病基础。蛋白质/氨基酸代谢的紊乱可能在 PF&S 的发展中起作用。在这项初步报告中,纳入了 68 名居住在社区的 70 岁及以上的老年人,其中 38 名患有 PF&S,30 名非肌少症、非虚弱对照者(非 PF&S)。他们是“与老年人肌少症和身体虚弱相关的生物标志物”(BIOSPHERE)研究的一部分。通过 UPLC-MS 测定了 37 种血清氨基酸及其衍生物。偏最小二乘判别分析(PLS-DA)用于表征 PF&S 的氨基酸谱。发现 PLS-DA 模型的最佳复杂度为三个潜在变量。正确分类的比例为 76.6±3.9%(PF&S 患者中为 75.1±4.6%;非 PF&S 患者中为 78.5±6.0%)。患有 PF&S 的老年人以天冬酰胺、天冬氨酸、瓜氨酸、乙醇胺、谷氨酸、肌氨酸和牛磺酸水平较高为特征。非 PF&S 参与者的特征是 α-氨基丁酸和蛋氨酸浓度较高。循环氨基酸及其衍生物的特征谱可用于区分患有 PF&S 的老年人。对这些模式的剖析可能为蛋白质/氨基酸紊乱在致残级联中的作用提供新的见解,并为干预措施提供新的潜在靶点。