National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, China.
National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, China; Center of Gerontology and Geriatrics, West China Hospital, Sichuan University, Chengdu, China.
Arch Gerontol Geriatr. 2021 Jan-Feb;92:104262. doi: 10.1016/j.archger.2020.104262. Epub 2020 Sep 23.
Increased evidence suggests chronic inflammation is significant in the progression of sarcopenia in older adults. In this study, we aimed to compare the level of systemic inflammation markers (White blood cells, neutrophils, lymphocytes, platelets and their derived ratios) between sarcopenic and non-sarcopenic individuals and investigate the association of these inflammatory markers with sarcopenia.
This cross-sectional study included 4224 adults (1514 men and 2710 women) from the West China Health and Aging Trend (WCHAT) study. Sarcopenia was defined according to the recommended diagnostic algorithm of the Asia Working Group for Sarcopenia (AWGS). The value of systemic inflammatory markers was based on laboratory data. Multiple logistic regression analysis was used to explore the association between inflammatory markers and sarcopenia after adjusting for covariates.
Among 4224 participants (mean age 62.3 ± 8.2 years, 64.2 % women), 814 (19.3 %) were diagnosed as sarcopenia. After adjusting for potential confounders, logistic regression analysis indicated that neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR) and systemic immune-inflammation index (SII) were significantly associated with sarcopenia. Participants in the highest NLR, PLR and SII value group had higher odds for sarcopenia than those in the lowest value group (OR [95 %CI]: 1.233 [1.002,1.517], 1.455 [1.177,1.799] and 1.268 [1.029,1.561], respectively).
Higher NLR, PLR, and SII level are associated with an increased prevalence of sarcopenia in middle-aged and older adults. Since these systemic inflammatory markers are inexpensive and can be obtained easily from routine blood tests, regular follow-up of NLR, PLR and SII may be an effective strategy in sarcopenia screening and management.
越来越多的证据表明,慢性炎症在老年人肌肉减少症的进展中起着重要作用。在这项研究中,我们旨在比较肌少症患者和非肌少症患者之间的系统性炎症标志物(白细胞、中性粒细胞、淋巴细胞、血小板及其衍生比值)水平,并探讨这些炎症标志物与肌少症的关系。
这项横断面研究纳入了来自华西健康与老龄化队列研究(WCHAT)的 4224 名成年人(男性 1514 名,女性 2710 名)。肌少症根据亚洲肌少症工作组(AWGS)的推荐诊断算法进行定义。系统炎症标志物的值基于实验室数据。采用多因素 logistic 回归分析调整协变量后,探讨炎症标志物与肌少症之间的关系。
在 4224 名参与者(平均年龄 62.3±8.2 岁,64.2%为女性)中,814 名(19.3%)被诊断为肌少症。在调整了潜在混杂因素后,logistic 回归分析表明,中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)和系统免疫炎症指数(SII)与肌少症显著相关。NLR、PLR 和 SII 值最高组的参与者发生肌少症的可能性高于最低组(比值比 [95%置信区间]:1.233 [1.002,1.517]、1.455 [1.177,1.799]和 1.268 [1.029,1.561])。
较高的 NLR、PLR 和 SII 水平与中年及以上人群肌少症的患病率增加有关。由于这些系统性炎症标志物价格低廉,且可从常规血液检查中轻易获得,因此定期监测 NLR、PLR 和 SII 可能是肌少症筛查和管理的有效策略。