Inflammatory and immunological markers and risk for mortality and cognitive impairment in a longitudinal study of older adults from the longevous project

M.R. Caldeira , C.M. Almada-Filho , M.C. Brunialti , R. Salomão , M.S. Cendoroglo
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Abstract

Senescence of the immunological system is characterized by alterations in immune system cells associated with aging, often linked to cognitive disorders and mortality.Objective:To determine the prevalence of immunological changes, including immunological risk profile (IRP), and its association with cognitive impairments or mortality in oldest-old individuals.Method:A longitudinal study of 201 older adults aged ≥80 years, able to walk unaided, with no cognitive or immunological impairment, and with no serious disease at baseline was conducted. Blood samples were collected at 2-year intervals between 2012 and 2014 during the morning period. High-sensitivity CRP testing was conducted. TCD4 and TCD8 cell counts were performed by flow cytometry and plasma cytokines by CytometricBeadArray (CBA) Human Enhanced Sensitive (BD Biosciences, San Jose, CA, USA) as per manufacturer directions. After the 2-year follow-up, an analysis of associations of test results with cognitive status, as measured by the Mini-Mental State Exam (MMSE), or with mortality, based on medical records and death certificates provided by relatives, was performed. Results:Mean age was 84.4 years.Higher IL6 and hs-CRP levels were observed in deceased participants that weremale (p = 0.016). Higher IL6 levels were associated with cognitive impairment in female participants (p = 0.008). CD4 (p-value <0.001) and CD4/CD8 ratio (p-value = 0.013) decreased, and lower CD4/CD8 values were associated with cognitive impairment in women (p = 0.045).Conclusion:In the independent oldest-old participants with controlled chronic diseases, both men and women aged equally, and not all exhibited inflammation. However, even slight changes in inflammatory markers can be associated with increased risk for mortality and cognitive decline.

Abstract Image

在长寿项目中对老年人进行的一项纵向研究中,炎症和免疫标志物、死亡率和认知障碍的风险
免疫系统衰老的特征是与衰老相关的免疫系统细胞的改变,通常与认知障碍和死亡有关。目的:确定免疫变化的患病率,包括免疫风险概况(IRP),及其与老年人认知障碍或死亡率的关系。方法:对201名年龄≥80岁、能够独立行走、无认知或免疫障碍、基线时无严重疾病的老年人进行纵向研究。在2012年至2014年的早晨,每隔两年采集一次血液样本。进行高敏CRP检测。TCD4和TCD8细胞计数采用流式细胞术,血浆细胞因子计数采用CytometricBeadArray (CBA) Human Enhanced Sensitive (BD Biosciences, San Jose, CA, USA)。经过2年的随访,对测试结果与认知状态(通过迷你精神状态检查(MMSE)测量)或基于医疗记录和亲属提供的死亡证明的死亡率之间的关系进行了分析。结果:平均年龄84.4岁。在死亡的女性参与者中观察到较高的il - 6和hs-CRP水平(p = 0.016)。较高的il - 6水平与女性参与者的认知障碍有关(p = 0.008)。CD4 (p值<;0.001)和CD4/CD8比值(p值= 0.013)降低,CD4/CD8值降低与女性认知功能障碍相关(p = 0.045)。结论:在控制慢性疾病的独立老年参与者中,男性和女性年龄相同,并不是所有人都表现出炎症。然而,即使炎症标志物的轻微变化也可能与死亡和认知能力下降的风险增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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