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免疫风险表型、认知功能障碍与高龄老人的生存:应激负荷对瑞典八旬和九旬老人的影响

An immune risk phenotype, cognitive impairment, and survival in very late life: impact of allostatic load in Swedish octogenarian and nonagenarian humans.

作者信息

Wikby Anders, Ferguson Frederick, Forsey Rosalyn, Thompson Julie, Strindhall Jan, Löfgren Sture, Nilsson Bengt-Olof, Ernerudh Jan, Pawelec Graham, Johansson Boo

机构信息

Department of Natural Science and Biomedicine, School of Health sciences, Jönköping University, Sweden.

出版信息

J Gerontol A Biol Sci Med Sci. 2005 May;60(5):556-65. doi: 10.1093/gerona/60.5.556.

DOI:10.1093/gerona/60.5.556
PMID:15972602
Abstract

In the previous OCTO longitudinal study, we identified an immune risk phenotype (IRP) of high CD8 and low CD4 numbers and poor proliferative response. We also demonstrated that cognitive impairment constitutes a major predictor of nonsurvival. In the present NONA longitudinal study, we simultaneously examine in a model of allostatic load IRP and compromised cognition in 4-year survival in a population-based sample (n = 138, 86-94 years). Immune system measurements consisted of determinations of T-cell subsets, plasma interleukin 6 and cytomegalovirus and Epstein-Barr virus serology. Interleukin 2 responsiveness to concanavalin A, using data from the previous OCTO (octogenarians) immune study, hereafter OCTO immune, was also examined. Cognitive status was rated using a battery of neuropsychological tests. Logistic regression indicated that the IRP and cognitive impairment together predicted 58% of observed deaths. IRP was associated with late differentiated CD8+CD28-CD27- cells (p < .001), decreased interleukin 2 responsiveness (p < .05) and persistent viral infection (p < .01). Cognitive impairment was associated with increased plasma interleukin 6 (p < .001). IRP individuals with cognitive impairment were all deceased at the follow-up, indicating an allostatic overload.

摘要

在之前的八旬老人纵向研究中,我们确定了一种免疫风险表型(IRP),其特征为CD8细胞数量高、CD4细胞数量低且增殖反应差。我们还证明,认知障碍是生存情况不佳的主要预测因素。在本次九旬老人纵向研究中,我们在一个基于人群的样本(n = 138,年龄86 - 94岁)中,同时在一种应激负荷模型中研究了IRP和认知功能受损对4年生存率的影响。免疫系统测量包括T细胞亚群测定、血浆白细胞介素6以及巨细胞病毒和EB病毒血清学检测。还利用之前八旬老人(OCTO)免疫研究(以下简称OCTO免疫研究)的数据,检测了白细胞介素2对伴刀豆球蛋白A的反应性。使用一系列神经心理学测试对认知状态进行评分。逻辑回归分析表明,IRP和认知障碍共同预测了58%的观察到的死亡情况。IRP与晚期分化的CD8 + CD28 - CD27 - 细胞有关(p < 0.001)、白细胞介素2反应性降低(p < 0.05)以及持续性病毒感染有关(p < 0.01)。认知障碍与血浆白细胞介素6升高有关(p < 0.001)。有认知障碍的IRP个体在随访时均已死亡,表明存在应激负荷过载。

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