Trollor Julian N, Smith Evelyn, Agars Emmeline, Kuan Stacey A, Baune Bernhard T, Campbell Lesley, Samaras Katherine, Crawford John, Lux Ora, Kochan Nicole A, Brodaty Henry, Sachdev Perminder
Department of Developmental Disability Neuropsychiatry, School of Psychiatry, University of New South Wales, 34 Botany Road, Sydney, NSW, Australia.
Age (Dordr). 2012 Oct;34(5):1295-308. doi: 10.1007/s11357-011-9301-x. Epub 2011 Aug 19.
Inflammation may contribute to cognitive decline and dementia. This study examined the cross-sectional relationships between markers of systemic inflammation (C-reactive protein, interleukins-1β, -6, -8, -10, -12, plasminogen activator inhibitor, serum amyloid A, tumour necrosis factor-α and vascular adhesion molecule-1) and cognitive function in 873 non-demented community-dwelling elderly participants aged 70-90 years. Regression analyses were performed to determine the relationships between cognitive domains and inflammatory markers, controlling for age, sex, education, cardiovascular risk factors, obesity and other metabolic factors, smoking, alcohol consumption, depression and presence of the apolipoprotein ε4 genotype. Regression analyses were repeated using four factors derived from a factor analysis of the cognitive tests. After Bonferroni correction for multiple testing, associations remained between raised levels of interleukin-12 and reduced performance in processing speed. Marked sex differences were noted in the abovementioned findings, with only females being significantly affected. Using the four factors derived from the factor analyses of cognitive test as dependent variables, interleukins-12 and -6 were both associated with the processing speed/executive function factor, even after controlling for relevant confounding factors. Thus, markers of systemic inflammation are related to cognitive deficits in a non-clinical community-dwelling elderly population, independent of depression, cardiovascular or metabolic risk factors, or presence of apolipoprotein ε4 genotype. Additional research is required to elucidate the pathophysiology and longitudinal development of these relationships.
炎症可能导致认知能力下降和痴呆。本研究调查了873名年龄在70至90岁之间、居住在社区且未患痴呆症的老年人中,全身炎症标志物(C反应蛋白、白细胞介素-1β、-6、-8、-10、-12、纤溶酶原激活物抑制剂、血清淀粉样蛋白A、肿瘤坏死因子-α和血管细胞黏附分子-1)与认知功能之间的横断面关系。进行回归分析以确定认知领域与炎症标志物之间的关系,并对年龄、性别、教育程度、心血管危险因素、肥胖及其他代谢因素、吸烟、饮酒、抑郁和载脂蛋白ε4基因型的存在情况进行了控制。使用从认知测试的因子分析中得出的四个因素重复进行回归分析。在对多重检验进行Bonferroni校正后,白细胞介素-12水平升高与处理速度降低之间仍存在关联。上述结果存在明显的性别差异,只有女性受到显著影响。以从认知测试的因子分析中得出的四个因素作为因变量,即使在控制了相关混杂因素后,白细胞介素-12和-6均与处理速度/执行功能因子相关。因此,在非临床社区居住老年人群中,全身炎症标志物与认知缺陷相关,独立于抑郁、心血管或代谢危险因素或载脂蛋白ε4基因型的存在情况。需要进一步的研究来阐明这些关系的病理生理学和纵向发展情况。