The association between systemic inflammation and cognitive performance in the elderly: the Sydney Memory and Ageing Study

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• 作者：Julian N. Trollor (14) j.trollor@unsw.edu.au
  Evelyn Smith (14)
  Emmeline Agars (1)
  Stacey A. Kuan (8)
  Bernhard T. Baune (9)
  Lesley Campbell (67)
  Katherine Samaras (67)
  John Crawford (4)
  Ora Lux (234)
  Nicole A. Kochan (24)
  Henry Brodaty (45)
  Perminder Sachdev (24)
• 关键词：Inflammation – ; Ageing – ; Cytokines – ; Inflammaging – ; Cognition – ; Dementia
• 刊名：AGE
• 出版年：2012
• 出版时间：October 2012
• 年：2012
• 卷：34
• 期：5
• 页码：1295-1308
• 全文大小：256.4 KB
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• 作者单位：1. Department of Developmental Disability Neuropsychiatry, School of Psychiatry, University of New South Wales, 34 Botany Road, Sydney, NSW, Australia2. Neuropsychiatric Institute, Prince of Wales Hospital, Randwick, NSW, Australia3. South-Eastern Area Laboratory Services, Prince of Wales Hospital, Avoca Street, Randwick, NSW 2031, Australia4. Brain and Aging Research Program, School of Psychiatry, University of New South Wales, Sydney, Australia5. Dementia Collaborative Research Centre, School of Psychiatry, University of New South Wales, Sydney, Australia6. Garvan Institute of Medical Research, Darlinghurst, NSW 2010, Australia7. Department of Endocrinology, St Vincent鈥檚 Hospital, Darlinghurst, NSW 2010, Australia8. The Benevolent Society, Paddington, 2021 Australia9. Discipline of Psychiatry, School of Medicine, University of Adelaide, Adelaide, SA, Australia
• ISSN：1574-4647

文摘

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.