Systemic Inflammation Is Associated with MCI and Its Subtypes: The Sydney Memory and Aging Study

被引:100
作者
Trollor, Julian N. [1 ,2 ]
Smith, Evelyn [1 ]
Baune, Bernhard T. [7 ]
Kochan, Nicole A. [2 ,4 ]
Campbell, Lesley [5 ,6 ]
Samaras, Katherine [5 ,6 ]
Crawford, John [2 ]
Brodaty, Henry [2 ,3 ]
Sachdev, Perminder [2 ,4 ]
机构
[1] Univ New S Wales, Dept Dev Disabil Neuropsychiat, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Psychiat, Brain & Aging Res Program, Sydney, NSW 2052, Australia
[3] Univ New S Wales, Sch Psychiat, Dementia Collaborat Res Ctr, Sydney, NSW 2052, Australia
[4] Prince Wales Hosp, Inst Neuropsychiat, Randwick, NSW 2031, Australia
[5] St Vincents Hosp, Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
[6] St Vincents Hosp, Dept Endocrinol, Darlinghurst, NSW 2010, Australia
[7] James Cook Univ, Sch Med & Dent, Dept Psychiat & Psychiat Neurosci, Townsville, Qld, Australia
基金
英国医学研究理事会;
关键词
Inflammation; Cytokines; Inflammatory markers; Mild cognitive impairment; Dementia; C-REACTIVE PROTEIN; MILD COGNITIVE IMPAIRMENT; TUMOR-NECROSIS-FACTOR; BODY-MASS INDEX; ONSET ALZHEIMERS-DISEASE; FACTOR-ALPHA; TNF-ALPHA; PROMOTER POLYMORPHISM; PLASMA-CONCENTRATION; GENERAL-POPULATION;
D O I
10.1159/000322092
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background/Aims: Raised low-grade systemic inflammation has been associated with dementia, and preliminary studies suggest an association with mild cognitive impairment (MCI). This study examines the relationship between systemic inflammation and MCI subtypes. Methods: We measured the inflammatory markers C-reactive protein, interleukins (IL)-1 beta, -6, -8, -10 and -12, plasminogen activator inhibitor-1 (PAI-1), serum amyloid A (SAA), tumor necrosis factor-alpha (TNF-alpha) and vascular adhesion molecule-1 (VCAM-1) in the Sydney Memory and Ageing Study (MAS) cohort, a longitudinal study of 1,037 Australians aged 70-90 years. Results: After adjusting for possible confounding variables, levels of TNF-alpha and SAA were higher in participants with MCI compared to cognitively normal individuals, and some sex differences were apparent. Nonamnestic multiple domain MCI was associated with higher levels of IL-1 beta and IL-12, TNF-alpha and SAA compared to cognitively normal, amnestic MCI (single and multiple domain) and nonamnestic single domain MCI. PAI-1 levels were higher in cognitively normal and nonamnestic multiple domain MCI than in amnestic multiple domain MCI. Conclusion: Our findings suggest an association between specific inflammatory markers and MCI subtypes, highlight sex differences in the association with MCI, and point to a discrete impact of systemic inflammation on cognition. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:569 / 578
页数:10
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