Changes in the plasma proteome at asymptomatic and symptomatic stages of autosomal dominant Alzheimer's disease

被引:31
|
作者
Muenchhoff, Julia [1 ]
Poljak, Anne [1 ,2 ,3 ]
Thalamuthu, Anbupalam [1 ]
Gupta, Veer B. [4 ,5 ]
Chatterjee, Pratishtha [4 ,5 ,6 ]
Raftery, Mark [2 ]
Masters, Colin L. [7 ]
Morris, John C. [8 ,9 ,10 ]
Bateman, Randall J. [8 ,9 ]
Fagan, Anne M. [8 ,9 ]
Martins, Ralph N. [4 ,5 ,6 ]
Sachdev, Perminder S. [1 ,11 ]
机构
[1] Univ New South Wales, Sch Psychiat, Ctr Hlth Brain Ageing, Sydney, NSW, Australia
[2] Univ New South Wales, Bioanalyt Mass Spectrometry Facil, Sydney, NSW, Australia
[3] Univ New South Wales, Sch Med Sci, Sydney, NSW, Australia
[4] Edith Cowan Univ, Sch Med Sci, Ctr Excellence Alzheimers Dis Res & Care, Joondalup, WA, Australia
[5] Hollywood Private Hosp, Sir James McCusker Alzheimers Dis Res Unit, Perth, WA, Australia
[6] Univ Western Australia, Sch Psychiat & Clin Neurosci, Perth, WA, Australia
[7] Univ Melbourne, Melbourne, Vic, Australia
[8] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[9] Washington Univ, Sch Med, Knight Alzheimers Dis Res Ctr, St Louis, MO USA
[10] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[11] Prince Wales Hosp, Inst Neuropsychiat, Sydney, NSW, Australia
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
HEPARIN-COFACTOR II; MILD COGNITIVE IMPAIRMENT; ESTIMATING EQUATIONS; CEREBROSPINAL-FLUID; ONSET; BIOMARKERS; INHIBITOR; DIAGNOSIS; RISK;
D O I
10.1038/srep29078
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The autosomal dominant form of Alzheimer's disease (ADAD) is far less prevalent than late onset Alzheimer's disease (LOAD), but enables well-informed prospective studies, since symptom onset is near certain and age of onset is predictable. Our aim was to discover plasma proteins associated with early AD pathology by investigating plasma protein changes at the asymptomatic and symptomatic stages of ADAD. Eighty-one proteins were compared across asymptomatic mutation carriers (aMC, n = 15), symptomatic mutation carriers (sMC, n = 8) and related noncarriers (NC, n = 12). Proteins were also tested for associations with cognitive measures, brain amyloid deposition and glucose metabolism. Fewer changes were observed at the asymptomatic than symptomatic stage with seven and 16 proteins altered significantly in aMC and sMC, respectively. This included complement components C3, C5, C6, apolipoproteins A-I, A-IV, C-I and M, histidine-rich glycoprotein, heparin cofactor II and attractin, which are involved in inflammation, lipid metabolism and vascular health. Proteins involved in lipid metabolism differed only at the symptomatic stage, whereas changes in inflammation and vascular health were evident at asymptomatic and symptomatic stages. Due to increasing evidence supporting the usefulness of ADAD as a model for LOAD, these proteins warrant further investigation into their potential association with early stages of LOAD.
引用
收藏
页数:11
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