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

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作者
Julia Muenchhoff
Anne Poljak
Anbupalam Thalamuthu
Veer B. Gupta
Pratishtha Chatterjee
Mark Raftery
Colin L. Masters
John C. Morris
Randall J. Bateman
Anne M. Fagan
Ralph N. Martins
Perminder S. Sachdev
机构
[1] Centre for Healthy Brain Ageing,Department of Neurology
[2] School of Psychiatry,Department of Pathology and Immunology
[3] University of New South Wales,undefined
[4] Bioanalytical Mass Spectrometry Facility,undefined
[5] University of New South Wales,undefined
[6] School of Medical Sciences,undefined
[7] University of New South Wales,undefined
[8] Centre of Excellence for Alzheimer’s disease Research & Care,undefined
[9] School of Medical Sciences,undefined
[10] Edith Cowan University,undefined
[11] Sir James McCusker Alzheimer’s Disease Research Unit (Hollywood Private Hospital),undefined
[12] School of Psychiatry and Clinical Neurosciences,undefined
[13] University of Western Australia,undefined
[14] University of Melbourne,undefined
[15] Washington University School of Medicine,undefined
[16] Knight Alzheimer’s Disease Research Center at Washington University School of Medicine,undefined
[17] Washington University School of Medicine,undefined
[18] Neuropsychiatric Institute,undefined
[19] Prince of Wales Hospital,undefined
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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.
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