Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery

被引:90
作者
Jaunmuktane, Zane [1 ,2 ]
Quaegebeur, Annelies [1 ]
Taipa, Ricardo [3 ]
Viana-Baptista, Miguel [4 ]
Barbosa, Raquel [4 ]
Koriath, Carolin [5 ]
Sciot, Raf [6 ]
Mead, Simon [7 ,8 ]
Brandner, Sebastian [1 ,5 ]
机构
[1] Univ Coll London Hosp NHS Fdn Trust, Natl Hosp Neurol & Neurosurg, Div Neuropathol, Queen Sq, London WC1N 3BG, England
[2] UCL Inst Neurol, Dept Mol Neurosci, Queen Sq, London WC1N 3BG, England
[3] Ctr Hosp Univ Porto, Dept Neurosci, Neuropathol Unit, Portuguese Brain Bank, P-4099001 Porto, Portugal
[4] Ctr Hosp Lisboa Ocidental, Dept Neurol, Hosp Egas Moniz, P-1449005 Lisbon, Portugal
[5] UCL Inst Neurol, Dept Neurodegenerat Dis, Queen Sq, London WC1N 3BG, England
[6] Univ Leuven, Dept Imaging & Pathol, B-3000 Louvain, Belgium
[7] UCL, Med Res Council, Prion Unit, UCL Inst Prion Dis, Queen Sq, London WC1N 3BG, England
[8] UCL Hosp NHS Fdn Trust, Natl Hosp Neurol & Neurosurg, Natl Prion Clin, Queen Sq, London WC1N 3BG, England
关键词
Cerebral amyloid angiopathy; CAA; Transmission; Prion diseases; Proteopathic seeding; Amyloid-beta; A beta; Neurosurgery; Decontamination; Intracerebral haemorrhage; Head trauma; Traumatic brain injury; TBI; CHRONIC TRAUMATIC ENCEPHALOPATHY; CREUTZFELDT-JAKOB-DISEASE; ALZHEIMERS ASSOCIATION GUIDELINES; INTRACEREBRAL HEMORRHAGE; NEUROPATHOLOGIC ASSESSMENT; BRAIN-INJURY; NATIONAL INSTITUTE; CODING VARIANTS; PRION DISEASES; HEAD TRAUMA;
D O I
10.1007/s00401-018-1822-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Amyloid-beta (A beta) is a peptide deposited in the brain parenchyma in Alzheimer's disease and in cerebral blood vessels, causing cerebral amyloid angiopathy (CAA). A beta pathology is transmissible experimentally in animals and through medical procedures in humans, such as contaminated growth hormone or dura mater transplantation in the context of iatrogenic prion disease. Here, we present four patients who underwent neurosurgical procedures during childhood or teenage years and presented with intracerebral haemorrhage approximately three decades later, caused by severe CAA. None of these patients carried pathogenic mutations associated with early A beta pathology development. In addition, we identified in the literature four patients with a history of neurosurgical intervention and subsequent development of CAA. These findings raise the possibility that A beta pathology may be transmissible, as prion disease is, through neurosurgical procedures.
引用
收藏
页码:671 / 679
页数:9
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