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In vivo characterisation of biochemical variants of amyloid β in subjects with idiopathic Normal Pressure Hydrocephalus and Alzheimer’s Disease Neuropathological Change
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för immunologi, genetik och patologi, Klinisk och experimentell patologi. Department of Pathology, Uppsala University Hospital, Sweden.ORCID-id: 0000-0003-1043-5385
Department of Neurology, University of Bonn, Germany.ORCID-id: 0000-0002-4678-2912
Department of Pathology, Uppsala University Hospital, Sweden.ORCID-id: 0000-0002-6249-569x
(Engelska)Ingår i: Journal of Alzheimer's Disease, ISSN 1387-2877, E-ISSN 1875-8908Artikel i tidskrift (Refereegranskat) Accepted
Nyckelord [en]
biochemical variants, amyloid β, idiopathic Normal Pressure Hydrocephalus, Alzheimer’s Disease Neuropathologic Change
Nationell ämneskategori
Annan medicinsk grundvetenskap
Forskningsämne
Patologi; Geriatrik
Identifikatorer
URN: urn:nbn:se:uu:diva-433959OAI: oai:DiVA.org:uu-433959DiVA, id: diva2:1525512
Tillgänglig från: 2021-02-03 Skapad: 2021-02-03 Senast uppdaterad: 2021-02-03
Ingår i avhandling
1. Alzheimer's Disease Neuropathological Change and neuronal and glial alterations in patients with idiopathic Normal Pressure Hydrocephalus
Öppna denna publikation i ny flik eller fönster >>Alzheimer's Disease Neuropathological Change and neuronal and glial alterations in patients with idiopathic Normal Pressure Hydrocephalus
2021 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Alzheimer’s disease Neuropathological Change (ADNC), i.e. amyloid β (Aβ) and hyperphosphorylated τ (HPτ), is seen in excess in the brains of subjects with AD. Idiopathic Normal Pressure Hydrocephalus (iNPH) lacks defined hallmark lesions, affects the elderly and leads to cognitive impairment, gait disturbance and urinary incontinence that can be treated with a ventriculoperitoneal shunt (VPS). A few centres around the world have obtained a brain biopsy from the area of VPS. It has been reported that the presence of ADNC in the biopsy is associated with progression to AD.

We confirm that majority of iNPH subjects display ADNC, and the ADNC increases in extent with age, in line with AD. The HPτ pathology is sparse in majority of cases. We observed remarkable neuronal survival and loss of matrix/synapses in subjects with iNPH (paper III).

When studying subjects with notable Aβ pathology (paper IV), we observed a stepwise increase of pyroglutamylated Aβ (pyAβ) and phosphorylated Aβ variants in iNPH. These two Aβ variants are associated with symptomatic AD and correlate with HPτ pathology. The pyAβ in the frontal cortex is a predictive marker for AD. Thus, notable Aβ pathology in presence of HPτ in iNPH is suggestive of a moderate level of ADNC.  

When assessing changes in the extent of pathology occurring during 21 months in a frontal cortex of a subject with iNPH and AD (paper II), HPτ pathology increased in parallel with neuronal and synaptic loss, whereas Aβ pathology and astroglial activity were stable over time. In contrast, we observed reduction of microglial markers, which might explain why anti-inflammatory treatment is effective only at an early stage of AD.

When assessing brain tissue, the section thickness must be standardised, as it affects the staining outcome and diagnosis (paper I).

In conclusion, we have demonstrated a progressive neurodegeneration of ADNC type in a population of iNPH subjects, mimicking what is seen in subjects with AD. A brain biopsy obtained from subjects with iNPH should be obligatory. This is because when ADNC is present in the biopsy, representing prodromal AD, contact with memory clinic should be initiated.

Ort, förlag, år, upplaga, sidor
Uppsala: Acta Universitatis Upsaliensis, 2021. s. 76
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 1719
Nyckelord
idiopathic Normal Pressure Hydrocephalus, Alzheimer’s disease, amyloid β, hyperphosphorylated τ
Nationell ämneskategori
Annan klinisk medicin
Forskningsämne
Patologi
Identifikatorer
urn:nbn:se:uu:diva-433963 (URN)978-91-513-1132-6 (ISBN)
Disputation
2021-03-27, Rudbecksalen, Rudbeckslaboratoriet, Dag Hammarskjölds väg 20, Uppsala, 09:15 (Engelska)
Opponent
Handledare
Tillgänglig från: 2021-03-05 Skapad: 2021-02-03 Senast uppdaterad: 2021-03-29

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Libard, SylwiaAlafuzoff, Irina

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Libard, SylwiaWalter, JochenAlafuzoff, Irina
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