Spatiotemporal characterization of Alzheimer disease pathology in living human brain tissue

Abstract Alzheimer disease begins in the brain many years before symptoms, but early changes are usually studied after death or indirectly through fluid and imaging biomarkers. Here we show that small brain biopsies collected during ventriculoperitoneal shunt surgery can be used to study Alzheimer disease pathology and protein turnover during life. We analysed biopsies from 18 individuals with suspected normal pressure hydrocephalus, alongside matched ventricular and lumbar cerebrospinal fluid and post-mortem control brain tissue. Amyloid plaques were present in 9 of 18 biopsies, while mature tau tangles were rare. Matrix-assisted laser desorption/ionization mass spectrometry imaging mapped amyloid plaque chemistry within tissue. Phosphorylated tau 217 was enriched around plaques, supporting a local relationship between amyloid and tau pathology. Stable isotope labelling, which tracks newly made proteins, detected rapid tau labelling within approximately 3 hours and estimated brain tau half-life at about 34 days. Amyloid plaques showed little detectable turnover.

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Publication Details

Journal
Nature Communications
Published
2026-09-24
DOI
https://doi.org/10.1038/s41467-026-76494-4
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Spatiotemporal characterization of Alzheimer disease pathology in living human brain tissue

Laurence Dale Watkins, Kaleigh F. Roberts, Nick C. Fox, Jörg Hanrieder et al.
Nature Communications
Alzheimer's disease research and treatments
article

Spatiotemporal characterization of Alzheimer disease pathology in living human brain tissue

Laurence Dale Watkins, Kaleigh F. Roberts, Nick C. Fox, Jörg Hanrieder, Alicja Szadziewska, Randall John Bateman, Chihiro Sato, Tatiana A. Giovannucci, Yingxin He, Eleanor M. Moncur, Fernando González‐Ortiz, Jack I. Wood, Elena Camporesi, Przemysław Radosław Kac, Donald L. Elbert, Aram Aslanyan, Lewis W. Thorne, Nicolas R. Barthélemy, Ross W. Paterson, Maciej Dulewicz, Srinivas Koutarapu, Junyue Ge, Henrik Zetterberg, Francesco Carletti, Soumya Mukherjee, Nupur Ghoshal, Eimear C. Murphy, Reid Coyle, Katherine Schwetye, Ahmed K. Toma, Claire A. Leckey, Kanza Tariq, Kaj Blennow
article en

Abstract

Abstract Alzheimer disease begins in the brain many years before symptoms, but early changes are usually studied after death or indirectly through fluid and imaging biomarkers. Here we show that small brain biopsies collected during ventriculoperitoneal shunt surgery can be used to study Alzheimer disease pathology and protein turnover during life. We analysed biopsies from 18 individuals with suspected normal pressure hydrocephalus, alongside matched ventricular and lumbar cerebrospinal fluid and post-mortem control brain tissue. Amyloid plaques were present in 9 of 18 biopsies, while mature tau tangles were rare. Matrix-assisted laser desorption/ionization mass spectrometry imaging mapped amyloid plaque chemistry within tissue. Phosphorylated tau 217 was enriched around plaques, supporting a local relationship between amyloid and tau pathology. Stable isotope labelling, which tracks newly made proteins, detected rapid tau labelling within approximately 3 hours and estimated brain tau half-life at about 34 days. Amyloid plaques showed little detectable turnover.

Nature CommunicationsVol. 17(1)
University of Science and Technology of China (CN), University of Washington (US), Washington University in St. Louis (US), Sahlgrenska University Hospital (SE), Sorbonne Université (FR), Institut des Sciences Moléculaires (FR), Darent Valley Hospital (GB), Pitié-Salpêtrière Hospital (FR), Hope Center for Neurological Disorders (US), UK Dementia Research Institute (GB), MRC Prion Unit (GB), National Hospital for Neurology and Neurosurgery (GB), Institut du Cerveau (FR), UCL Queen Square Institute of Neurology (GB), University College London (GB), Seattle University (US), University of Gothenburg (SE)
Good health and well-being
Openalex Percentile: Top 12%
Alzheimer's disease research and treatments
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