Operationalizing postmortem pathology-MRI association studies in Alzheimer's disease and related disorders with MRI-guided histology sampling.

Authors

Athalye C,Bahena A,Khandelwal P,Emrani S,Trotman W,Levorse LM,Khodakarami Z,Ohm DT,Teunissen-Bermeo E,Capp N,Sadaghiani S,Arezoumandan S,Lim SA,Prabhakaran K,Ittyerah R,Robinson JL,Schuck T,Lee EB,Tisdall MD,Das SR,Wolk DA,Irwin DJ,Yushkevich PA

Affiliations (5)

  • Department of Bioengineering, University of Pennsylvania, Philadelphia, USA. [email protected].
  • Department of Neurology, University of Pennsylvania, Philadelphia, USA.
  • Department of Bioengineering, University of Pennsylvania, Philadelphia, USA.
  • Department of Radiology, University of Pennsylvania, Philadelphia, USA.
  • Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, USA.

Abstract

Postmortem neuropathological examination, while the gold standard for diagnosing neurodegenerative diseases, often relies on limited regional sampling that may miss critical areas affected by Alzheimer's disease and related disorders. Ultra-high resolution postmortem MRI can help identify regions that fall outside the diagnostic sampling criteria for additional histopathologic evaluation. However, there are no standardized guidelines for integrating histology and MRI in a traditional brain bank. We developed a comprehensive protocol for whole hemisphere postmortem 7T MRI-guided histopathological sampling with whole-slide digital imaging and histopathological analysis, providing a reliable pipeline for high-volume brain banking in heterogeneous brain tissue. Our method uses patient-specific 3D printed molds built from postmortem MRI, allowing standardized tissue processing with a permanent spatial reference frame. To facilitate pathology-MRI association studies, we created a semi-automated MRI to histology registration pipeline and developed a quantitative pathology scoring system using weakly supervised deep learning. We validated this protocol on a cohort of 29 brains with diagnosis on the AD spectrum that revealed correlations between cortical thickness and phosphorylated tau accumulation. This pipeline has broad applicability across neuropathological research and brain banking, facilitating large-scale studies that integrate histology with neuroimaging. The innovations presented here provide a scalable and reproducible approach to studying postmortem brain pathology, with implications for advancing diagnostic and therapeutic strategies for Alzheimer's disease and related disorders.

Topics

Alzheimer DiseaseMagnetic Resonance ImagingBrainJournal Article

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