Assessing subcortical, brainstem and cerebellar metabolic patterns using [18F]FDG PET-CT imaging in dementia with Lewy bodies

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Authors: Daniël S. L. Loewenstein, Max van Grinsven, Cécile de Pont, Anne I.J. Arens, P. L. J. Dautzenberg, Astrid M. van Strien, Osama Sabri, Swen Hesse, Michael Rullmann, Dylan Henssen, for the Alzheimer's Disease Neuroimaging Initiative (ADNI), Michael Weiner
+88 more Paul Aisen, Ronald Petersen, Clifford R. Jack, William Jagust, Susan Landau, Monica Rivera-Mindt, Ozioma Okonkwo, Leslie M. Shaw, Edward B. Lee, Arthur W. Toga, Laurel Beckett, Danielle Harvey, Robert C. Green, Andrew J. Saykin, Kwangsik Nho, Richard J. Perrin, Duygu Tosun, Pallavi Sachdev, Erin Drake, Tom Montine, Rachel Nosheny, Diana Truran Sacrey, Juliet Fockler, Melanie J. Miller, Catherine Cat Conti, Winnie Kwang, Chengshi Jin, Adam Diaz, Miriam T. Ashford, Derek Flenniken, Adrienne Kormos, Michael Rafii, Rema Raman, Gustavo Jimenez, Michael Donohue, Jennifer Salazar, Andrea Fidell, Virginia Boatwright, Justin Robison, Caileigh Zimmerman, Yuliana Cabrera, Sarah Walter, Taylor Clanton, Elizabeth Shaffer, Caitlin Webb, Lindsey Hergesheimer, Stephanie Smith, Sheila Ogwang, Olusegun Adegoke, Payam Mahboubi, Jeremy Pizzola, Cecily Jenkins, Naomi Saito, Kedir Adem Hussen, Hannatu Amaza, Mai Seng Thao, Shaniya Parkins, Omobolanle Ayo, Matt Glittenberg, Isabella Hoang, Kaori Kubo Germano, Joe Strong, Trinity Weisensel, Fabiola Magana, Lisa Thomas, Vanessa Guzman, Adeyinka Ajayi, Joseph Di Benedetto, Sandra Talavera, Joel Felmlee, Nick C. Fox, Paul Thompson, Charles DeCarli, Arvin Forghanian-Arani, Bret Borowski, Calvin Reyes, Caitie Hedberg, Chad Ward, Christopher Schwarz, Denise Reyes, Jeff Gunter, John Moore-Weiss, Kejal Kantarci, Leonard C. Matoush, Matthew Senjem, Prashanthi Vemuri, Robert Reid, Ian Malone
Cited by: 1
References: 62

Abstract

Abstract Purpose Numerous clinical features of Dementia with Lewy Bodies (DLB) are attributed to dysfunction in subcortical anatomy. Despite this, [ 18 F]FDG PET imaging as a diagnostic tool for DLB largely relies on the metabolic signature of the occipital lobe, precuneus, and posterior cingulate cortex. This study aimed to assess subcortical brain metabolism in patients with DLB using [ 18 F]FDG PET imaging. Methods Patients diagnosed with probable DLB were included from both a prospectively maintained regional database ( n = 33), and the ADNI database ( n = 43). Using statistical parametric mapping (SPM) analysis, metabolic activity was compared with a cohort of subjects exhibiting normal brain metabolism ( n = 19). A sub-analysis was conducted with disease progression included as a covariate. Results Hypermetabolism was observed in various subcortical regions, notably in the dentate nucleus, anterolateral thalamus, and regions of the superior cerebellar peduncle. Increased metabolism was also detected in the mesencephalic tectum, likely representing heightened activity in the superior colliculus. All findings were reproduced in the ADNI cohort and were found to be dependent on the DLB disease stage. Additionally, the well-established cortical hypometabolic signature of DLB pathology was evident, validating our methods and findings. Conclusion Increased metabolic activity is evident in a variety of brainstem, cerebellar, and subcortical regions in patients with DLB. The dentatorubrothalamic tract, in particular, emerges as a structure of interest that connects these structures and potentially helps in understanding DLB pathophysiology. Correction for disease stage eliminated this pattern, suggesting a driver associated with disease progression.

Fields of Study & Subjects

Dementia and Cognitive Impairment Research Neurological and metabolic disorders Cerebrospinal fluid and hydrocephalus

Publication details

Journal / source
European Journal of Nuclear Medicine and Molecular Imaging
Publisher
Springer Science and Business Media LLC
Volume
53
Issue
11
Pages
6167–6183
Publication date
8 June 2026
Language
EN