학술논문
Associations between sex, body mass index and the individual microglial response in Alzheimer’s disease
Document Type
article
Author
Gloria Biechele; Boris-Stephan Rauchmann; Daniel Janowitz; Katharina Buerger; Nicolai Franzmeier; Endy Weidinger; Selim Guersel; Sebastian Schuster; Anika Finze; Stefanie Harris; Simon Lindner; Nathalie L. Albert; Christian Wetzel; Rainer Rupprecht; Axel Rominger; Carla Palleis; Sabrina Katzdobler; Lena Burow; Carolin Kurz; Mirlind Zaganjori; Lena-Katharina Trappmann; Oliver Goldhardt; Timo Grimmer; Jan Haeckert; Daniel Keeser; Sophia Stoecklein; Estrella Morenas-Rodriguez; Peter Bartenstein; Johannes Levin; Günter U. Höglinger; Mikael Simons; Robert Perneczky; Matthias Brendel
Source
Journal of Neuroinflammation, Vol 21, Iss 1, Pp 1-15 (2024)
Subject
Language
English
ISSN
1742-2094
Abstract
Abstract Background and objectives 18-kDa translocator protein position-emission-tomography (TSPO-PET) imaging emerged for in vivo assessment of neuroinflammation in Alzheimer’s disease (AD) research. Sex and obesity effects on TSPO-PET binding have been reported for cognitively normal humans (CN), but such effects have not yet been systematically evaluated in patients with AD. Thus, we aimed to investigate the impact of sex and obesity on the relationship between β-amyloid-accumulation and microglial activation in AD. Methods 49 patients with AD (29 females, all Aβ-positive) and 15 Aβ-negative CN (8 female) underwent TSPO-PET ([18F]GE-180) and β-amyloid-PET ([18F]flutemetamol) imaging. In 24 patients with AD (14 females), tau-PET ([18F]PI-2620) was additionally available. The brain was parcellated into 218 cortical regions and standardized-uptake-value-ratios (SUVr, cerebellar reference) were calculated. Per region and tracer, the regional increase of PET SUVr (z-score) was calculated for AD against CN. The regression derived linear effect of regional Aβ-PET on TSPO-PET was used to determine the Aβ-plaque-dependent microglial response (slope) and the Aβ-plaque-independent microglial response (intercept) at the individual patient level. All read-outs were compared between sexes and tested for a moderation effect of sex on associations with body mass index (BMI). Results In AD, females showed higher mean cortical TSPO-PET z-scores (0.91 ± 0.49; males 0.30 ± 0.75; p = 0.002), while Aβ-PET z-scores were similar. The Aβ-plaque-independent microglial response was stronger in females with AD (+ 0.37 ± 0.38; males with AD − 0.33 ± 0.87; p = 0.006), pronounced at the prodromal stage. On the contrary, the Aβ-plaque-dependent microglial response was not different between sexes. The Aβ-plaque-independent microglial response was significantly associated with tau-PET in females (Braak-II regions: r = 0.757, p = 0.003), but not in males. BMI and the Aβ-plaque-independent microglial response were significantly associated in females (r = 0.44, p = 0.018) but not in males (BMI*sex interaction: F (3,52) = 3.077, p = 0.005). Conclusion While microglia response to fibrillar Aβ is similar between sexes, women with AD show a stronger Aβ-plaque-independent microglia response. This sex difference in Aβ-independent microglial activation may be associated with tau accumulation. BMI is positively associated with the Aβ-plaque-independent microglia response in females with AD but not in males, indicating that sex and obesity need to be considered when studying neuroinflammation in AD.