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Jiang, Xueyan; Hu, Xiaochen; Daamen, Marcel; Wang, Xiaoqi; Fan, Chunqiu; Meiberth, Dix; Spottke, Annika; Roeske, Sandra; Fliessbach, Klaus; Spruth, Eike Jakob; Altenstein, Slawek; Lohse, Andrea; Hansen, Niels; Glanz, Wenzel; Incesoy, Enise I. I.; Dobisch, Laura; Janowitz, Daniel; Rauchmann, Boris-Stephan; Ramirez, Alfredo; Kilimann, Ingo; Munk, Matthias H. H.; Wang, Xiao; Schneider, Luisa-Sophie; Gabelin, Tatjana; Roy, Nina; Wolfsgruber, Steffen; Kleineidam, Luca; Hetzer, Stefan; Dechent, Peter; Ewers, Michael; Scheffler, Klaus; Amthauer, Holger; Buchert, Ralph; Essler, Markus; Drzezga, Alexander; Rominger, Axel; Krause, Bernd J. J.; Reimold, Matthias; Priller, Josef; Schneider, Anja; Wiltfang, Jens; Buerger, Katharina; Perneczky, Robert; Teipel, Stefan; Laske, Christoph; Peters, Oliver; Duezel, Emrah; Wagner, Michael; Jiang, Jiehui; Jessen, Frank; Boecker, Henning und Han, Ying (2023): Altered limbic functional connectivity in individuals with subjective cognitive decline: Converging and diverging findings across Chinese and German cohorts. In: Alzheimers & Dementia, Bd. 19, Nr. 11: S. 4922-4934 [PDF, 1MB]

Abstract

INTRODUCTION: It remains unclear whether functional brain networks are consistently altered in individuals with subjective cognitive decline (SCD) of diverse ethnic and cultural backgrounds and whether the network alterations are associated with an amyloid burden. METHODS: Cross-sectional resting-state functional magnetic resonance imaging connectivity (FC) and amyloid-positron emission tomography (PET) data from the Chinese Sino Longitudinal Study on Cognitive Decline and German DZNE Longitudinal Cognitive Impairment and Dementia cohorts were analyzed. RESULTS: Limbic FC, particularly hippocampal connectivity with right insula, was consistently higher in SCD than in controls, and correlated with SCD-plus features. Smaller SCD subcohorts with PET showed inconsistent amyloid positivity rates and FC-amyloid associations across cohorts. DISCUSSION: Our results suggest an early adaptation of the limbic network in SCD, which may reflect increased awareness of cognitive decline, irrespective of amyloid pathology. Different amyloid positivity rates may indicate a heterogeneous underlying etiology in Eastern and Western SCD cohorts when applying current research criteria. Future studies should identify culture-specific features to enrich preclinical Alzheimer's disease in non-Western populations.

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