| Literature DB >> 27109158 |
Yujin Jeon1, Binna Kim1, Jieun E Kim1,2, Bori R Kim1,2, Soonhyun Ban1,2, Jee Hyang Jeong3, Oran Kwon4, Sandy Jeong Rhie5, Chang-Won Ahn6, Jong-Hoon Kim6, Sung Ug Jung6, Soo-Hyun Park6, In Kyoon Lyoo1,2,5, Sujung Yoon1,2.
Abstract
This randomized, double-blind, placebo-controlled trial examined whether the administration of ganglioside, an active ingredient of deer bone extract, can improve working memory performance by increasing gray matter volume and functional connectivity in the default mode network (DMN) in individuals with subjective cognitive impairment. Seventy-five individuals with subjective cognitive impairment were chosen to receive either ganglioside (330[Formula: see text][Formula: see text]g/day or 660[Formula: see text][Formula: see text]g/day) or a placebo for 8 weeks. Changes in working memory performance with treatment of either ganglioside or placebo were assessed as cognitive outcome measures. Using voxel-based morphometry and functional connectivity analyses, changes in gray matter volume and functional connectivity in the DMN were also assessed as brain outcome measures. Improvement in working memory performance was greater in the ganglioside group than in the placebo group. The ganglioside group, relative to the placebo group, showed greater increases in gray matter volume and functional connectivity in the DMN. A significant relationship between increased functional connectivity of the precuneus and improved working memory performance was observed in the ganglioside group. The current findings suggest that ganglioside has cognitive-enhancing effects in individuals with subjective cognitive impairment. Ganglioside-induced increases in gray matter volume and functional connectivity in the DMN may partly be responsible for the potential nootropic effects of ganglioside. The clinical trial was registered with ClinicalTrials.gov (identifier: NCT02379481).Entities:
Keywords: Deer Bone Extract; Default Mode Network; Ganglioside; Subjective Cognitive Impairment; Working Memory
Mesh:
Substances:
Year: 2016 PMID: 27109158 DOI: 10.1142/S0192415X16500270
Source DB: PubMed Journal: Am J Chin Med ISSN: 0192-415X Impact factor: 4.667