Evidence map›Paper›PMID 40426276›Full record

ArticleCNS neuroscience & therapeutics2025

Differences in Glucose Metabolism Between Single Memory Domain and Multidomain Subjective Cognitive Decline: A Longitudinal Study From SILCODE.

Min Wei, Luyao Wang, Xianfeng Yu, Wenjing Hu, Min Wang, Qi Zhang, Tengfei Guo, Jiayi Zhong, Chenyang Li, Jiehui Jiang and 1 more

Abstract read
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Article in CNS neuroscience & therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Min WeiDepartment of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, China.
Luyao WangInstitute of Biomedical Engineering, School of Life Sciences, Shanghai University, Shanghai, China.
Xianfeng YuDepartment of Neurology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Wenjing HuInstitute of Biomedical Engineering, School of Life Sciences, Shanghai University, Shanghai, China.
Min WangInstitute of Biomedical Engineering, School of Life Sciences, Shanghai University, Shanghai, China.
Qi ZhangInstitute of Biomedical Engineering, School of Life Sciences, Shanghai University, Shanghai, China.
Tengfei GuoInstitute of Biomedical Engineering, Shenzhen Bay Laboratory, Shenzhen, China.
Jiayi ZhongInstitute of Biomedical Engineering, School of Life Sciences, Shanghai University, Shanghai, China.
Chenyang LiInstitute of Biomedical Engineering, School of Life Sciences, Shanghai University, Shanghai, China.
Jiehui JiangInstitute of Biomedical Engineering, School of Life Sciences, Shanghai University, Shanghai, China.ORCID 0000-0003-4948-3683
Ying HanDepartment of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, China.ORCID 0000-0003-0377-7424

Funding

National Natural Science Foundation of China 82020108013National Natural Science Foundation of China 82327809Shenzhen Bay Scholars ProgramSino-German Cooperation M-0759STI2030-Major Projects 2022ZD0211800Tianchi Scholars Program
6 · The paper itself

Abstract

backgroundGlucose metabolism and plasma biomarkers have emerged as important early markers in Alzheimer's disease. Different subtypes (single memory domain, multidomain) of subjective cognitive decline (SCD) may represent distinct stages of disease progression, but the differences in glucose metabolism remain unclear. This study focused on exploring the differences in glucose metabolism between different SCD subtypes and the correlation with plasma biomarkers based on

methodsIn this study, thirty-three normal controls (NCs), thirty-five individuals with single memory domain SCD (sd-SCD), thirty-nine individuals with multidomain SCD (md-SCD), and twenty-one cognitively impaired (CI) individuals were involved. We investigated the standardized uptake value ratio (SUVR) and voxel differences between the sd-SCD and md-SCD groups followed by FDR and GRF corrections, with an average follow-up time of 44.98 ± 16.49 months. Correlation analyses were employed to assess relationships between FDG-PET SUVR and neuropsychological scales as well as plasma biomarkers. Finally, Kaplan-Meier survival analysis was used to investigate the risk of cognitive decline conversion among SCD subgroups.

resultsAfter controlling for the effects of covariates, the following brain regions showed voxel differences and lower SUVR in md-SCD groups, including right anterior cingulate and paracingulate gyri (ACG.R, p = 0.003), left anterior cingulate and paracingulate gyri (ACG.L, p = 0.003), right middle temporal gyrus (MTG.R, p = 0.004), and right inferior temporal gyrus (ITG.R, p = 0.001), compared to the sd-SCD group. SUVR of ACG.R was correlated with plasma Aβ42/40 (r = 0.435, p = 0.006) and AVLT-N7 score (r = 0.347, p = 0.031) in the md-SCD group while none of the correlations existed in the sd-SCD group. SUVR of MTG.R was also correlated with the AVLT-N7 score (r = 0.246, p = 0.035) across SCD individuals. The SCD individuals with positive plasma Aβ42/40, p-tau181, and glucose metabolism in above four regions, or those in the md-SCD group showed an elevated risk of cognitive conversion in comparison to the controls.

conclusionsDifferences in glucose metabolism could be observed between the md-SCD and sd-SCD groups. SCD participants in the md-SCD group, or those with positive biomarkers, might represent a higher risk of cognitive decline conversion.

Indexed as

BrainCognitive DysfunctionGlucoseMemoryAgedAmyloid beta-PeptidesBiomarkersFemaleFluorodeoxyglucose F18HumansLongitudinal StudiesMaleMiddle AgedNeuropsychological TestsPositron-Emission Tomographytau ProteinsAmyloid beta-PeptidesBiomarkersFluorodeoxyglucose F18Glucosetau ProteinsAlzheimer's diseaseFDG‐PETplasma AD biomarkerssubjective cognitive decline

Identifiers

PMID40426276
PMCPMC12116337

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.