Evidence map›Paper›PMID 31937364›Full record

ArticleAlzheimer's research & therapy2020

Effects of gene mutation and disease progression on representative neural circuits in familial Alzheimer's disease.

Meina Quan, Tan Zhao, Yi Tang, Ping Luo, Wei Wang, Qi Qin, Tingting Li, Qigeng Wang, Jiliang Fang, Jianping Jia

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03653156 recruitingnot on this map

China Cognition and Aging Study: a Multi-center, National-wide, Longitudinal Study in China

Typeobservational_patient_registrySponsorCapital Medical UniversityRan2000 to 2038Enrolled100,000ConditionsMild Cognitive Impairment(MCI), Alzheimer Disease, Late Onset, Familial Alzheimer Disease (FAD), Vascular Dementia (VaD)
NCT03657732 recruitingnot on this map

A Multi-center Longitudinal Cohort Study of Familial Alzheimer's Disease in China

Typeobservational_patient_registrySponsorCapital Medical UniversityRan2005 to 2038Enrolled40,000ConditionsAlzheimer Disease, Familial Alzheimer Disease (FAD)
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 27 citations in OpenAlex.

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  15. Biphasic cortical macro- and microstructural changes in autosomal dominant Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Meina QuanInnovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, People's Republic of China.
Tan ZhaoInnovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, People's Republic of China.
Yi TangInnovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, People's Republic of China.
Ping LuoGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Wei WangInnovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, People's Republic of China.
Qi QinInnovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, People's Republic of China.
Tingting LiInnovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, People's Republic of China.
Qigeng WangInnovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, People's Republic of China.
Jiliang FangGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Jianping JiaInnovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, People's Republic of China. jjp@ccmu.edu.cn.ORCID 0000-0003-4624-0336
Capital Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

Beijing Municipal Administration of Hospitals SML20150801Beijing Municipal Commission of Health and Family Planning PXM2018_026283_000002Beijing Municipal Human Resources and Social Security Bureau the Beijing Scholars ProgramBeijing Municipal Science & Technology Commission for the Beijing Brain Initiative Z161100000216137Key Programme 81530036National Key Scientific Instrument and Equipment Development Projects of China 31627803
6 · The paper itself

Abstract

backgroundAlthough structural and functional changes of the striatum and hippocampus are present in familial Alzheimer's disease, little is known about the effects of specific gene mutation or disease progression on their related neural circuits. This study was to evaluate the effects of known pathogenic gene mutation and disease progression on the striatum- and hippocampus-related neural circuits, including frontostriatal and hippocampus-posterior cingulate cortex (PCC) pathways.

methodsA total of 102 healthy mutation non-carriers, 40 presymptomatic mutation carriers (PMC), and 30 symptomatic mutation carriers (SMC) of amyloid precursor protein (APP), presenilin 1 (PS1), or presenilin 2 gene, with T1 structural MRI, diffusion tensor imaging, and resting-state functional MRI were included. Representative neural circuits and their key nodes were obtained, including bilateral caudate-rostral middle frontal gyrus (rMFG), putamen-rMFG, and hippocampus-PCC. Volumes, diffusion indices, and functional connectivity of circuits were compared between groups and correlated with neuropsychological and clinical measures.

resultsIn PMC, APP gene mutation carriers showed impaired diffusion indices of caudate-rMFG and putamen-rMFG circuits; PS1 gene mutation carriers showed increased fiber numbers of putamen-rMFG circuit. SMC showed increased diffusivity of the left hippocampus-PCC circuit and volume reduction of all regions as compared with PMC. Imaging measures especially axial diffusivity of the representative circuits were correlated with neuropsychological measures.

conclusionsAPP and PS1 gene mutations affect frontostriatal circuits in a different manner in familial Alzheimer's disease; disease progression primarily affects the structure of hippocampus-PCC circuit. The structural connectivity of both frontostriatal and hippocampus-PCC circuits is associated with general cognitive function. Such findings may provide further information about the imaging biomarkers for early identification and prognosis of familial Alzheimer's disease, and pave the way for early diagnosis, gene- or circuit-targeted treatment, and even prevention.

Indexed as

AdultAlzheimer DiseaseAmyloid beta-Protein PrecursorBrainDisease ProgressionFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedMutationNeural PathwaysPresenilin-1Presenilin-2Amyloid beta-Protein PrecursorPresenilin-1Presenilin-2PSEN1 protein, humanPSEN2 protein, humanDiffusion tensor imagingFamilial Alzheimer’s diseaseGene mutationNeural circuitsResting-state functional MRI

Identifiers

PMID31937364
PMCPMC6961388
OpenAlexW3095333145

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.