Evidence map›Paper›PMID 35368064›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2023

Mapping cerebral atrophic trajectory from amnestic mild cognitive impairment to Alzheimer's disease.

Xiaotong Wei, Xiaotong Du, Yingying Xie, Xinjun Suo, Xiaoxi He, Hao Ding, Yu Zhang, Yi Ji, Chao Chai, Meng Liang and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 12% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 12 citations in OpenAlex.

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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

14 authors at 2 institutions in 1 country.

Xiaotong WeiDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Xiaotong DuDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Yingying XieDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Xinjun SuoDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Xiaoxi HeDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Hao DingDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Yu ZhangDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Yi JiDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Chao ChaiDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Meng LiangDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Chunshui YuDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Yong LiuSchool of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing 100876, China.
Wen QinDepartment of Radiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Alzheimer’s Disease Neuroimaging Initiative
Tianjin Medical University General Hospital · CNBeijing University of Posts and Telecommunications · CN

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
NIA NIH HHS U01 AG024904NIH HHS U01 AG024904
6 · The paper itself

Abstract

Alzheimer's disease (AD) patients suffer progressive cerebral atrophy before dementia onset. However, the region-specific atrophic processes and the influences of age and apolipoprotein E (APOE) on atrophic trajectory are still unclear. By mapping the region-specific nonlinear atrophic trajectory of whole cerebrum from amnestic mild cognitive impairment (aMCI) to AD based on longitudinal structural magnetic resonance imaging data from Alzheimer's disease Neuroimaging Initiative (ADNI) database, we unraveled a quadratic accelerated atrophic trajectory of 68 cerebral regions from aMCI to AD, especially in the superior temporal pole, caudate, and hippocampus. Besides, interaction analyses demonstrated that APOE ε4 carriers had faster atrophic rates than noncarriers in 8 regions, including the caudate, hippocampus, insula, etc.; younger patients progressed faster than older patients in 32 regions, especially for the superior temporal pole, hippocampus, and superior temporal gyrus; and 15 regions demonstrated complex interaction among age, APOE, and disease progression, including the caudate, hippocampus, etc. (P < 0.05/68, Bonferroni correction). Finally, Cox proportional hazards regression model based on the identified region-specific biomarkers could effectively predict the time to AD conversion within 10 years. In summary, cerebral atrophic trajectory mapping could help a comprehensive understanding of AD development and offer potential biomarkers for predicting AD conversion.

Indexed as

Alzheimer DiseaseCognitive DysfunctionApolipoproteins EAtrophyBiomarkersDisease ProgressionHumansMagnetic Resonance ImagingApolipoproteins EBiomarkersAgingAlzheimer’s diseaseapolipoprotein Eatrophic trajectorymild cognitive impairment

Identifiers

PMID35368064
PMCPMC9930625
OpenAlexW4226066060

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.