Evidence map›Paper›PMID 42434592›Full record

ArticleFrontiers in aging neuroscience2026

Trajectories and timing of accelerated decline in specific memory domains preceding Alzheimer's disease.

Xianxian Long, Meng Rong, Shushu Long, Shuqin Wen, Luhui Mo, Mingming Xu, Zeyun Zhang, Qinqi Nie

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Xianxian LongShenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Meng RongFuyang Center for Disease Control and Prevention, Fuyang, China.
Shushu LongFujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Shuqin WenShenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Luhui MoShenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Mingming XuShenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Zeyun ZhangDepartment of Scientific Research, Department of Neurology, Xiang'an Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Qinqi NieShenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Memory impairment is a hallmark feature of Alzheimer's disease (AD) and may emerge years before clinical diagnosis. However, the temporal sequence and acceleration patterns of decline across specific memory domains during the preclinical stage remain incompletely understood. This study aimed to characterize the longitudinal dynamics of four distinct memory processes in individuals progressing to clinical AD, and to identify the temporal sequence of continually accelerated decline. Methods: We analyzed longitudinal data from 382 participants in the Alzheimer's Disease Neuroimaging Initiative (ADNI) who converted from cognitively normal or mild cognitive impairment to AD. Generalized additive mixed models (GAMMs) were employed to characterize the nonlinear trajectories of four Rey Auditory Verbal Learning Test (RAVLT) derived scores over time prior to AD diagnosis, adjusting for key demographics and genetic factors. The finite difference method was applied to identify time points of continually accelerated decline from the fitted curves. Sensitivity analyses additionally adjusted for stroke and emotional incontinence, replicating all steps. Results: Our analysis revealed distinct nonlinear progression patterns across memory domains. All trajectories significantly deviated from linearity (Edf > 1, Conclusion: The decline in four memory tests among individuals with preclinical AD followed nonlinear trajectories, with learning memory exhibiting the earliest continuously accelerated decline. Higher education was associated with better immediate memory performance, while the APOE-ε4 genotype specifically exacerbated impairments in learning memory and retention loss.

Indexed as

Alzheimer’s diseasegeneralized additive mixed modelsinfluencing factorslongitudinal studymemory trajectory

Identifiers

PMID42434592
PMCPMC13352412

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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.