Evidence map›Paper›PMID 37000849›Full record

ArticlePloS one2023

White matter hyperintensities in cholinergic pathways may predict poorer responsiveness to acetylcholinesterase inhibitor treatment for Alzheimer's disease.

Li-Hua Lee, Shu-Ching Wu, Cheng-Feng Ho, Wan-Lin Liang, Yi-Chien Liu, Chia-Ju Chou

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

6 authors at 3 institutions in 2 countries.

Li-Hua LeeDepartment of Neurology, Cardinal Tien Hospital, New Taipei City, Taipei, Taiwan.ORCID 0000-0003-0111-2808
Shu-Ching WuDepartment of Neurology, Cardinal Tien Hospital, New Taipei City, Taipei, Taiwan.
Cheng-Feng HoDepartment of Radiology, Cardinal Tien Hospital, New Taipei City, Taipei, Taiwan.
Wan-Lin LiangDepartment of Medical Research, Far Eastern Hospital, New Taipei City, Taipei, Taiwan.
Yi-Chien LiuDepartment of Neurology, Cardinal Tien Hospital, New Taipei City, Taipei, Taiwan.ORCID 0000-0003-2579-740X
Chia-Ju ChouDepartment of Neurology, Cardinal Tien Hospital, New Taipei City, Taipei, Taiwan.
Cardinal Tien Hospital · TWFar Eastern Memorial Hospital · TWFu Jen Catholic University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcetylcholinesterase inhibitor (AChEI) drug regimens are the mainstay treatment options for patients with Alzheimer's disease (AD). Herein, We examined the association between clinical response to AChEI and white matter hyperintensities on magnetic resonance imaging (MRI) scan at baseline.

methodsBetween 2020 and 2021, we recruited 101 individuals with a clinical diagnosis of probable AD. Each participant underwent complete neuropsychological testing and 3T (Telsa) brain magnetic resonance imaging. Responsiveness to AChEI, as assessed after 12 months, was designated as less than two points of regression in Mini-Mental State Examination scores (MMSE) and stable clinical dementia rating scale. We also evaluated MRI images by examining scores on the Cholinergic Pathways Hyperintensities Scale (CHIPS), Fazekas scale, and medial temporal atrophy (MTA) scale.

resultsIn our cohort, 52 patients (51.4%) were classified as responders. We observed significantly higher CHIPS scores in the nonresponder group (21.1 ± 12.9 vs. 14.9 ± 9.2, P = 0.007). Age at baseline, education level, sex, Clinical Dementia Rating sum of boxes scores, and three neuroimaging parameters were tested in regression models. Only CHIPS scores predicted clinical response to AChEI treatment.

conclusionWMHs in the cholinergic pathways, not diffuse white matter lesions or hippocampal atrophy, correlated with poorer responsiveness to AChEI treatment. Therefore, further investigation into the role of the cholinergic pathway in AD is warranted.

Indexed as

Alzheimer DiseaseWhite MatterAcetylcholinesteraseAtrophyCholinergic AgentsCholinesterase InhibitorsHumansMagnetic Resonance ImagingNeuropsychological TestsAcetylcholinesteraseCholinergic AgentsCholinesterase Inhibitors

Identifiers

PMID37000849
PMCPMC10065432
OpenAlexW4362471531

What OpenQuestion holds

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LicenceCC BY
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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.