Evidence map›Paper›PMID 39567427›Full record

ReviewMolecular and cellular biochemistry2025

The neuroinflammatory role of microRNAs in Alzheimer's disease: pathological insights to therapeutic potential.

Wenjia Liu, Xin Rao, Wen Sun, Xiaodong Chen, Liyang Yu, Jiangtao Zhang, Jiong Chen, Xiaorong Zheng

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular and cellular biochemistry, 2025. 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
–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

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.

  1. Article
  2. 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.

Wenjia LiuSchool of Electronics and Information, Hangzhou Dianzi University, Hangzhou, 310018, China.
Xin RaoSchool of Electronics and Information, Hangzhou Dianzi University, Hangzhou, 310018, China. raoxin1992@hdu.edu.cn.
Wen SunSchool of Electronics and Information, Hangzhou Dianzi University, Hangzhou, 310018, China.
Xiaodong ChenSchool of Electronics and Information, Hangzhou Dianzi University, Hangzhou, 310018, China. xiaodongchen@hdu.edu.cn.
Liyang YuSchool of Electronics and Information, Hangzhou Dianzi University, Hangzhou, 310018, China.
Jiangtao ZhangDepartment of Geriatrics, Tongde Hospital of Zhejiang Province, Hangzhou, 310012, China. 18969125501@163.com.
Jiong ChenDepartment of Geriatrics, Tongde Hospital of Zhejiang Province, Hangzhou, 310012, China.
Xiaorong ZhengBlood Purification Center, The Second Affiliated Hospital of Jiaxing University, Jiaxing, 314000, China.

Funding

National Key R&D Program of China 2023YFC2412001National Natural Science Foundation of China 62101171Natural Science Foundation of Zhejiang Province LQ22F010015
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a neurodegenerative disease and the most common cause of dementia, contributing to around 60-80% of cases. The main pathophysiology of AD is characterized by an abnormal accumulation of protein aggregates extracellularly (beta-amyloid plaques) and intracellularly (neurofibrillary tangles of hyperphosphorylated tau). However, an increasing number of studies have also suggested neuroinflammation may have a crucial role in precipitating the cascade reactions that result in the development of AD neuropathology. In particular, several studies indicate microRNAs (miRNAs) can act as regulatory factors for neuroinflammation in AD, with potential to affect the occurrence and/or progression of AD inflammation by targeting the expression of multiple genes. Therefore, miRNAs may have potential as therapeutic targets for AD, which requires more research. This article will review the existing studies on miRNAs that have been identified to regulate neuroinflammation, aiming to gain further insights into the specific regulatory processes of miRNAs, highlight the diagnostic and therapeutic potential of miRNAs as biomarkers in AD, as well as current challenges, and suggest the further work to bridge the gap in knowledge to utilize miRNAs as therapeutic targets for AD.

Indexed as

Alzheimer DiseaseMicroRNAsNeuroinflammatory DiseasesAnimalsBiomarkersHumansInflammationBiomarkersMicroRNAsAlzheimer’s diseaseDiagnostic potentialMicroRNANeuroinflammationRegulatorTherapeutic target

Identifiers

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.