Evidence map›Paper›PMID 36875702›Full record

ArticleFrontiers in aging neuroscience2023

lncRNA-associated ceRNA network revealing the potential regulatory roles of ferroptosis and immune infiltration in Alzheimer's disease.

Yejun Tan, Wang Tang, Wenbiao Xiao, Roujie Huang, Xin Li, Weijun Peng, Kuipo Yan, Yuan Cao, Yi Zeng, Jin Kang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

10 citing papers in PubMed, 20 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

10 authors at 4 institutions in 2 countries.

Yejun TanDepartment of Rheumatology and Immunology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Wang TangDepartment of Geriatrics, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Wenbiao XiaoDepartment of Geriatrics, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Roujie HuangDepartment of Rheumatology and Immunology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Xin LiHunan Key Laboratory of Skin Cancer and Psoriasis, Hunan Engineering Research Center of Skin Health and Disease, Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Weijun PengDepartment of Integrated Traditional Chinese and Western Medicine, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Kuipo YanDepartment of Cardiology, The First Affiliated Hospital of Henan University of CM, Zhengzhou, Henan, China.
Yuan CaoDepartment of Geriatrics, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Yi ZengDepartment of Geriatrics, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Jin KangDepartment of Rheumatology and Immunology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Second Xiangya Hospital of Central South University · CNCentral South University · CNFirst Affiliated Hospital of Henan University · CNUniversity of Minnesota · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Alzheimer's disease (AD) is the most common form of dementia characterized by a prominent cognitive deterioration of sufficient magnitude to impair daily living. Increasing studies indicate that non-coding RNAs (ncRNAs) are involved in ferroptosis and AD progression. However, the role of ferroptosis-related ncRNAs in AD remains unexplored. Methods: We obtained the intersection of differentially expressed genes in GSE5281 (brain tissue expression profile of patients with AD) from the GEO database and ferroptosis-related genes (FRGs) from the ferrDb database. Least absolute shrinkage and selection operator model along with weighted gene co-expression network analysis screened for FRGs highly associated with AD. Results: A total of five FRGs were identified and further validated in GSE29378 (area under the curve = 0.877, 95% confidence interval = 0.794-0.960). A competing endogenous RNA (ceRNA) network of ferroptosis-related hub genes ( Conclusion: We constructed a novel ferroptosis-related signature model including mRNAs, miRNAs and lncRNAs, and characterized its association with immune infiltration in AD. The model provides novel ideas for the pathologic mechanism elucidation and targeted therapy development of AD.

Indexed as

Alzheimer’s diseasebiomarkerceRNAferroptosisimmune infiltrationlncRNAs

Identifiers

PMID36875702
PMCPMC9979855
OpenAlexW4321082506

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LicenceCC BY
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Registered trials

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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.