Evidence map›Paper›PMID 37332019›Full record

ArticleCell & bioscience2023

Integrating host transcriptomic signatures for distinguishing autoimmune encephalitis in cerebrospinal fluid by metagenomic sequencing.

Siyuan Fan, Xiangyan He, Zhongyi Zhu, Lu Chen, Yijun Zou, Zhonglin Chen, Jialin Yu, Weijun Chen, Hongzhi Guan, Jinmin Ma

Open access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 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
0.8field-weighted citation impact, top 26% 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

10 authors at 4 institutions in 2 countries.

Siyuan Fan *Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, 100730, China.
Xiangyan He *Clinical Laboratory of BGI Health, BGI-Shenzhen, Shenzhen, 518083, China.
Zhongyi Zhu *Clinical Laboratory of BGI Health, BGI-Shenzhen, Shenzhen, 518083, China.
Lu ChenBeijing Macro & Micro-Test Bio-Tech Co., Ltd., Beijing, 101300, China.
Yijun ZouCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.
Zhonglin ChenBGI PathoGenesis Pharmaceutical Technology, BGI-Shenzhen, Shenzhen, 518083, China.
Jialin YuBGI PathoGenesis Pharmaceutical Technology, BGI-Shenzhen, Shenzhen, 518083, China.
Weijun ChenClinical Laboratory of BGI Health, BGI-Shenzhen, Shenzhen, 518083, China. chenwj@bgi.com.
Hongzhi GuanPeking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, 100730, China. pumchghz@126.com.
Jinmin MaClinical Laboratory of BGI Health, BGI-Shenzhen, Shenzhen, 518083, China. majinmin@genomics.cn.ORCID http://orcid.org/0000-0002-7993-7001
BGI Group (China) · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNBeijing Biocytogen (China) · CNUniversity of Chinese Academy of Sciences · CN

Funding

CAMS Innovations Fund for Medical Sciences CIFMS 2021-I2M-1-003National Natural Science Foundation of China 82161138018
6 · The paper itself

Abstract

backgroundThe early accurate diagnoses for autoimmune encephalitis (AE) and infectious encephalitis (IE) are essential since the treatments for them are different. This study aims to discover some specific and sensitive biomarkers to distinguish AE from IE at early stage to give specific treatments for good outcomes.

resultsWe compared the host gene expression profiles and microbial diversities of cerebrospinal fluid (CSF) from 41 patients with IE and 18 patients with AE through meta-transcriptomic sequencing. Significant differences were found in host gene expression profiles and microbial diversities in CSF between patients with AE and patients with IE. The most significantly upregulated genes in patients with IE were enriched in pathways related with immune response such as neutrophil degranulation, antigen processing and presentation and adaptive immune system. In contrast, those upregulated genes in patients with AE were mainly involved in sensory organ development such as olfactory transduction, as well as synaptic transmission and signaling. Based on the differentially expressed genes, a classifier consisting of 5 host genes showed outstanding performance with an area under the receiver operating characteristic (ROC) curve (AUC) of 0.95.

conclusionsThis study provides a promising classifier and is the first to investigate transcriptomic signatures for differentiating AE from IE by using meta-transcriptomic next-generation sequencing technology.

Indexed as

Autoimmune encephalitisCerebrospinal fluidInfectious encephalitisNext-generation sequencing (NGS)Transcriptomic signatures

Identifiers

PMID37332019
PMCPMC10278324
OpenAlexW4381158396

What OpenQuestion holds

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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.