Evidence map›Paper›PMID 36172367›Full record

ArticleFrontiers in immunology2022

Identification of diagnostic mRNA biomarkers in whole blood for ankylosing spondylitis using WGCNA and machine learning feature selection.

Yaguang Han, Yiqin Zhou, Haobo Li, Zhenyu Gong, Ziye Liu, Huan Wang, Bo Wang, Xiaojian Ye, Yi Liu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. 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

9 authors at 4 institutions in 2 countries.

Yaguang HanDepartment of Orthopaedics, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Yiqin ZhouDepartment of Orthopaedics, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Haobo LiDepartment of Orthopaedics, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Zhenyu GongDepartment of Neurosurgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Ziye LiuDepartment of Orthopaedics, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Huan WangDepartment of Orthopaedics, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Bo WangDepartment of Orthopaedics, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Xiaojian YeDepartment of Orthopaedics, Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yi LiuDepartment of Orthopaedics, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Shanghai Changzheng Hospital · CNSecond Military Medical University · CNShanghai Jiao Tong University · CNKlinikum rechts der Isar · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ankylosing spondylitis (AS) is a common inflammatory spondyloarthritis affecting the spine and sacroiliac joint that finally results in sclerosis of the axial skeleton. Aside from human leukocyte antigen B27, transcriptomic biomarkers in blood for AS diagnosis still remain unknown. Hence, this study aimed to investigate credible AS-specific mRNA biomarkers from the whole blood of AS patients by analyzing an mRNA expression profile (GSE73754) downloaded Gene Expression Omnibus, which includes AS and healthy control blood samples. Weighted gene co-expression network analysis was performed and revealed three mRNA modules associated with AS. By performing gene set enrichment analysis, the functional annotations of these modules revealed immune biological processes that occur in AS. Several feature mRNAs were identified by analyzing the hubs of the protein-protein interaction network, which was based on the intersection between differentially expressed mRNAs and mRNA modules. A machine learning-based feature selection method, SVM-RFE, was used to further screen out 13 key feature mRNAs. After verifying by qPCR, IL17RA, Sqstm1, Picalm, Eif4e, Srrt, Lrrfip1, Synj1 and Cxcr6 were found to be significant for AS diagnosis. Among them, Cxcr6, IL17RA and Lrrfip1 were correlated with severity of AS symptoms. In conclusion, our findings provide a framework for identifying the key mRNAs in whole blood of AS that is conducive for the development of novel diagnostic markers for AS.

Indexed as

Spondylitis, AnkylosingBiomarkersEukaryotic Initiation Factor-4EHLA AntigensHumansMachine LearningRNA, MessengerSequestosome-1 ProteinBiomarkersEukaryotic Initiation Factor-4EHLA AntigensRNA, MessengerSequestosome-1 Proteinankylosing spondylitis (AS)mRNAs biomarkersrecursive feature elimination (RFE)support vector machineweighted gene co-expression network analysis (WGCBA)

Identifiers

PMID36172367
PMCPMC9510835
OpenAlexW4295328998

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.