Evidence map›Paper›PMID 37686413›Full record

ArticleInternational journal of molecular sciences2023

Elevation of Metrnβ and Its Association with Disease Activity in Systemic Lupus Erythematosus.

Chen Zhang, Shijie Cai, Ying Li, Xiaoyan Xu, Yonghui Liu, Huaiyu Qiao, Chun-Kwok Wong, Guoqiu Wu, Hui Jin, Xun Gao

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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 3 institutions in 2 countries.

Chen ZhangCenter of Clinical Laboratory Medicine, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Shijie CaiDepartment of Laboratory Medicine, Medical School of Southeast University, Nanjing 210009, China.
Ying LiCenter of Clinical Laboratory Medicine, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Xiaoyan XuDepartment of Rheumatology, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Yonghui LiuCenter of Clinical Laboratory Medicine, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Huaiyu QiaoCenter of Clinical Laboratory Medicine, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Chun-Kwok WongDepartment of Chemical Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.ORCID 0000-0002-5637-8331
Guoqiu WuCenter of Clinical Laboratory Medicine, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Hui JinDepartment of Epidemiology and Health Statistics, School of Public Health, Southeast University, Nanjing 210009, China.
Xun GaoCenter of Clinical Laboratory Medicine, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Zhongda Hospital Southeast University · CNSoutheast University · CNChinese University of Hong Kong · HK

Funding

Special Funds for Research in Laboratory Medicine, Jiangsu Medical Association, Nanjing, China SYH-3201160-0054 (2023001)
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is an auto-immune disease, the pathogenesis of which remains to be fully addressed. Metrnβ is a novel cytokine involved in the pathogenesis of inflammatory disease, but its regulatory roles in SLE are unclear. We aimed to comprehensively investigate the clinical value of Metrnβ in SLE. A massive elevation of circulating Metrnβ levels was observed in SLE, and patients with an active phase displayed higher Metrnβ concentrations than those with inactive phases. Additionally, we found that Metrnβ expression was positively correlated with clinical indicators of SLE. Longitudinal cytokine and chemokine profiles revealed a disturbed immune response in SLE, with high activity profiles displayed severe pathogenic inflammation, and a positive correlation of the serum Metrnβ with CXCL9, IL10, IL18 and IL1RA was observed as well. Moreover, Metrnβ expressions exhibited an inverse correlation with Treg and B10. Of note, a significant decrease of ILC2 was found in SLE, and there was a negative correlation of Metrnβ with ILC2 as well. Further ROC analysis showed that the area under the curve (AUC) for Metrnβ was 0.8250 (95% CI: 0.7379-0.9121), with a cutoff value of 1131 pg/mL to effectively distinguish SLE patients from healthy controls. Our study herein demonstrated for the first time that Metrnβ values were increased and were immunologically correlated with SLE activity, which could be utilized as an alternative biomarker for the early identification and predicting of the immuno-response of SLE.

Indexed as

Autoimmune DiseasesLupus Erythematosus, SystemicCytokinesHumansImmunity, InnateLymphocytesCytokinesILC2Metrnβpathogenesissystemic lupus erythematosus

Identifiers

PMID37686413
PMCPMC10563073
OpenAlexW4386409216

What Socratic 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 Socratic graph.