Evidence map›Paper›PMID 31594897›Full record

SynthesisBMJ open2019

Serum soluble urokinase type plasminogen activated receptor and focal segmental glomerulosclerosis: a systematic review and meta-analysis.

Tiankui Shuai, Yan Pei Jing, Qiangru Huang, Huaiyu Xiong, Jingjing Liu, Lei Zhu, Kehu Yang, Liu Jian

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Kynurenine pathway in kidney diseases.Pharmacological reports : PR · 2022
    Review
  3. Review
  4. MicroRNAs as Biomarkers for Nephrotic Syndrome.International journal of molecular sciences · 2020
    Review
  5. 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 at 2 institutions in 2 countries.

Tiankui Shuai *Department of Intensive Care Unit, Lanzhou University First Affiliated Hospital, Lanzhou, China.
Yan Pei Jing *Evidence-Based Medicine Center, School of Basic Medical Sciences, Lanzhou University, Lanzhou, China.
Qiangru HuangDepartment of Intensive Care Unit, Lanzhou University First Affiliated Hospital, Lanzhou, China.
Huaiyu XiongDepartment of Intensive Care Unit, Lanzhou University First Affiliated Hospital, Lanzhou, China.
Jingjing LiuDepartment of Intensive Care Unit, Lanzhou University First Affiliated Hospital, Lanzhou, China.
Lei ZhuDepartment of Intensive Care Unit, Lanzhou University First Affiliated Hospital, Lanzhou, China.
Kehu YangEvidence-Based Medicine Center, School of Basic Medical Sciences, Lanzhou University, Lanzhou, China medecinliu@sina.com kehuyangebm2006@126.com.
Liu JianDepartment of Intensive Care Unit, Lanzhou University First Affiliated Hospital, Lanzhou, China medecinliu@sina.com kehuyangebm2006@126.com.ORCID 0000-0002-1825-571X
First Hospital of Lanzhou University · CNGansu Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSoluble urokinase plasminogen activated receptor (suPAR) is a biomarker that may predict the occurrence of focal segmental glomerulosclerosis (FSGS); however, there is still controversy about whether suPAR can predict FSGS. In this study, we performed a systematic evaluation and meta-analysis to prove whether suPAR can predict FSGS, and to detect a threshold concentration of suPAR that can be used to diagnose FSGS. In addition, a threshold concentration of suPAR for the diagnosis of FSGS was proposed.

designSystematic review and meta-analysis. DATA SOURCES: We systematically searched PubMed, Embase, Cochrane Library, Web of Science and China Biology Medicine databases for studies published from the inception dates to 1 December 2018. ELIGIBILITY CRITERIA: (1) Data involving the suPAR level were from blood samples; (2) FSGS was diagnosed by biopsy; and (3) randomised controlled trials, cohort studies, case-control studies and cross-sectional studies. DATA EXTRACTION AND SYNTHESIS: Initially, a total of 364 studies were searched, among which 29 studies were finally included. In addition, seven studies described the cut-off value of suPAR, which ranged from 2992.6 to 5500 pg/mL.

resultsThe results showed that the suPAR levels in the primary FSGS group were significantly higher when compared with that in the normal control group (p

conclusionOur results suggested that suPAR might be a potential biomarker for predicting primary and secondary FSGS. In addition, our data showed that a suPAR concentration of 3000 pg/mL might be used as a threshold for the diagnosis of FSGS. TRIAL REGISTRATION NUMBER: CRD42019120948.

Indexed as

Glomerulosclerosis, Focal SegmentalBiomarkersHumansPredictive Value of TestsPrognosisReceptors, Urokinase Plasminogen ActivatorBiomarkersReceptors, Urokinase Plasminogen Activatorfocal segmental glomerulosclerosisnephrology

Identifiers

PMID31594897
PMCPMC6797292
OpenAlexW2979470778

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.