Evidence map›Paper›PMID 30729666›Full record

Trial reportJournal of cellular and molecular medicine2019

Serum semaphorin 7A is associated with the risk of acute atherothrombotic stroke.

Tao You, Zhengbao Zhu, Xiaowei Zheng, Nimei Zeng, Shuhong Hu, Yifei Liu, Lijie Ren, Qiongyu Lu, Chaojun Tang, Changgeng Ruan and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Axon guidance molecules in immunometabolic diseases.Inflammation and regeneration · 2022
    Review
  8. Role of Semaphorins in Ischemic Stroke.Frontiers in molecular neuroscience · 2022
    Review
  9. Article
  10. Mapping pleiotropic loci using a fast-sequential testing algorithm.European journal of human genetics : EJHG · 2021
    Article
  11. Common Polymorphisms in theFrontiers in cardiovascular medicine · 2021
    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

12 authors.

Tao YouCyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
Zhengbao ZhuDepartment of Epidemiology, School of Public Health, Medical College of Soochow University, Suzhou, China.
Xiaowei ZhengDepartment of Epidemiology, School of Public Health, Medical College of Soochow University, Suzhou, China.
Nimei ZengDepartment of Epidemiology, School of Public Health, Medical College of Soochow University, Suzhou, China.
Shuhong HuCyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
Yifei LiuCyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
Lijie RenCyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
Qiongyu LuCyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
Chaojun TangCyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
Changgeng RuanCyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
Yonghong ZhangDepartment of Epidemiology, School of Public Health, Medical College of Soochow University, Suzhou, China.
Li ZhuCyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.ORCID 0000-0003-2040-294X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Semaphorin 7A (Sema7A), a neural guidance cue, was recently identified to regulate atherosclerosis in mice. However, the clinical relevance of Sema7A with atherosclerotic diseases remains unknown. The aim of this study was to investigate the association between serum Sema7A and the risk of acute atherothrombotic stroke (AAS). We measured serum concentrations of Sema7A in 105 newly onset AAS cases and 105 age- and sex-matched controls, showing that median Sema7A level in AAS cases was over three times of that in controls (5.86 vs 1.66 ng/mL). Adjusted for hypertension, body mass index, fasting blood glucose, total cholesterol, triglyceride, high-density lipoprotein (HDL)-cholesterol, low-density lipoprotein (LDL)-cholesterol, current smoking and alcohol consumption, multivariate logistic regression showed that higher Sema7A was independently associated with the odds of AAS (OR = 6.40, 95% CI: 2.88-14.25). Each 1-standard deviation increase in Sema7A was associated with a threefold higher odds of AAS (OR = 3.42, 95% CI: 1.84-6.35). Importantly, adding Sema7A to a multivariate logistic model containing conventional cardiovascular risk factors improved the area under receiver operating characteristic curves from 0.831 to 0.891 for the association with AAS. In conclusion, elevated serum Sema7A is independently associated with the risk of AAS, suggesting that it may play a potential role in AAS.

Indexed as

Antigens, CDAtherosclerosisBiomarkersCase-Control StudiesFemaleGPI-Linked ProteinsHumansMalePrognosisRisk FactorsSemaphorinsStrokeAntigens, CDBiomarkersGPI-Linked ProteinsSEMA7A protein, humanSemaphorinsacute atherothrombotic strokerisk factorsemaphorin 7A

Identifiers

PMID30729666
PMCPMC6433662

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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.