Evidence map›Paper›PMID 29379005›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2018

Association of Single-Nucleotide Polymorphisms of C-Reactive Protein Gene with Susceptibility to Infantile Sepsis in Southern China.

Chunyi Liu, Ping Jin, Yong Luo, Jinji Xu, Chengxiang Kong, Juan Chen, Hongbo Xie, Gang Zhou

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  3. TheInfection and drug resistance · 2021
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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

8 authors at 1 institution in 1 country.

Chunyi LiuDepartment of Pediatrics, Shenzhen Baoan District Maternity and Child Care Service Centre, Shenzhen, Guangdong, China (mainland).
Ping JinDepartment of Pediatrics, Shenzhen Baoan District Maternity and Child Care Service Centre, Shenzhen, Guangdong, China (mainland).
Yong LuoDepartment of Pediatrics, Shenzhen Baoan District Maternity and Child Care Service Centre, Shenzhen, Guangdong, China (mainland).
Jinji XuDepartment of Pediatrics, Shenzhen Baoan District Maternity and Child Care Service Centre, Shenzhen, Guangdong, China (mainland).
Chengxiang KongDepartment of Pediatrics, Shenzhen Baoan District Maternity and Child Care Service Centre, Shenzhen, Guangdong, China (mainland).
Juan ChenDepartment of Pediatrics, Shenzhen Baoan District Maternity and Child Care Service Centre, Shenzhen, Guangdong, China (mainland).
Hongbo XieDepartment of Pediatrics, Shenzhen Baoan District Maternity and Child Care Service Centre, Shenzhen, Guangdong, China (mainland).
Gang ZhouDepartment of Pediatrics, Shenzhen Baoan District Maternity and Child Care Service Centre, Shenzhen, Guangdong, China (mainland).
Shenzhen Maternity and Child Healthcare Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND C-reactive protein (CRP) is an important biomarker of sepsis. Several single-nucleotide polymorphisms (SNPs) in the CRP gene can determine plasma CRP levels and are risk factors in many diseases, such as cancer, arteritis, and diabetes. However, it is unknown whether polymorphisms in CRP are associated with susceptibility to and outcome of infantile sepsis. We explored the effect of these SNPs on CRP response in infantile sepsis, and compared genetic data on patients with sepsis. MATERIAL AND METHODS A total of 49 infants with sepsis and 20 healthy infants were enrolled during hospitalization, and 3 SNPs in the CRP gene region (rs1205, rs2808530, and rs3091244) were genotyped and then analyzed for associations with CRP levels and sepsis. RESULTS The CRP means concentration results showed that mean CRP concentration was different in the 4 groups (healthy, sepsis, severe sepsis, and septic shock) and was positively correlated with the severity of infantile sepsis. There was also a difference in CRP SNP rs1205 between infants with septic shock and healthy infants, and between infants with septic shock and infants with sepsis. No differences were observed in SNP rs2808630 and SNP rs3091244. CONCLUSIONS Our study suggests that rs1205 genetic variability in the CRP gene determines the CRP levels in sepsis of different severities, while SNP rs3091244 and SNP rs2808630 are not associated with sepsis. However, the results of the present study on SNP rs1205, rs3091244, and rs2808630 in the CRP gene should be interpreted with caution due to limited sample size and sample heterogeneity. Large-scale, well-designed studies are needed to validate our findings.

Indexed as

Genetic Predisposition to DiseaseChinaChi-Square DistributionC-Reactive ProteinFemaleHumansInfantMalePolymorphism, Single NucleotideSepsisC-Reactive Protein

Identifiers

PMID29379005
PMCPMC5800323
OpenAlexW2786660489

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.