Evidence map›Paper›PMID 29320990›Full record

ArticleBMC infectious diseases2018

Correlation between polymorphisms in toll-like receptor genes and the activity of hepatitis B virus among treatment-naïve patients: a case-control study in a Han Chinese population.

Yong Lin, Zheng-Xiang Gao, Xu Shen, Mei-Jun Chen, Yan-Ting Li, Shu-Lian Li, Hui-Ling Lin, Qi-Feng Zhao, Fan Liu, Jian-Jun Niu

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

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  8. Journal of personalized medicine · 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

10 authors at 3 institutions in 1 country.

Yong LinCenter of Clinical Laboratory, Zhongshan Hospital, Medical College of Xiamen University, 201-209 Hubin South Road, Siming District, Xiamen City, 361004, Fujian Province, People's Republic of China.
Zheng-Xiang GaoCenter of Clinical Laboratory, Zhongshan Hospital, Medical College of Xiamen University, 201-209 Hubin South Road, Siming District, Xiamen City, 361004, Fujian Province, People's Republic of China.
Xu ShenCenter of Clinical Laboratory, Zhongshan Hospital, Medical College of Xiamen University, 201-209 Hubin South Road, Siming District, Xiamen City, 361004, Fujian Province, People's Republic of China.
Mei-Jun ChenCenter of Clinical Laboratory, Zhongshan Hospital, Medical College of Xiamen University, 201-209 Hubin South Road, Siming District, Xiamen City, 361004, Fujian Province, People's Republic of China.
Yan-Ting LiCenter of Clinical Laboratory, Zhongshan Hospital, Medical College of Xiamen University, 201-209 Hubin South Road, Siming District, Xiamen City, 361004, Fujian Province, People's Republic of China.
Shu-Lian LiXiamen Huli District Maternity and Child Care Hospital, Xiamen, Fujian Province, China.
Hui-Ling LinXiamen Huli District Maternity and Child Care Hospital, Xiamen, Fujian Province, China.
Qi-Feng ZhaoCenter of Clinical Laboratory, Zhongshan Hospital, Medical College of Xiamen University, 201-209 Hubin South Road, Siming District, Xiamen City, 361004, Fujian Province, People's Republic of China.
Fan LiuCenter of Clinical Laboratory, Zhongshan Hospital, Medical College of Xiamen University, 201-209 Hubin South Road, Siming District, Xiamen City, 361004, Fujian Province, People's Republic of China.
Jian-Jun NiuCenter of Clinical Laboratory, Zhongshan Hospital, Medical College of Xiamen University, 201-209 Hubin South Road, Siming District, Xiamen City, 361004, Fujian Province, People's Republic of China. niujianjun62@163.com.
Zhongshan Hospital of Xiamen University · CNXiamen University · CNXiamen Maternal and Child Health Hospital · CN

Funding

National Natural Science Foundation of China 81471970Natural Science Foundation of Fujian Province (CN) 2015J01529Xiamen Municipal Bureau of Science and Technology 3502Z20154015Xiamen Municipal Bureau of Science and Technology (CN) 3502Z20144022Xiamen Municipal Bureau of Science and Technology (CN) WSK2010-01
6 · The paper itself

Abstract

backgroundBecause of the high prevalence and absence of cure for infection, chronic hepatitis B virus (HBV) infection has been acknowledged as a pressing public health issue. Toll-like receptors (TLRs) activate the human innate immune system and the polymorphisms in TLRs may alter their function. The present study aimed to investigate the association between TLR polymorphisms and disease progression of chronic HBV infection.

methodsDuring the study period, 211 treatment-naïve patients with chronic HBV infection were recruited, and blood samples were collected from each individual. Matrix-assisted laser desorption/ionization time of flight mass spectrometry was employed to genotype the selected TLR polymorphisms after human genome extraction. In addition, HbsAg, TNF-α, and IL-6 levels were quantified using enzyme linked immunosorbent assay (ELISA). Statistical analyses were conducted to investigate the association between TLR polymorphisms and hepatitis activity, liver function parameters, HbsAg level, and cytokine level.

resultsWe did not observe any mutations in rs4986790, rs4986791, and rs5743708 among all study subjects. A logistic regression revealed that mutations in rs3804099 and rs4696480 were associated with milder hepatitis activity. Consistent with the logistic regression, improved liver function parameters and reduced level of both HbsAg and cytokines were also correlated with the mutant carriers of rs3804099 and rs4696480.

conclusionsTLR mutations were significantly associated with milder hepatitis activity among patients with chronic HBV infection. Therefore, we conclude that the activation of TLR pathways may further intensify the inflammation of hepatocytes, and leads to progression of disease.

Indexed as

Polymorphism, Single NucleotideAdultAsian PeopleCase-Control StudiesCytokinesFemaleHepatitis B, ChronicHepatitis B Surface AntigensHepatitis B virusHumansInterleukin-6Liver Function TestsMaleMutationToll-Like Receptor 2Toll-Like ReceptorsCytokinesHepatitis B Surface AntigensIL6 protein, humanInterleukin-6TLR2 protein, humanToll-Like Receptor 2Toll-Like ReceptorsTumor Necrosis Factor-alphaHepatitis activityHepatitis B virusImmune responseToll-like receptors

Identifiers

PMID29320990
PMCPMC5764005
OpenAlexW2782817149

What OpenQuestion holds

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LicenceCC BY
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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.