Evidence map›Paper›PMID 27427388›Full record

ArticleJournal of molecular neuroscience : MN2016

TLR7 rs2897827 Polymorphism Affects TLR7 Gene mRNA Expression and Serum Apolipoprotein A1 Level of Ischemic Stroke Patients in a Chinese Han Population.

Lian Gu, Jinying Zhou, Jinjing Tan, Li Su, Qiugui Wei, Haiyun Jiang, Baoyun Liang, Qianli Tang

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2016. 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
0.2field-weighted citation impact, top 42% 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, 3 citations in OpenAlex.

  1. 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 4 institutions in 1 country.

Lian GuFirst Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.
Jinying ZhouFirst Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.
Jinjing TanFirst Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.
Li SuSchool of Public Health, Guangxi Medical University, Nanning, Guangxi, China.
Qiugui WeiFirst Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.
Haiyun JiangFirst Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.
Baoyun LiangFirst Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.
Qianli TangYou Jiang Medical University for Nationalities, 98 Chengxiang Road, Baise, Guangxi, 533000, China. tangqianli2015@163.com.
Guangxi University of Chinese Medicine · CNThe First Affiliated Hospital of Guangxi University of Traditional Chinese Medicine · CNAffiliated Hospital of Youjiang Medical University for Nationalities · CNGuangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stroke is a multi-factorial disorder that has become the leading cause of death and disability worldwide. Previous studies reported that TLR7 mRNA expression is associated with poor outcome of ischemic stroke (IS). This study aimed to assess whether TLR7 mRNA expression affects IS occurrence, as well as the association of TLR7 rs2897827 with susceptibility to IS and TLR7 mRNA expression and serum apolipoprotein and lipid levels in a Chinese Han population. A total of 816 stroke patients and 816 healthy controls were included in this study. mRNA expression was determined by quantitative real-time PCR. The Sequenom MassARRAY iPLEX platform was used to genotype the TLR7 rs2897827 polymorphism. TLR7 mRNA expression of the IS cases was statistically significantly higher than that of the controls in the male or female group (male, P = 0.014; female, P = 0.025). In the male IS cases, TLR7 mRNA expression of the T allele carriers was statistically significantly higher than that of the C allele carriers (P = 0.018). However, a significant difference was not observed in the female cases (P = 0.545). In either the male or female group, the distribution of genotype or allele had no statistical significance (P > 0.050). The ApoA1 level of the T carriers was statistically significantly higher than the C carriers in males (t = -2.383, P = 0.020); however, the ApoB and lipid levels were not associated with rs2897827 (P > 0.050). In female patients, no significant difference was observed between different genotypic/allelic carriers in serum apolipoprotein and lipid levels (all P > 0.050). The expression of the TLR7 gene may affect IS occurrence. TLR7 gene rs2897827 may influence TLR7 mRNA expression and the plasma ApoA1 level in male IS patients.

Indexed as

Polymorphism, Single NucleotideAgedAllelesApolipoprotein A-IBrain IschemiaCase-Control StudiesChinaFemaleHeterozygoteHumansMaleMiddle AgedRNA, MessengerStrokeToll-Like Receptor 7Apolipoprotein A-IRNA, MessengerTLR7 protein, humanToll-Like Receptor 7Ischemic strokemRNA expressionPolymorphismSerum apolipoprotein levelToll-like receptor 7

Identifiers

PMID27427388
OpenAlexW2494312779

What OpenQuestion holds

Textmetadata
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.