Evidence map›Paper›PMID 23987125›Full record

ArticleLipids in health and disease2013

Associations of genetic polymorphisms of SAA1 with cerebral infarction.

Li-Jun Zhang, Bin Yuan, He-Hua Li, Sheng-Bo Tao, Hai-Qing Yan, Li Chang, Jian-Hua Zhao

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. [Association of rs4638289 and rs7131332 polymorphisms of the serum amyloid A1 gene with Kawasaki disease].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2020
    Article
  4. Review
  5. Association of CYP2J2 gene polymorphisms with ischemic stroke.International journal of clinical and experimental medicine · 2015
    Article
  6. SAA1 gene variants and childhood obesity in China.Lipids in health and disease · 2013
    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

7 authors at 2 institutions in 1 country.

Li-Jun ZhangDepartment of Neurology, First Affiliated Hospital of Xinxiang Medical College, Xinxiang, Henan 453100, P R, China. zhaojianhua_z@126.com.
Bin Yuan
He-Hua Li
Sheng-Bo Tao
Hai-Qing Yan
Li Chang
Jian-Hua Zhao
Xinxiang Medical University · CNFirst Affiliated Hospital of Xinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSerum amyloid A protein (SAA) is both an inflammatory factor and an apolipoprotein. However, the relation between genetic polymorphisms of SAA and cerebral infarction (CI) remains unclear. METHODS AND

resultsThe previously reported 4 Single Nucleotide Polymorphisms (rs12218, rs4638289, rs7131332, and rs11603089) of SAA1 gene were genotyped by TaqMan method in a case-control study including 287 cerebral infarction patients and 376 control subjects. We found rs12218 CC genotype and rs7131332 AA genotype were more frequent among CI patients than among controls (9.76% versus 3.19%, P = 0.001; 32.75% versus 24.20%; p = 0.017; respectively). After adjustment of confounding factors such as sex, age, smoking, drinking, hypertension, diabetes, and lipids profile, the difference remained significant in rs12218 (P < 0.01, OR = 2.106, 95% CI: 1.811-7.121).

conclusionGenetic polymorphism of SAA1 may be a genetic maker of cerebral infarction in Chinese.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAgedAllelesAsian PeopleCase-Control StudiesCerebral InfarctionFemaleGene ExpressionGene FrequencyGenetic MarkersHumansMaleMiddle AgedSerum Amyloid A ProteinGenetic MarkersSAA1 protein, humanSerum Amyloid A Protein

Identifiers

PMID23987125
PMCPMC3765816
OpenAlexW2139933668

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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.