Evidence map›Paper›PMID 36570009›Full record

ArticlePeerJ2022

Genetic analysis of DNA methylation in dyslipidemia: a case-control study.

Shuai Liu, Yang Li, Xian Wei, Dilare Adi, Yong-Tao Wang, Min Han, Fen Liu, Bang-Dang Chen, Xiao-Mei Li, Yi-Ning Yang and 2 more

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Methylation status ofEpigenomics · 2024
    Article
  4. Article
  5. 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 at 2 institutions in 1 country.

Shuai Liu *First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Yang Li *First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Xian WeiFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Dilare AdiFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Yong-Tao WangFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Min HanFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Fen LiuFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Bang-Dang ChenFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Xiao-Mei LiFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Yi-Ning YangFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Zhen-Yan FuFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Yi-Tong MaFirst Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
First Affiliated Hospital of Xinjiang Medical University · CNXinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Coronary heart disease has become the leading cause of death in developed countries, and dyslipidemia is closely associated with the risk of cardiovascular disease. Dyslipidemia is caused by the abnormal regulation of several genes and signaling pathways, and dyslipidemia is influenced mainly by genetic variation. Methods: A case-control research method was used in this study. The patient's blood samples were collected at the Heart Center of the First Affiliated Hospital of Xinjiang Medical University. In the Xinjiang Han population, 100 cases of hyperlipidemia and 80 cases of the control group were selected. The two groups were age and gender-matched. Quantitative methylation analysis of CpG sites in the gene promoter regions of six genes was performed by Solexa high-throughput sequencing. Results: The DNA methylation levels of 23 CpG sites in six genes were shown to be associated with hyperlipidemia, and a total of 20 DNA methylation haplotypes showed statistically significant differences between the two groups. When compared with the control group, the dyslipidemia group had significantly higher levels of methylation in the Conclusion: The findings of this study reveal that the DNA methylation of

Indexed as

Coronary DiseaseDyslipidemiasCase-Control StudiesDNA MethylationHaplotypesHumansCoronary artery diseaseCpGDNA methylationDyslipidemiaGRINAHaplotype

Identifiers

PMID36570009
PMCPMC9774006
OpenAlexW4312212144

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.