Evidence map›Paper›PMID 28846698›Full record

ArticlePloS one2017

Association between mitochondrial DNA variations and schizophrenia in the northern Chinese Han population.

Feng-Ling Xu, Mei Ding, Jun Yao, Zhang-Sen Shi, Xue Wu, Jing-Jing Zhang, Hao Pang, Jia-Xin Xing, Jin-Feng Xuan, Bao-Jie Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. A meta-analysis of data associatingNeuropsychiatric disease and treatment · 2018
    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

10 authors at 1 institution in 1 country.

Feng-Ling XuSchool of Forensic Medicine, China Medical University, Shenyang, China.
Mei DingSchool of Forensic Medicine, China Medical University, Shenyang, China.
Jun YaoSchool of Forensic Medicine, China Medical University, Shenyang, China.
Zhang-Sen ShiSchool of Forensic Medicine, China Medical University, Shenyang, China.
Xue WuSchool of Forensic Medicine, China Medical University, Shenyang, China.
Jing-Jing ZhangSchool of Forensic Medicine, China Medical University, Shenyang, China.
Hao PangSchool of Forensic Medicine, China Medical University, Shenyang, China.
Jia-Xin XingSchool of Forensic Medicine, China Medical University, Shenyang, China.
Jin-Feng XuanSchool of Forensic Medicine, China Medical University, Shenyang, China.
Bao-Jie WangSchool of Forensic Medicine, China Medical University, Shenyang, China.ORCID http://orcid.org/0000-0003-1931-423X
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To determine whether mitochondrial DNA (mtDNA) variations are associated with schizophrenia, 313 patients with schizophrenia and 326 unaffected participants of the northern Chinese Han population were included in a prospective study. Single-nucleotide polymorphisms (SNPs) including C5178A, A10398G, G13708A, and C13928G were analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Hypervariable regions I and II (HVSI and HVSII) were analyzed by sequencing. The results showed that the 4 SNPs and 11 haplotypes, composed of the 4 SNPs, did not differ significantly between patient and control groups. No significant association between haplogroups and the risk of schizophrenia was ascertained after Bonferroni correction. Drawing a conclusion, there was no evidence of an association between mtDNA (the 4 SNPs and the control region) and schizophrenia in the northern Chinese Han population.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdultAsian PeopleChinaDNA, MitochondrialFemaleGenetic Association StudiesHaplotypesHumansMaleMiddle AgedSchizophreniaDNA, Mitochondrial

Identifiers

PMID28846698
PMCPMC5573569
OpenAlexW2748660694

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.