Evidence map›Paper›PMID 26024530›Full record

Trial reportPloS one2015

Deletion of a 4977-bp Fragment in the Mitochondrial Genome Is Associated with Mitochondrial Disease Severity.

Yanchun Zhang, Yinan Ma, Dingfang Bu, Hui Liu, Changyu Xia, Ying Zhang, Sainan Zhu, Hong Pan, Pei Pei, Xuefei Zheng and 3 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Yanchun ZhangDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Yinan MaDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Dingfang BuDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Hui LiuDepartment of Respiratory, Beijing Children's Hospital, Beijing, 100045, China.
Changyu XiaDepartment of Clinical Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Ying ZhangDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Sainan ZhuDepartment of Biostatistics, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Hong PanDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Pei PeiDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Xuefei ZhengDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Songtao WangDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Yufeng XuDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Yu QiDepartment of Central Laboratory, Peking University First Hospital, No. 8, West District, Beijing, 100034, China.
Peking University · CNPeking University First Hospital · CNBeijing Children’s Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large deletions in mitochondrial DNA (mtDNA) may be involved in the pathogenesis of mitochondrial disease. In this study, we investigated the relationship between a 4,977-bp deletion in the mitochondrial genome (ΔmtDNA(4977)) and the severity of clinical symptoms in patients with mitochondrial disease lacking known point mutations. A total of 160 patients with mitochondrial disease and 101 healthy controls were recruited for this study. The copy numbers of ΔmtDNA(4977) and wild-type mtDNA were determined by real-time quantitative PCR and analyzed using Spearman's bivariate correlation analysis, t-tests, or one-way ANOVA. The overall ΔmtDNA(4977) copy number per cell and the proportion of mtDNA(4977) relative to the total wild-type mtDNA, increased with patient age and symptom severity. Surprisingly, the total mtDNA copy number decreased with increasing symptom severity. Our analyses revealed that increases in the proportion and total copy number of ΔmtDNA(4977) in the blood may be associated with disease severity in patients with mitochondrial dysfunction.

Indexed as

Base SequenceGenome, MitochondrialSequence DeletionAdolescentAdultChildChild, PreschoolDNA, MitochondrialHumansInfantMaleMetabolism, Inborn ErrorsMitochondrial DiseasesSeverity of Illness IndexDNA, Mitochondrial

Identifiers

PMID26024530
PMCPMC4449107
OpenAlexW1589231011

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.