Evidence map›Paper›PMID 26463265›Full record

ArticleAnnals of neurology2015

Growth differentiation factor 15 as a useful biomarker for mitochondrial disorders.

Shuichi Yatsuga, Yasunori Fujita, Akiko Ishii, Yoshihiro Fukumoto, Hajime Arahata, Tatsuyuki Kakuma, Toshio Kojima, Masafumi Ito, Masashi Tanaka, Reo Saiki and 1 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Annals of neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02745938 (GDF-15 as a Biomarker for Mitochondrial Disease), which is not on this map. Cited by 163 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
163citing papers in PubMed, 3 pooled it
11.8field-weighted citation impact, top 1% 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.

NCT02745938 completednot on this mapstarted 2016, after this paper: background citation

GDF-15 as a Biomarker for Mitochondrial Disease

TypeobservationalSponsorRigshospitalet, DenmarkRan2016 to 2017Enrolled97ConditionsMitochondrial Disease, Metabolic Myopathy, Muscular Dystrophy
3 · Its place in the literature

Who cites it

163 citing papers in PubMed, 3 syntheses or guidelines pooled it, 282 citations in OpenAlex.

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103 more citing papers are in PubMed but not listed here.

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

11 authors at 5 institutions in 1 country.

Shuichi YatsugaDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Yasunori FujitaResearch Team for Mechanism of Aging, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Akiko IshiiDepartment of Neurology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Yoshihiro FukumotoDivision of Cardiovascular Medicine, Department of Internal Medicine, Kurume University School of Medicine, Fukuoka, Japan.
Hajime ArahataDepartment of Neurology, Neuro-Muscular Center, National Omuta Hospital, Fukuoka, Japan.
Tatsuyuki KakumaDepartment of Biostatistics, Kurume University Graduate School of Medicine, Kurume, Japan.
Toshio KojimaHealth Care Center, Toyohashi University of Technology, Toyohashi, Japan.
Masafumi ItoResearch Team for Mechanism of Aging, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Masashi TanakaDepartment of Genomics for Longevity and Health, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Reo SaikiDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Yasutoshi KogaDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Kurume University · JPTokyo Metropolitan Institute of Gerontology · JPOmuta hospital · JPToyohashi University of Technology · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe diagnosis of mitochondrial disorders (MDs) is occasionally difficult because patients often present with solitary, or a combination of, symptoms caused by each organ insufficiency, which may be the result of respiratory chain enzyme deficiency. Growth differentiation factor 15 (GDF-15) has been reported to be elevated in serum of patients with MDs. In this study, we investigated whether GDF-15 is a more useful biomarker for MDs than several conventional biomarkers.

methodsWe measured the serum levels of GDF-15 and fibroblast growth factor 21 (FGF-21), as well as other biomarkers, in 48 MD patients and in 146 healthy controls in Japan. GDF-15 and FGF-21 concentrations were measured by enzyme-linked immunosorbant assay and compared with lactate, pyruvate, creatine kinase, and the lactate-to-pyruvate ratio. We calculated sensitivity and specificity and also evaluated the correlation based on two rating scales, including the Newcastle Mitochondrial Disease Rating Scale (NMDAS).

resultsMean GDF-15 concentration was 6-fold higher in MD patients compared to healthy controls (2,711 ± 2,459 pg/ml vs 462.5 ± 141.0 pg/mL; p < 0.001). Using a receiver operating characteristic curve, the area under the curve was significantly higher for GDF-15 than FGF-21 and other conventional biomarkers. Our date suggest that GDF-15 is the most useful biomarker for MDs of the biomarkers examined, and it is associated with MD severity.

interpretationOur results suggest that measurement of GDF-15 is the most useful first-line test to indicate the patients who have the mitochondrial respiratory chain deficiency.

Indexed as

AdolescentAdultBiomarkersChildCreatine KinaseFemaleFibroblast Growth FactorsGrowth Differentiation Factor 15HumansLactic AcidMaleMELAS SyndromeMiddle AgedMitochondrial DiseasesPyruvic AcidROC CurveBiomarkersCreatine Kinasefibroblast growth factor 21Fibroblast Growth FactorsGDF15 protein, humanGrowth Differentiation Factor 15Lactic AcidPyruvic Acid

Identifiers

PMID26463265
PMCPMC5057301
OpenAlexW1903699046

What OpenQuestion holds

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Registered trials

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.