Evidence map›Paper›PMID 25004141›Full record

ArticlePloS one2014

Quantitative analyses of schizophrenia-associated metabolites in serum: serum D-lactate levels are negatively correlated with gamma-glutamylcysteine in medicated schizophrenia patients.

Takeshi Fukushima, Hideaki Iizuka, Ayaka Yokota, Takehiro Suzuki, Chihiro Ohno, Yumiko Kono, Minami Nishikiori, Ayaka Seki, Hideaki Ichiba, Yoshinori Watanabe and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 5 pooled it
4.6field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 5 syntheses or guidelines pooled it, 101 citations in OpenAlex.

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  18. Schizophrenia and Glutathione: A Challenging Story.Journal of personalized medicine · 2023
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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

15 authors at 3 institutions in 1 country.

Takeshi FukushimaDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Hideaki IizukaDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Ayaka YokotaDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Takehiro SuzukiDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Chihiro OhnoDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Yumiko KonoDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Minami NishikioriDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Ayaka SekiDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Hideaki IchibaDepartment of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Yoshinori WatanabeNanko Clinic of Psychiatry, Himorogi group, Medical Corporation JISENKAI, Shirakawa-shi, Fukushima, Japan.
Seiji HongoNanko Clinic of Psychiatry, Himorogi group, Medical Corporation JISENKAI, Shirakawa-shi, Fukushima, Japan.
Mamoru UtsunomiyaPublic Interest Incorporated Foundation, Sumiyoshi-kaiseikai Sumiyoshi hospital, Koufu-shi, Yamanashi, Japan.
Masaki NakataniPublic Interest Incorporated Foundation, Sumiyoshi-kaiseikai Sumiyoshi hospital, Koufu-shi, Yamanashi, Japan.
Kiyomi SadamotoDepartment of Clinical Pharmacy, Yokohama College of Pharmacy, Yokohama-shi, Kanagawa, Japan.
Takashi YoshioDepartment of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Funabashi-shi, Chiba, Japan.
Toho University · JPKishokai Medical Corporation · JPYokohama University of Pharmacy · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The serum levels of several metabolites are significantly altered in schizophrenia patients. In this study, we performed a targeted analysis of 34 candidate metabolites in schizophrenia patients (n = 25) and compared them with those in age- and gender-matched healthy subjects (n = 27). Orthogonal partial least square-discriminant analysis revealed that complete separation between controls and patients was achieved based on these metabolites. We found that the levels of γ-glutamylcysteine (γ-GluCys), linoleic acid, arachidonic acid, D-serine, 3-hydroxybutyrate, glutathione (GSH), 5-hydroxytryptamine, threonine, and tyrosine were significantly lower, while D-lactate, tryptophan, kynurenine, and glutamate levels were significantly higher in schizophrenia patients compared to controls. Using receiver operating characteristics (ROC) curve analysis, the sensitivity, specificity, and the area under curve of γ-GluCys, a precursor of GSH, and D-lactate, a terminal metabolite of methylglyoxal, were 88.00%, 81.48%, and 0.8874, and 88.00%, 77.78%, and 0.8415, respectively. In addition, serum levels of D-lactate were negatively correlated with γ-GluCys levels in patients, but not in controls. The present results suggest that oxidative stress-induced damage may be involved in the pathogenesis of schizophrenia.

Indexed as

MetabolomeMetabolomicsAdolescentAdultCase-Control StudiesDipeptidesFemaleGlutathioneHumansLactatesMaleROC CurveSchizophreniaYoung AdultDipeptidesgamma-glutamylcysteineGlutathioneLactates

Identifiers

PMID25004141
PMCPMC4086900
OpenAlexW2081803015

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.