Evidence map›Paper›PMID 26894921›Full record

ArticlePloS one2016

Niacin Skin Sensitivity Is Increased in Adolescents at Ultra-High Risk for Psychosis.

Gregor E Berger, Stefan Smesny, Miriam R Schäfer, Berko Milleit, Kerstin Langbein, Uta-Christina Hipler, Christine Milleit, Claudia M Klier, Monika Schlögelhofer, Magdalena Holub and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 3 pooled it
2.0field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 3 syntheses or guidelines pooled it, 46 citations in OpenAlex.

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  14. Meat Intake and the Dose of Vitamin BInternational journal of tryptophan research : IJTR · 2017
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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 6 institutions in 4 countries.

Gregor E BergerUniversity Hospital of Child and Adolescent Psychiatry, University of Zurich, Neumünsterallee 9, 8032 Zurich, Switzerland.
Stefan SmesnyDepartment of Psychiatry, Jena University Hospital, Philosophenweg 3, D-07743 Jena, Germany.
Miriam R SchäferOrygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Victoria 3052, Melbourne, Australia.
Berko MilleitDepartment of Psychiatry, Jena University Hospital, Philosophenweg 3, D-07743 Jena, Germany.
Kerstin LangbeinDepartment of Psychiatry, Jena University Hospital, Philosophenweg 3, D-07743 Jena, Germany.
Uta-Christina HiplerDepartment of Dermatology, University Hospital Jena, Erfurter Straße 35, D-07743 Jena, Germany.
Christine MilleitDepartment of Psychiatry, Jena University Hospital, Philosophenweg 3, D-07743 Jena, Germany.
Claudia M KlierDepartment of Child and Adolescent Psychiatry, Medical University of Vienna, Währingergürtel 18-20, A-1090 Vienna, Austria.
Monika SchlögelhoferDepartment of Child and Adolescent Psychiatry, Medical University of Vienna, Währingergürtel 18-20, A-1090 Vienna, Austria.
Magdalena HolubDepartment of Nutritional Sciences, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria.
Ingrid HolzerDepartment of Nutritional Sciences, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria.
Michael BerkDeakin University of Melbourne, School of Medicine, Barwon Health, Geelong, Australia.
Patrick D McGorryOrygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Victoria 3052, Melbourne, Australia.
Heinrich SauerDepartment of Psychiatry, Jena University Hospital, Philosophenweg 3, D-07743 Jena, Germany.
G Paul AmmingerOrygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Victoria 3052, Melbourne, Australia.
Jena University Hospital · DEMedical University of Vienna · ATOrygen Youth Health · AUUniversity of Melbourne · AUUniversity of Vienna · ATDeakin University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost studies provide evidence that the skin flush response to nicotinic acid (niacin) stimulation is impaired in schizophrenia. However, only little is known about niacin sensitivity in the ultra-high risk (UHR) phase of psychotic disorders.

methodsWe compared visual ratings of niacin sensitivity between adolescents at UHR for psychosis according to the one year transition outcome (UHR-T n = 11; UHR-NT n = 55) with healthy controls (HC n = 25) and first episode schizophrenia patients (FEP n = 25) treated with atypical antipsychotics.

resultsContrary to our hypothesis niacin sensitivity of the entire UHR group was not attenuated, but significantly increased compared to the HC group, whereas no difference could be found between the UHR-T and UHR-NT groups. As expected, niacin sensitivity of FEP was attenuated compared to HC group. In UHR individuals niacin sensitivity was inversely correlated with omega-6 and -9 fatty acids (FA), but positively correlated with phospholipase A2 (inPLA2) activity, a marker of membrane lipid repair/remodelling.

conclusionsIncreased niacin sensitivity in UHR states likely indicates an impaired balance of eicosanoids and omega-6/-9 FA at a membrane level. Our findings suggest that the emergence of psychosis is associated with an increased mobilisation of eicosanoids prior to the transition to psychosis possibly reflecting a "pro-inflammatory state", whereas thereafter eicosanoid mobilisation seems to be attenuated. Potential treatment implications for the UHR state should be further investigated.

Indexed as

AdolescentAdultEnzyme ActivationFatty AcidsFemaleFlushingHumansIntracellular SpaceMaleNiacinPhospholipases A2Psychotic DisordersRiskSkinYoung AdultFatty AcidsNiacinPhospholipases A2

Identifiers

PMID26894921
PMCPMC4764507
OpenAlexW2286213955

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.