Evidence map›Paper›PMID 28656371›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2017

Cerebrospinal fluid monoamine metabolite profiles in bipolar disorder, ADHD, and controls.

Erik Pålsson, Carl Sellgren, Eleonore Rydén, Ruth Kizza, Aurimantas Pelanis, Henrik Zetterberg, Kaj Blennow, Mikael Landén

Open access · hybridAbstract read
In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Article
  7. Five-year outcomes of ADHD diagnosed in adulthood.Scandinavian journal of psychology · 2021
    Article
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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

8 authors at 4 institutions in 3 countries.

Erik PålssonDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, POB 431, 405 30, Göteburg, Sweden. erik.palsson@neuro.gu.se.ORCID 0000-0002-0345-3430
Carl SellgrenStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Eleonore RydénSection of Psychiatry, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Ruth KizzaSection of Psychiatry, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Aurimantas PelanisSahlgrenska University Hospital, Göteburg, Sweden.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, POB 431, 405 30, Göteburg, Sweden.
Kaj BlennowDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, POB 431, 405 30, Göteburg, Sweden.
Mikael LandénDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, POB 431, 405 30, Göteburg, Sweden.
Karolinska Institutet · SESahlgrenska University Hospital · SEBroad Institute · USUniversity of Gothenburg · SE

Funding

Stiftelsen för Strategisk Forskning KF10-0039Swedish Federal Government under the LUA/ALF agreement ALF 20130032Swedish Federal Government under the LUA/ALF agreement ALFGBG-142041Swedish Federal Government under the LUA/ALF agreement ALFGBG-441051Vetenskapsrådet 2013-2546Vetenskapsrådet K2010-61P-21568-01-4Vetenskapsrådet K2013-61X-14002Vetenskapsrådet K2014-62X-14647-12-51
6 · The paper itself

Abstract

Alterations in monoaminergic signaling are suggested as key aspects of the pathophysiology in bipolar disorder and ADHD, but it is not known if the monoamine metabolic profile differs between these disorders. One method to study monoaminergic systems in humans is to measure monoamine end-point metabolite concentrations in cerebrospinal fluid (CSF). Here, we analyzed CSF monoamine metabolite concentrations in 103 adults with bipolar disorder, 72 adults with ADHD, and 113 controls. Individuals with bipolar disorder had significantly higher homovanillic acid (HVA, 264 ± 112 nmol/L, p < 0.001) and 5-hydroxyindoleacetic acid (5-HIAA, 116 ± 42 nmol/L, p = 0.001) concentration, but lower 3-methoxy-4-hydroxyphenylethyleneglycol (MHPG, 38 ± 8 nmol/L, p < 0.001) concentrations than controls (HVA, 206 ± 70 nmol/L; 5-HIAA, 98 ± 31 nmol/L; and MHPG, 42 ± 7 nmol/L). Higher HVA concentrations were associated with a history of psychosis in the bipolar disorder sample. Subjects with ADHD had higher HVA (240 ± 94 nmol/L, p < 0.001) concentrations compared with controls. In addition, SSRI treatment was associated with lower 5-HIAA concentrations in both patient groups. A power analysis indicated that for within-group comparisons, only large effects would be reliably detectable. Thus, there may be moderate-to-small effects caused by medication that were not detected due to the limited size of the sub-groups in these analyses. In conclusion, the present study suggests disorder-specific alterations of CSF monoamine metabolite concentrations in patients with bipolar disorder and ADHD compared with controls; these differences were independent of acute symptoms and medication effects.

Indexed as

AdultAttention Deficit Disorder with HyperactivityBiogenic MonoaminesBiomarkersBipolar DisorderFemaleHumansMaleSelective Serotonin Reuptake InhibitorsBiogenic MonoaminesBiomarkersSelective Serotonin Reuptake InhibitorsADHDBipolar disorderCerebrospinal fluidDopamineMonoaminesNorepinephrineSerotonin

Identifiers

PMID28656371
PMCPMC5565665
OpenAlexW2732755502

What OpenQuestion holds

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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.