Evidence map›Paper›PMID 28230325›Full record

ArticleBipolar disorders2017

Serum phosphatidylinositol as a biomarker for bipolar disorder liability.

Emma Em Knowles, Peter J Meikle, Kevin Huynh, Harald Hh Göring, Rene L Olvera, Samuel R Mathias, Ravi Duggirala, Laura Almasy, John Blangero, Joanne E Curran and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Bipolar disorders, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  7. Untargeted Lipidomics Study of Bipolar Disorder Patients in Serbia.International journal of molecular sciences · 2023
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  19. Disentangling the genetic overlap between cholesterol and suicide risk.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
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 6 institutions in 2 countries.

Emma Em KnowlesDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0003-0642-267X
Peter J MeikleBaker Heart and Diabetes Institute, Melbourne, Vic., Australia.
Kevin HuynhBaker Heart and Diabetes Institute, Melbourne, Vic., Australia.
Harald Hh GöringSouth Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX, USA.
Rene L OlveraDepartment of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Samuel R MathiasDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Ravi DuggiralaSouth Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX, USA.
Laura AlmasyDepartment of Genetics, University of Pennsylvania and Department of Biomedical and Health Informatics at Children's Hospital of Philadelphia, PA, USA.
John BlangeroSouth Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX, USA.
Joanne E CurranSouth Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX, USA.
David C GlahnDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
The University of Texas Rio Grande Valley · USBaker Heart and Diabetes Institute · AUYale University · USChildren's Hospital of Philadelphia · USHartford Hospital · USThe University of Texas Health Science Center at San Antonio · US

Funding

SOLAR-Eclipse Computational Tools for Imaging GeneticsR01EB015611 · NIBIB · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KOCHUNOV, PETER V. · 2012 to 2024
$5.0M
Genetics of Brain Structure and FunctionR01MH078111 · NIMH · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 2006 to 2014
$4.5M
Genetics of Brain Structure and Function: Genome-Wide AssociationR01MH083824 · NIMH · YALE UNIVERSITY · PI GLAHN, DAVID C · 2008 to 2013
$3.3M
NIBIB NIH HHS R01 EB015611NIMH NIH HHS R01 MH078111NIMH NIH HHS R01 MH083824
6 · The paper itself

Abstract

objectivesIndividuals with bipolar disorder (BPD) exhibit alterations in their phospholipid levels. It is unclear whether these alterations are a secondary consequence of illness state, or if phospholipids and illness risk overlap genetically. If the latter were true, then phospholipids might provide key insights into the pathophysiology of the illness. Therefore, we rank-ordered phospholipid classes by their genetic overlap with BPD risk in order to establish which class might be most informative in terms of increasing our understanding of illness pathophysiology.

methodsAnalyses were conducted in a sample of 558 individuals, unselected for BPD, from 38 extended pedigrees (average family size=14.79, range=2-82). We calculated a coefficient of relatedness for all family members of nine individuals with BPD in the sample (N=185); this coefficient was set to be zero in unrelated individuals (N=373). Then, under an endophenotype ranking value (ERV) approach, this scalar index was tested against 13 serum-based phospholipid concentrations in order to rank-order lipid classes by their respective overlap with BPD risk.

resultsThe phosphatidylinositol class was significantly heritable (h

conclusionsWe identified a peripheral biomarker, serum-based phosphatidylinositol, which exhibits a significant association with BPD risk. Therefore, given that phosphatidylinositol and BPD risk share partially common etiology, it seems that this lipid class warrants further investigation, not only in terms of treatment, but also as a promising diagnostic and risk marker.

Indexed as

Bipolar DisorderAdultBiomarkersEndophenotypesFamilyFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedPedigreePhosphatidylinositolsPsychiatric Status Rating ScalesQuantitative Trait, HeritableRisk FactorsTandem Mass SpectrometryBiomarkersPhosphatidylinositolsbipolarfamily studygeneticslipidomephosphatidylinositol

Identifiers

PMID28230325
PMCPMC5798864
OpenAlexW2591499495

What OpenQuestion holds

Textmetadata
LicenceTDM
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.