Evidence map›Paper›PMID 30082891›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2018

Disentangling the genetic overlap between cholesterol and suicide risk.

Emma E M Knowles, Joanne E Curran, Peter J Meikle, Kevin Huynh, Samuel R Mathias, Harald H H Göring, John L VandeBerg, Michael C Mahaney, Maria Jalbrzikowski, Marian K Mosior and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018. 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
1.1field-weighted citation impact, top 28% 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, 34 citations in OpenAlex.

  1. Identifying the Lipidomic Effects of a Rare Loss-of-Function Deletion inCirculation. Genomic and precision medicine · 2021
    Trial
  2. Low 5HTJournal of neurochemistry · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Biological Basis for the Formation of Suicidal Behavior: A Review.Medical journal of the Islamic Republic of Iran · 2025
    Review
  8. Article
  9. Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2022
    Article
  10. Review
  11. Article
  12. Article
  13. Development of a Suicide Prediction Model for the Elderly Using Health Screening Data.International journal of environmental research and public health · 2021
    Article
  14. Review
  15. Are Lipids Possible Markers of Suicide Behaviors?Journal of clinical medicine · 2021
    Review
  16. Lipids and Suicide Risk.Current topics in behavioral neurosciences · 2020
    Article
  17. Article
  18. Review
  19. 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

16 authors at 8 institutions in 2 countries.

Emma E M KnowlesDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA. emma.knowles@yale.edu.ORCID http://orcid.org/0000-0003-0642-267X
Joanne E CurranSouth Texas Diabetes and Obesity Institute and Department of Human Genetics, University of Texas of the Rio Grande Valley School of Medicine, Brownsville, TX, USA.
Peter J MeikleBaker IDI Heart and Diabetes Institute, Melbourne, Australia.
Kevin HuynhBaker IDI Heart and Diabetes Institute, Melbourne, Australia.
Samuel R MathiasDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Harald H H GöringSouth Texas Diabetes and Obesity Institute and Department of Human Genetics, University of Texas of the Rio Grande Valley School of Medicine, Brownsville, TX, USA.
John L VandeBergSouth Texas Diabetes and Obesity Institute and Department of Human Genetics, University of Texas of the Rio Grande Valley School of Medicine, Brownsville, TX, USA.
Michael C MahaneySouth Texas Diabetes and Obesity Institute and Department of Human Genetics, University of Texas of the Rio Grande Valley School of Medicine, Brownsville, TX, USA.
Maria JalbrzikowskiDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
Marian K MosiorDiabetes and Complications Therapeutic Area, Eli Lilly and Company, Indianapolis, IN, USA.
Laura F MichaelDiabetes and Complications Therapeutic Area, Eli Lilly and Company, Indianapolis, IN, USA.
Rene L OlveraDepartment of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Ravi DuggiralaSouth Texas Diabetes and Obesity Institute and Department of Human Genetics, University of Texas of the Rio Grande Valley School of Medicine, Brownsville, TX, USA.
Laura AlmasyDepartment of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
David C GlahnDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
John BlangeroSouth Texas Diabetes and Obesity Institute and Department of Human Genetics, University of Texas of the Rio Grande Valley School of Medicine, Brownsville, TX, USA.
The University of Texas Rio Grande Valley · USBaker Heart and Diabetes Institute · AUEli Lilly (United States) · USYale University · USChildren's Hospital of Philadelphia · USHartford Hospital · USThe University of Texas Health Science Center at San Antonio · USUniversity of Pittsburgh · US

Funding

Whole Genome Sequencing to Identify Causal Genetic Variants Influencing CVD RiskR01HL113323 · NHLBI · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI BLANGERO, JOHN, CURRAN, JOANNE E. · 2012 to 2016
$8.2M
Quantitative Trait Locus Mapping in Human PedigreesR37MH059490 · NIMH · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 2001 to 2010
$6.8M
Genetics of Brain Structure and FunctionR01MH078111 · NIMH · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 2006 to 2014
$4.5M
Genetics of Brain Structure and FunctionR01MH078143 · NIMH · YALE UNIVERSITY · PI GLAHN, DAVID C · 2006 to 2014
$4.3M
Construction of a Biomedical Research Facility at the U*C06RR020547 · NCRR · UNIV/TEXAS BROWNSVILLE & SOUTHMOST COLL · PI KROUSE, JOHN H · 2010 to 2010
$4.0M
Genetics of Brain Structure and Function: Genome-Wide AssociationR01MH083824 · NIMH · YALE UNIVERSITY · PI GLAHN, DAVID C · 2008 to 2013
$3.3M
Neurodevelopmental variation of intrinsic functional connectivity and its relationship to psychosis risk and gene expression - SupplementK01MH112774 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JALBRZIKOWSKI, MARIA · 2017 to 2022
$884k
QUANTITATIVE TRAIT LOCUS MAPPING IN HUMAN PEDIGREESR01MH059490 · NIMH · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI BLANGERO, JOHN · 1998 to 2000
$426k
NCRR NIH HHS C06 RR020547NHLBI NIH HHS R01 HL113323NIMH NIH HHS K01 MH112774NIMH NIH HHS R01 MH059490NIMH NIH HHS R01 MH078111NIMH NIH HHS R01 MH078143NIMH NIH HHS R01 MH083824NIMH NIH HHS R37 MH059490U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH059490U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH078111U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH078143U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH083824
6 · The paper itself

Abstract

Suicide is major public health concern; one million individuals worldwide die by suicide each year of which there are many more attempts. Thus, it is imperative that robust and reliable indicators, or biomarkers, of suicide risk be identified so that individuals at risk can be identified and provided appropriate interventions as quickly as possible. Previous work has revealed a relationship between low levels of circulating cholesterol and suicide risk, implicating cholesterol level as one such potential biomarker, but the factors underlying this relationship remain unknown. In the present study, we applied a combination of bivariate polygenic and coefficient-of-relatedness analysis, followed by mediation analysis, in a large sample of Mexican-American individuals from extended pedigrees [N = 1897; 96 pedigrees (average size = 19.17 individuals, range = 2-189) 60% female; mean age = 42.58 years, range = 18-97 years, sd = 15.75 years] with no exclusion criteria for any given psychiatric disorder. We observed that total esterified cholesterol measured at the time of psychiatric assessment shared a significant genetic overlap with risk for suicide attempt (ρ

Indexed as

Suicidal IdeationAdolescentAdultAgedAged, 80 and overCholesterolCohort StudiesDisease SusceptibilityFemaleGenetic Predisposition to DiseaseHumansMaleMental DisordersMiddle AgedPedigreeRisk FactorsCholesterol

Identifiers

PMID30082891
PMCPMC6224547
OpenAlexW2884827489

What OpenQuestion holds

Textmetadata
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.