Evidence map›Paper›PMID 20724716›Full record

ArticleStroke2010

Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses.

Peter Kochunov, David Glahn, Jack Lancaster, Anderson Winkler, Jack W Kent, Rene L Olvera, Shelley A Cole, Thomas D Dyer, Laura Almasy, Ravi Duggirala and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Stroke, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. The genetic and environmental etiology of novel frequency-driven regional parcellations of abnormal white matter.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2025
    Article
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  6. Cardiovascular risks impact human brainProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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  9. Article
  10. Epigenetic Age Acceleration Assessed with Human White-Matter Images.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Blood and CSF biomarkers in brain subcortical ischemic vascular disease: Involved pathways and clinical applicability.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2016
    Review
  15. 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

12 authors at 1 institution in 1 country.

Peter KochunovDip ABMP, Research Imaging Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78284, USA. kochunov@uthscsa.edu
David Glahn
Jack Lancaster
Anderson Winkler
Jack W Kent
Rene L Olvera
Shelley A Cole
Thomas D Dyer
Laura Almasy
Ravi Duggirala
Peter T Fox
John Blangero
Neuropsychiatric Research Institute · US

Funding

PEDIGREE ANALYSIS OF LIPOPROTEIN PHENOTYPESP01HL045522 · NHLBI · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 1991 to 2012
$27.6M
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 Function: Genome-Wide AssociationR01MH083824 · NIMH · YALE UNIVERSITY · PI GLAHN, DAVID C · 2008 to 2013
$3.3M
COMBINING NEUROIMAGING AND GENETICS FOR HERITABILITY MEASUREMENTSK01EB006395 · NIBIB · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI KOCHUNOV, PETER V. · 2007 to 2011
$733k
NHLBI NIH HHS P01 HL045522NHLBI NIH HHS P01HL045522NIBIB NIH HHS K01 EB006395NIMH NIH HHS R01MH0708143NIMH NIH HHS R01 MH078111NIMH NIH HHS R01MH078111NIMH NIH HHS R01 MH083824NIMH NIH HHS R01MH083824NIMH NIH HHS R37 MH059490NIMH NIH HHS R37MH059490
6 · The paper itself

Abstract

background and purposeThe volume of T2-hyperintense white matter (HWM) is an important neuroimaging marker of cerebral integrity with a demonstrated high heritability. Pathophysiology studies have shown that the regional, ependymal, and subcortical HWM lesions are associated with elevated arterial pulse pressure and arterial blood pressure (BP), respectively. We performed bivariate, whole-genome linkage analyses for HWM volumes and BP measurements to identify chromosomal regions that contribute jointly to both traits in a population of healthy Mexican Americans. Our aims were to localize novel quantitative trait loci acting pleiotropically on these phenotypes and to replicate previous genetic findings on whole brain HWM volume and BP measurements.

methodsBP measurements and volumes of whole-brain (WB), subcortical, and ependymal HWM lesions, measured from high-resolution (1 mm(3)) 3-dimensional fluid-attenuated inversion recovery images, served as focal quantitative phenotypes. Data were collected from 357 (218 females; mean age=47.9±13.2 years) members of large extended families who participated in the San Antonio Family Heart Study.

resultsBivariate genomewide linkage analyses localized a significant quantitative trait locus influencing WB and regional (ependymal) HWM volumes and pulse pressure and systolic BP to chromosomal location 1q24 between markers D1S196 and D1S1619. Several other chromosomal regions (1q42, 10q24-q26, and 15q26) exhibited suggestive linkages. The results of the post hoc analyses that excluded 55 subjects taking antihypertensive medication showed no substantive differences from the results obtained in the full cohort.

conclusionsThis study confirms several previously observed quantitative trait loci influencing BP and cerebral integrity and identifies a novel significant quantitative trait locus at chromosome 1q24. The genetic results strongly support a role for pleiotropically acting genes jointly influencing BP and cerebral white matter integrity.

Indexed as

Genetic LinkageGenetic LociAdultAgedAged, 80 and overBlood PressureBrainFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansLod ScoreMagnetic Resonance ImagingMaleMexican Americans

Identifiers

PMID20724716
PMCPMC3084627
OpenAlexW2116887309

What OpenQuestion holds

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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.