Evidence map›Paper›PMID 28402004›Full record

ArticleHuman brain mapping2017

The VEGF gene polymorphism impacts brain volume and arterial blood volume.

Hikaru Takeuchi, Hiroaki Tomita, Yasuyuki Taki, Yoshie Kikuchi, Chiaki Ono, Zhiqian Yu, Atsushi Sekiguchi, Rui Nouchi, Yuka Kotozaki, Seishu Nakagawa and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Human brain mapping, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. The Janus Face of VEGF in Stroke.International journal of molecular sciences · 2018
    Review
  8. The Chinese herbal formulaNeuropsychiatric disease and treatment · 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

20 authors at 2 institutions in 1 country.

Hikaru TakeuchiDivision of Developmental Cognitive Neuroscience, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0002-8022-9694
Hiroaki TomitaDepartment of Disaster Psychiatry, International Research Institute of Disaster Science, Tohoku University, Sendai, Japan.
Yasuyuki TakiDivision of Developmental Cognitive Neuroscience, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.
Yoshie KikuchiDepartment of Disaster Psychiatry, International Research Institute of Disaster Science, Tohoku University, Sendai, Japan.
Chiaki OnoDepartment of Disaster Psychiatry, International Research Institute of Disaster Science, Tohoku University, Sendai, Japan.
Zhiqian YuDepartment of Disaster Psychiatry, International Research Institute of Disaster Science, Tohoku University, Sendai, Japan.
Atsushi SekiguchiDivision of Medical Neuroimage Analysis, Department of Community Medical Supports, Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Rui NouchiHuman and Social Response Research Division, International Research Institute of Disaster Science, Tohoku University, Sendai, Japan.
Yuka KotozakiSmart Ageing International Research Center, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.
Seishu NakagawaDepartment of Functional Brain Imaging, Institute of Development, Aging and Cancer, Tohoku University, Sendai Japan.
Carlos Makoto MiyauchiGraduate School of Arts and Sciences, Department of General Systems Studies, The University of Tokyo, Tokyo, Japan.
Kunio IizukaDepartment of Functional Brain Imaging, Institute of Development, Aging and Cancer, Tohoku University, Sendai Japan.
Ryoichi YokoyamaDepartment of Functional Brain Imaging, Institute of Development, Aging and Cancer, Tohoku University, Sendai Japan.
Takamitsu ShinadaDepartment of Functional Brain Imaging, Institute of Development, Aging and Cancer, Tohoku University, Sendai Japan.
Yuki YamamotoDepartment of Functional Brain Imaging, Institute of Development, Aging and Cancer, Tohoku University, Sendai Japan.
Sugiko HanawaDepartment of Functional Brain Imaging, Institute of Development, Aging and Cancer, Tohoku University, Sendai Japan.
Tsuyoshi ArakiSmart Ageing International Research Center, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.
Keiko KunitokiFaculty of Medicine, Tohoku University, Sendai, Japan.
Yuko SassaDivision of Developmental Cognitive Neuroscience, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.
Ryuta KawashimaDivision of Developmental Cognitive Neuroscience, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.
Tohoku University · JPTokyo University of the Arts · JP

Funding

Grant-in-Aid for Young Scientists (A) from the Ministry of Education, Culture, Sports, Science, and TechnologyJST/RISTEX, JST/CRESTKAKENHI 23700306KAKENHI 25700012
6 · The paper itself

Abstract

Vascular endothelial growth factor (VEGF) plays a critical role in the angiogenesis and proliferation of various types of cells such as neurons, astroglia, and endothelial cells in the brain. A common polymorphism in the VEGF gene (-2578 C/A) is associated with circulating VEGF levels, cancers and Alzheimer's disease. Nonetheless, the effects of this polymorphism on normal human brain volume, arterial blood volume, and blood supply remain unclear. In this study, the effects of this polymorphism on the total gray matter volume (TGMV) and total white matter volume (TWMV) using T1-weighted structural images and the total arterial blood volume (TABV) and mean cerebral blood flow (mCBF) during rest using arterial spin labeling (ASL) in 765 young adult humans were investigated. Voxel-by-voxel whole-brain analyses of these measures were also performed. Multiple regression analyses with age and sex as covariates revealed that the VEGF genotype (number of C alleles) was significantly and positively correlated with TGMV, TWMV, and TABV as well as with regional gray and white matter volumes in widespread areas and regional arterial blood volume in some areas with high arterial blood volume. However, these regional associations were not seen when the corresponding global signal was included as a covariate in the multiple regression analyses, indicating that we failed to obtain evidence of region-specific associations between these brain measures and the genotype. The results suggest that the VEGF-2578C allele, is associated with changes in the vascular system that lead to increased blood volume and larger brain volume. Hum Brain Mapp 38:3516-3526, 2017. © 2017 Wiley Periodicals, Inc.

Indexed as

blood volumebrainbrain volumepolymorphismVEGF

Identifiers

PMID28402004
PMCPMC6866916
OpenAlexW2605397563

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.