Evidence map›Paper›PMID 24026422›Full record

ArticleHuman genetics2014

Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography.

Mary Ellen I Koran, Timothy J Hohman, Tricia A Thornton-Wells

Open access · greenAbstract read
In one paragraph

Article in Human genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  13. Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2016
    Article
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  20. Dantrolene, a treatment for Alzheimer disease?Alzheimer disease and associated disorders
    Review
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

3 authors at 2 institutions in 1 country.

Mary Ellen I KoranMedical Scientist Training Program, Center for Human Genetics and Research, Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, TN, 37232, USA, maryellen.koran@gmail.com.
Timothy J Hohman
Tricia A Thornton-Wells
Vanderbilt University Medical Center · USCenter for Human Genetics · US

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
RECRUITMENT COREU19AG010483 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FELDMAN, HOWARD · 2013 to 2020
$80.6M
UC Davis Alzheimer's Disease Core CenterP30AG010129 · NIA · UNIVERSITY OF CALIFORNIA DAVIS · PI DECARLI, CHARLES · 1991 to 2020
$28.3M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Program in NeurogenomicsT32MH065215 · NIMH · VANDERBILT UNIVERSITY · PI ROGER J COLBRAN · 2002 to 2026
$6.4M
Recruitment of Faculty for Genetic Aging ResearchP30AG036445 · NIA · VANDERBILT UNIVERSITY · PI HAINES, JONATHAN L · 2009 to 2010
$977k
"MR Morphometrics and Cognitive Decline Rate in Large-Scale Aging Studies"K01AG030514 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CARMICHAEL, OWEN T. · 2008 to 2012
$495k
NIA NIH HHS K01 AG030514NIA NIH HHS P30 AG010129NIA NIH HHS P30 AG036445NIA NIH HHS U01 AG024904NIA NIH HHS U19 AG010483NIA NIH HHS U24 AG021886NIGMS NIH HHS T32 GM007347NIGMS NIH HHS T32 GM07347NIMH NIH HHS T32 MH065215NIMH NIH HHS T32 MH65215
6 · The paper itself

Abstract

Late-onset Alzheimer's disease (LOAD) is known to have a complex, oligogenic etiology, with considerable genetic heterogeneity. We investigated the influence of genetic interactions between genes in the Alzheimer's disease (AD) pathway on amyloid-beta (Aβ) deposition as measured by PiB or AV-45 ligand positron emission tomography (PET) to aid in understanding LOAD's genetic etiology. Subsets of the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohorts were used for discovery and for two independent validation analyses. A significant interaction between RYR3 and CACNA1C was confirmed in all three of the independent ADNI datasets. Both genes encode calcium channels expressed in the brain. The results shown here support previous animal studies implicating interactions between these calcium channels in amyloidogenesis and suggest that the pathological cascade of this disease may be modified by interactions in the amyloid-calcium axis. Future work focusing on the mechanisms of such relationships may inform targets for clinical intervention.

Indexed as

Epistasis, GeneticPositron-Emission TomographyAgedAged, 80 and overAlzheimer DiseaseAmyloid beta-PeptidesApolipoprotein E4BrainCalcium Channels, L-TypeChromosome MappingFemaleGenotypeHomeostasisHumansMalePolymorphism, Single NucleotideAmyloid beta-PeptidesApolipoprotein E4CACNA1C protein, humanCalcium Channels, L-TypeRyanodine Receptor Calcium Release Channel

Identifiers

PMID24026422
PMCPMC4045094
OpenAlexW2115469076

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.