Evidence map›Paper›PMID 24650791›Full record

ArticleNeurobiology of aging2014

Genetic variation of oxidative phosphorylation genes in stroke and Alzheimer's disease.

Alessandro Biffi, Mert R Sabuncu, Rahul S Desikan, Nick Schmansky, David H Salat, Jonathan Rosand, Christopher D Anderson, Alzheimer's disease Neuroimaging Initiative (ADNI)

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of aging, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Mitochondria in Alzheimer's Disease Pathogenesis.Life (Basel, Switzerland) · 2024
    Review
  4. Article
  5. Review
  6. Article
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  10. Review
  11. Article
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  13. Article
  14. Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2015
    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

8 authors at 4 institutions in 1 country.

Alessandro BiffiDivision of Neurocritical Care and Emergency Neurology, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA; Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, USA. Electronic address: abiffi@partners.org.
Mert R SabuncuAthinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA, USA; Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, MA, USA.
Rahul S DesikanDepartment of Radiology, University of California, San Diego, CA, USA.
Nick SchmanskyAthinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA, USA.
David H SalatDivision of Neurocritical Care and Emergency Neurology, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA.
Jonathan RosandDivision of Neurocritical Care and Emergency Neurology, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA; Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, USA.
Christopher D AndersonDivision of Neurocritical Care and Emergency Neurology, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA; Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, USA.
Alzheimer's disease Neuroimaging Initiative (ADNI)
Broad Institute · USMassachusetts General Hospital · USUniversity of California San Diego · USVA Boston Healthcare System · US

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
RECRUITMENT COREU19AG010483 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FELDMAN, HOWARD · 2013 to 2020
$80.6M
Smartphone-Based "Burst" Cognitive AssessmentsP01AG003991 · NIA · WASHINGTON UNIVERSITY · PI Suzanne Elizabeth Schindler · 1985 to 2026
$69.5M
WASHINGTON UNIVERSITY ALZHEIMERS DISEASE RESEARCH CENTERP50AG005681 · NIA · WASHINGTON UNIVERSITY · PI MORRIS, JOHN · 1985 to 2019
$52.1M
Ethnic/Racial Variation in Intracerebral Hemorrhage (ERICH)U01NS069763 · NINDS · UNIVERSITY OF CINCINNATI · PI ANDERSON, CHRISTOPHER DAVID, DEMEL, STACIE · 2010 to 2024
$34.2M
MORPHOMETRY BIOMEDICAL INFORMATICS RESEARCH NETWORKU24RR021382 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI ROSEN, BRUCE R · 2004 to 2008
$24.1M
ULTRAHIGH FIELD TECHNOLOGY FOR FUNCTIONAL IMAGINGP41RR014075 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI ROSEN, BRUCE R · 1999 to 2011
$16.4M
The NINDS International Stroke Genetics Consortium StudyU01NS069208 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI HOWARD, GEORGE, KITTNER, STEVEN J · 2010 to 2013
$9.4M
Vascular Dysfunction in Cerebral Amyloid AngiopathyR01AG026484 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI GREENBERG, STEVEN M · 2005 to 2019
$7.5M
Prospective Neuroimaging in Huntington's DiseaseR01NS042861 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ROSAS, HERMINIA DIANA · 2003 to 2013
$5.6M
Cerebrovascular Contributions to Brain Aging and DementiaR01NR010827 · NINR · MASSACHUSETTS GENERAL HOSPITAL · PI SALAT, DAVID H · 2007 to 2017
$5.0M
Gene Discovery for Warfarin-Related Intracerebral HemorrhageR01NS059727 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ROSAND, JONATHAN · 2008 to 2012
$4.2M
NCRR NIH HHS P41 RR014075NCRR NIH HHS P41-RR014075NCRR NIH HHS P41-RR14075NCRR NIH HHS R01 RR016594NCRR NIH HHS R01 RR16594-01A1NCRR NIH HHS U24 RR021382NHLBI NIH HHS K23 HL093023NHLBI NIH HHS R01 HL093023NIA NIH HHS AG021910NIA NIH HHS AG02238NIA NIH HHS F30 AG041681NIA NIH HHS P01 AG003991NIA NIH HHS P01AG03991NIA NIH HHS P50 AG005681NIA NIH HHS P50AG05681NIA NIH HHS R01 AG021910NIA NIH HHS R01 AG026484NIA NIH HHS R01-AG026484NIA NIH HHS R01 AG031224NIA NIH HHS R01AG031224NIA NIH HHS U01 AG024904NIA NIH HHS U01AG024904NIA NIH HHS U19 AG010483NIBIB NIH HHS 1K25EB013649-01NIBIB NIH HHS K25 EB013649NIBIB NIH HHS R01 EB001550NIBIB NIH HHS R01 EB006758NIBIB NIH HHS R01EB006758NIBIB NIH HHS T32 EB005970NIDA NIH HHS R33 DA026104NIDA NIH HHS R33-DA026104NINDS NIH HHS K23 NS086873NINDS NIH HHS R01 NS042861NINDS NIH HHS R01-NS042861NINDS NIH HHS R01 NS052585NINDS NIH HHS R01 NS052585-01NINDS NIH HHS R01 NS052585E01NINDS NIH HHS R01 NS059727NINDS NIH HHS R01NS059727NINDS NIH HHS R01 NS063925NINDS NIH HHS R01NS063925NINDS NIH HHS R01 NS070834NINDS NIH HHS R01-NS070834NINDS NIH HHS R01 NS070963NINDS NIH HHS R01-NS070963NINDS NIH HHS U01 NS069208NINDS NIH HHS U01NS069208NINDS NIH HHS U01 NS069763NINDS NIH HHS U01NS069763NINR NIH HHS R01 NR010827
6 · The paper itself

Abstract

Previous research implicates alterations in oxidative phosphorylation (OXPHOS) in the development of Alzheimer's disease (AD). We sought to test whether genetic variants within OXPHOS genes increase the risk of AD. We first used gene-set enrichment analysis to identify associations, and then applied a previously replicated stroke genetic risk score to determine if OXPHOS genetic overlap exists between stroke and AD. Gene-set enrichment analysis identified associations between variation in OXPHOS genes and AD versus control status (p = 0.012). Conversion from cognitively normal controls to mild cognitive impairment was also associated with the OXPHOS gene-set (p = 0.045). Subset analyses demonstrated association for complex I genes (p < 0.05), but not for complexes II-V. Among neuroimaging measures, hippocampal volume and entorhinal cortex thickness were associated with OXPHOS genes (all p < 0.025). The stroke genetic risk score demonstrated association with clinical status, baseline and longitudinal imaging measures (p < 0.05). OXPHOS genetic variation influences clinical status and neuroimaging intermediates of AD. OXPHOS genetic variants associated with stroke are also linked to AD progression. Further studies are needed to explore functional consequences of these OXPHOS variants.

Indexed as

Genetic Association StudiesOxidative PhosphorylationAgedAlzheimer DiseaseCognitive DysfunctionElectron Transport Complex IEntorhinal CortexFemaleGenetic VariationHippocampusHumansMagnetic Resonance ImagingMaleNeuroimagingOrgan SizePolymorphism, Single NucleotideElectron Transport Complex IAlzheimer's diseaseGenesMitochondriaOXPHOSStroke

Identifiers

PMID24650791
PMCPMC4329419
OpenAlexW2080544548

What OpenQuestion holds

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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.