Evidence map›Paper›PMID 24985533›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2014

APOE ε4 influences β-amyloid deposition in primary progressive aphasia and speech apraxia.

Keith A Josephs, Joseph R Duffy, Edythe A Strand, Mary M Machulda, Matthew L Senjem, Val J Lowe, Clifford R Jack, Jennifer L Whitwell

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. An Update on Apraxia of Speech.Current neurology and neuroscience reports · 2023
    Review
  6. Article
  7. Article
  8. Frontiers in neuroscience · 2023
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Longitudinal flortaucipir ([Cortex; a journal devoted to the study of the nervous system and behavior · 2020
    Article
  15. Article
  16. Article
  17. FTD spectrum: Neuroimaging across the FTD spectrum.Progress in molecular biology and translational science · 2019
    Review
  18. [Annals of neurology · 2018
    Article
  19. Tau-PET imaging with [18F]AV-1451 in primary progressive apraxia of speech.Cortex; a journal devoted to the study of the nervous system and behavior · 2018
    Article
  20. 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

8 authors at 3 institutions in 1 country.

Keith A JosephsDivision of Behavioral Neurology, Department of Neurology, Mayo Clinic, Rochester, MN, USA; Division of Movement Disorders, Department of Neurology, Mayo Clinic, Rochester, MN, USA. Electronic address: Josephs.keith@mayo.edu.
Joseph R DuffyDivision of Speech Pathology, Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Edythe A StrandDivision of Speech Pathology, Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Mary M MachuldaDivision of Neuropsychology, Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA.
Matthew L SenjemDepartment of Information Technology, Mayo Clinic, Rochester, MN, USA.
Val J LoweDivision of Nuclear Medicine, Department of Radiology, Mayo Clinic, Rochester, MN, USA.
Clifford R JackDivision of Neuroradiology, Department of Radiology, Mayo Clinic, Rochester, MN, USA.
Jennifer L WhitwellDivision of Neuroradiology, Department of Radiology, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic · USMayo Clinic in Arizona · USWinnMed · US

Funding

PIB PET Scanning in Speech and Language Based DementiasR01DC010367 · NIDCD · MAYO CLINIC ROCHESTER · PI JOSEPHS, KEITH A · 2010 to 2014
$1.7M
NIDCD NIH HHS R01 DC010367
6 · The paper itself

Abstract

backgroundApolipoprotein E ε4 (APOE ε4) is a risk factor for β-amyloid deposition in Alzheimer's disease dementia. Its influence on β-amyloid deposition in speech and language disorders, including primary progressive aphasia (PPA), is unclear.

methodsOne hundred thirty subjects with PPA or progressive speech apraxia underwent APOE genotyping and Pittsburgh compound B (PiB) PET scanning. The relationship between APOE ε4 and PiB status, as well as severity and regional distribution of PiB, was assessed.

resultsForty-five subjects had an APOE ε4 allele and 60 subjects were PiB-positive. The odds ratio for a subject with APOE ε4 being PiB-positive compared with a subject without APOE ε4 being PiB-positive was 10.2 (95% confidence interval, 4.4-25.5; P < .0001). The APOE ε4 allele did not influence regional PiB distribution or severity.

conclusionAPOE ε4 increases the risk of β-amyloid deposition in PPA and progressive speech apraxia but does not influence regional β-amyloid distribution or severity.

Indexed as

AgedAged, 80 and overAmyloid beta-PeptidesAniline CompoundsAphasia, Primary ProgressiveApolipoprotein E4ApraxiasBrain MappingFemaleHumansMaleMiddle AgedPositron-Emission TomographyThiazoles2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazoleAmyloid beta-PeptidesAniline CompoundsApolipoprotein E4ThiazolesApolipoproteinLogopenic aphasiaPittsburgh compound BPrimary progressive aphasiaSpeech apraxia

Identifiers

PMID24985533
PMCPMC4254054
OpenAlexW2016105622

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.