Evidence map›Paper›PMID 33068458›Full record

ArticleEuropean journal of neurology2021

Association of amyloid angiopathy with microbleeds in logopenic progressive aphasia: an imaging-pathology study.

M Buciuc, J R Duffy, M M Machulda, A J Spychalla, J L Gunter, C R Jack, C Giannini, A Raghunathan, D W Dickson, K A Josephs and 1 more

Open access · greenAbstract read
In one paragraph

Article in European journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

M BuciucDepartment of Neurology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0003-4826-5430
J R DuffyDepartment of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
M M MachuldaDepartment of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota, USA.
A J SpychallaDepartment of Radiology, Mayo Clinic, Rochester, Minnesota, USA.
J L GunterDepartment of Radiology, Mayo Clinic, Rochester, Minnesota, USA.
C R JackDepartment of Radiology, Mayo Clinic, Rochester, Minnesota, USA.
C GianniniDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
A RaghunathanDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
D W DicksonDepartment of Neuroscience, Mayo Clinic, Jacksonville, Florida, USA.
K A JosephsDepartment of Neurology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0003-2930-8634
J L WhitwellDepartment of Radiology, Mayo Clinic, Rochester, Minnesota, USA.
Mayo Clinic · USJacksonville College · US

Funding

Molecular and structural imaging in atypical Alzheimer's disease: a longitudinal studyR01AG050603 · NIA · MAYO CLINIC ROCHESTER · PI WHITWELL, JENNIFER LOUISE · 2016 to 2025
$5.9M
PIB PET Scanning in Speech and Language Based DementiasR01DC010367 · NIDCD · MAYO CLINIC ROCHESTER · PI JOSEPHS, KEITH A · 2010 to 2014
$1.7M
NIA NIH HHS R01 AG050603NIDCD NIH HHS R01 DC010367NIH HHS NIRG-12-242215NIH HHS R01-AG50603NIH HHS R01-DC10367
6 · The paper itself

Abstract

background and purposeCerebral microbleeds (MB) and superficial siderosis (SS) are frequent neuroimaging findings in patients with logopenic progressive aphasia (LPA), often with frontal lobe predilection. Cerebral amyloid angiopathy (CAA) is hypothesized to be the major pathologic determinant of MB/SS in these patients; however, neuroimaging-pathologic data are limited.

methodsAll patients who had been prospectively recruited by the Neurodegenerative Research Group at the Mayo Clinic (Rochester, MN) between 2010 and 2015 and met the following inclusion criteria were included: (i) received an antemortem LPA diagnosis, (ii) had a gradient-recalled echo T2*-weighted magnetic resonance imaging (MRI) performed, (iii) died and completed a brain autopsy. Demographic, genetic, neuroimaging, and clinical and pathologic characteristics were compared between patients with/without MB/SS. Two-tailed Fisher exact and Wilcoxon rank sum tests were used for comparison of categorical and continuous variables, respectively.

resultsThirteen patients met inclusion criteria, six (46%) had MB/SS on MRI. Moderate/severe CAA was associated with the presence of MB/SS (p = 0.029). As expected, MB/SS most frequently involved the frontal lobes, followed by the parietal lobes. No clear associations were found between regional MB/SS distribution and regional distribution of CAA or hypometabolism on [

conclusionsThe presence of MB/SS is a strong indicator of underlying moderate/severe CAA in LPA, although the biological mechanisms underlying the topographic distribution of MB/SS remain unclear.

Indexed as

AphasiaCerebral Amyloid AngiopathyCerebral HemorrhageHumansMagnetic Resonance ImagingPositron-Emission Tomographyatypical Alzheimer’s diseasecerebral amyloid angiopathylogopenic progressive aphasiamagnetic resonance imagingmicrobleedspositron emission tomography

Identifiers

PMID33068458
PMCPMC8174551
OpenAlexW3092836587

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.