Evidence map›Paper›PMID 39233675›Full record

ArticleFrontiers in neurology2024

Boundary-based registration improves sensitivity for detecting hypoperfusion in sporadic frontotemporal lobar degeneration.

Sylvia Mihailescu, Quinn Hlava, Philip A Cook, Maria Luisa Mandelli, Suzee E Lee, Bradley F Boeve, Bradford C Dickerson, Maria Luisa Gorno-Tempini, Emily Rogalski, Murray Grossman and 3 more

Abstract read
In one paragraph

Article in Frontiers in neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Sylvia MihailescuSchool of Engineering and Applied Sciences, University of Pennsylvania, Philadelphia, PA, United States.
Quinn HlavaDepartment of Neurology, University of Pennsylvania, Philadelphia, PA, United States.
Philip A CookDepartment of Radiology, University of Pennsylvania, Philadelphia, PA, United States.
Maria Luisa MandelliMemory and Aging Center, Department of Neurology, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
Suzee E LeeMemory and Aging Center, Department of Neurology, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
Bradley F BoeveDepartment of Neurology, Mayo Clinic, Rochester, MN, United States.
Bradford C DickersonDepartment of Neurology, Massachusetts General Hospital, Boston, MA, United States.
Maria Luisa Gorno-TempiniMemory and Aging Center, Department of Neurology, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, United States.
Emily RogalskiHealthy Aging & Alzheimer's Care Center, University of Chicago, Chicago, IL, United States.
Murray GrossmanDepartment of Neurology, University of Pennsylvania, Philadelphia, PA, United States.
James GeeDepartment of Radiology, University of Pennsylvania, Philadelphia, PA, United States.
Corey T McMillanDepartment of Neurology, University of Pennsylvania, Philadelphia, PA, United States.
Christopher A OlmDepartment of Neurology, University of Pennsylvania, Philadelphia, PA, United States.

Funding

Technology and Remote Assessment CoreU19AG063911 · NIA · MAYO CLINIC ROCHESTER · PI ADAM L. BOXER, Bradley F Boeve · 2019 to 2026
$120.9M
Understanding Environmental Contributions to Heterogeneity in bvFTD.P01AG066597 · NIA · UNIVERSITY OF PENNSYLVANIA · PI David John Irwin, Corey T McMillan · 2020 to 2026
$18.8M
Connectomic imaging in familial and sporadic frontotemporal degenerationU01AG052943 · NIA · UNIVERSITY OF PENNSYLVANIA · PI GORNO TEMPINI, MARIA LUISA, GROSSMAN, MURRAY · 2016 to 2019
$5.9M
NIA NIH HHS P01 AG066597NIA NIH HHS U01 AG052943NIA NIH HHS U19 AG063911
6 · The paper itself

Abstract

Introduction: Frontotemporal lobar degeneration (FTLD) is associated with FTLD due to tau (FTLD-tau) or TDP (FTLD-TDP) inclusions found at autopsy. Arterial Spin Labeling (ASL) MRI is often acquired in the same session as a structural T1-weighted image (T1w), enabling detection of regional changes in cerebral blood flow (CBF). We hypothesize that ASL-T1w registration with more degrees of freedom using boundary-based registration (BBR) will better align ASL and T1w images and show increased sensitivity to regional hypoperfusion differences compared to manual registration in patient participants. We hypothesize that hypoperfusion will be associated with a clinical measure of disease severity, the FTLD-modified clinical dementia rating scale sum-of-boxes (FTLD-CDR). Materials and methods: Patients with sporadic likely FTLD-tau (sFTLD-tau; Results: All registration methods demonstrated significant hypoperfusion in frontal and temporal regions in each patient group relative to controls. All registration methods detected hypoperfusion in the left insular cortex, middle temporal gyrus, and temporal pole in sFTLD-TDP relative to sFTLD-tau. FTLD-CDR had an inverse association with CBF in right temporal and orbitofrontal ROIs in sFTLD-TDP. Manual+BBR performed similarly to FLIRT+BBR. Discussion: ASL is sensitive to distinct regions of hypoperfusion in patient participants relative to controls, and in patients with sFTLD-TDP relative to sFTLD-tau, and decreasing perfusion is associated with increasing disease severity, at least in sFTLD-TDP. BBR can register ASL-T1w images adequately for controls and patients.

Indexed as

arterial spin labelingboundary-based registrationcerebral blood flowfrontotemporal lobar degenerationimage registration

Identifiers

PMID39233675
PMCPMC11371585

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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.