Evidence map›Paper›PMID 41503006›Full record

ArticleImaging neuroscience (Cambridge, Mass.)2026

Detecting patterns of atrophy in cognitively impaired individuals using portable, low-field MRI.

Ava Farnan, Annabel J Sorby-Adams, Jennifer Guo, John R Dickson, Liliana Ramirez Gomez, Amanda DeSenna, John E Kirsch, Joel Smith, Emma Peasley, Jeremy Ford and 11 more

Abstract read
In one paragraph

Article in Imaging neuroscience (Cambridge, Mass.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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

21 authors.

Ava FarnanDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.ORCID 0009-0002-5189-1563
Annabel J Sorby-AdamsDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Jennifer GuoDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
John R DicksonDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Liliana Ramirez GomezDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Amanda DeSennaDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
John E KirschAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Joel SmithDepartment of Neurology, Center for Brain & Mind Health, Yale New Haven Hospital and Yale School of Medicine, New Haven, CT, United States.
Emma PeasleyDepartment of Neurology, Center for Brain & Mind Health, Yale New Haven Hospital and Yale School of Medicine, New Haven, CT, United States.
Jeremy FordDivision of Neuroradiology, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Seyedmehdi PayabvashDepartment of Radiology, Colombia University, New York, NY, United States.
Gordon SzeDivision of Neuroradiology, Department of Radiology and Biomedical Imaging, Yale New Haven Hospital and Yale University School of Medicine, New Haven, CT, United States.
Arman Fesharaki-ZadehDepartment of Neurology, Center for Brain & Mind Health, Yale New Haven Hospital and Yale School of Medicine, New Haven, CT, United States.
Christopher van DyckDepartment of Neurology, Center for Brain & Mind Health, Yale New Haven Hospital and Yale School of Medicine, New Haven, CT, United States.
Matthew S RosenAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Kevin N ShethDepartment of Neurology, Center for Brain & Mind Health, Yale New Haven Hospital and Yale School of Medicine, New Haven, CT, United States.
J Eugenio IglesiasAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Adam de HavenonDepartment of Neurology, Center for Brain & Mind Health, Yale New Haven Hospital and Yale School of Medicine, New Haven, CT, United States.
Alberto Serrano PozoDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Teresa Gomez-IslaDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
W Taylor KimberlyDepartment of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.ORCID 0000-0002-2519-8530

Funding

Functionally guided adult whole brain cell atlas in human and NHPUM1MH130981 · NIMH · ALLEN INSTITUTE · PI Ed Lein, Hongkui Zeng · 2022 to 2026
$91.9M
Portable, Low Field Brain Magnetic Resonance Imaging (MRI) for Acute StrokeR01EB031114 · NIBIB · YALE UNIVERSITY · PI William Taylor Kimberly, Matthew Scot Rosen · 2022 to 2026
$3.5M
NIBIB NIH HHS R01 EB031114NIMH NIH HHS UM1 MH130981
6 · The paper itself

Abstract

Low-field MRI (LF-MRI) is an emerging neuroimaging approach for evaluating patients with dementia, offering greater accessibility and lower cost, albeit with reduced image resolution. In this study, we deployed LF-MRI in an outpatient clinic and analyzed images with a multi-functional artificial intelligence (AI) algorithm (WMH-SynthSeg) to generate segmentation volumes of 16 brain regions. We validated the accuracy of the quantifications compared with conventional, high-field (HF) MRI in healthy volunteers and subsequently applied the algorithm to aged subjects with mild cognitive impairment (MCI) or dementia due to Alzheimer's disease (AD), and to similarly aged subjects with cognitive impairment and vascular comorbidities (VC). Agreement between HF- and LF-derived brain volumes was high across cohorts and brain regions, with the highest correlations in the cortex, white matter, lateral ventricles, third ventricle, caudate, and amygdala (all r > 0.80, p < 0.001). The MCI and AD cohorts showed regional atrophy relative to the VC cohort, including the cortex, hippocampus, amygdala, putamen, and nucleus accumbens (all p < 0.001) but not the caudate, ventral diencephalon, and fourth ventricle (p > 0.05). Taken together, LF-MRI paired with an AI segmentation algorithm can generate brain volumes comparable with those derived from conventional MRI, allowing for differentiation between VC and AD/MCI subgroups. Our findings demonstrate that LF-MRI could be used at the point-of-care for evaluation of patients with dementia of different etiologies.

Indexed as

artificial intelligencedementialow-field MRIsegmentation

Identifiers

PMID41503006
PMCPMC12770908

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.