Evidence map›Paper›PMID 39714256›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2024

The early-onset Alzheimer's disease MRI signature: a replication and extension analysis in early-stage AD.

Rashi I Mehta, Cierra M Keith, Camila Vieira Ligo Teixeira, Patrick D Worhunsky, Holly E Phelps, Melanie Ward, Mark Miller, R Osvaldo Navia, Stephanie Pockl, Nafiisah Rajabalee and 5 more

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

15 authors.

Rashi I MehtaRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.ORCID 0000-0002-2532-7435
Cierra M KeithRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Camila Vieira Ligo TeixeiraRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Patrick D WorhunskyRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Holly E PhelpsRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Melanie WardRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Mark MillerRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
R Osvaldo NaviaRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Stephanie PocklRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Nafiisah RajabaleeRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Michelle M ColemanRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Pierre-François D'HaeseRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Ali R RezaiRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Kirk C WilhelmsenRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.
Marc W HautRockefeller Neuroscience Institute 33 Medical Center Dr. Morgantown, WV 26505, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early-onset Alzheimer's disease (EOAD) is less investigated than the more common late-onset Alzheimer's disease (LOAD) despite its more aggressive course. A cortical signature of EOAD was recently proposed and may facilitate EOAD investigation. Here, we aimed to validate this proposed MRI biomarker of EOAD neurodegeneration in an Appalachian clinical cohort. We also compared differences in EOAD signature atrophy in participants with biomarker-positive EOAD, LOAD, early-onset non-AD pathologies, and cognitively normal individuals. Cortical thinning was reliably detected in eight of nine signature areas of persons with EOAD relative to cognitively normal individuals despite very early disease stage. Additionally, individuals with EOAD showed thinner cortex in most signature regions relative to those with early-onset non-AD pathologies. EOAD and LOAD showed similar cortical atrophy within most EOAD signature regions. Whole-brain vertex-wise cortical analyses supported these findings. Furthermore, signature cortical atrophy showed expected relationships with measures of global and specific cognitive and functional status. This investigation further validates and expands upon the recently defined EOAD signature and suggests its robustness within a rural population, even at early disease stage. Larger scale and longitudinal studies employing this marker of EOAD neurodegeneration are needed to further understand clinical effects and appropriate management of persons with EOAD.

Indexed as

Alzheimer DiseaseAtrophyMagnetic Resonance ImagingAgedAge of OnsetBrainCerebral CortexCohort StudiesFemaleHumansMaleMiddle Agedamyloidcortical thicknessearly-onset Alzheimer’s diseaseMRIneuroimaging

Identifiers

PMID39714256
PMCPMC11664631

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.