Evidence map›Paper›PMID 32350336›Full record

ArticleScientific reports2020

Identifying a subtype of Alzheimer's disease characterised by predominant right focal cortical atrophy.

Ko Woon Kim, Seongbeom Park, Hyunjin Jo, Soo Hyun Cho, Seung Joo Kim, Yeshin Kim, Hyemin Jang, Duk L Na, Sang Won Seo, Hee Jin Kim

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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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

10 authors at 2 institutions in 1 country.

Ko Woon Kim *Department of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Seongbeom Park *Department of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Hyunjin JoDepartment of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.ORCID http://orcid.org/0000-0001-9563-1849
Soo Hyun ChoDepartment of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Seung Joo KimDepartment of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Yeshin KimDepartment of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Hyemin JangDepartment of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.ORCID http://orcid.org/0000-0003-3152-1274
Duk L NaDepartment of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Sang Won SeoDepartment of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Hee Jin KimDepartment of Neurology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea. evekhj@gmail.com.
Samsung Medical Center · KRChangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to identify an Alzheimer's disease (AD) subtype with right predominant focal atrophy. We recruited 17 amyloid PET positive logopenic variant primary progressive aphasia (lvPPA) and 226 amyloid PET positive AD patients. To identify AD with right focal atrophy (Rt-AD), we selected cortical areas that showed more atrophy in lvPPA than in AD and calculated an asymmetry index (AI) for this area in each individual. Using a receiver operating characteristic curve, we found that the optimal AI cut-off to discriminate lvPPA from AD was -3.1 (mean AI - 1.00 standard deviation) (sensitivity 88.2, specificity 89.8). We identified 32 Rt-AD patients whose AI was above mean AI + 1.00 standard deviation, 38 Lt-AD patients whose AI was lower than mean AI - 1.00 standard deviation, and 173 Symmetric-AD patients whose AI was within mean AI ± 1.00 standard deviation. We characterized clinical and cognitive profiles of Rt-AD patients by comparing with those of Lt-AD and Symmetric-AD patients. Compared to Symmetric-AD patients, Rt-AD patients had asymmetric focal atrophy in the right temporoparietal area and showed poor performance on visuospatial function testing (p = 0.009). Our findings suggested that there is an AD variant characterized by right focal atrophy and visuospatial dysfunction.

Indexed as

AgedAlzheimer DiseaseAtrophyCerebral CortexFemaleHumansMaleMiddle AgedNeuropsychological Tests

Identifiers

PMID32350336
PMCPMC7190862
OpenAlexW3022348530

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.