Evidence map›Paper›PMID 31591842›Full record

ArticleJournal of clinical neurology (Seoul, Korea)2019

Relationships between [¹⁸F]-THK5351 Retention and Language Functions in Primary Progressive Aphasia.

Hye Jin Jeong, Cindy W Yoon, Seongho Seo, Sang Yoon Lee, Mee Kyung Suh, Ha Eun Seo, Woo Ram Kim, Hyon Lee, Jae Hyeok Heo, Yeong Bae Lee and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical neurology (Seoul, Korea), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Clinical application of MAO-B PET usingGeriatrics & gerontology international · 2024
    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 at 5 institutions in 1 country.

Hye Jin Jeong *Neuroscience Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0003-3765-8546
Cindy W Yoon *Department of Neurology, Inha University School of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0002-4697-6610
Seongho SeoDepartment of Neuroscience, College of Medicine, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0001-7894-0535
Sang Yoon LeeDepartment of Neuroscience, College of Medicine, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0002-6029-8553
Mee Kyung SuhDepartment of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-2558-8018
Ha Eun SeoNeuroscience Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0003-4452-0908
Woo Ram KimNeuroscience Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0003-1361-4426
Hyon LeeDepartment of Neurology, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0002-0273-8960
Jae Hyeok HeoDepartment of Neurology, Seoul Medical Center, Seoul, Korea.ORCID https://orcid.org/0000-0003-4848-0528
Yeong Bae LeeDepartment of Neurology, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0001-5952-1423
Kee Hyung ParkDepartment of Neurology, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0001-6847-6679
Seong Hye ChoiDepartment of Neurology, Inha University School of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0002-4180-8626
Tatsuo IdoNeuroscience Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0002-2825-9343
Kyoung Min LeeDepartment of Neurology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-6168-8385
Young NohDepartment of Neurology, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0002-9633-3314
Gachon University · KRInha University · KRSamsung Medical Center · KRSeoul Medical Center · KRSeoul National University Hospital · KR

Funding

Korea Health Industry Development Institute HI14C1135National Research Foundation of Korea NRF-2014M3C7033998National Research Foundation of Korea NRF-2018M3C7A1056889
6 · The paper itself

Abstract

background and purposeThere are three distinct subtypes of primary progressive aphasia (PPA): the nonfluent/agrammatic variant (nfvPPA), the semantic variant (svPPA), and the logopenic variant (lvPPA). We sought to characterize the pattern of [¹⁸F]-THK5351 retention across all three subtypes and determine the topography of [¹⁸F]-THK5351 retention correlated with each neurolinguistic score.

methodsWe enrolled 50 participants, comprising 13 PPA patients (3 nfvPPA, 5 svPPA, and 5 lvPPA) and 37 subjects with normal cognition (NC) who underwent 3.0-tesla magnetic resonance imaging, [¹⁸F]-THK5351 positron-emission tomography scans, and detailed neuropsychological tests. The PPA patients additionally participated in extensive neurolinguistic tests. Voxel-wise and region-of-interest-based analyses were performed to analyze [¹⁸F]-THK5351 retention.

resultsThe nfvPPA patients exhibited higher [¹⁸F]-THK5351 retention in the the left inferior frontal and precentral gyri. In svPPA patients, [¹⁸F]-THK5351 retention was elevated in the anteroinferior and lateral temporal cortices compared to the NC group (left>right). The lvPPA patients exhibited predominant [¹⁸F]-THK5351 retention in the inferior parietal, lateral temporal, and dorsolateral prefrontal cortices, and the precuneus (left>right). [¹⁸F]-THK5351 retention in the left inferior frontal area was associated with lower fluency scores. Comprehension was correlated with [¹⁸F]-THK5351 retention in the left temporal cortices. Repetition was associated with [¹⁸F]-THK5351 retention in the left inferior parietal and posterior temporal areas, while naming difficulty was correlated with retention in the left fusiform and temporal cortices.

conclusionsThe pattern of [¹⁸F]-THK5351 retention was well matched with clinical and radiological findings for each PPA subtype, in agreement with the anatomical and functional location of each language domain.

Indexed as

languageneurofibrillary tanglespositron-emission tomographyprimary progressive aphasia

Identifiers

PMID31591842
PMCPMC6785468
OpenAlexW2977249618

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.