Evidence map›Paper›PMID 35079008›Full record

ArticleScientific reports2022

A combination of multiple autoantibodies is associated with the risk of Alzheimer's disease and cognitive impairment.

Sung-Mi Shim, Young Ho Koh, Jong-Hoon Kim, Jae-Pil Jeon

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  3. The role of autoantibodies in Alzheimer's disease: Pathogenetic connections or epiphenomena?Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Sung-Mi ShimDivision of Brain Disease Research, Department of Chronic Disease Convergence Research, Korea National Institute of Health, Osong-eup, Chungcheongbuk-do, 28159, Republic of Korea.
Young Ho KohDivision of Brain Disease Research, Department of Chronic Disease Convergence Research, Korea National Institute of Health, Osong-eup, Chungcheongbuk-do, 28159, Republic of Korea.
Jong-Hoon KimDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea.
Jae-Pil JeonDivision of Brain Disease Research, Department of Chronic Disease Convergence Research, Korea National Institute of Health, Osong-eup, Chungcheongbuk-do, 28159, Republic of Korea. jaepiljeon@hanmail.net.
Korea National Institute of Health · KRKorea University · KR

Funding

Korea National Institute of Health, the Korea Center for Disease Control and Prevention 2016-NG62003-00
6 · The paper itself

Abstract

Autoantibodies are self-antigen reactive antibodies that play diverse roles in the normal immune system, tissue homeostasis, and autoimmune and neurodegenerative diseases. Anti-neuronal autoantibodies have been detected in neurodegenerative disease serum, with unclear significance. To identify diagnostic biomarkers of Alzheimer's disease (AD), we analyzed serum autoantibody profiles of the HuProt proteome microarray using the discovery set of cognitively normal control (NC, n = 5) and AD (n = 5) subjects. Approximately 1.5-fold higher numbers of autoantibodies were detected in the AD group (98.0 ± 39.9/person) than the NC group (66.0 ± 39.6/person). Of the autoantigen candidates detected in the HuProt microarray, five autoantigens were finally selected for the ELISA-based validation experiment using the validation set including age- and gender-matched normal (NC, n = 44), mild cognitive impairment (MCI, n = 44) and AD (n = 44) subjects. The serum levels of four autoantibodies including anti-ATCAY, HIST1H3F, NME7 and PAIP2 IgG were significantly different among NC, MCI and/or AD groups. Specifically, the anti-ATCAY autoantibody level was significantly higher in the AD (p = 0.003) and MCI (p = 0.015) groups compared to the NC group. The anti-ATCAY autoantibody level was also significantly correlated with neuropsychological scores of MMSE (r

Indexed as

AgedAged, 80 and overAlzheimer DiseaseAutoantibodiesBiomarkersCase-Control StudiesCognitive DysfunctionCohort StudiesFemaleHumansImmunoglobulin GMaleProteomeRepublic of KoreaRisk FactorsAutoantibodiesBiomarkersImmunoglobulin GProteome

Identifiers

PMID35079008
PMCPMC8789802
OpenAlexW4210765944

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.