Evidence map›Paper›PMID 36349274›Full record

ArticleOpen forum infectious diseases2022

Use of Anti-Glycopeptidolipid-Core Antibodies Serology for Diagnosis and Monitoring of

A G Hernandez, A E Brunton, M Ato, K Morimoto, S Machida, E Henkle, K L Winthrop

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Core outcome domains forERJ open research · 2025
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  6. Detection ofInfection and drug resistance · 2023
    Article
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

7 authors at 3 institutions in 2 countries.

A G HernandezCenter for Infectious Disease Studies, School of Public Health, Oregon Health & Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0002-3079-4695
A E BruntonCenter for Infectious Disease Studies, School of Public Health, Oregon Health & Science University, Portland, Oregon, USA.
M AtoDepartment of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Aoba-cho, Higashimurayama, Tokyo, Japan.
K MorimotoRespiratory Disease Center, Fukujuji Hospital, Japan Anti-Tuberculosis Association, Matsuyama, Kiyose City, Tokyo, Japan.
S MachidaDepartment of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Aoba-cho, Higashimurayama, Tokyo, Japan.
E HenkleCenter for Infectious Disease Studies, School of Public Health, Oregon Health & Science University, Portland, Oregon, USA.
K L WinthropCenter for Infectious Disease Studies, School of Public Health, Oregon Health & Science University, Portland, Oregon, USA.
Oregon Health & Science University · USNational Institute of Infectious Diseases · JPJapan Anti Tuberculosis Association · JP

Funding

Oregon Clinical and Translational Research Institute - The National COVID Cohort Collaborative (N3C)UL1TR002369 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Cynthia D Morris, Christopher G. Slatore · 2017 to 2026
$78.4M
NCATS NIH HHS UL1 TR002369
6 · The paper itself

Abstract

Background: There is an unmet need for rapid, accurate, and noninvasive assays for diagnosis and monitoring of Methods: We identified serum samples from MAC patients starting treatment at enrollment and control subjects with or without bronchiectasis within OHSU's NTM Biobank. We conducted diagnostic test accuracy. Changes in mean levels of anti-GPL-core IgA antibodies between 0 and 3, 6, or 12 months after treatment start were assessed using the Student's paired Results: We included 25 MAC patients and 18 controls. At baseline, IgA antibody concentrations in MAC patients (3.40 ± 6.77 U/mL) were significantly higher than in controls without bronchiectasis (0.14 ± 0.03 U/mL, Conclusions: Anti-GPL-core IgA antibody levels are relatively specific for MAC-PD and decrease with treatment. Larger studies are warranted to evaluate the role of IgA serology in monitoring treatment response or for disease relapse/reinfection.

Indexed as

epidemiologylung diseasesnontuberculous mycobacteriaserodiagnosis

Identifiers

PMID36349274
PMCPMC9636853
OpenAlexW4307060725

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.