Evidence map›Paper›PMID 38946998›Full record

ArticleResearch square2024

Differences in the DNA Methylome of T cells in Adults With Asthma of Varying Severity.

Yixuan Liao, Raymond Cavalcante, Jonathan Waller, Furong Deng, Anne Scruggs, Yvonne Huang, Ulus Atasoy, Yahong Chen, Steven Huang

Abstract readPreprint
In one paragraph

Article in Research square, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Yixuan LiaoPeking University Third Hospital.
Raymond CavalcanteUniversity of Michigan-Ann Arbor.
Jonathan WallerUniversity of Michigan-Ann Arbor.
Furong DengPeking University Third Hospital.
Anne ScruggsUniversity of Michigan-Ann Arbor.
Yvonne HuangUniversity of Michigan-Ann Arbor.
Ulus AtasoyUniversity of Michigan-Ann Arbor.
Yahong ChenPeking University Third Hospital.
Steven HuangUniversity of Michigan-Ann Arbor.

Funding

The Role of KCNMB1 and the Large Conductance Potassium (BK) Channel in Myofibroblast Differentiation and Pulmonary FibrosisR01HL127203 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HUANG, STEVEN K · 2015 to 2024
$4.4M
Heterogeneity and Regulation of the DNA Methylome in IPF Mesenchymal CellsR01HL162963 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STEVEN K HUANG · 2023 to 2026
$2.7M
NHLBI NIH HHS R01 HL127203NHLBI NIH HHS R01 HL162963
6 · The paper itself

Abstract

Background: DNA methylation plays a critical role in asthma development, but differences in DNA methylation among adults with varying asthma severity or asthma endotypes are less well-defined. Objective: To examine how DNA methylomic patterns differ among adults with asthma based on asthma severity and airway inflammation. Methods: Peripheral blood T cells from 35 adults with asthma in Beijing, China were serially collected over time (130 samples total) and analyzed for global DNA methylation using the Illumina MethylationEPIC Array. Differential methylation was compared among subjects with varying airway inflammation and severity, as measured by fraction of exhaled nitric oxide, forced expiratory volume in one second (FEV1), and Asthma Control Test (ACT) scores. Results: Significant differences in DNA methylation were noted among subjects with different degrees of airway inflammation and asthma severity. These differences in DNA methylation were annotated to genes that were enriched in pathways related to asthma or T cell function and included gene ontology categories related to MHC class II assembly, T cell activation, interleukin (IL)-1, and IL-12. Genes related to P450 drug metabolism, glutathione metabolism, and developmental pathways were also differentially methylated in comparisons between subjects with high vs low FEV1 and ACT. Notable genes that were differentially methylated based on asthma severity included Conclusion: These findings demonstrate how adults with asthma of varying severity possess differences in peripheral blood T cell DNA methylation that contribute to the phenotype and severity of their overall disease.

Indexed as

DNA methylationEpigeneticsFraction of Exhaled Nitric OxideParticulate Matter

Identifiers

PMID38946998
PMCPMC11213176

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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.