Evidence map›Paper›PMID 34573331›Full record

ArticleGenes2021

Thousands of CpGs Show DNA Methylation Differences in ACPA-Positive Individuals.

Yixiao Zeng, Kaiqiong Zhao, Kathleen Oros Klein, Xiaojian Shao, Marvin J Fritzler, Marie Hudson, Inés Colmegna, Tomi Pastinen, Sasha Bernatsky, Celia M T Greenwood

Abstract read
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Yixiao ZengPhD Program in Quantitative Life Sciences, Interfaculty Studies, McGill University, Montréal, QC H3A 1E3, Canada.
Kaiqiong ZhaoLady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC H3T 1E2, Canada.
Kathleen Oros KleinLady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC H3T 1E2, Canada.
Xiaojian ShaoDigital Technologies Research Centre, National Research Council Canada, Ottawa, ON K1A 0R6, Canada.
Marvin J FritzlerCumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada.
Marie HudsonLady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC H3T 1E2, Canada.
Inés ColmegnaDepartment of Medicine, McGill University, Montréal, QC H4A 3J1, Canada.
Tomi PastinenDepartment of Human Genetics, McGill University, Montréal, QC H3A 0C7, Canada.
Sasha BernatskyDepartment of Medicine, McGill University, Montréal, QC H4A 3J1, Canada.
Celia M T GreenwoodPhD Program in Quantitative Life Sciences, Interfaculty Studies, McGill University, Montréal, QC H3A 1E3, Canada.ORCID 0000-0002-2427-5696

Funding

CIHR 130344
6 · The paper itself

Abstract

High levels of anti-citrullinated protein antibodies (ACPA) are often observed prior to a diagnosis of rheumatoid arthritis (RA). We undertook a replication study to confirm CpG sites showing evidence of differential methylation in subjects positive vs. negative for ACPA, in a new subset of 112 individuals sampled from the population cohort and biobank CARTaGENE in Quebec, Canada. Targeted custom capture bisulfite sequencing was conducted at approximately 5.3 million CpGs located in regulatory or hypomethylated regions from whole blood; library and protocol improvements had been instituted between the original and this replication study, enabling better coverage and additional identification of differentially methylated regions (DMRs). Using binomial regression models, we identified 19,472 ACPA-associated differentially methylated cytosines (DMCs), of which 430 overlapped with the 1909 DMCs reported by the original study; 814 DMRs of relevance were clustered by grouping adjacent DMCs into regions. Furthermore, we performed an additional integrative analysis by looking at the DMRs that overlap with RA related loci published in the GWAS Catalog, and protein-coding genes associated with these DMRs were enriched in the biological process of cell adhesion and involved in immune-related pathways.

Indexed as

CpG IslandsDNA MethylationAnti-Citrullinated Protein AntibodiesArthritis, RheumatoidCytosineDatabases, FactualEpigenomeFemaleGene OntologyGenome-Wide Association StudyHumansMaleMiddle AgedPolymorphism, Single NucleotideAnti-Citrullinated Protein AntibodiesCytosineanti-citrullinated protein antibody positivitycell adhesiondifferentially methylated cytosinesdifferentially methylated regionsDNA methylationrheumatoid arthritistargeted bisulfite sequencing

Identifiers

PMID34573331
PMCPMC8472734

What OpenQuestion holds

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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.