Lupus & antiphospholipid syndrome

Patients with systemic lupus erythematosus (SLE) have an increased bisphenol A methylation score linked to SLE risk genes and selected clinical subphenotypes

RMD OpenPublished Case-control epigenetic association study

Authors' conclusion

Our findings reveal a novel association between BPA exposure and DNA methylation changes in SLE, with potential implications for the regulation of immune-related gene expression.

Study context

Population
Swedish patients with SLE and healthy controlsdiscovery n=747
Comparison
Patients with SLE vs healthy controls
Outcome
Methylation at BPA-sensitive CpG sites: BPASLE score (3 CpGs co-localised with SLE risk loci) and BPAAll score (19 CpGs)
Methodological detailsdiscovery and replication cohorts, meta-analysis, Illumina HM450k bead chip
  • Discovery and replication cohorts
  • Meta-analysis
  • Illumina HM450k bead chip

Main finding

As reported in the abstract

BPASLE score, SLE vs controls

Odds ratio

1.34

P = 4.6×10-13

discovery cohort

Odds ratio

1.28

P = 1.1×10-5

replication cohort

Odds ratio

1.32

P = 3.3×10-17

meta-analysis

Observational data: associations, not effects.

Further findings

OutcomeORP value
BPAAll score, SLE vs controlsSLE vs Controls · discovery cohort1.05P = 2.3×10-3
BPAAll score, SLE vs controlsSLE vs Controls · replication cohort1.04P = 0.12
BPAAll score, SLE vs controlsSLE vs Controls · meta-analysis1.05P = 7.0×10-4

Association of scores with clinical data

Both scores associated with prednisolone treatment
P < 0.001
BPASLE score associated with serositis and autoantibodies
P < 0.05

Transcriptomic data from Bisphenol A (BPA)-treated cells

Enrichment in pathways such as interferon and mitogen-activated protein kinase signalling

Original publication

Patients with systemic lupus erythematosus (SLE) have an increased bisphenol A methylation score linked to SLE risk genes and selected clinical subphenotypes. RMD Open. Published 25 September 2025. doi:10.1136/rmdopen-2025-006021

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