Cardio-oncology & otherCohort study

Clonal Hematopoiesis and Risk of New-Onset Myocarditis and Pericarditis

JAMA CardiolPublished

  • Prospective cohort study
  • population-based
  • UK Biobank

Authors' conclusion

In this study, CHIP was a strong risk factor for myocarditis and pericarditis among middle-aged adults.

Study context

Population
UK Biobank participants with whole-exome sequencing, no prevalent CVD or hematological malignancy; enrolled 2006–2010382 developed myocarditis or pericarditis
Participants
335,426 participants
Exposure
Clonal hematopoiesis of indeterminate potential (CHIP) vs no CHIP
  • Any CHIPn = 11,057
  • Large CHIPn = 7,271
Outcome
Composite of:
  • Incident myocarditis
  • Pericarditis
Follow-up
Median 13.6 (IQR, 12.8-14.2) years

Main finding

As reported in the abstract

Incident myocarditis or pericarditis
Each group vs no CHIPMultivariable-adjusted HR (95% CI)P value
Any CHIP
1.75(1.14–2.68)
P = 0.01
Large CHIP
2.07(1.28–3.33)
P = 0.003

Observational data: associations, not effects.

Further findings

OutcomeHR (95% CI)P value
Pericarditis, DNMT3A CHIP2.22 (1.17–4.21)P = 0.01
Myocarditis, TET2 CHIP3.65 (1.16–11.49)P = 0.03
Outcomefold risk (95% CI)P value
Noncardiac immune-mediated inflammatory diseases · no evidence for reverse causation1.27 (1.16–1.39)P < 0.001

Other CVD (eg, CAD, HF)

CHIP associated with myocarditis and pericarditis more strongly than with other CVD

Original publication

Clonal Hematopoiesis and Risk of New-Onset Myocarditis and Pericarditis. JAMA Cardiol. Published 1 November 2025. doi:10.1001/jamacardio.2025.3369

Summarised from the published abstract; every number is checked against it