Arrhythmias & electrophysiology

The Heritability of Supraventricular Tachycardia

JACC Clin ElectrophysiolPublished

  • classical biometrical twin study design
  • nationwide
  • Danish Twin Registry and the Danish National Patient Registry
+2 more
  • nationwide
  • Danish Twin Registry and the Danish National Patient Registry

Authors' conclusion

Based on a large nationwide population of monozygotic and same-sex dizygotic twins, this is the first study to quantify the genetic and environmental contributions to SVT.

Study context

Population
Monozygotic and same-sex dizygotic twin pairs born in Denmark, in which one or both members were diagnosed with supraventricular tachycardia (SVT) between 1977 and 2024twin pairs, at least one SVT diagnosis in 663 twin pairs · monozygotic pairs 12,006 · dizygotic pairs 20,318
Participants
32,324 participants
Exposure
risk of SVT in monozygotic co-twins compared with dizygotic co-twins
  • monozygotic co-twinsn = 12,006
  • dizygotic co-twinsn = 20,318reference

Main finding

As reported in the abstract

Risk of SVT in the co-twin after an SVT diagnosis in the index-twin
monozygotic co-twins vs dizygotic co-twinsHazard ratio (95% CI)P value
Risk of SVT in the co-twin after an SVT diagnosis in the index-twin
3.61(1.35–9.63)
P = 0.01
adjusting for age and sex
3.3(1.24–8.89)
P = 0.01

Observational data: associations, not effects.

Further findings

Probandwise concordance rate

  • Probandwise concordance rate: P < 0.001

Biometrical models: attribution of SVT risk

genetics
35%
unique environmental components
65%

Original publication

The Heritability of Supraventricular Tachycardia. JACC Clin Electrophysiol. Published 22 January 2026. doi:10.1016/j.jacep.2025.12.021

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