QT dispersion in amyloidosis due to familial Mediterranean fever

Udi Nussinovitch1, Naomi Nussinovitch, Moshe Nussinovitch

  • 1The Heller Institute of Medical Research, and Department of Medicine F, Sheba Medical Center, Tel Hashomer Israel and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. enussi@yahoo.com

Insights

Familial Mediterranean fever (FMF) with amyloidosis did not show increased QT or JT dispersion compared to healthy individuals. This suggests repolarization dispersion may not be a significant marker in FMF-associated amyloidosis.

Area of Science:

  • Cardiology
  • Genetics
  • Internal Medicine

Background:

  • Cardiac amyloid deposition is a potential complication of familial Mediterranean fever (FMF).
  • QT dispersion (QTd) is a recognized marker for cardiac arrhythmias.
  • Previous studies suggest a link between amyloidosis and increased QTd.

Purpose of the Study:

  • To investigate repolarization dispersion in patients with familial Mediterranean fever (FMF) and amyloidosis.
  • To compare electrocardiographic findings between FMF-amyloidosis patients and healthy controls.

Main Methods:

  • 12-lead electrocardiography was performed on 18 FMF-amyloidosis patients and 18 age/sex-matched controls.
  • Repolarization and dispersion parameters, including QTd and JT dispersion, were computed using specialized software.
  • Averaging of 5 beats was used for parameter calculation.

Main Results:

  • No statistically significant differences were observed in average corrected QT interval, average QTd, QT dispersion ratio, JT dispersion, or JT corrected dispersion between the FMF-amyloidosis group and the control group.
  • Both groups exhibited similar repolarization and dispersion parameters.

Conclusions:

  • Patients with FMF-amyloidosis appear to have similar QT and JT dispersion parameters to healthy subjects.
  • Further research and extended follow-up are needed to determine the prognostic value of repolarization dispersion in FMF-associated amyloidosis.