Bundle Branch Blocks and Fragmented QRS Complex in Iranian Patients with Systemic Sclerosis

Ali Javinani1, Zahra Javady Nejad1, Farhad Gharibdoost1

  • 1Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Insights

Bundle branch blocks (BBBs) and fragmented QRS (fQRS) were more common in Iranian systemic sclerosis (SSc) patients. These cardiac conduction abnormalities may indicate an independent SSc cardiac pathophysiology.

Area of Science:

  • Cardiology
  • Rheumatology
  • Systemic Sclerosis (SSc) research

Background:

  • Cardiac involvement in systemic sclerosis (SSc) is a severe manifestation, often due to myocardial collagen deposition leading to conduction abnormalities.
  • Bundle branch blocks (BBBs) and fragmented QRS (fQRS) are ECG markers that may reflect cardiac damage.
  • Investigating these markers in SSc patients can elucidate the cardiac pathophysiology specific to the disease.

Purpose of the Study:

  • To determine the prevalence of bundle branch blocks (BBBs) and fragmented QRS (fQRS) in Iranian patients with systemic sclerosis (SSc).
  • To explore the clinical significance and associations of these ECG abnormalities with SSc characteristics and cardiovascular risk factors.

Main Methods:

  • Forty-one SSc patients were enrolled from an outpatient clinic.
  • Standard 12-lead electrocardiograms (ECGs) were analyzed for BBBs and fQRS.
  • Framingham risk scores were calculated; associations with SSc subtypes, disease duration, and Medsger severity scores were assessed.

Main Results:

  • The prevalence of BBBs was 26.8% and fQRS was 36.6% in the study population.
  • Fragmented QRS (fQRS) showed a significant association with the limited cutaneous SSc subtype (OR: 0.100, P=0.028).
  • Neither BBBs nor fQRS were associated with Framingham risk scores or other demographic/clinical variables.

Conclusions:

  • Bundle branch blocks (BBBs) and fragmented QRS (fQRS) are prevalent in Iranian SSc patients.
  • These findings suggest that cardiac conduction abnormalities in SSc may arise from a pathophysiology independent of other organ involvements or traditional cardiovascular risk factors.
  • Further research into the specific cardiac mechanisms in SSc is warranted.

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