Electrocardiographic abnormalities in infants born from mothers with autoimmune diseases--a multicentre prospective

M Gerosa1, R Cimaz, M Stramba-Badiale

  • 1Allergy, Clinical Immunology & Rheumatology Unit, IRCCS Istituto Auxologico Italiano, Via Spagnoletto, 3, 20149 Milan, Italy.

Insights

Congenital heart block (CHB) is rare in infants of anti-Ro/SSA-positive mothers. However, electrocardiographic (ECG) abnormalities like AV block and QTc prolongation are common in these infants, regardless of maternal factors.

Area of Science:

  • Maternal-fetal medicine
  • Neonatal cardiology
  • Autoimmune disease in pregnancy

Background:

  • Anti-Ro/SSA antibodies can cross the placenta, potentially affecting fetal and neonatal cardiac function.
  • Congenital heart block (CHB) is a known complication, but its prevalence and other ECG abnormalities require further assessment.

Purpose of the Study:

  • To determine the incidence of CHB and other ECG abnormalities in infants born to anti-Ro/SSA-positive women.
  • To compare ECG findings in infants of anti-Ro/SSA-positive mothers with those of anti-Ro/SSA-negative mothers and healthy controls.

Main Methods:

  • Prospective follow-up of pregnant women (60 anti-Ro-positive, 36 anti-Ro-negative) with weekly fetal echocardiography.
  • Infant ECG and/or ECG-Holter monitoring at 1, 3, 6, and 12 months.
  • Comparison with a control group of 200 neonates.

Main Results:

  • One case of CHB and one case of second-degree atrioventricular (AV) block occurred in the anti-Ro-positive group.
  • Transient first-degree AV block was significantly more prevalent in the anti-Ro-positive group versus controls (P = 0.002).
  • QTc interval prolongation was frequent in both anti-Ro-positive and -negative groups compared to controls (P < 0.001), with similar Holter findings.

Conclusions:

  • The occurrence of CHB in newborns of anti-Ro/SSA-positive mothers is low.
  • ECG abnormalities, including first-degree AV block and QTc prolongation, are frequent in infants of mothers with autoimmune diseases, irrespective of maternal factors.
Abstract