The pregnancy-associated spontaneous coronary artery dissection in a young woman with a novel missense mutation in NOTCH1: a case report

BMC Med Genet. 2020 Jun 1;21(1):119. doi: 10.1186/s12881-020-01058-2.

Abstract

Background: Spontaneous coronary artery dissection (SCAD) is frequently reported as a disorder that primarily affects women without risk factors for cardiovascular disease. Although it has been recognized as one of the genetically mediated vascular disorders, the genetic pathogenesis of SCAD remains obscure to date.

Case presentation: In this report, we presented a rare case of pregnancy-associated SCAD in a young woman that occurred in multiple coronary arteries within a short period. The initial conservative management and then intravascular ultrasound-guided primary percutaneous coronary intervention (PCI) were adopted to achieve optimal results of revascularization in affected coronary arteries and avoid potential risks for PCI-associated complications. We further performed the whole-exome sequencing and Sanger sequencing and, for the first time, reported a novel heterozygous missense variant, c.4574 C > T (p.Arg1438Cys), in the NOTCH1 gene. This variant has never been documented in the medical literature and was predicted as being potentially damaging or disease-causing variant.

Conclusions: We described a rare case of recurrent SCAD in a young woman after baby delivery. The initial conservative management and PCI with multiple stent implantations were successfully implemented to achieve optimal results of revascularization in coronary arteries. We, for the first time, identified a novel missense variant in the NOTCH1 gene, which appears to be a potential predisposing factor for artery fragility.

Keywords: Myocardial infarction; NOTCH 1 variant; Pregnancy; Primary percutaneous coronary intervention; Spontaneous coronary artery dissection.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Alleles
  • Amino Acid Sequence
  • Coronary Angiography
  • Coronary Vessel Anomalies / diagnosis*
  • Coronary Vessel Anomalies / etiology*
  • Coronary Vessel Anomalies / therapy
  • DNA Mutational Analysis
  • Disease Susceptibility*
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Models, Molecular
  • Mutation, Missense*
  • Pregnancy
  • Pregnancy Complications, Cardiovascular*
  • Protein Conformation
  • Receptor, Notch1 / chemistry
  • Receptor, Notch1 / genetics*
  • Structure-Activity Relationship
  • Symptom Assessment
  • Ultrasonography, Interventional
  • Vascular Diseases / congenital*
  • Vascular Diseases / diagnosis
  • Vascular Diseases / etiology
  • Vascular Diseases / therapy

Substances

  • NOTCH1 protein, human
  • Receptor, Notch1

Supplementary concepts

  • Coronary Artery Dissection, Spontaneous