Genetic profiling and cardiovascular phenotypic spectrum in a Chinese cohort of Loeys-Dietz syndrome patients

Abstract

Background: Loeys-Dietz syndrome (LDS) is a rare connective tissue disorder for which 6 genes in the TGF-β pathway have been identified as causative. With the widespread use of genetic testing, the range of known clinical and genetic profiles has broadened, but these features have not been fully elucidated thus far. Methods and results: Using gene panel sequencing or whole exome sequencing, we identified 54 unique rare variants in LDS genes in 57 patients with thoracic aneurysms/dissections, including 27 pathogenic mutations (P + LP) and 27 variants of unknown significance (VUS LP + VUS). Genotype-phenotype correlation analysis revealed that carriers with P/LP/ VUS LP variants in TGFBR1/TGFBR2/SMAD3 genes had significantly more severe cardiovascular features (cardiovascular death/dissection) than carriers with VUSs in these 3 genes at an early age and had less favorable eventfree survival. Additionally, carriers with VUS in combination with other risk factors, such as hypertension, might be prone to developing an aortic dissection, as indicated by the fact that 5/8 (62.5%) patients with VUSs in our cohort developed aortic dissections in the presence of hypertension, compared with 25.0% (3/12) in the absence of hypertension (p = 0.047). Conclusions: To date, this was the largest cohort of LDS patients ever reported in China, and the present study expanded the known mutation and phenotypic spectra of LDS, which might help refine our knowledge of LDS.

Loeys‑Dietz syndrome associated with a heterozygous mutation in TGFBR2 in a female infant: A case report

“…While the pathogenesis of LDS remains unclear, mutations in the transforming growth factor β receptor 1 (TGFBR1) and TGFBR2 genes identified in 2005 are the first known causative factors (5). Subsequently, other genes in the TGF-β signaling pathway, including SMAD3, transforming growth factor β (TGFB)2, SMAD2 and TGFB3, have been reported to be associated with LDS (6). Furthermore, LDS is subdivided into five clinical subtypes based on the pathogenic genes involved (Table I).…”

“…Vascular dilatation occurs mainly in the sinus node, which is further prone to aortic dissection or even rupture. A study reported early dissection during a young age in patients with TGFBR1, TGFBR2 or SMAD3 mutations (6).…”