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Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier.

Authors :
Perik MHAM
Govaerts E
Laga S
Goovaerts I
Saenen J
Van Craenenbroeck E
Meester JAN
Luyckx I
Rodrigus I
Verstraeten A
Van Laer L
Loeys BL
Source :
Frontiers in genetics [Front Genet] 2023 Aug 31; Vol. 14, pp. 1251675. Date of Electronic Publication: 2023 Aug 31 (Print Publication: 2023).
Publication Year :
2023

Abstract

Background: TGFB3 variants cause Loeys-Dietz syndrome type 5, a syndromic form of thoracic aortic aneurysm and dissection. The exact disease phenotype is hard to delineate because of few identified cases and highly variable clinical representation. Methodology: We provide the results of a haplotype analysis and a medical record review of clinical features of 27 individuals from 5 different families, originating from the Campine region in Flanders, carrying the NM_003239.5( TGFB3 ):c.787G>C p.(Asp263His) likely pathogenic variant, dbSNP:rs796051886, ClinVar:203492. The Asp <superscript>263</superscript> residue is essential for integrin binding to the Arg-Gly-Asp (RGD) motif of the TGFβ3-cytokine. Results: The haplotype analysis revealed a shared haplotype of minimum 1.92 Mb and maximum 4.14 Mb, suggesting a common founder originating >400 years ago. Variable clinical features included connective tissue manifestations, non-aneurysmal cardiovascular problems such as hypertrophic cardiomyopathy, bicuspid aortic valve, mitral valve disease, and septal defects. Remarkably, only in 4 out of the 27 variant-harboring individuals, significant aortic involvement was observed. In one family, a 31-year-old male presented with type A dissection. In another family, the male proband (65 years) underwent a Bentall procedure because of bicuspid aortic valve insufficiency combined with sinus of Valsalva of 50 mm, while an 80-year-old male relative had an aortic diameter of 43 mm. In a third family, the father of the proband (75 years) presented with ascending aortic aneurysm (44 mm). Conclusion: The low penetrance (15%) of aortic aneurysm/dissection suggests that haploinsufficiency alone by the TGFB3 variant may not result in aneurysm development but that additional factors are required to provoke the aneurysm phenotype.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Perik, Govaerts, Laga, Goovaerts, Saenen, Van Craenenbroeck, Meester, Luyckx, Rodrigus, Verstraeten, Van Laer and Loeys.)

Details

Language :
English
ISSN :
1664-8021
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in genetics
Publication Type :
Academic Journal
Accession number :
37719708
Full Text :
https://doi.org/10.3389/fgene.2023.1251675