Details

Autor(en) / Beteiligte

• Aubart, Melodie
• Gazal, Steven
• Arnaud, Pauline
• Benarroch, Louise
• Gross, Marie-Sylvie
• Buratti, Julien
• Boland, Anne
• Meyer, Vincent
• Zouali, Habib
• Hanna, Nadine
• Milleron, Olivier
• Stheneur, Chantal
• Bourgeron, Thomas
• Desguerre, Isabelle
• Jacob, Marie-Paule
• Gouya, Laurent
• Génin, Emmanuelle
• Deleuze, Jean-François
• Jondeau, Guillaume
• Boileau, Catherine

Titel

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability

Ist Teil von

• European journal of human genetics : EJHG, 2018-12, Vol.26 (12), p.1759-1772

Ort / Verlag

England: Nature Publishing Group

Erscheinungsjahr

2018

Link zum Volltext

Quelle

Free E-Journal (出版社公開部分のみ）

Beschreibungen/Notizen

• Marfan syndrome (MFS) is a rare autosomal dominant connective tissue disorder related to variants in the FBN1 gene. Prognosis is related to aortic risk of dissection following aneurysm. MFS clinical variability is notable, for age of onset as well as severity and number of clinical manifestations. To identify genetic modifiers, we combined genome-wide approaches in 1070 clinically well-characterized FBN1 disease-causing variant carriers: (1) an FBN1 eQTL analysis in 80 fibroblasts of FBN1 stop variant carriers, (2) a linkage analysis, (3) a kinship matrix association study in 14 clinically concordant and discordant sib-pairs, (4) a genome-wide association study and (5) a whole exome sequencing in 98 extreme phenotype samples.Three genetic mechanisms of variability were found. A new genotype/phenotype correlation with an excess of loss-of-cysteine variants (P = 0.004) in severely affected subjects. A second pathogenic event in another thoracic aortic aneurysm gene or the COL4A1 gene (known to be involved in cerebral aneurysm) was found in nine individuals. A polygenic model involving at least nine modifier loci (named gMod-M1-9) was observed through cross-mapping of results. Notably, gMod-M2 which co-localizes with PRKG1, in which activating variants have already been described in thoracic aortic aneurysm, and gMod-M3 co-localized with a metalloprotease (proteins of extra-cellular matrix regulation) cluster. Our results represent a major advance in understanding the complex genetic architecture of MFS and provide the first steps toward prediction of clinical evolution.