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Next-generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy.

Hui LiuAnna-Gaëlle Giguet-ValardThomas SimonetEmmanuelle Szenker-RaviLaetitia LambertCatherine Vincent-DelormeSophie ScheideckerMélanie FradinFanny Morice-PicardSophie NaudionViorica Ciorna-MonferratoEstelle ColinFlorence FellmannSophie BlessonPierre-Simon JoukChristine FrancannetFlorence PetitSébastien MouttonDaphné LehalleNicolas ChassaingLoubna El ZeinAnne BazinClaire BénéteauTania Attié-BitachSylvie M HanuMarie-Pierre BrechardJean ChiesaLaurent PasquierCaroline Rooryck-ThamboLionel Van MaldergemChristelle CabrolSalima El ChehadehAlexandre VasiljevicBertrand IsidorCarine AbelJulien ThevenonSylvie Di FilippoAdeline Vigouroux-CasteraJocelyne AttiaChloé QuelinSylvie OdentJuliette PiardFabienne GiulianoAudrey PutouxPhilippe Khau Van KienCatherine YardinRenaud TouraineBruno ReversadePatrice Bouvagnet
Published in: Human mutation (2020)
Herein, we report the screening of a large panel of genes in a series of 80 fetuses with congenital heart defects (CHDs) and/or heterotaxy and no cytogenetic anomalies. There were 49 males (61%/39%), with a family history in 28 cases (35%) and no parental consanguinity in 77 cases (96%). All fetuses had complex CHD except one who had heterotaxy and midline anomalies while 52 cases (65%) had heterotaxy in addition to CHD. Altogether, 29 cases (36%) had extracardiac and extra-heterotaxy anomalies. A pathogenic variant was found in 10/80 (12.5%) cases with a higher percentage in the heterotaxy group (8/52 cases, 15%) compared with the non-heterotaxy group (2/28 cases, 7%), and in 3 cases with extracardiac and extra-heterotaxy anomalies (3/29, 10%). The inheritance was recessive in six genes (DNAI1, GDF1, MMP21, MYH6, NEK8, and ZIC3) and dominant in two genes (SHH and TAB2). A homozygous pathogenic variant was found in three cases including only one case with known consanguinity. In conclusion, after removing fetuses with cytogenetic anomalies, next-generation sequencing discovered a causal variant in 12.5% of fetal cases with CHD and/or heterotaxy. Genetic counseling for future pregnancies was greatly improved. Surprisingly, unexpected consanguinity accounts for 20% of cases with identified pathogenic variants.
Keyphrases
  • gene expression
  • heart failure
  • dna methylation
  • transcription factor
  • hepatitis c virus
  • atrial fibrillation
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