Literature DB >> 29444212

Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation.

Alexandre Vivanti1, Augustin Ozanne2, Cynthia Grondin1, Guillaume Saliou3, Loic Quevarec1, Helène Maurey4, Patrick Aubourg4, Alexandra Benachi5, Marta Gut6,7, Ivo Gut6,7, Jelena Martinovic8, Marie Victoire Sénat9, Marcel Tawk10, Judith Melki1.   

Abstract

See Meschia (doi:10.1093/brain/awy066) for a scientific commentary on this article.Vein of Galen aneurysmal malformation is a congenital anomaly of the cerebral vasculature representing 30% of all paediatric vascular malformations. We conducted whole exome sequencing in 19 unrelated patients presenting this malformation and subsequently screened candidate genes in a cohort of 32 additional patients using either targeted exome or Sanger sequencing. In a cohort of 51 patients, we found five affected individuals with heterozygous mutations in EPHB4 including de novo frameshift (p.His191Alafs*32) or inherited deleterious splice or missense mutations predicted to be pathogenic by in silico tools. Knockdown of ephb4 in zebrafish embryos leads to specific anomalies of dorsal cranial vessels including the dorsal longitudinal vein, which is the orthologue of the median prosencephalic vein and the embryonic precursor of the vein of Galen. This model allowed us to investigate EPHB4 loss-of-function mutations in this disease by the ability to rescue the brain vascular defect in knockdown zebrafish co-injected with wild-type, but not truncated EPHB4, mimicking the p.His191Alafs mutation. Our data showed that in both species, loss of function mutations of EPHB4 result in specific and similar brain vascular development anomalies. Recently, EPHB4 germline mutations have been reported in non-immune hydrops fetalis and in cutaneous capillary malformation-arteriovenous malformation. Here, we show that EPHB4 mutations are also responsible for vein of Galen aneurysmal malformation, indicating that heterozygous germline mutations of EPHB4 result in a large clinical spectrum. The identification of EPHB4 pathogenic mutations in patients presenting capillary malformation or vein of Galen aneurysmal malformation should lead to careful follow-up of pregnancy of carriers for early detection of anomaly of the cerebral vasculature in order to propose optimal neonatal care. Endovascular embolization indeed greatly improved the prognosis of patients.

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Year:  2018        PMID: 29444212     DOI: 10.1093/brain/awy020

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  13 in total

1.  A theory for polymicrogyria and brain arteriovenous malformations in HHT.

Authors:  Jesse M Klostranec; Long Chen; Shobhit Mathur; Jamie McDonald; Marie E Faughnan; Felix Ratjen; Timo Krings
Journal:  Neurology       Date:  2019-01-01       Impact factor: 9.910

Review 2.  Childhood stroke.

Authors:  Peter B Sporns; Heather J Fullerton; Sarah Lee; Helen Kim; Warren D Lo; Mark T Mackay; Moritz Wildgruber
Journal:  Nat Rev Dis Primers       Date:  2022-02-24       Impact factor: 52.329

3.  Mutations in EPHB4 cause human venous valve aplasia.

Authors:  Oliver Lyons; James Walker; Christopher Seet; Mohammed Ikram; Adam Kuchta; Andrew Arnold; Magda Hernández-Vásquez; Maike Frye; Gema Vizcay-Barrena; Roland A Fleck; Ashish S Patel; Soundrie Padayachee; Peter Mortimer; Steve Jeffery; Siren Berland; Sahar Mansour; Pia Ostergaard; Taija Makinen; Bijan Modarai; Prakash Saha; Alberto Smith
Journal:  JCI Insight       Date:  2021-09-22

Review 4.  Genetics of brain arteriovenous malformations and cerebral cavernous malformations.

Authors:  Hiroki Hongo; Satoru Miyawaki; Yu Teranishi; Daiichiro Ishigami; Kenta Ohara; Yu Sakai; Daisuke Shimada; Motoyuki Umekawa; Satoshi Koizumi; Hideaki Ono; Hirofumi Nakatomi; Nobuhito Saito
Journal:  J Hum Genet       Date:  2022-07-13       Impact factor: 3.755

5.  Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly.

Authors:  Dong Li; Tara L Wenger; Christoph Seiler; Michael E March; Alvaro Gutierrez-Uzquiza; Charlly Kao; Elizabeth Bhoj; Lifeng Tian; Misha Rosenbach; Yichuan Liu; Nora Robinson; Mechenzie Behr; Rosetta Chiavacci; Cuiping Hou; Tiancheng Wang; Marina Bakay; Renata Pellegrino da Silva; Jonathan A Perkins; Patrick Sleiman; Michael A Levine; Patricia J Hicks; Maxim Itkin; Yoav Dori; Hakon Hakonarson
Journal:  Hum Mol Genet       Date:  2018-09-15       Impact factor: 6.150

6.  Endothelial EphB4 maintains vascular integrity and transport function in adult heart.

Authors:  Guillermo Luxán; Jonas Stewen; Mara E Pitulescu; Ralf H Adams; Noelia Díaz; Katsuhiro Kato; Sathish K Maney; Anusha Aravamudhan; Frank Berkenfeld; Nina Nagelmann; Hannes Ca Drexler; Dagmar Zeuschner; Cornelius Faber; Hermann Schillers; Sven Hermann; John Wiseman; Juan M Vaquerizas
Journal:  Elife       Date:  2019-11-29       Impact factor: 8.140

Review 7.  EphrinB2-EphB4-RASA1 Signaling in Human Cerebrovascular Development and Disease.

Authors:  Xue Zeng; Ava Hunt; Sheng Chih Jin; Daniel Duran; Jonathan Gaillard; Kristopher T Kahle
Journal:  Trends Mol Med       Date:  2019-02-25       Impact factor: 11.951

8.  Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes.

Authors:  Kazim Ogmen; Ege Sackey; Silvia Martin-Almedina; Dionysios Grigoriadis; Christina Karapouliou; Noeline Nadarajah; Cathrine Ebbing; Jenny Lord; Rhiannon Mellis; Fanny Kortuem; Mary Beth Dinulos; Cassandra Polun; Sherri Bale; Giles Atton; Alexandra Robinson; Hallvard Reigstad; Gunnar Houge; Axel von der Wense; Wolf-Henning Becker; Steve Jeffery; Peter S Mortimer; Kristiana Gordon; Katherine S Josephs; Sarah Robart; Mark D Kilby; Stephanie Vallee; Jerome L Gorski; Maja Hempel; Siren Berland; Sahar Mansour; Pia Ostergaard
Journal:  Genet Med       Date:  2021-04-16       Impact factor: 8.822

Review 9.  Systemic and CNS manifestations of inherited cerebrovascular malformations.

Authors:  Blaine L Hart; Marc C Mabray; Leslie Morrison; Kevin J Whitehead; Helen Kim
Journal:  Clin Imaging       Date:  2021-01-20       Impact factor: 2.420

Review 10.  Zebrafish Vascular Development: General and Tissue-Specific Regulation.

Authors:  Hiroyuki Nakajima; Ayano Chiba; Moe Fukumoto; Nanami Morooka; Naoki Mochizuki
Journal:  J Lipid Atheroscler       Date:  2021-03-02
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