Literature DB >> 34999808

NT5E mutation in sisters who underwent aortic valve replacements for aortic stenosis.

Tetsuro Uchida1, Atsushi Yamashita1, Ai Ishizawa1, Mitsuaki Sadahiro1, Nobuyoshi Azuma2, Tadashi Kaname3.   

Abstract

Mutations of the NT5E gene encoding the cluster of differentiation 73 (CD73) protein have been found in patients with characteristic calcification of joints and arteries (CALJA). CD73 plays a protective role against aortic valve calcification; therefore, its deletion results in aortic valve calcification. However, to date, there are no reports of a patient with CALJA with aortic stenosis. In this study, we describe 2 extremely rare cases of sisters with identical NT5E gene mutation patterns, both of whom developed late-onset severe aortic stenosis and limb ischaemia. Both patients underwent aortic valve replacement and bilateral distal arterial bypass surgeries successfully. They were genetically diagnosed with CALJA based on the NT5E mutation. Our report suggests that NT5E mutations should be considered in patients requiring aortic valve replacement for a calcified aortic valve and bypass surgery for specific calcified and occluded arteries.
© The Author(s) 2021. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.

Entities:  

Keywords:  Aortic stenosis; Aortic valve replacement; NT5E gene mutation

Mesh:

Substances:

Year:  2021        PMID: 34999808      PMCID: PMC8932508          DOI: 10.1093/icvts/ivab229

Source DB:  PubMed          Journal:  Interact Cardiovasc Thorac Surg        ISSN: 1569-9285


  8 in total

1.  NT5E mutations and arterial calcifications.

Authors:  Cynthia St Hilaire; Shira G Ziegler; Thomas C Markello; Alfredo Brusco; Catherine Groden; Fred Gill; Hannah Carlson-Donohoe; Robert J Lederman; Marcus Y Chen; Dan Yang; Michael P Siegenthaler; Carlo Arduino; Cecilia Mancini; Bernard Freudenthal; Horia C Stanescu; Anselm A Zdebik; R Krishna Chaganti; Robert L Nussbaum; Robert Kleta; William A Gahl; Manfred Boehm
Journal:  N Engl J Med       Date:  2011-02-03       Impact factor: 91.245

2.  Deletion of CD73 in mice leads to aortic valve dysfunction.

Authors:  P Zukowska; B Kutryb-Zajac; A Jasztal; M Toczek; M Zabielska; T Borkowski; Z Khalpey; R T Smolenski; E M Slominska
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2017-02-10       Impact factor: 5.187

3.  Calcification of joints and arteries: second report with novel NT5E mutations and expansion of the phenotype.

Authors:  Zeng Zhang; Jin-Wei He; Wen-Zhen Fu; Chang-Qing Zhang; Zhen-Lin Zhang
Journal:  J Hum Genet       Date:  2015-07-16       Impact factor: 3.172

4.  Isolated arterial calcifications of the lower extremities: A clue for NT5E mutation.

Authors:  Tjerk de Nijs; Juliette Albuisson; Charlotte W Ockeloen; Anne Legrand; Xavier Jeunemaitre; Leo J Schultze Kool; Niels P Riksen
Journal:  Int J Cardiol       Date:  2016-03-19       Impact factor: 4.164

5.  Calcification of joints and arteries with novel NT5E mutations with involvement of upper extremity arteries.

Authors:  Kenji Yoshioka; Shunsuke Kuroda; Kentaro Takahashi; Tetsuo Sasano; Tetsushi Furukawa; Akihiko Matsumura
Journal:  Vasc Med       Date:  2017-08-19       Impact factor: 3.239

6.  Polymorphism in exon 6 of the human NT5E gene is associated with aortic valve calcification.

Authors:  Zdzislaw Kochan; Joanna Karbowska; Patrycja Gogga; Barbara Kutryb-Zajac; Ewa M Slominska; Ryszard T Smolenski
Journal:  Nucleosides Nucleotides Nucleic Acids       Date:  2016-12       Impact factor: 1.381

7.  Arterial Calcification Due to Deficiency of CD73 (ACDC) As One of Rheumatic Diseases Associated With Periarticular Calcification.

Authors:  Naomi Ichikawa; Atsuo Taniguchi; Hirotaka Kaneko; Manabu Kawamoto; Chieko Sekita; Ayako Nakajima; Hisashi Yamanaka
Journal:  J Clin Rheumatol       Date:  2015-06       Impact factor: 3.517

8.  Definitive diagnosis of mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome caused by a recurrent de novo mutation in the POLD1 gene.

Authors:  Haruka Sasaki; Kumiko Yanagi; Satoshi Ugi; Kunihisa Kobayashi; Kumiko Ohkubo; Yuji Tajiri; Hiroshi Maegawa; Atsunori Kashiwagi; Tadashi Kaname
Journal:  Endocr J       Date:  2017-12-02       Impact factor: 2.349

  8 in total

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