Literature DB >> 9538314

Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect.

M Chessa1, G Butera, P Bonhoeffer, L Iserin, J Kachaner, S Lyonnet, A Munnich, D Sidi, D Bonnet.   

Abstract

OBJECTIVE: To compare the morphology of the pulmonary vessels in tetralogy of Fallot or pulmonary atresia-ventricular septal defect (PA-VSD) with (del22q) and without 22Q11 deletion (non-del22q). PATIENTS: 94 consecutive infants (54 with tetralogy of Fallot, 40 with PA-VSD) were studied using ultrasound and catheterisation. MOLECULAR INVESTIGATIONS: Identification of the 22q deletion was performed either by fluorescent in situ hybridisation or polymerisation chain reaction genotyping.
RESULTS: 25 patients were del22q (16/40 (40%) PA-VSD v 9/54 (17%) tetralogy of Fallot; p < 0.02). Major aortopulmonary collateral arteries was more common in patients with PA-VSD-del22q (p < 0.03). Such collaterals were identified in 13 patients: 10 del22q and three non-del22q (p < 0.001). The size of the right and left pulmonary arteries expressed as a standard deviation (SD) difference of the normal range was -4.2 (quartiles -5.3 and -2.9) for PA-VSD del22q, and -2.6 (-3.1 and -1.8) for PA-VSD non-del22q (p = 0.02). The mean (SD) difference between the measured and theoretical Nakata index was -373 (94) for PA-VSD del22q v -245 (93) in PA-VSD non-del22q (p = 0.0002). In tetralogy of Fallot patients with and without del22q, the size of the pulmonary arteries was similar (p = 0.6).
CONCLUSIONS: A "specific" phenotype could be defined in patients with deletion: PA-VSD, major aortopulmonary collateral arteries with complex loop morphology, and small central pulmonary arteries. Differences in the morphology of the pulmonary vessels may indicate a different timing of the faulty developmental pathway in patients with and without 22q11 deletion.

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Mesh:

Year:  1998        PMID: 9538314      PMCID: PMC1728608          DOI: 10.1136/hrt.79.2.186

Source DB:  PubMed          Journal:  Heart        ISSN: 1355-6037            Impact factor:   5.994


  25 in total

1.  Dinucleotide repeat polymorphism at the D22S264 locus.

Authors:  C Marineau; M Aubry; J P Julien; G A Rouleau
Journal:  Nucleic Acids Res       Date:  1992-03-25       Impact factor: 16.971

2.  Pathogenesis of persistent truncus arteriosus and dextroposed aorta in the chick embryo after neural crest ablation.

Authors:  M Nishibatake; M L Kirby; L H Van Mierop
Journal:  Circulation       Date:  1987-01       Impact factor: 29.690

3.  Cardiac morphogenesis--recent research advances.

Authors:  M L Kirby
Journal:  Pediatr Res       Date:  1987-03       Impact factor: 3.756

4.  Neural crest cells contribute to normal aorticopulmonary septation.

Authors:  M L Kirby; T F Gale; D E Stewart
Journal:  Science       Date:  1983-06-03       Impact factor: 47.728

5.  Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

Authors:  P J Scambler; A H Carey; R K Wyse; S Roach; J P Dumanski; M Nordenskjold; R Williamson
Journal:  Genomics       Date:  1991-05       Impact factor: 5.736

6.  Microsatellite DNA markers detects 95% of chromosome 22q11 deletions.

Authors:  D Bonnet; V Cormier-Daire; J Kachaner; I Szezepanski; P Souillard; D Sidi; A Munnich; S Lyonnet
Journal:  Am J Med Genet       Date:  1997-01-20

7.  A new method for the quantitative standardization of cross-sectional areas of the pulmonary arteries in congenital heart diseases with decreased pulmonary blood flow.

Authors:  S Nakata; Y Imai; Y Takanashi; H Kurosawa; K Tezuka; M Nakazawa; M Ando; A Takao
Journal:  J Thorac Cardiovasc Surg       Date:  1984-10       Impact factor: 5.209

8.  Cardiovascular malformations in DiGeorge syndrome (congenital absence of hypoplasia of the thymus).

Authors:  P Moerman; P Goddeeris; J Lauwerijns; L G Van der Hauwaert
Journal:  Br Heart J       Date:  1980-10

9.  Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.

Authors:  D A Driscoll; N B Spinner; M L Budarf; D M McDonald-McGinn; E H Zackai; R B Goldberg; R J Shprintzen; H M Saal; J Zonana; M C Jones
Journal:  Am J Med Genet       Date:  1992-09-15

Review 10.  Mesenchymal derivatives from the neural crest.

Authors:  H Nakamura
Journal:  Arch Histol Jpn       Date:  1982-05
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  13 in total

1.  22q11.2 Deletion Status and Perioperative Outcomes for Tetralogy of Fallot with Pulmonary Atresia and Multiple Aortopulmonary Collateral Vessels.

Authors:  Laura Mercer-Rosa; Okan U Elci; Nelangi M Pinto; Ronn E Tanel; Elizabeth Goldmuntz
Journal:  Pediatr Cardiol       Date:  2018-03-08       Impact factor: 1.655

2.  Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot.

Authors:  Sara Piran; Anne S Bassett; Jasmine Grewal; Jodi-Ann Swaby; Chantal Morel; Erwin N Oechslin; Andrew N Redington; Peter P Liu; Candice K Silversides
Journal:  Am Heart J       Date:  2011-01       Impact factor: 4.749

Review 3.  Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

Authors:  Marta Unolt; Paolo Versacci; Silvia Anaclerio; Caterina Lambiase; Giulio Calcagni; Matteo Trezzi; Adriano Carotti; Terrence Blaine Crowley; Elaine H Zackai; Elizabeth Goldmuntz; James William Gaynor; Maria Cristina Digilio; Donna M McDonald-McGinn; Bruno Marino
Journal:  Am J Med Genet A       Date:  2018-04-16       Impact factor: 2.802

4.  Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.

Authors:  Fabíola P Monteiro; Társis P Vieira; Ilária C Sgardioli; Miriam C Molck; Ana Paula Damiano; Josiane Souza; Isabella L Monlleó; Marshall I B Fontes; Agnes C Fett-Conte; Têmis M Félix; Gabriela F Leal; Erlane M Ribeiro; Claudio E M Banzato; Clarissa de R Dantas; Iscia Lopes-Cendes; Vera Lúcia Gil-da-Silva-Lopes
Journal:  Eur J Pediatr       Date:  2013-02-26       Impact factor: 3.183

5.  Pulmonary atresia with intact ventricular septum and major aortopulmonary collaterals: association with deletion 22q11.2.

Authors:  C Li; A E Chudley; R Soni; A Divekar
Journal:  Pediatr Cardiol       Date:  2003-07-29       Impact factor: 1.655

6.  Prenatally diagnosed pulmonary atresia with ventricular septal defect: echocardiography, genetics, associated anomalies and outcome.

Authors:  S Vesel; S Rollings; A Jones; N Callaghan; J Simpson; G K Sharland
Journal:  Heart       Date:  2006-03-17       Impact factor: 5.994

7.  Management of Pulmonary Atresia with Ventricular Septal Defect.

Authors:  Douglas D. Mair; Franciso J. Puga
Journal:  Curr Treat Options Cardiovasc Med       Date:  2003-10

8.  Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.

Authors:  Lidia Ziolkowska; Wanda Kawalec; Anna Turska-Kmiec; Malgorzata Krajewska-Walasek; Grazyna Brzezinska-Rajszys; Jadwiga Daszkowska; Bogdan Maruszewski; Piotr Burczynski
Journal:  Eur J Pediatr       Date:  2008-01-03       Impact factor: 3.183

9.  The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome.

Authors:  A Kyburz; U Bauersfeld; A Schinzel; M Riegel; M Hug; M Tomaske; E R Valsangiacomo Büchel
Journal:  Pediatr Cardiol       Date:  2007-09-29       Impact factor: 1.655

10.  Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome).

Authors:  Mc Digilio; B Marino; R Capolino; B Dallapiccola
Journal:  Images Paediatr Cardiol       Date:  2005-04
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