Literature DB >> 18172682

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

Lidia Ziolkowska1, Wanda Kawalec, Anna Turska-Kmiec, Malgorzata Krajewska-Walasek, Grazyna Brzezinska-Rajszys, Jadwiga Daszkowska, Bogdan Maruszewski, Piotr Burczynski.   

Abstract

The association of conotruncal heart defects with 22q11.2 chromosomal microdeletions is well established. However, it is not clear whether particular types of conotruncal malformations or additional cardiovascular anomalies are associated with microdeletions. In addition, cardiac surgery outcome in children with conotruncal defects and del22q11.2 is not well described. We prospectively enrolled 214 children with conotruncal defects: 126 with tetralogy of Fallot (TOF), 18 with pulmonary atresia-ventricular septal defect (PA-VSD), 15 with truncus arteriosus communis (TAC) type I, one with interrupted aortic arch (IAA) type B, and 54 with the transposition of great arteries, who were consecutively hospitalized at the Pediatric Cardiology Department between 2003 and 2005. 22q11.2 microdeletion was identified by fluorescence in situ hybridization. The postoperative course following cardiac surgery was compared in patients with TOF and its more severe form, PA-VSD, with/without del22q11.2 (groups A and B) and TAC with/without del22q11.2 (groups C and D). In 15 of 214 patients, 22q11.2 microdeletion was diagnosed (in 11 with TOF/PA-VSD, in three with TAC, in one with IAA type B). In patients with TOF/PA-VSD and microdeletion anatomic features that were significantly associated with 22q11.2, deletion included right aortic arch (p = 0.018), aberrant right subclavian artery (p < 0.001), and major aortopulmonary collateral arteries (p = 0.016). A complicated postoperative course was more frequent and mortality was higher in patients with conotruncal defects and with/without microdeletion. We conclude that additional cardiovascular anomalies are significantly more frequent in children with 22q11.2 microdeletion and TOF/PA-VSD. Children with conotruncal heart defects and 22q11.2 microdeletion more frequently experienced complicated postoperative course after cardiac surgery.

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Year:  2008        PMID: 18172682     DOI: 10.1007/s00431-007-0645-2

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  19 in total

1.  22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin.

Authors:  S Fokstuen; U Arbenz; S Artan; F Dutly; U Bauersfeld; L Brecevic; M Fasnacht; B Röthlisberger; A Schinzel
Journal:  Clin Genet       Date:  1998-01       Impact factor: 4.438

2.  Operative mortality and frequency of coexistent anomalies in interruption of the aortic arch.

Authors:  C B Powell; F M Stone; D L Atkins; D G Watson; J H Moller
Journal:  Am J Cardiol       Date:  1997-04-15       Impact factor: 2.778

3.  Abnormalities in lymphocyte populations in infants with neural crest cardiovascular defects.

Authors:  D K Rhoden; L Leatherbury; S Helman; M Gaffney; W B Strong; M F Guill
Journal:  Pediatr Cardiol       Date:  1996 May-Jun       Impact factor: 1.655

4.  Early and intermediate outcomes after repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries: experience with 85 patients.

Authors:  V M Reddy; D B McElhinney; Z Amin; P Moore; A J Parry; D F Teitel; F L Hanley
Journal:  Circulation       Date:  2000-04-18       Impact factor: 29.690

5.  22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.

Authors:  F Amati; A Mari; M C Digilio; R Mingarelli; B Marino; A Giannotti; G Novelli; B Dallapiccola
Journal:  Hum Genet       Date:  1995-05       Impact factor: 4.132

6.  Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Authors:  J Burn; A Takao; D Wilson; I Cross; K Momma; R Wadey; P Scambler; J Goodship
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

7.  Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.

Authors:  K Momma; C Kondo; R Matsuoka
Journal:  J Am Coll Cardiol       Date:  1996-01       Impact factor: 24.094

8.  Results of a policy of primary repair of truncus arteriosus in the neonate.

Authors:  E L Bove; F M Lupinetti; A K Pridjian; R H Beekman; L B Callow; A R Snider; A Rosenthal
Journal:  J Thorac Cardiovasc Surg       Date:  1993-06       Impact factor: 5.209

9.  Anatomic patterns of conotruncal defects associated with deletion 22q11.

Authors:  B Marino; M C Digilio; A Toscano; S Anaclerio; A Giannotti; C Feltri; M A de Ioris; A Angioni; B Dallapiccola
Journal:  Genet Med       Date:  2001 Jan-Feb       Impact factor: 8.822

10.  Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Authors:  A K Ryan; J A Goodship; D I Wilson; N Philip; A Levy; H Seidel; S Schuffenhauer; H Oechsler; B Belohradsky; M Prieur; A Aurias; F L Raymond; J Clayton-Smith; E Hatchwell; C McKeown; F A Beemer; B Dallapiccola; G Novelli; J A Hurst; J Ignatius; A J Green; R M Winter; L Brueton; K Brøndum-Nielsen; P J Scambler
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

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  20 in total

Review 1.  How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease.

Authors:  Alvin J Chin; Jean-Pierre Saint-Jeannet; Cecilia W Lo
Journal:  Mech Dev       Date:  2012-05-26       Impact factor: 1.882

Review 2.  CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes.

Authors:  Benjamin J Landis; David S Cooper; Robert B Hinton
Journal:  Cardiol Young       Date:  2015-09-08       Impact factor: 1.093

3.  Hospital Survival After Surgical Repair of Truncus Arteriosus with Interrupted Aortic Arch: Results from a Multi-institutional Database.

Authors:  Brandon A Jones; Mark R Conaway; Michael C Spaeder; Peter N Dean
Journal:  Pediatr Cardiol       Date:  2021-03-30       Impact factor: 1.655

4.  The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome.

Authors:  Goran Cuturilo; Danijela Drakulic; Ida Jovanovic; Slobodan Ilic; Jasna Kalanj; Irena Vulicevic; Misela Raus; Dejan Skoric; Marija Mijovic; Biljana Medjo; Snezana Rsovac; Milena Stevanovic
Journal:  Pediatr Cardiol       Date:  2017-09-22       Impact factor: 1.655

Review 5.  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

Review 6.  22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects.

Authors:  Carolina Putotto; Flaminia Pugnaloni; Marta Unolt; Stella Maiolo; Matteo Trezzi; Maria Cristina Digilio; Annapaola Cirillo; Giuseppe Limongelli; Bruno Marino; Giulio Calcagni; Paolo Versacci
Journal:  Children (Basel)       Date:  2022-05-25

7.  Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India.

Authors:  Ashutosh Halder; Manish Jain; Isha Chaudhary; Madhulika Kabra
Journal:  BMC Med Genet       Date:  2010-06-23       Impact factor: 2.103

8.  22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases.

Authors:  Shabnam Peyvandi; Philip J Lupo; Jennifer Garbarini; Stacy Woyciechowski; Sharon Edman; Beverly S Emanuel; Laura E Mitchell; Elizabeth Goldmuntz
Journal:  Pediatr Cardiol       Date:  2013-04-21       Impact factor: 1.655

Review 9.  The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review.

Authors:  Diana Cárdenas-Nieto; Maribel Forero-Castro; Clara Esteban-Pérez; Julio Martínez-Lozano; Ignacio Briceño-Balcázar
Journal:  J Pediatr Genet       Date:  2019-10-23

10.  Cardiac abnormalities and facial anthropometric measurements in children from the Free State and Northern Cape provinces of South Africa with chromosome 22q11.2 microdeletion.

Authors:  S C Brown; B D Henderson; D A Buys; M Theron; M A Long; F Smit
Journal:  Cardiovasc J Afr       Date:  2010 Jan-Feb       Impact factor: 1.167

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