Prenatal cardiac biometry and flow assessment in fetuses with bicuspid aortic valve at 20 weeks' gestation: multicenter cohort study.


Journal

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
ISSN: 1469-0705
Titre abrégé: Ultrasound Obstet Gynecol
Pays: England
ID NLM: 9108340

Informations de publication

Date de publication:
Dec 2021
Historique:
revised: 14 04 2021
received: 10 02 2021
accepted: 28 04 2021
pubmed: 18 5 2021
medline: 28 12 2021
entrez: 17 5 2021
Statut: ppublish

Résumé

To investigate prenatal changes in cardiac biometric and flow parameters in fetuses with bicuspid aortic valve (BAV) diagnosed neonatally compared with controls with normal cardiac anatomy. This analysis was conducted as part of the Copenhagen Baby Heart Study, a multicenter cohort study of 25 556 neonates that underwent second-trimester anomaly scan at 18 + 0 to 22 + 6 weeks' gestation and neonatal echocardiography within 4 weeks after birth, in Copenhagen University Hospital Herlev, Hvidovre Hospital and Rigshospitalet in greater Copenhagen, between April 2016 and October 2018. From February 2017 (Rigshospitalet) and September 2017 (Herlev and Hvidovre hospitals), the protocol for second-trimester screening of the heart was extended to include evaluation of the four-chamber view, with assessment of flow across the atrioventricular valves, sagittal view of the aortic arch and midumbilical artery and ductus venosus pulsatility indices. All images were evaluated by two investigators, and cardiac biometric and flow parameters were measured and compared between cases with BAV and controls. All cases with neonatal BAV were assessed by a specialist. Maternal characteristics and first- and second-trimester biomarkers were also compared between the two groups. Fifty-five infants with BAV and 8316 controls with normal cardiac anatomy were identified during the study period and assessed using the extended prenatal cardiac imaging protocol. There were three times as many mothers who smoked before pregnancy in the group with BAV as in the control group (9.1% vs 2.7%; P = 0.003). All other baseline characteristics were similar between the two groups. Fetuses with BAV, compared with controls, had a significantly larger diameter of the aorta at the level of the aortic valve (3.1 mm vs 3.0 mm (mean difference, 0.12 mm (95% CI, 0.03-0.21 mm))) and the pulmonary artery at the level of the pulmonary valve (4.1 mm vs 3.9 mm (mean difference, 0.15 mm (95% CI, 0.03-0.28 mm))). Following conversion of the diameter measurements of the aorta and pulmonary artery to Z-scores and Bonferroni correction, the differences between the two groups were no longer statistically significant. Pregnancy-associated plasma protein-A (PAPP-A) multiples of the median (MoM) was significantly lower in the BAV group than in the control group (0.85 vs 1.03; P = 0.04). Our findings suggest that fetuses with BAV may have a larger aortic diameter at the level of the aortic valve, measured in the left-ventricular-outflow-tract view, and a larger pulmonary artery diameter at the level of the pulmonary valve, measured in the three-vessel view, at 20 weeks' gestation. Moreover, we found an association of maternal smoking and low PAPP-A MoM with BAV. © 2021 International Society of Ultrasound in Obstetrics and Gynecology.

Identifiants

pubmed: 33998082
doi: 10.1002/uog.23670
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

846-852

Subventions

Organisme : Rigshospitalet

Informations de copyright

© 2021 International Society of Ultrasound in Obstetrics and Gynecology.

Références

Sillesen AS, Vøgg O, Pihl C, Raja AA, Sundberg K, Vedel C, Zingenberg H, Jørgensen FS, Vejlstrup N, Iversen K, Bundgaard H. Prevalence of Bicuspid Aortic Valve and Associated Aortopathy in Newborns in Copenhagen, Denmark. JAMA 2021; 325: 561-567.
Tzemos N, Therrien J, Yip J, Thanassoulis G, Tremblay S, Jamorski MT, Webb GD, Siu SC. Outcomes in adults with bicuspid aortic valves. JAMA 2008; 300: 1317-1325.
Michelena HI, Desjardins VA, Avierinos JF, Russo A, Nkomo VT, Sundt TM, Pellikka PA, Tajik AJ, Enriquez-Sarano M. Natural history of asymptomatic patients with normally functioning or minimally dysfunctional bicuspid aortic valve in the community. Circulation 2008; 117: 2776-2784.
Aquila I, Frati G, Sciarretta S, Dellegrottaglie S, Torella D, Torella M. New imaging techniques project the cellular and molecular alterations underlying bicuspid aortic valve development. J Mol Cell Cardiol 2019; 129: 197-207.
Jiao J, Tian W, Qiu P, Norton EL, Wang MM, Chen YE, Yang B. Induced pluripotent stem cells with NOTCH1 gene mutation show impaired differentiation into smooth muscle and endothelial cells: Implications for bicuspid aortic valve-related aortopathy. J Thorac Cardiovasc Surg 2018; 156: 515-522.e1.
Laforest B, Nemer M. Genetic insights into bicuspid aortic valve formation. Cardiol Res Pract 2012; 2012: 180297.
Galian-Gay L, Carro Hevia A, Teixido-Tura G, Rodriguez Palomares J, Gutierrez-Moreno L, Maldonado G, Gonzalez-Alujas MT, Sao-Aviles A, Gallego P, Calvo-Iglesias F, Bermejo J, Robledo-Carmona J, Sanchez V, Saura D, Sevilla T, Burillo-Sanz S, Guala A, Garcia-Dorado D, Evangelista A. Familial clustering of bicuspid aortic valve and its relationship with aortic dilation in first-degree relatives. Heart 2019; 105: 603-608.
Piatti F, Sturla F, Bissell MM, Pirola S, Lombardi M, Nesteruk I, Della Corte A, Redaelli ACL, Votta E. 4D Flow Analysis of BAV-Related Fluid-Dynamic Alterations: Evidences of Wall Shear Stress Alterations in Absence of Clinically-Relevant Aortic Anatomical Remodeling. Front Physiol 2017; 8: 441.
Sievers HH, Sievers HL. Aortopathy in bicuspid aortic valve disease - genes or hemodynamics? or Scylla and Charybdis? Eur J Cardiothorac Surg 2011; 39: 803-804.
Girdauskas E, Borger MA, Secknus MA, Girdauskas G, Kuntze T. Is aortopathy in bicuspid aortic valve disease a congenital defect or a result of abnormal hemodynamics? A critical reappraisal of a one-sided argument. Eur J Cardiothorac Surg 2011; 39: 809-814.
Broberg CS, Therrien J. Understanding and treating aortopathy in bicuspid aortic valve. Trends Cardiovasc Med 2015; 25: 445-451.
Chau AC, Jones A, Sutherland M, Lilje C, Sernich S, Hagan J, Miller J. Characteristics of Isolated Ventricular Septal Defects Less Likely to Close In Utero. J Ultrasound Med 2018; 37: 1891-1898.
Paladini D, Russo MG, Vassallo M, Tartaglione A, Pacileo G, Martinelli P, Calabro R. Ultrasound evaluation of aortic valve anatomy in the fetus. Ultrasound Obstet Gynecol 2002; 20: 30-34.
Sillesen A-S, Raja AA, Pihl C, Vøgg ROB, Hedegaard M, Emmersen P, Sundberg K, Tabor A, Vedel C, Zingenberg H, Kruse C, Wilken-Jensen C, Nielsen TH, Jøorgensen FS, Jeppesen DL, Søndergaard L, Kamstrup PR, Nordestgaard BG, Frikke-Schmidt R, Vejlstrup N, Boyd HA, Bundgaard H, Iversen K. Copenhagen Baby Heart Study: a population study of newborns with prenatal inclusion. Eur J Epidemiol 2019; 34: 79-90.
DFMS. National Guideline on the 2nd-trimester anomaly scan: Danish Fetal Medicine Society; 2017 [Available from: https://static1.squarespace.com/static/5d8120d60fe9717b4299a867/t/5dd57d655828035255a60bf3/1574272361493/gennemscanningaffostret.pdf.
Robinson HP, Fleming JE. A critical evaluation of sonar “crown-rump length” measurements. Br J Obstet Gynaecol 1975; 82: 702-710.
Ward C. Clinical significance of the bicuspid aortic valve. Heart 2000; 83: 81-85.
Borger MA, Fedak PWM, Stephens EH, Gleason TG, Girdauskas E, Ikonomidis JS, Khoynezhad A, Siu SC, Verma S, Hope MD, Cameron DE, Hammer DF, Coselli JS, Moon MR, Sundt TM, Barker AJ, Markl M, Della Corte A, Michelena HI, Elefteriades JA. The American Association for Thoracic Surgery consensus guidelines on bicuspid aortic valve-related aortopathy: Full online-only version. J Thorac Cardiovasc Surg 2018; 156: e41-e74.
Peterson JC, Chughtai M, Wisse LJ, Gittenberger-de Groot AC, Feng Q, Goumans M-JTH, VanMunsteren JC, Jongbloed MRM, DeRuiter MC. Bicuspid aortic valve formation: Nos3 mutation leads to abnormal lineage patterning of neural crest cells and the second heart field. Dis Model Mech 2018; 11: dmm034637.
Li W, Zhou J, Chen Y, Zhang G, Jiang P, Hong L, Shen Y, Wang X, Gong X. Cigarette smoke enhances initiation and progression of lung cancer by mutating Notch1/2 and dysregulating downstream signaling molecules. Oncotarget 2017; 8: 115128-115139.
Garg V, Muth AN, Ransom JF, Schluterman MK, Barnes R, King IN, Grossfeld PD, Srivastava D. Mutations in NOTCH1 cause aortic valve disease. Nature 2005; 437: 270-274.
Bonachea EM, Zender G, White P, Corsmeier D, Newsom D, Fitzgerald-Butt S, Garg V, McBride KL. Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve. BMC Med Genomics 2014; 7: 56.
Llurba E, Syngelaki A, Sanchez O, Carreras E, Cabero L, Nicolaides KH. Maternal serum placental growth factor at 11-13 weeks' gestation and fetal cardiac defects. Ultrasound Obstet Gynecol 2013; 42: 169-174.
Fantasia I, Kasapoglu D, Kasapoglu T, Syngelaki A, Akolekar R, Nicolaides KH. Fetal major cardiac defects and placental dysfunction at 11-13 weeks' gestation. Ultrasound Obstet Gynecol 2018; 51: 194-198.

Auteurs

C Vedel (C)

Center of Fetal Medicine and Pregnancy, Department of Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark.

L Rode (L)

Department of Clinical Biochemistry, Copenhagen University Hospital Rigshospitalet, Glostrup, Denmark.

H Bundgaard (H)

University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark.
Department of Cardiology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

K Iversen (K)

University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark.
Department of Cardiology, Copenhagen University Hospital Herlev, Herlev, Denmark.

F S Jørgensen (FS)

University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark.
Fetal Medicine Unit, Department of Obstetrics and Gynecology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.

O B Petersen (OB)

Center of Fetal Medicine and Pregnancy, Department of Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark.

A-S Sillesen (AS)

Department of Cardiology, Copenhagen University Hospital Herlev, Herlev, Denmark.

K Sundberg (K)

Center of Fetal Medicine and Pregnancy, Department of Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

N Vejlstrup (N)

Department of Cardiology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

H Zingenberg (H)

Department of Obstetrics and Gynecology, Copenhagen University Hospital Herlev, Herlev, Denmark.

A Tabor (A)

Center of Fetal Medicine and Pregnancy, Department of Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark.

C K Ekelund (CK)

Center of Fetal Medicine and Pregnancy, Department of Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH