Lack of association between folate receptor autoantibodies and conotruncal congenital heart defects.

Abstract:

:Conotruncal cardiac defects are partially prevented by maternal folic acid supplementation. However, the biochemical mechanism is unknown. Maternal autoantibodies to folate receptors, previously associated with increased risk for neural tube defects, also may account for this effect. This study aimed to examine the titers of folate receptor-blocking autoantibodies in mothers of children with conotruncal congenital heart defects and to compare them with those in the general population. Serum samples were obtained from 22 women whose pregnancies were complicated by conotruncal congenital heart malformations. Groups of samples were analyzed for autoantibodies against [(3)H] folic acid-labeled folate receptors, quantitative amounts of immunoglobulin G (IgG) and IgM autoantibodies to the folate receptor, and for ability to block-bind folic acid to receptors. No elevated levels of antibodies binding to [(3)H] folic acid-labeled folate receptors were found. No difference was found in antifolate receptor alpha-IgG or IgM median levels between cases (261 vs. 240 μg/mL) and control subjects (773 vs. 924 μg/mL). There was no increased blocking of folic acid binding between cases [0.69 ng/mL; 95 % confidence interval (CI), 0.006-0.01] and control subjects (0.69 ng/mL; 95 % CI, 0.003-0.013). Although epidemiologic evidence suggests that periconceptual folic acid may prevent many conotruncal congenital heart defects, the current study suggests that this effect is unlikely to be explained by the presence of maternal autoantibodies to folate receptor. These data suggest that a strategy of screening women for such autoantibodies will not identify a high-risk group of women to target for supplemental folic acid to prevent congenital heart defects.

journal_name

Pediatr Cardiol

journal_title

Pediatric cardiology

authors

Lewandowski LB,Sanghavi D

doi

10.1007/s00246-012-0485-3

subject

Has Abstract

pub_date

2013-03-01 00:00:00

pages

512-7

issue

3

eissn

0172-0643

issn

1432-1971

journal_volume

34

pub_type

杂志文章
  • Increasing Burden of Lyme Carditis in United States Children's Hospitals.

    abstract::We sought to characterize the shifting epidemiology and resource utilization of Lyme disease and associated carditis in US children's hospitals. We hypothesized that the Lyme carditis burden has increased and that hospitalizations for Lyme carditis are costlier than those for Lyme disease without carditis. The PHIS da...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-019-02250-9

    authors: Beach CM,Hart SA,Nowalk A,Feingold B,Kurland K,Arora G

    更新日期:2020-02-01 00:00:00

  • Device closure of secundum atrial septal defects in infants weighing less than 8 kg.

    abstract::This study aimed to assess the technical aspects of atrial septal defect (ASD) closure using the Amplatzer septal occluder (ASO) and the Gore Helex septal occluder (GHSO) for infants weighing less than 8 kg and to determine the safety, effectiveness, and near-to-intermediate-term outcome of the closure. The Mid-Atlant...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00246-014-0905-7

    authors: Bishnoi RN,Everett AD,Ringel RE,Owada CY,Holzer RJ,Chisolm JL,Radtke WA,Scott Lim D,Rhodes JF Jr,Coulson JD

    更新日期:2014-10-01 00:00:00

  • Heart rate and systolic time intervals in healthy newborn infants: longitudinal study.

    abstract::To determine the influence of heart rate (HR) on systolic time intervals (STI) in neonates, serial measurements of right ventricular (RVSTI) and left ventricular systolic time intervals (LVSTI) were made on 30 healthy term newborn infants at age 4-8 h, 24-30 h, eight days, and four weeks. STI was related to HR and age...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02336549

    authors: Lindner W,Döhlemann C,Schneider K,Versmold H

    更新日期:1985-01-01 00:00:00

  • Magnetocardiographic localization of ventricular pre-excitation in a child with a congenital heart defect.

    abstract::Magnetocardiographic mapping was performed on a 2-year-old boy who suffered from the Wolff-Parkinson-White syndrome in association with a complex congenital heart defect. The pre-excitation site was determined noninvasively from the measured cardiac magnetic fields. The location was in the same anatomic region as foun...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02310333

    authors: Nenonen J,Rovamo L,Toivonen L,Ilmoniemi R,Järvinen A,Leiniö M,Montonen J,Nisula L

    更新日期:1995-01-01 00:00:00

  • Aneurysm of the fossa ovalis in infants: a pathologic study.

    abstract::An aneurysm of the fossa ovalis was identified at autopsy in 17 infants. In each case the aneurysm of the fossa ovalis was considered to have resulted from excessive elevation of pressure in that atrium contralateral to the side into which the aneurysm bulged. The aneurysms were divided into two types: intrinsic (thre...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02282740

    authors: Topaz O,Feigl A,Edwards JE

    更新日期:1985-01-01 00:00:00

  • Epidemiology, etiology, and management of Kawasaki disease: state of the art.

    abstract::Since its first description in Japan 30 years ago, Kawasaki disease has been reported worldwide. Although an infectious etiology is suspected based on the epidemiology and clinical features, a causative agent has not been identified. The majority of the morbidity and mortality associated with this condition is attribu...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s002469900436

    authors: Laupland KB,Dele Davies H

    更新日期:1999-05-01 00:00:00

  • Right Ventricular Pressure Overload and Pathophysiology of Growing Porcine Biomodel.

    abstract::The primary objective was to create a clinically relevant model of right ventricular hypertension and to study right ventricular myocardial pathophysiology in growing organism. The secondary objective was to analyse the effect of oral enoximone (phosphodiesterase inhibitor) therapy on right ventricular haemodynamic pa...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-016-1463-y

    authors: Kobr J,Slavik Z,Uemura H,Saeed I,Furck A,Pizingerová K,Fremuth J,Tonar Z

    更新日期:2016-12-01 00:00:00

  • A patient with kawasaki disease showing severe tricuspid regurgitation and left ventricular dysfunction in the acute phase.

    abstract::We encountered a male aged 6 years 4 months with Kawasaki disease (KD) with severe tricuspid regurgitation and left ventricular dysfunction in the acute phase. His clinical course and findings of endomyocardial biopsy suggested that myocarditis was the cause of left ventricular dysfunction and responsible for the deve...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-002-0137-0

    authors: Shinohara T,Tanihira Y

    更新日期:2003-01-01 00:00:00

  • Transposition of Great Arteries with Complex Coronary Artery Variants: Time-Related Events Following Arterial Switch Operation.

    abstract::Coronary artery anatomy represents a challenging and, often, determining predictor of outcome in an arterial switch operation (ASO). Impact of specific coronary artery variants, such as single, intramural and inverted, on time-related events following ASO, is, yet, to be determined. We sought to compare early and late...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-016-1543-z

    authors: Al Anani S,Fughhi I,Taqatqa A,Elzein C,Ilbawi MN,Polimenakos AC

    更新日期:2017-03-01 00:00:00

  • Catecholaminergic Ventricular Tachycardia, Pregnancy and Teenager: Are They Compatible?

    abstract::Arrhythmias in pregnancy are becoming more common given more available and effective medical, ablation and device treatment options. Several changes associated with pregnancy, increased blood volume, cardiac output, and heart rate secondary to an increased sympathetic state, facilitate more frequent occurrences of arr...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-015-1232-3

    authors: Friday KP,Moak JP,Fries MH,Iqbal SN

    更新日期:2015-10-01 00:00:00

  • Pattern of recovery for transient complete heart block after open heart surgery for congenital heart disease: duration alone predicts risk of late complete heart block.

    abstract::Transient complete heart block (TCHB) is defined as complete interruption of atrioventricular conduction (AVC) after cardiac surgery followed by return of conduction. This study aimed to assess the risk for the development of late complete heart block (LCHB) after recovery of TCHB and to examine the electrocardiograph...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0595-y

    authors: Aziz PF,Serwer GA,Bradley DJ,LaPage MJ,Hirsch JC,Bove EL,Ohye RG,Dick M 2nd

    更新日期:2013-04-01 00:00:00

  • Longitudinal observations of left ventricular end-diastolic dimension in children using echocardiography.

    abstract::Previous studies have evaluated left ventricular dimensions in children using two-dimensional echocardiography, but there is little information on gender differences and on the longitudinal development of the dimensions of the left ventricle. Our objective was to assess, by two-dimensional echocardiography, the normal...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02505207

    authors: Nagasawa H,Arakaki Y,Yamada O,Nakajima T,Kamiya T

    更新日期:1996-05-01 00:00:00

  • Successful combined orthotopic liver transplant and transcatheter management of atrial septal defect, patent ductus arteriosus, and peripheral pulmonic stenosis in a small infant with Alagille syndrome.

    abstract::We report on a 4-kg infant with Alagille syndrome and congenital heart disease consisting of atrial septal defect (ASD), patent ductus arteriosus (PDA), and severe peripheral pulmonic stenosis. He underwent successful orthotopic liver transplant along with catheter closure of the ASD and PDA using the Amplatzer device...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:

    authors: Harris M,Cao QL,Waight D,Hijazi ZM

    更新日期:2002-11-01 00:00:00

  • Double-outlet single ventricle and an abdominal vascular mass: in utero diagnosis with pathological confirmation.

    abstract::A fetal echocardiographic scan was performed when routine prenatal ultrasound screening failed to identify four cardiac chambers. The scan showed a single ventricle with an associated circoid varicosity. Because of these anomalies, amniocentesis was suggested and trisomy 18 confirmed. The presence of major cardiac str...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF00794843

    authors: Duncan WJ,George D,Ezzat W,Wallace K,Van den Beuken B

    更新日期:1993-01-01 00:00:00

  • Polymorphism 677C → T MTHFR gene in Mexican mothers of children with complex congenital heart disease.

    abstract::Congenital heart defects (CHD) are the third leading cause of death in children <1 year of age in Mexico where there is a high prevalence of the 677C → T polymorphism of the MTHFR gene. This is important because the homozygous 677T/T MTHFR gene and deficiency of folic acid (FA) intake have been associated with CHD. Ou...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0380-y

    authors: Balderrábano-Saucedo NA,Sánchez-Urbina R,Sierra-Ramírez JA,García-Hernández N,Sánchez-Boiso A,Klunder-Klunder M,Arenas-Aranda D,Bravo-Hernández G,Noriega-Zapata P,Vizcaíno-Alarcón A

    更新日期:2013-01-01 00:00:00

  • A triad: cardiac rhabdomyosarcoma, stroke and tamponade.

    abstract::The case report describes a 9-year-old boy who presented with an acute cerebrovascular accident and was found to have cardiac tamponade caused by cardiac rhabdomyosarcoma. Symptoms of rhabdomyosarcoma can be indolent and nonspecific, even with metastatic disease. Echocardiography and cardiac magnetic resonance imaging...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0549-4

    authors: Ashraf T,Day TG,Marek J,Hughes M,Giardini A

    更新日期:2013-03-01 00:00:00

  • Congenital giant aneurysm of the left innominate vein: is surgical treatment required?

    abstract::Congenital aneurysms of the thoracic venous system are rare. In particular, innominate venous aneurysms are extremely rare. We describe a 16-year-old girl whose chest x-ray suggested a mediastinal tumor. Three-dimensional contrast-enhancement magnetic resonance venography showed a giant sacciform aneurysm of the left ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-003-0499-y

    authors: Tsuji A,Katada Y,Tanimoto M,Fujita I

    更新日期:2004-07-01 00:00:00

  • Association of Hematocrit and Red Blood Cell Transfusion with Outcomes in Infants Undergoing Norwood Operation.

    abstract::The objective of this study was to investigate the association between red blood cell (RBC) transfusion and hematocrit values with outcomes in infants undergoing Norwood operation. This study included infants ≤2 months of age who underwent Norwood operation with either a modified Blalock-Taussig shunt or a right ventr...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-015-1147-z

    authors: Gupta P,King C,Benjamin L,Goodhart T,Robertson MJ,Gossett JM,Pesek GA,DasGupta R

    更新日期:2015-08-01 00:00:00

  • Exercise stress echocardiography after childhood Ross surgery: functional outcome in 26 patients from a single institution.

    abstract::Adult studies suggest a better functional outcome after aortic valve replacement with a pulmonary autograft compared with mechanical or homograft valves. Little is known about functional results after Ross surgery in growing children. This study reports formal exercise stress echocardiographic data from 26 pediatric R...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0218-7

    authors: Pauliks LB,Brian Clark J,Rogerson A,DiPietro A,Myers JL,Cyran SE

    更新日期:2012-06-01 00:00:00

  • Outcomes following electroanatomic mapping and ablation for the treatment of ectopic atrial tachycardia in the pediatric population.

    abstract::Ectopic atrial tachycardia (EAT) is often resistant to medical therapy, with radiofrequency ablation (RFA) being a preferred treatment option. Three-dimensional (3-D) electroanatomic mapping was introduced as a tool for improved substrate localization, although there are no published data with this technology in pedia...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00246-007-9137-4

    authors: Cummings RM,Mahle WT,Strieper MJ,Campbell RM,Costello L,Balfour V,Burchfield A,Frias PA

    更新日期:2008-03-01 00:00:00

  • Echocardiographic abnormalities in familial dysautonomia.

    abstract::Sudden death accounts for up to 43% of all deaths in patients with familial dysautonomia (FD). The classic features of FD, namely, autonomic dysfunction, high blood pressure, and blood pressure labiality, are all risk factors for cardiac remodeling and hypertrophy. Myocardial remodeling and hypertrophy are independent...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-009-9497-z

    authors: Nussinovitch U,Katz U,Nussinovitch M,Blieden L,Nussinovitch N

    更新日期:2009-11-01 00:00:00

  • Rho-kinase in development and heart failure: insights from genetic models.

    abstract::Rho-kinase (ROCK) belongs to the AGC (protein kinase A/protein kinase G/protein kinase C, PKA/PKG/PKC) family of serine/threonine kinases and is a major downstream effector of small GTPase RhoA. Rho-kinase is involved in a wide range of fundamental cellular functions such as contraction, adhesion, migration, and proli...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-011-9920-0

    authors: Shi J,Zhang L,Wei L

    更新日期:2011-03-01 00:00:00

  • Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary tale.

    abstract::A two-year-old child who had had palliative surgery as a neonate for an absent right atrioventricular connection and double-inlet ventricle was shown to be developmentally retarded. Trisomy for the short arm of chromosome 8 was demonstrated, resulting from a familial 8:13 translocation, with a high risk of recurrence....

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02306750

    authors: Burn J,Baraitser M,Hughes DT,Saldana-Garcia P,Taylor JF

    更新日期:1984-01-01 00:00:00

  • The Challenge of Hammock Mitral Valve During Infancy: Precise Preoperative Advanced Imaging and Three-Dimensional Modeling Augments Customized Operative Valve Reconstruction.

    abstract::Hammock mitral valve (MV), also known as anomalous mitral arcade, is a rare congenital anomaly. We report a case of a 10-month-old child who presented with congestive heart failure and was found to have severe mitral stenosis (MS) secondary to a hammock MV anomaly. Detailed advanced imaging with cardiac MRI and three-...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-017-1797-0

    authors: VanLoozen D,McCafferty S,Lutin WA,Polimenakos AC

    更新日期:2018-03-01 00:00:00

  • Noninvasive measurement of cardiac output in critically ill children.

    abstract::This study was performed to evaluate the hemodynamic status of children admitted to the intensive care unit, using suprasternal and transesophageal Doppler ultrasound, and to establish a suitable noninvasive technique to monitor trends in cardiac output in critically ill children. Twenty children were studied over a p...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-001-0014-2

    authors: Mohan UR,Britto J,Habibi P,de MC,Nadel S

    更新日期:2002-01-01 00:00:00

  • Beta-blocker therapy failures in symptomatic probands with genotyped long-QT syndrome.

    abstract::Beta-blocker therapy is one of the principal therapies for congenital long-QT syndrome (LQTS). However, breakthrough cardiac events occur while being treated with beta-blockers. We sought to determine the frequency of and clinical correlates underlying beta-blocker therapy failures in genotyped, symptomatic LQTS proba...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-003-0567-3

    authors: Chatrath R,Bell CM,Ackerman MJ

    更新日期:2004-09-01 00:00:00

  • VO2@RER1.0: a novel submaximal cardiopulmonary exercise index.

    abstract::Maximal oxygen consumption (VO2max) is the "gold standard" by which to assess functional capacity; however, it is effort dependent. VO2@RER1.0 is defined when VO2 = VCO2. Between December 22, 1997 and November 9, 2004, 305 pediatric subjects underwent cycle ergometer cardiopulmonary exercise testing, exercised to exha...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-009-9544-9

    authors: Chin C,Kazmucha J,Kim N,Suryani R,Olson I

    更新日期:2010-01-01 00:00:00

  • Hemodynamic assessment in patients with one-and-a-half ventricle repair revealed by four-dimensional flow magnetic resonance imaging.

    abstract::We report hemodynamic findings in two patients with pulmonary atresia and intact ventricular septum (PAIVS) after "one-and-a-half ventricle repair" and placement of a bidirectional Glenn shunt using four-dimensional (4D) flow magnetic resonance imaging. Quantification of flow and analysis of flow patterns revealed the...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0288-6

    authors: Uribe S,Bächler P,Valverde I,Crelier GR,Beerbaum P,Tejos C,Irarrazaval P

    更新日期:2013-02-01 00:00:00

  • Primary pulmonary artery sarcoma in two children.

    abstract::The clinical and pathological features of primary pulmonary artery sarcoma in two children are reported. The first patient presented with right ventricular outflow obstruction and underwent successful surgical resection of his tumor. The second patient developed cardiac arrest following a relatively short period of sy...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02078416

    authors: Farooki ZQ,Chang CH,Jackson WL,Clapp SK,Hakimi M,Arciniegas E,Pinsky WW

    更新日期:1988-01-01 00:00:00

  • Defibrillator implantation in a child with long QT syndrome.

    abstract::We report the placement of an implantable cardiac defibrillator as preventative treatment in a 2-year-old with long QT syndrome. ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-003-5230-5

    authors: Brachlow A,Bell M

    更新日期:2004-07-01 00:00:00