Abnormal Brain Development in Newborns with Congenital Heart Disease

Children who survive surgical repair of congenital heart defects often have abnormal neurodevelopment. In this comparison of 41 term newborns with congenital heart disease and 16 controls, abnormalities in brain maturation were present before cardiac surgery. In newborns with congenital heart diseas...

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Published inThe New England journal of medicine Vol. 357; no. 19; pp. 1928 - 1938
Main Authors Miller, Steven P, McQuillen, Patrick S, Hamrick, Shannon, Xu, Duan, Glidden, David V, Charlton, Natalie, Karl, Tom, Azakie, Anthony, Ferriero, Donna M, Barkovich, A. James, Vigneron, Daniel B
Format Journal Article
LanguageEnglish
Published Boston, MA Massachusetts Medical Society 08.11.2007
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Online AccessGet full text
ISSN0028-4793
1533-4406
1533-4406
DOI10.1056/NEJMoa067393

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Abstract Children who survive surgical repair of congenital heart defects often have abnormal neurodevelopment. In this comparison of 41 term newborns with congenital heart disease and 16 controls, abnormalities in brain maturation were present before cardiac surgery. In newborns with congenital heart disease, abnormalities in brain maturation were present before cardiac surgery. In the United States, severe congenital heart disease is a common cause of childhood morbidity, occurring in 6 to 8 infants per 1000 live births. 1 Although most forms of congenital heart disease are now amenable to early surgical repair, deficits that impair widespread neurodevelopmental domains are identified in up to half of childhood survivors: fine motor skills, visuospatial skills, and cognition, including memory, attention, and higher-order language skills. 2 – 5 Despite the importance of these functional impairments at a public health level, the underlying basis of the deficits is largely unknown. Although studies of brain injury in newborns with congenital heart . . .
AbstractList Congenital heart disease in newborns is associated with global impairment in development. We characterized brain metabolism and microstructure, as measures of brain maturation, in newborns with congenital heart disease before they underwent heart surgery.BACKGROUNDCongenital heart disease in newborns is associated with global impairment in development. We characterized brain metabolism and microstructure, as measures of brain maturation, in newborns with congenital heart disease before they underwent heart surgery.We studied 41 term newborns with congenital heart disease--29 who had transposition of the great arteries and 12 who had single-ventricle physiology--with the use of magnetic resonance imaging (MRI), magnetic resonance spectroscopy (MRS), and diffusion tensor imaging (DTI) before cardiac surgery. We calculated the ratio of N-acetylaspartate to choline (which increases with brain maturation), the ratio of lactate to choline (which decreases with maturation), average diffusivity (which decreases with maturation), and fractional anisotropy of white-matter tracts (which increases with maturation). We compared these findings with those in 16 control newborns of a similar gestational age.METHODSWe studied 41 term newborns with congenital heart disease--29 who had transposition of the great arteries and 12 who had single-ventricle physiology--with the use of magnetic resonance imaging (MRI), magnetic resonance spectroscopy (MRS), and diffusion tensor imaging (DTI) before cardiac surgery. We calculated the ratio of N-acetylaspartate to choline (which increases with brain maturation), the ratio of lactate to choline (which decreases with maturation), average diffusivity (which decreases with maturation), and fractional anisotropy of white-matter tracts (which increases with maturation). We compared these findings with those in 16 control newborns of a similar gestational age.As compared with control newborns, those with congenital heart disease had a decrease of 10% in the ratio of N-acetylaspartate to choline (P=0.003), an increase of 28% in the ratio of lactate to choline (P=0.08), an increase of 4% in average diffusivity (P<0.001), and a decrease of 12% in white-matter fractional anisotropy (P<0.001). Preoperative brain injury, as seen on MRI, was not significantly associated with findings on MRS or DTI. White-matter injury was observed in 13 newborns with congenital heart disease (32%) and in no control newborns.RESULTSAs compared with control newborns, those with congenital heart disease had a decrease of 10% in the ratio of N-acetylaspartate to choline (P=0.003), an increase of 28% in the ratio of lactate to choline (P=0.08), an increase of 4% in average diffusivity (P<0.001), and a decrease of 12% in white-matter fractional anisotropy (P<0.001). Preoperative brain injury, as seen on MRI, was not significantly associated with findings on MRS or DTI. White-matter injury was observed in 13 newborns with congenital heart disease (32%) and in no control newborns.Term newborns with congenital heart disease have widespread brain abnormalities before they undergo cardiac surgery. The imaging findings in such newborns are similar to those in premature newborns and may reflect abnormal brain development in utero.CONCLUSIONSTerm newborns with congenital heart disease have widespread brain abnormalities before they undergo cardiac surgery. The imaging findings in such newborns are similar to those in premature newborns and may reflect abnormal brain development in utero.
Congenital heart disease in newborns is associated with global impairment in development. We characterized brain metabolism and microstructure, as measures of brain maturation, in newborns with congenital heart disease before they underwent heart surgery. We studied 41 term newborns with congenital heart disease--29 who had transposition of the great arteries and 12 who had single-ventricle physiology--with the use of magnetic resonance imaging (MRI), magnetic resonance spectroscopy (MRS), and diffusion tensor imaging (DTI) before cardiac surgery. We calculated the ratio of N-acetylaspartate to choline (which increases with brain maturation), the ratio of lactate to choline (which decreases with maturation), average diffusivity (which decreases with maturation), and fractional anisotropy of white-matter tracts (which increases with maturation). We compared these findings with those in 16 control newborns of a similar gestational age. As compared with control newborns, those with congenital heart disease had a decrease of 10% in the ratio of N-acetylaspartate to choline (P=0.003), an increase of 28% in the ratio of lactate to choline (P=0.08), an increase of 4% in average diffusivity (P<0.001), and a decrease of 12% in white-matter fractional anisotropy (P<0.001). Preoperative brain injury, as seen on MRI, was not significantly associated with findings on MRS or DTI. White-matter injury was observed in 13 newborns with congenital heart disease (32%) and in no control newborns. Term newborns with congenital heart disease have widespread brain abnormalities before they undergo cardiac surgery. The imaging findings in such newborns are similar to those in premature newborns and may reflect abnormal brain development in utero.
Children who survive surgical repair of congenital heart defects often have abnormal neurodevelopment. In this comparison of 41 term newborns with congenital heart disease and 16 controls, abnormalities in brain maturation were present before cardiac surgery. In newborns with congenital heart disease, abnormalities in brain maturation were present before cardiac surgery. In the United States, severe congenital heart disease is a common cause of childhood morbidity, occurring in 6 to 8 infants per 1000 live births. 1 Although most forms of congenital heart disease are now amenable to early surgical repair, deficits that impair widespread neurodevelopmental domains are identified in up to half of childhood survivors: fine motor skills, visuospatial skills, and cognition, including memory, attention, and higher-order language skills. 2 – 5 Despite the importance of these functional impairments at a public health level, the underlying basis of the deficits is largely unknown. Although studies of brain injury in newborns with congenital heart . . .
Background Congenital heart disease in newborns is associated with global impairment in development. We characterized brain metabolism and microstructure, as measures of brain maturation, in newborns with congenital heart disease before they underwent heart surgery. Methods We studied 41 term newborns with congenital heart disease -- 29 who had transposition of the great arteries and 12 who had single-ventricle physiology -- with the use of magnetic resonance imaging (MRI), magnetic resonance spectroscopy (MRS), and diffusion tensor imaging (DTI) before cardiac surgery. We calculated the ratio of N -acetylaspartate to choline (which increases with brain maturation), the ratio of lactate to choline (which decreases with maturation), average diffusivity (which decreases with maturation), and fractional anisotropy of white-matter tracts (which increases with maturation). We compared these findings with those in 16 control newborns of a similar gestational age. Results As compared with control newborns, those with congenital heart disease had a decrease of 10% in the ratio of N -acetylaspartate to choline (P=0.003), an increase of 28% in the ratio of lactate to choline (P=0.08), an increase of 4% in average diffusivity (P<0.001), and a decrease of 12% in white-matter fractional anisotropy (P<0.001). Preoperative brain injury, as seen on MRI, was not significantly associated with findings on MRS or DTI. White-matter injury was observed in 13 newborns with congenital heart disease (32%) and in no control newborns. Conclusions Term newborns with congenital heart disease have widespread brain abnormalities before they undergo cardiac surgery. The imaging findings in such newborns are similar to those in premature newborns and may reflect abnormal brain development in utero. [PUBLICATION ABSTRACT]
Author Ferriero, Donna M
McQuillen, Patrick S
Karl, Tom
Miller, Steven P
Hamrick, Shannon
Xu, Duan
Glidden, David V
Charlton, Natalie
Vigneron, Daniel B
Azakie, Anthony
Barkovich, A. James
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  fullname: Hamrick, Shannon
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  surname: Xu
  fullname: Xu, Duan
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  givenname: David V
  surname: Glidden
  fullname: Glidden, David V
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  givenname: Natalie
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  surname: Karl
  fullname: Karl, Tom
– sequence: 8
  givenname: Anthony
  surname: Azakie
  fullname: Azakie, Anthony
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  givenname: Donna M
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  fullname: Barkovich, A. James
– sequence: 11
  givenname: Daniel B
  surname: Vigneron
  fullname: Vigneron, Daniel B
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19216185$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/17989385$$D View this record in MEDLINE/PubMed
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Keywords Medicine
Brain
Newborn diseases
Development
Cardiovascular disease
Congenital cardiopathy
Encephalon
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Copyright 2007 Massachusetts Medical Society.
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Snippet Children who survive surgical repair of congenital heart defects often have abnormal neurodevelopment. In this comparison of 41 term newborns with congenital...
Congenital heart disease in newborns is associated with global impairment in development. We characterized brain metabolism and microstructure, as measures of...
Background Congenital heart disease in newborns is associated with global impairment in development. We characterized brain metabolism and microstructure, as...
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SubjectTerms Babies
Biological and medical sciences
Brain
Brain - anatomy & histology
Brain - embryology
Brain - metabolism
Brain - pathology
Brain Diseases - diagnosis
Brain Diseases - etiology
Cardiovascular disease
Case-Control Studies
Congenital diseases
Diffusion Magnetic Resonance Imaging
Female
General aspects
Gestational Age
Heart Defects, Congenital - complications
Heart Ventricles - abnormalities
Humans
Imaging, Three-Dimensional
Infant, Newborn
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
Medical sciences
Prenatal development
Prospective Studies
Transposition of Great Vessels - complications
Title Abnormal Brain Development in Newborns with Congenital Heart Disease
URI http://dx.doi.org/10.1056/NEJMoa067393
https://www.ncbi.nlm.nih.gov/pubmed/17989385
https://www.proquest.com/docview/223929594
https://www.proquest.com/docview/68490447
Volume 357
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