TY - JOUR
T1 - Regional Brain Growth Trajectories in Fetuses with Congenital Heart Disease
AU - Rollins, Caitlin K.
AU - Ortinau, Cynthia M.
AU - Stopp, Christian
AU - Friedman, Kevin G.
AU - Tworetzky, Wayne
AU - Gagoski, Borjan
AU - Velasco-Annis, Clemente
AU - Afacan, Onur
AU - Vasung, Lana
AU - Beaute, Jeanette I.
AU - Rofeberg, Valerie
AU - Estroff, Judy A.
AU - Grant, P. Ellen
AU - Soul, Janet S.
AU - Yang, Edward
AU - Wypij, David
AU - Gholipour, Ali
AU - Warfield, Simon K.
AU - Newburger, Jane W.
N1 - Funding Information:
The authors acknowledge contributions from Carol Barnewolt, Reem Chamseddine, Maggie Mittleman, and Sarah Perelman. Research reported in this publication was supported the National Institutes of Health (NIH), including the National Institute of Neurological Disorders and Stroke K23NS101120 (C.K.R.), the National Heart, Lung, and Blood Institute K23HL141602 (C.M.O.), National Institute of Biomedical Imaging and Bioengineering R01EB013248 (S.K.W.), R01EB018988 and R01NS106030 (A.G.), and a National Heart, Lung, and Blood Institute Pediatric Heart Network Scholar Award (C.K.R.); the American Academy of Neurology Clinical Research Training Fellowship (C.K.R.); the Brain and Behavior Research Foundation NARSAD Young Investigator (C.K.R.) and Distinguished Investigator (S.K.W.) Awards; the McKnight Foundation Technological Innovations in Neuroscience Award (A.G.); Office of Faculty Development at Boston Children's Hospital Career Development Awards (A.G. and C.K.R.); and the Mend A Heart Foundation (C.M.O.). The content does not necessarily represent the official views of the NIH or other funding agencies.
Publisher Copyright:
© 2020 American Neurological Association
PY - 2021/1
Y1 - 2021/1
N2 - Objective: Congenital heart disease (CHD) is associated with abnormal brain development in utero. We applied innovative fetal magnetic resonance imaging (MRI) techniques to determine whether reduced fetal cerebral substrate delivery impacts the brain globally, or in a region-specific pattern. Our novel design included two control groups, one with and the other without a family history of CHD, to explore the contribution of shared genes and/or fetal environment to brain development. Methods: From 2014 to 2018, we enrolled 179 pregnant women into 4 groups: “HLHS/TGA” fetuses with hypoplastic left heart syndrome (HLHS) or transposition of the great arteries (TGA), diagnoses with lowest fetal cerebral substrate delivery; “CHD-other,” with other CHD diagnoses; “CHD-related,” healthy with a CHD family history; and “optimal control,” healthy without a family history. Two MRIs were obtained between 18 and 40 weeks gestation. Random effect regression models assessed group differences in brain volumes and relationships to hemodynamic variables. Results: HLHS/TGA (n = 24), CHD-other (50), and CHD-related (34) groups each had generally smaller brain volumes than the optimal controls (71). Compared with CHD-related, the HLHS/TGA group had smaller subplate (−13.3% [standard error = 4.3%], p < 0.01) and intermediate (−13.7% [4.3%], p < 0.01) zones, with a similar trend in ventricular zone (−7.1% [1.9%], p = 0.07). These volumetric reductions were associated with lower cerebral substrate delivery. Interpretation: Fetuses with CHD, especially those with lowest cerebral substrate delivery, show a region-specific pattern of small brain volumes and impaired brain growth before 32 weeks gestation. The brains of fetuses with CHD were more similar to those of CHD-related than optimal controls, suggesting genetic or environmental factors also contribute. ANN NEUROL 2021;89:143–157.
AB - Objective: Congenital heart disease (CHD) is associated with abnormal brain development in utero. We applied innovative fetal magnetic resonance imaging (MRI) techniques to determine whether reduced fetal cerebral substrate delivery impacts the brain globally, or in a region-specific pattern. Our novel design included two control groups, one with and the other without a family history of CHD, to explore the contribution of shared genes and/or fetal environment to brain development. Methods: From 2014 to 2018, we enrolled 179 pregnant women into 4 groups: “HLHS/TGA” fetuses with hypoplastic left heart syndrome (HLHS) or transposition of the great arteries (TGA), diagnoses with lowest fetal cerebral substrate delivery; “CHD-other,” with other CHD diagnoses; “CHD-related,” healthy with a CHD family history; and “optimal control,” healthy without a family history. Two MRIs were obtained between 18 and 40 weeks gestation. Random effect regression models assessed group differences in brain volumes and relationships to hemodynamic variables. Results: HLHS/TGA (n = 24), CHD-other (50), and CHD-related (34) groups each had generally smaller brain volumes than the optimal controls (71). Compared with CHD-related, the HLHS/TGA group had smaller subplate (−13.3% [standard error = 4.3%], p < 0.01) and intermediate (−13.7% [4.3%], p < 0.01) zones, with a similar trend in ventricular zone (−7.1% [1.9%], p = 0.07). These volumetric reductions were associated with lower cerebral substrate delivery. Interpretation: Fetuses with CHD, especially those with lowest cerebral substrate delivery, show a region-specific pattern of small brain volumes and impaired brain growth before 32 weeks gestation. The brains of fetuses with CHD were more similar to those of CHD-related than optimal controls, suggesting genetic or environmental factors also contribute. ANN NEUROL 2021;89:143–157.
UR - http://www.scopus.com/inward/record.url?scp=85096774219&partnerID=8YFLogxK
U2 - 10.1002/ana.25940
DO - 10.1002/ana.25940
M3 - Article
C2 - 33084086
AN - SCOPUS:85096774219
SN - 0364-5134
VL - 89
SP - 143
EP - 157
JO - Annals of Neurology
JF - Annals of Neurology
IS - 1
ER -