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Combining neuroanatomical features to support diagnosis of fetal alcohol spectrum disorders.
Fraize, Justine; Garzón, Pauline; Ntorkou, Alexandra; Kerdreux, Eliot; Boespflug-Tanguy, Odile; Beggiato, Anita; Delorme, Richard; Hertz-Pannier, Lucie; Elmaleh-Berges, Monique; Germanaud, David.
Afiliação
  • Fraize J; CEA Paris-Saclay, Frederic Joliot Institute, NeuroSpin, UNIACT, Gif-sur-Yvette, France.
  • Garzón P; Université Paris Cité, Inserm, NeuroDiderot, InDEV, Paris, France.
  • Ntorkou A; CEA Paris-Saclay, Frederic Joliot Institute, NeuroSpin, UNIACT, Gif-sur-Yvette, France.
  • Kerdreux E; Université Paris Cité, Inserm, NeuroDiderot, InDEV, Paris, France.
  • Boespflug-Tanguy O; Department of Paediatric Radiologic, Centre of Excellence InovAND, Robert-Debré Hospital, AP-HP, Paris, France.
  • Beggiato A; CEA Paris-Saclay, Frederic Joliot Institute, NeuroSpin, UNIACT, Gif-sur-Yvette, France.
  • Delorme R; Université Paris Cité, Inserm, NeuroDiderot, InDEV, Paris, France.
  • Hertz-Pannier L; Université Paris Cité, Inserm, NeuroDiderot, NeuroDEV, Paris, France.
  • Elmaleh-Berges M; Department of Child and Adolescent Psychiatry, Centre of Excellence InovAND, Robert-Debré Hospital, AP-HP, Paris, France.
  • Germanaud D; Department of Child and Adolescent Psychiatry, Centre of Excellence InovAND, Robert-Debré Hospital, AP-HP, Paris, France.
Dev Med Child Neurol ; 65(4): 551-562, 2023 04.
Article em En | MEDLINE | ID: mdl-36137006
ABSTRACT

AIM:

To identify easily accessible neuroanatomical abnormalities useful for diagnosing fetal alcohol spectrum disorders (FASD) in fetal alcohol syndrome (FAS) but more importantly for the probabilistic diagnosis of non-syndromic forms (NS-FASD).

METHOD:

We retrospectively collected monocentric data from 52 individuals with FAS, 37 with NS-FASD, and 94 paired typically developing individuals (6-20 years, 99 males, 84 females). On brain T1-weighted magnetic resonance imaging, we measured brain size, corpus callosum length and thicknesses, vermis height, then evaluated vermis foliation (Likert scale). For each parameter, we established variations with age and brain size in comparison individuals (growth and scaling charts), then identified participants with abnormal measurements (<10th centile).

RESULTS:

According to growth charts, there was an excess of FAS with abnormally small brain, isthmus, splenium, and vermis. According to scaling charts, this excess remained only for isthmus thickness and vermis height. The vermis foliation was pathological in 18% of those with FASD but in no comparison individual. Overall, 39% of those with FAS, 27% with NS-FASD, but only 2% of comparison individuals presented with two FAS-recurrent abnormalities, and 19% of those with FAS had all three. Considering the number of anomalies, there was a higher likelihood of a causal link with alcohol in 14% of those with NS-FASD.

INTERPRETATION:

Our results suggest that adding an explicit composite neuroanatomical-radiological criterion for FASD diagnosis may improve its specificity, especially in NS-FASD. WHAT THIS PAPER ADDS Neuroanatomical anomalies independent of microcephaly can be measured with clinical-imaging tools. Small-for-age brain, small-for-brain-size callosal isthmus or vermian height, and disrupted vermis foliation are fetal alcohol syndrome (FAS)-recurrent anomalies. Associations of these anomalies are frequent in fetal alcohol spectrum disorder (FASD) even without FAS, while exceptional in typically developing individuals. These associations support higher likelihood of causal link with alcohol in some individuals with non-syndromic FASD. A new explicit and composite neuroanatomical-radiological criterion can improve the specificity of FASD diagnosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos do Espectro Alcoólico Fetal Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos do Espectro Alcoólico Fetal Idioma: En Ano de publicação: 2023 Tipo de documento: Article