| Literature DB >> 28856627 |
Caroline Dejean de la Bâtie1, Valérie Barbier2, Célina Roda2, Anaïs Brassier2, Jean-Baptiste Arnoux2, Vassili Valayannopoulos2, Anne-Sophie Guemann2, Clément Pontoizeau3, Stéphanie Gobin4, Florence Habarou3, Florence Lacaille5, Jean-Paul Bonnefont4, Pierre Canouï1, Chris Ottolenghi3, Pascale De Lonlay2, Lisa Ouss6.
Abstract
Propionic acidemia is the result of a deficiency in propionyl-CoA carboxylase activity. Chronic neurologic and cognitive complications frequently occur, but the psychiatric evolution of the disorder is not well documented. We conducted a pedopsychiatric evaluation of 19 children, adolescents and young adults, aged between 2 and 25 years, using ADI-R, CARS-T, as well as ADOS when autism spectrum disorder was suspected. Previous psychometric examinations were also taken into consideration. Thirteen patients had an IQ < 80. Two patients presented with autism and two additional patients with other autism spectrum disorders. Five patients did not fulfill diagnostic criteria for autism spectrum disorder but showed difficulties indicative of a broader autism phenotype (BAP). Four other patients had severe anxiety manifestations related to their disease. Two patients presented with acute psychotic episodes. The number of decompensations in the first 3 years of life was lower in patients with autism spectrum disorder or related symptoms. These patients were also older when they were assessed (median age of 15 years old versus 11 years old). There was no significant correlation between 3-hydroxypropionate levels during the first 6 years of life and autism spectrum disorder diagnosis. In conclusion, autism spectrum disorder is frequent in patients with propionic acidemia. These patients should undergo in-depth psychiatric evaluation and be screened for autism spectrum disorder. Further studies are needed to understand the underlying mechanisms.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28856627 DOI: 10.1007/s10545-017-0070-2
Source DB: PubMed Journal: J Inherit Metab Dis ISSN: 0141-8955 Impact factor: 4.982