Service de Pédopsychiatrie, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, 149 rue de Sèvres, 75015, Paris, France.
Reference Center of Inherited Metabolic Diseases, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
J Inherit Metab Dis. 2018 Jul;41(4):623-629. doi: 10.1007/s10545-017-0070-2. Epub 2017 Aug 30.
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.
丙酸血症是由于丙酰基辅酶 A 羧化酶活性缺乏所致。慢性神经认知并发症常发生,但该疾病的精神科演变尚未得到充分记录。我们对 19 名年龄在 2 至 25 岁的儿童、青少年和年轻人进行了儿童精神科评估,使用了 ADI-R、CARS-T,以及在怀疑自闭症谱系障碍时使用了 ADOS。还考虑了之前的心理测量检查。13 名患者的智商<80。2 名患者表现出自闭症,另外 2 名患者则表现出其他自闭症谱系障碍。5 名患者未达到自闭症谱系障碍的诊断标准,但表现出广泛自闭症表型(BAP)的困难。另外 4 名患者则表现出与疾病相关的严重焦虑症状。2 名患者出现急性精神病发作。在生命的前 3 年内,有自闭症谱系障碍或相关症状的患者的病情恶化次数较少。这些患者在接受评估时年龄也较大(自闭症谱系障碍或相关症状患者的中位年龄为 15 岁,而无自闭症谱系障碍患者的中位年龄为 11 岁)。生命的前 6 年内 3-羟丙酸水平与自闭症谱系障碍诊断之间无显著相关性。总之,丙酸血症患者中自闭症谱系障碍较为常见。这些患者应进行深入的精神科评估,并筛查自闭症谱系障碍。需要进一步研究以了解潜在的机制。