Pontoizeau Clément, Habarou Florence, Brassier Anaïs, Veauville-Merllié Alice, Grisel Coraline, Arnoux Jean-Baptiste, Vianey-Saban Christine, Barouki Robert, Chadefaux-Vekemans Bernadette, Acquaviva Cécile, de Lonlay Pascale, Ottolenghi Chris
Centre de Référence des Maladies Héréditaires du Métabolisme, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, University of Paris Descartes, Institut Imagine, Paris, France.
Service de Biochimie Métabolomique et Protéomique, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, 149 rue de Sèvres, 75015, Paris, France.
JIMD Rep. 2016;27:39-45. doi: 10.1007/8904_2015_481. Epub 2015 Sep 27.
Classical neonatal-onset glutaric aciduria type 2 (MAD deficiency) is a severe disorder of mitochondrial fatty acid oxidation associated with poor survival. Secondary dysfunction of acyl-CoA dehydrogenases may result from deficiency for riboflavin transporters, leading to severe disorders that, nevertheless, are treatable by riboflavin supplementation. In the last 10 years, we identified nine newborns with biochemical features consistent with MAD deficiency, only four of whom survived past the neonatal period. A likely iatrogenic cause of riboflavin deficiency was found in two premature newborns having parenteral nutrition, one of whom recovered upon multivitamin supplementation, whereas the other died before diagnosis. Four other patients had demonstrated mutations involving ETF or ETF-DH flavoproteins, whereas the remaining three patients presumably had secondary deficiencies of unknown mechanism. Interestingly, six newborns among the seven tested for plasma amino acids had pronounced hyperprolinemia. In one case, because the initial diagnostic workup did not include organic acids and acylcarnitine profiling, clinical presentation and hyperprolinemia suggested the diagnosis. Analysis of our full cohort of >50,000 samples from >30,000 patients suggests that the proline/alanine ratio may be a good marker of MAD deficiency and could contribute to a more effective management of the treatable forms.
经典型新生儿期发病的2型戊二酸尿症(中链酰基辅酶A脱氢酶缺乏症)是一种严重的线粒体脂肪酸氧化障碍疾病,存活率较低。酰基辅酶A脱氢酶的继发性功能障碍可能源于核黄素转运蛋白缺乏,导致严重疾病,不过通过补充核黄素可进行治疗。在过去10年中,我们鉴定出9名具有与中链酰基辅酶A脱氢酶缺乏症相符的生化特征的新生儿,其中只有4名存活至新生儿期之后。在两名接受肠外营养的早产新生儿中发现了可能的医源性核黄素缺乏原因,其中一名在补充多种维生素后康复,而另一名在诊断前死亡。另外4名患者表现出涉及电子传递黄素蛋白或电子传递黄素蛋白-泛醌氧化还原酶的突变,而其余3名患者可能存在机制不明的继发性缺乏。有趣的是,在7名接受血浆氨基酸检测的新生儿中,有6名患有明显的高脯氨酸血症。在1例中,由于初始诊断检查未包括有机酸和酰基肉碱分析,临床表现和高脯氨酸血症提示了诊断。对我们来自30,000多名患者的超过50,000份样本的完整队列分析表明,脯氨酸/丙氨酸比值可能是中链酰基辅酶A脱氢酶缺乏症的良好标志物,有助于更有效地管理可治疗形式的疾病。