Organic acidemias in the neonatal period: 30 years of experience in a referral center for inborn errors of metabolism.

Yagmur Unsal, Murat Yurdakok, Sule Yigit, Hasan Tolga Celik, Ali Dursun, Hatice Serap Sivri, Aysegul Tokatli, Turgay Coskun
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引用次数: 2

Abstract

Objectives: Neonatal-onset organic acidemias (OAs) account for 80% of neonatal intensive care unit (NICU) admissions due to inborn errors of metabolism. The aim of this study is to analyze clinical features and follow-up of neonates diagnosed with OAs in a metabolic referral center, focusing on perinatal characteristics and the impact of first the metabolic crisis on long-term outcome.

Methods: Perinatal features, clinical and laboratory characteristics on admission and follow-up of 108 neonates diagnosed with OAs were retrospectively analyzed. Global developmental delay, abnormal electroencephalogram (EEG) or brain magnetic resonance imaging (MRI), chronic complications, and overall mortality. Associations between clinical findings on admission and outcome measures were evaluated.

Results: Most prevalent OA was maple syrup urine disease (MSUD) (34.3%). Neonates with methylmalonic acidemia (MMA) had significantly lower birth weight (p<0.001). Metabolic acidosis with increased anion gap was more frequent in MMA and propionic acidemia (PA) (p=0.003). 89.1% of OAs were admitted for recurrent metabolic crisis. 46% had chronic non-neurologic complications; 19.3% of MMA had chronic kidney disease. Abnormal findings were present in 26/34 of EEG, 19/29 of MRI studies, and 32/33 of developmental screening tests. Metabolic acidosis on admission was associated with increased incidence of abnormal EEG (p=0.005) and overall mortality (p<0.001). Severe hyperammonemia in MMA was associated with overall mortality (33.3%) (p=0.047). Patients diagnosed between 2007-2017 had lower overall mortality compared to earlier years (p<0.001).

Conclusions: Metabolic acidosis and hyperammonemia are emerging predictors of poor outcome and mortality. Based on a large number of infants from a single center, survival in neonatal-onset OA has increased over the course of 30 years, but long-term complications and neurodevelopmental results remain similar. While prompt onset of more effective treatment may improve survival, newer treatment modalities are urgently needed for prevention and treatment of chronic complications.

新生儿期有机酸血症:先天性代谢错误转诊中心30年的经验。
目的:新生儿发病的有机酸血症(OAs)占新生儿重症监护病房(NICU)入院人数的80%,原因是先天性代谢错误。本研究的目的是分析代谢转诊中心诊断为OAs的新生儿的临床特征和随访,重点关注围产期特征和首次代谢危机对长期预后的影响。方法:回顾性分析108例OAs新生儿的围生期特征、入院及随访时的临床、实验室特征。整体发育迟缓,脑电图(EEG)或脑磁共振成像(MRI)异常,慢性并发症和总死亡率。评估入院时的临床表现与结果测量之间的关系。结果:OA以枫糖浆尿病(MSUD)为主(34.3%)。结论:代谢性酸中毒和高氨血症是不良预后和死亡率的新预测因素。基于来自单一中心的大量婴儿,在30年的过程中,新生儿发病OA的生存率有所增加,但长期并发症和神经发育结果仍然相似。虽然及时开始更有效的治疗可以提高生存率,但迫切需要新的治疗方式来预防和治疗慢性并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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