Organic acidemias in the neonatal period: 30 years of experience in a referral center for inborn errors of metabolism
Author:
Unsal Yagmur1ORCID, Yurdakok Murat2ORCID, Yigit Sule2ORCID, Celik Hasan Tolga2ORCID, Dursun Ali3ORCID, Sivri Hatice Serap3, Tokatli Aysegul3, Coskun Turgay3ORCID
Affiliation:
1. Division of Pediatric Endocrinology, Department of Pediatrics , Hacettepe University Faculty of Medicine , Ankara , Turkey 2. Division of Neonatology, Department of Pediatrics , Hacettepe University Faculty of Medicine , Ankara , Turkey 3. Division of Pediatric Metabolism, Department of Pediatrics , Hacettepe University Faculty of Medicine , Ankara , Turkey
Abstract
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.
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Reference45 articles.
1. Leonard, JV, Morris, AA. Inborn errors of metabolism around time of birth. Lancet 2000;356:583–7, https://doi.org/10.1016/s0140-6736(00)02591-5. 2. Nyhan, WL, Borsop, BA, Ozand, PT. Organic acidemias. Introduction. In: Atlas of metabolic diseases. London: Chapman and Hall Medical; 2005: 1–7. 3. Villani, GR, Gallo, G, Scolamiero, E, Salvatore, F, Ruoppolo, M. “Classical organic acidurias”: diagnosis and pathogenesis. Clin Exp Med 2017;17:305–23, https://doi.org/10.1007/s10238-016-0435-0. 4. Huang, X, Yang, L, Tong, F, Yang, R, Zhao, Z. Screening for inborn errors of metabolism in high-risk children: a 3-year pilot study in Zhejiang Province, China. BMC Pediatr 2012;12:18, https://doi.org/10.1186/1471-2431-12-18. 5. Han, B, Nie, W, Sun, M, Liu, Y, Cao, Z. Clinical presentation, molecular analysis and follow-up of patients with mut methylmalonic acidemia in Shandong province, China. Pediatr Neonatol 2020;61:148–54, https://doi.org/10.1016/j.pedneo.2019.07.004.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|