Objective To understand distribution characteristics of the concentration of relevant indicators in neonatal methylmalonic academia (MMA) screening by tandem mass spectrometry technology, and to evaluate the application value of 3-hydroxyhexadecenoyl carnitine (C16:1-OH) in the interpretation of MMA diseases, so as to provide basis for improving the positive predictive value of MMA screening and screening efficiency. Methods A total of 185 239 local newborns born between October 2013 and July 2019 were conducted MMA screening using tandem mass spectrometry technology.The levels of MMA disease-related indicators were compared among children in different gender, gestational age and birth weight groups.The initial screening levels were compared with re-examination indicator levels of confirmed samples. Results A total of 44 cases were diagnosed, 5 cases with simple type, 39 cases with combined type, and the overall prevalence was about 0.023 7%(44/185 239).Grouped by gender, gestational age and birth weight, free carnitine (C0), propionyl carnitine (C3), propionyl carnitine/free carnitine (C3/C0), propionyl carnitine/acetyl carnitine (C3/C2), C16:1-OH and methionine (MET) and other index concentration value distribution differences were statistically significant (P<0.001).Compared with the results of initial screening, the level of C3/C2 in the re-examination samples was significantly higher (Z=5.10,P<0.001), while the C16:1-OH level in the re-examination samples was significantly lower (Z=5.236, P<0.001).The area under the ROC curve of the C16:1-OH indicator was 0.951 (95%CI: 0.914 - 0.987), and the weight index was approximately 15.46. Conclusions When screening MMA in neonates, medical staff are suggested give comprehensive interpretation based on the time of blood collection, birth weight and gestational age so as to reduce the positive rate of initial screening.The C16:1-OH indicator is helpful in the interpretation of MMA disease in the primary screening sample (blood sampling from 3 to 7 days after birth), and can effectively improve the positive predictive value and screening efficiency, thereby achieving early diagnosis, early treatment, and reducing the rate of disability.
Key words
neonatal disease screening /
methylmalonic acidemia /
3~7 days after birth /
C16:1-OH
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References
[1] 顾学范.临床遗传代谢病[M].北京:人民卫生出版社,2015.
[2] 刘明芳.聊城地区应用串联质谱技术筛查新生儿甲基丙二酸血症分析[J].中国优生与遗传杂志,2018,26(2):29-30.
[3] 吴海兰,董世霄,刘红,等.新生儿甲基丙二酸血症的临床特点分析[J].山西大学学报,2018,49(1):48-52.
[4] 王卫平.儿科学[M].北京:人民卫生出版社,2018.
[5] 王彩君,张耀东,康文清,等.新生儿甲基丙二酸血症基因及临床分析[J].中华实用诊断与治疗杂志,2018,32(12):1181-1183.
[6] 蔡奥捷,宗亚楠,刘宁,等.单纯型甲基丙二酸血症家系MUT 基因分析及在产前诊断中的应用[J].中华围产医学杂志,2016,19(9):688-694.
[7] 叶军.新生儿遗传代谢病筛查发展及诊治规范[J].中国计划生育和妇产科,2016,8(1):6-13.
[8] 董丽萍,牟凯,朱峰.山东鲁中地区新生儿体内游离肉碱及酰基肉碱的变化特点[J].中国妇幼保健杂志,2016,31(13):2671-2675.
[9] Cheng KH, Liu MY, Kao CH,et al.Newborn screening for methylmalonic aciduria by tandem mass spectrometry: 7 years' experience from two centers in taiwan[J].J Chin Med Assoc,2010,73(6):314-318.
[10] 孙英梅,李文杰.甲基丙二酸血症临床诊治研究进展[J].中国儿童保健杂志,2017,25(2):147-150.
[11] Malvagia S, Haynes CA, Grisotto L,et al.Heptadecanoylcarnitine (C17) a novel candidate biomarker for propionic and methylmalonic acidemias during expanded newborn screening[J].Clin Chim Acta,2015, 450(23): 342-348.