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发育医学电子杂志  2023, Vol. 11 Issue (1): 14-18    DOI: 10.3969/j.issn.2095-5340.2023.01.003
  围产医学   论著 |新生儿 |
河北省石家庄市新生儿短链酰基辅酶A脱氢酶缺乏症筛查及基因突变分析
贾立云 封露露 封纪珍 弓苗 马翠霞
石家庄市妇幼保健院 遗传科,河北石家庄 050000
Screening and gene mutation analysis of neonates with short-chain acyl-coenzyme Adehydrogenase deficiency in Shijiazhuang city of Hebei province
Jia Liyun, Feng Lulu, Feng Jizhen, et al
Department of Genetics, Shijiazhuang Maternaland Child Health Hospital, Hebei, Shijiazhuang 050000, China)
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摘要 【摘要】 目的  了解短链酰基辅酶A 脱氢酶缺乏症(short-chain acyl-coenzyme A dehydrogenase
deficiency,SCADD)在河北省石家庄市新生儿中的患病率和临床特征,以及酰基辅酶A 脱氢酶(acylcoenzymeA dehydrogenase,ACADS)基因突变情况。 方法 2014 年1 月至2021 年12 月,河北省石家庄市共分娩185 683 例活产新生儿,行串联质谱筛查,检测丁酰基肉碱(butylcarnitine,C4)、C4/ 乙酰基肉碱(acetylcarnitine,C2)、C4/ 丙酰基肉碱(propionylcarnitine,C3)。筛查阳性患儿进一步行基因检测,Sanger 测序进行验证。185 683 例活产新生儿中,纳入118 502 例出生胎龄信息准确完整的新生儿,分
为早产儿组(5 597 例)、足月儿组(112 369 例)、过期产儿组(536 例),比较3 组间C4、C4/C2 及C4/C3 水平。统计学方法采用单因素方差分析、t 检验和Pearson 相关性分析。 结果  185 683 例新生儿中,确诊4 例SCADD 患儿,患病率为1/46 421。基因检测到ACADS 基因2 例复合杂合突变、1 例纯合突变及
1 例杂合突变;发现了4 种突变位点,分别为:c.625 G>A、c.1031A>G 、c.1157 G>A 和c.1130 C>T,均为已知突变。4 例患儿初筛C4 水平为0.65~0.84 μmol/L。随访4 例确诊患儿的生长发育情况,未出现临床表现。早产儿、足月儿、过期产儿组的C4 分别为(0.192±0.073)、(0.168±0.058)、(0.158±0.052) μmol/L(F=447.700,P<0.001);C4/C2 分别为0.011 5±0.004 7、0.010 6±0.004 0、0.010 4±0.003 8(F=110.200,P<0.001);C4/C3 分别为0.117 5±0.071 4、0.116 1±0.056 3、0.118 0±0.059 3(F=2.481,P=0.084)。早产儿C4、C4/C2 水平均高于足月儿(P 值均<0.001);过期产儿C4 水平低于足月儿(P<0.001)。出生胎龄与C4 水平、C4/C2 值均呈负相关(r 值分别为-0.119 与-0.036,P 值均<0.001)。 结论 串联质谱联合基因测序技术可及早确诊SCADD 患儿。河北省石家庄市新生儿的SCADD 患病率为1/46 421 ;检测到4 种ACADS 基因已知突变位点。
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关键词:  新生儿筛查  串联质谱  基因测序技术  酰基辅酶A 脱氢酶  基因突变    
Abstract: 【Abstract】 Objective To investigate the prevalence and clinical characteristics of short-chain acylcoenzymeA dehydrogenase deficiency (SCADD) and the gene mutation of acyl-coenzyme A dehydrogenase(ACADS) in Shijiazhuang city of Hebei province. Method From January 2014 to December 2021, a totalof 185 683 neonates in Shijiazhuang city of Hebei province were screened by tandem mass spectrometry to detectbutylcarnitine (C4), C4/acetylcarnitine (C2), C4/propionyl carnitine (C3). The positive children were furthertested for gene detection and verified by Sanger sequencing. Among 185 683 neonates, 118 502 neonateswith accurate and complete birth age information were divided into premature neonates group (n=5 597),term neonates group (n=112 369) and post term neonates group (n=536), and compared by the level of C4, C4/C2and C4/C3. One-way ANOVA test, t-test and Pearson correlation analysis were performed for statisticalanalysis. Result Four children with SCADD were diagnosed in 185 683 neonates, with a prevalence of1/46 421. Two cases with complex heterozygous mutations, one case with homozygous mutation and onecase with heterozygous mutation of ACADS gene were found. Four mutation sites were found, c.625 G>A,c.1031A>G, c.1157 G>A and c.1130 C>T, all of which were known mutations. The C4 level of the fourchildren in initial screening was 0.65-0.84 μmol/L. No clinical symptoms appeared during the follow-upperiod of the four children. The C4 levels in premature, term and post term neonates were (0.192±0.073),(0.168±0.058) and (0.158±0.052) μmol/L, respectively (F=447.700, P<0.001). The values of C4/C2 were0.011 5±0.004 7, 0.010 6±0.004 0 and 0.010 4±0.003 8 (F=110.200, P<0.001). The values of C4/C3were 0.117 5±0.071 4, 0.116 1±0.056 3 and 0.118 0±0.059 3 (F=2.481, P=0.084). The levels of C4 andC4/C2 in premature neonates were higher than those in term neonates (all P<0.001); the level of C4 in postterm neonates was lower than that in term neonates (P<0.001). The gestational age at birth was negativelycorrelated with C4 level and C4/C2 value (r= -0.119 and -0.036, all P<0.001). Conclusion Tandem massspectrometry combined with gene sequencing technology can confirm the diagnosis of children with SCADDin time. The prevalence of SCADD in Shijiazhuang city of Hebei province is 1/46 421; and four knownmutation sites of ACADS gene were detected.
Key words:  Neonatal screening    Tandem mass spectrometry    Gene sequencing technology    ACADS    Gene mutation
收稿日期:  2022-07-18                出版日期:  2023-01-31      发布日期:  2023-01-30      期的出版日期:  2023-01-31
通讯作者:  封纪珍    E-mail:  jlygmr@163.com
引用本文:    
贾立云 封露露 封纪珍 弓苗 马翠霞. 河北省石家庄市新生儿短链酰基辅酶A脱氢酶缺乏症筛查及基因突变分析[J]. 发育医学电子杂志, 2023, 11(1): 14-18.
Jia Liyun, Feng Lulu, Feng Jizhen, et al. Screening and gene mutation analysis of neonates with short-chain acyl-coenzyme Adehydrogenase deficiency in Shijiazhuang city of Hebei province. Journal of Developmental Medicine(Electronic Version), 2023, 11(1): 14-18.
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[1] Society of Neonatologist, Chinese Medical Doctor Association. Consensus recommendations on the prevention and early management of respiratory distress syndrome in preterm infants[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 129 -131 .
[2] Professional Committee of Respiratory, Society of Neonatologist, Chinese Medical Doctor Association. Clinical application recommendations for heated humidified high flow nasal cannula[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 132 -135 .
[3] YAN Jun, ZHU Xing-wang, SHI Yuan. Application progress of noninvasive ventilate technique for premature infants[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 136 -140 .
[4] GU Min-fang, YANG Chuan-zhong. Progress of intrapartum resuscitation for premature infants[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 141 -145 .
[5] LIU Shu-hua, SHEN Yue-bo, LIU Cui-qing, MA Li. The efficacy of pulmonary surfactant for pulmonary function in premature tension pneumothorax[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 146 -151 .
[6] GAO Xiao-hui, MAO Jian. Clinical features of non-oliguric hyperkalemia in extremely low birth weight infants[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 152 -158 .
[7] XIA Yao-fang, YANG Juan , TIAN Bao-li, et al. Value of amplitude-integrated electroencephalography in monitoring acute period of neonatal bilirubin encephalopathy and prognostic assessment[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 159 -163 .
[8] WANG Li-rong, SUN Xiao-yan, ZHU Ruo-xin, et al. Epidemiological investigation and analysis of women aged 40-55 years old with osteoporosis in Gansu province[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 164 -167 .
[9] CHEN Ru-yue, SHEN Yun-yan, CHEN Qing , et al. Five cases about Henoch-Schönlein purpura complicated with central nervous system injury in children and literatures review[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 168 -171 .
[10] ZHANG Ai-run, FANG Xiao-yi. Lung function testing of bronchopulmonary dysplasia for infants and children[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 172 -176 .
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