Expanded Newborn Screening for Inborn Errors of Metabolism and Genetic Characteristics in a Chinese Population
The incidence of inborn errors of metabolisms (IEMs) varies dramatically in different countries and regions. Expanded newborn screening for IEMs by tandem mass spectrometry (MS/MS) is an efficient approach for early diagnosis and presymptomatic treatment to prevent severe permanent sequelae and deat...
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Published in | Frontiers in genetics Vol. 9; p. 122 |
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Main Authors | , , , , , |
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Language | English |
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Abstract | The incidence of inborn errors of metabolisms (IEMs) varies dramatically in different countries and regions. Expanded newborn screening for IEMs by tandem mass spectrometry (MS/MS) is an efficient approach for early diagnosis and presymptomatic treatment to prevent severe permanent sequelae and death. To determine the characteristics of IEMs and IEMs-associated mutations in newborns in Jining area, China, 48,297 healthy neonates were recruited for expanded newborn screening by MS/MS. The incidence of IEMs was 1/1178 in Jining, while methylmalonic acidemia, phenylketonuria, and primary carnitine deficiency ranked the top 3 of all detected IEMs. Thirty mutations in nine IEMs-associated genes were identified in 28 confirmed cases. As 19 cases with the mutations in phenylalanine hydroxylase (
), solute carrier family 22 member 5 (
), and methylmalonic aciduria (cobalamin deficiency) cblC type with homocystinuria (
) genes, respectively, it suggested that mutations in the
,
, and
genes are the predominant causes of IEMs, leading to the high incidence of phenylketonuria, primary carnitine deficiency, and methylmalonic acidemia, respectively. Our work indicated that the overall incidence of IEMs is high and the mutations in
,
, and
genes are the leading causes of IEMs in Jining area. Therefore, it is critical to increase the coverage of expanded newborn screening by MS/MS and prenatal genetic consulting in Jining area. |
---|---|
AbstractList | The incidence of inborn errors of metabolisms (IEMs) varies dramatically in different countries and regions. Expanded newborn screening for IEMs by tandem mass spectrometry (MS/MS) is an efficient approach for early diagnosis and presymptomatic treatment to prevent severe permanent sequelae and death. To determine the characteristics of IEMs and IEMs-associated mutations in newborns in Jining area, China, 48,297 healthy neonates were recruited for expanded newborn screening by MS/MS. The incidence of IEMs was 1/1178 in Jining, while methylmalonic acidemia, phenylketonuria, and primary carnitine deficiency ranked the top 3 of all detected IEMs. Thirty mutations in nine IEMs-associated genes were identified in 28 confirmed cases. As 19 cases with the mutations in phenylalanine hydroxylase (PAH), solute carrier family 22 member 5 (SLC22A5), and methylmalonic aciduria (cobalamin deficiency) cblC type with homocystinuria (MMACHC) genes, respectively, it suggested that mutations in the PAH, SLC22A5, and MMACHC genes are the predominant causes of IEMs, leading to the high incidence of phenylketonuria, primary carnitine deficiency, and methylmalonic acidemia, respectively. Our work indicated that the overall incidence of IEMs is high and the mutations in PAH, SLC22A5, and MMACHC genes are the leading causes of IEMs in Jining area. Therefore, it is critical to increase the coverage of expanded newborn screening by MS/MS and prenatal genetic consulting in Jining area. The incidence of inborn errors of metabolisms (IEMs) varies dramatically in different countries and regions. Expanded newborn screening for IEMs by tandem mass spectrometry (MS/MS) is an efficient approach for early diagnosis and presymptomatic treatment to prevent severe permanent sequelae and death. To determine the characteristics of IEMs and IEMs-associated mutations in newborns in Jining area, China, 48,297 healthy neonates were recruited for expanded newborn screening by MS/MS. The incidence of IEMs was 1/1178 in Jining, while methylmalonic acidemia, phenylketonuria, and primary carnitine deficiency ranked the top 3 of all detected IEMs. Thirty mutations in nine IEMs-associated genes were identified in 28 confirmed cases. As 19 cases with the mutations in phenylalanine hydroxylase ( PAH ), solute carrier family 22 member 5 ( SLC22A5 ), and methylmalonic aciduria (cobalamin deficiency) cblC type with homocystinuria ( MMACHC ) genes, respectively, it suggested that mutations in the PAH , SLC22A5 , and MMACHC genes are the predominant causes of IEMs, leading to the high incidence of phenylketonuria, primary carnitine deficiency, and methylmalonic acidemia, respectively. Our work indicated that the overall incidence of IEMs is high and the mutations in PAH , SLC22A5 , and MMACHC genes are the leading causes of IEMs in Jining area. Therefore, it is critical to increase the coverage of expanded newborn screening by MS/MS and prenatal genetic consulting in Jining area. The incidence of inborn errors of metabolisms (IEMs) varies dramatically in different countries and regions. Expanded newborn screening for IEMs by tandem mass spectrometry (MS/MS) is an efficient approach for early diagnosis and presymptomatic treatment to prevent severe permanent sequelae and death. To determine the characteristics of IEMs and IEMs-associated mutations in newborns in Jining area, China, 48,297 healthy neonates were recruited for expanded newborn screening by MS/MS. The incidence of IEMs was 1/1178 in Jining, while methylmalonic acidemia, phenylketonuria, and primary carnitine deficiency ranked the top 3 of all detected IEMs. Thirty mutations in nine IEMs-associated genes were identified in 28 confirmed cases. As 19 cases with the mutations in phenylalanine hydroxylase ( ), solute carrier family 22 member 5 ( ), and methylmalonic aciduria (cobalamin deficiency) cblC type with homocystinuria ( ) genes, respectively, it suggested that mutations in the , , and genes are the predominant causes of IEMs, leading to the high incidence of phenylketonuria, primary carnitine deficiency, and methylmalonic acidemia, respectively. Our work indicated that the overall incidence of IEMs is high and the mutations in , , and genes are the leading causes of IEMs in Jining area. Therefore, it is critical to increase the coverage of expanded newborn screening by MS/MS and prenatal genetic consulting in Jining area. The incidence of inborn errors of metabolisms (IEMs) varies dramatically in different countries and regions. Expanded newborn screening for IEMs by tandem mass spectrometry (MS/MS) is an efficient approach for early diagnosis and presymptomatic treatment to prevent severe permanent sequelae and death. To determine the characteristics of IEMs and IEMs-associated mutations in newborns in Jining area, China, 48,297 healthy neonates were recruited for expanded newborn screening by MS/MS. The incidence of IEMs was 1/1178 in Jining, while methylmalonic acidemia, phenylketonuria, and primary carnitine deficiency ranked the top 3 of all detected IEMs. Thirty mutations in nine IEMs-associated genes were identified in 28 confirmed cases. As 19 cases with the mutations in phenylalanine hydroxylase (PAH), solute carrier family 22 member 5 (SLC22A5), and methylmalonic aciduria (cobalamin deficiency) cblC type with homocystinuria (MMACHC) genes, respectively, it suggested that mutations in the PAH, SLC22A5, and MMACHC genes are the predominant causes of IEMs, leading to the high incidence of phenylketonuria, primary carnitine deficiency, and methylmalonic acidemia, respectively. Our work indicated that the overall incidence of IEMs is high and the mutations in PAH, SLC22A5, and MMACHC genes are the leading causes of IEMs in Jining area. Therefore, it is critical to increase the coverage of expanded newborn screening by MS/MS and prenatal genetic consulting in Jining area.The incidence of inborn errors of metabolisms (IEMs) varies dramatically in different countries and regions. Expanded newborn screening for IEMs by tandem mass spectrometry (MS/MS) is an efficient approach for early diagnosis and presymptomatic treatment to prevent severe permanent sequelae and death. To determine the characteristics of IEMs and IEMs-associated mutations in newborns in Jining area, China, 48,297 healthy neonates were recruited for expanded newborn screening by MS/MS. The incidence of IEMs was 1/1178 in Jining, while methylmalonic acidemia, phenylketonuria, and primary carnitine deficiency ranked the top 3 of all detected IEMs. Thirty mutations in nine IEMs-associated genes were identified in 28 confirmed cases. As 19 cases with the mutations in phenylalanine hydroxylase (PAH), solute carrier family 22 member 5 (SLC22A5), and methylmalonic aciduria (cobalamin deficiency) cblC type with homocystinuria (MMACHC) genes, respectively, it suggested that mutations in the PAH, SLC22A5, and MMACHC genes are the predominant causes of IEMs, leading to the high incidence of phenylketonuria, primary carnitine deficiency, and methylmalonic acidemia, respectively. Our work indicated that the overall incidence of IEMs is high and the mutations in PAH, SLC22A5, and MMACHC genes are the leading causes of IEMs in Jining area. Therefore, it is critical to increase the coverage of expanded newborn screening by MS/MS and prenatal genetic consulting in Jining area. |
Author | Chen, Xigui Guo, Kejian Kong, Qingsheng Liu, Chuanxin Zhou, Xuan Wu, Yili |
AuthorAffiliation | 1 Jining Maternal and Child Health Care Hospital , Jining , China 3 Shandong Key Laboratory of Behavioral Medicine, Jining Medical University , Jining , China 2 Department of Psychiatry, Jining Medical University , Jining , China 4 Collaborative Innovation Center for Birth Defect Research and Transformation of Shandong Province, Jining Medical University , Jining , China 5 Department of Biochemistry, Jining Medical University , Jining , China |
AuthorAffiliation_xml | – name: 2 Department of Psychiatry, Jining Medical University , Jining , China – name: 4 Collaborative Innovation Center for Birth Defect Research and Transformation of Shandong Province, Jining Medical University , Jining , China – name: 5 Department of Biochemistry, Jining Medical University , Jining , China – name: 1 Jining Maternal and Child Health Care Hospital , Jining , China – name: 3 Shandong Key Laboratory of Behavioral Medicine, Jining Medical University , Jining , China |
Author_xml | – sequence: 1 givenname: Kejian surname: Guo fullname: Guo, Kejian – sequence: 2 givenname: Xuan surname: Zhou fullname: Zhou, Xuan – sequence: 3 givenname: Xigui surname: Chen fullname: Chen, Xigui – sequence: 4 givenname: Yili surname: Wu fullname: Wu, Yili – sequence: 5 givenname: Chuanxin surname: Liu fullname: Liu, Chuanxin – sequence: 6 givenname: Qingsheng surname: Kong fullname: Kong, Qingsheng |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29731766$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1203/PDR.0b013e3181c9fb85 10.16190/j.cnki.45-1211/r.2013.05.055 10.1097/GIM.0b013e31820d5e67 10.1016/j.clinbiochem.2017.10.016 10.1542/peds.105.1.e10 10.1186/s13023-015-0283-0 10.1515/jpem-2016-0028 10.1155/2015/259627 10.1111/cge.12112 10.1007/8904_2011_119 10.1186/1750-1172-6-44 10.1136/adc.2005.091637 10.13404/j.cnki.cjbhh.2016.03.036 10.1159/000331469 10.1373/clinchem.2009.131300 10.1016/j.cccn.2004.11.032 10.1007/s12035-017-0459-9 10.1016/j.braindev.2015.10.016 10.1111/j.1399-0004.2008.01071.x 10.4103/0256-4947.65254 10.1177/0969141315618229 10.1016/j.jpeds.2011.04.011 10.1186/1750-1172-7-68 10.1016/j.ymgme.2008.07.001 10.1039/c4mb00729h 10.1016/j.ymgme.2014.07.018 10.1093/hmg/8.12.2247 10.1515/jpem-2017-0003 |
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Copyright | Copyright © 2018 Guo, Zhou, Chen, Wu, Liu and Kong. 2018 Guo, Zhou, Chen, Wu, Liu and Kong |
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Keywords | inborn errors of metabolism IEMs-associated gene mutation newborn screening incidence of IEMs |
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Snippet | The incidence of inborn errors of metabolisms (IEMs) varies dramatically in different countries and regions. Expanded newborn screening for IEMs by tandem mass... |
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SubjectTerms | Genetics IEMs-associated gene mutation inborn errors of metabolism incidence of IEMs newborn screening |
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Title | Expanded Newborn Screening for Inborn Errors of Metabolism and Genetic Characteristics in a Chinese Population |
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