Retrospective Review of Positive Newborn Screening Results for Isovaleric Acidemia and Development of a Strategy to Improve the Efficacy of Newborn Screening in the UK

被引:0
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作者
Carling, Rachel S. [1 ,2 ]
Hedgethorne, Katy [1 ]
Chakrapani, Anupam [3 ]
Hall, Patricia L. [4 ]
Flynn, Nick [5 ]
Greenfield, Toby [6 ]
Moat, Stuart J. [7 ,8 ]
Ssali, Joshua [9 ]
Shakespeare, Lynette [10 ]
Taj, Nazia [11 ]
Wu, Teresa H. Y. [12 ]
Anderson, Mark [13 ]
Ghosh, Arunabha [14 ]
Lemonde, Hugh [15 ]
Pierre, Germaine [16 ]
Sharrard, Mark [17 ]
Sreekantam, Sreevidya [18 ]
Bonham, James R. [10 ]
机构
[1] Guys & St Thomas NHSFT, Biochem Sci, Synnovis, London SE1 7EH, England
[2] Kings Coll London, GKT Sch Med Educ, London WC2R 2LS, England
[3] Great Ormond St Hosp NHSFT, Dept Metab Med, London WC1N 3JH, England
[4] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[5] Cambridge Univ Hosp NHSFT, Biochem Genet Unit, Cambridge CB2 0QQ, England
[6] Portsmouth Hosp Trust, Portsmouth PO6 3LY, England
[7] Univ Hosp Wales, Dept Med Biochem Immunol & Toxicol, Cardiff CF14 4XW, Wales
[8] Cardiff Univ, Sch Med, Cardiff CF14 4XN, Wales
[9] Epsom & St Helier Hosp, South West Thames Newborn Screening, Carshalton SM5 1AA, England
[10] Sheffield Childrens NHSFT, Clin Chem, Sheffield S10 2TH, England
[11] Oxford Univ Hosp NHSFT, Dept Clin Biochem, Oxford OX3 9DU, England
[12] Manchester Univ NHSFT, Willink Biochem Genet Lab, Genom Med, Manchester M13 9WL, England
[13] Great North Childrens Hosp, Newcastle Tyne Hosp NHSFT, Newcastle Upon Tyne NE1 4LP, England
[14] Manchester Univ NHSFT, Willink Biochem Genet Unit, Manchester M13 9WL, England
[15] Guys & St Thomas NHSFT, Evelina London Childrens Hosp, Dept Paediat Metab Med, London SE1 7EH, England
[16] Univ Hosp Bristol & Weston NHSFT, Bristol BS1 3NU, England
[17] Sheffield Childrens NHSFT, Paediat Med, Sheffield S10 2TH, England
[18] Birmingham Womens & Childrens Hosp, Birmingham B4 6NH, England
关键词
isovaleric acidemia; false positive; newborn screening; inherited metabolic disease; TANDEM MASS-SPECTROMETRY; DRIED BLOOD SPOTS;
D O I
10.3390/ijns10010024
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Since the UK commenced newborn screening for isovaleric acidemia in 2015, changes in prescribing have increased the incidence of false positive (FP) results due to pivaloylcarnitine. A review of screening results between 2015 and 2022 identified 24 true positive (TP) and 84 FP cases, with pivalate interference confirmed in 76/84. Initial C5 carnitine (C5C) did not discriminate between FP and TP with median (range) C5C of 2.9 (2.0-9.6) and 4.0 (1.8->70) mu mol/L, respectively, and neither did Precision Newborn Screening via Collaborative Laboratory Integrated Reports (CLIR), which identified only 1/47 FP cases. However, among the TP cases, disease severity showed a correlation with initial C5C in 'asymptomatic' individuals (n = 17), demonstrating a median (range) C5C of 3.0 (1.8-7.1) whilst 'clinically affected' patients (n = 7), showed a median (range) C5C of 13.9 (7.7-70) mu mol/L. These findings allowed the introduction of dual cut-off values into the screening algorithm to reduce the incidence of FPs, with initial C5C results >= 5 mu mol/L triggering urgent referral, and those >2.0 and <5.0 <mu>mol/L prompting second-tier C5-isobar testing. This will avoid delayed referral in babies at particular risk whilst reducing the FP rate for the remainder.
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页数:8
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