Introduction of a Novel Cut-off in Newborn Screening of Galactosemia; A Cohort Study

被引:0
作者
Naseri, Reyhaneh [1 ,2 ]
Beyzaei, Zahra [3 ]
Geramizadeh, Bita [3 ,4 ]
机构
[1] Shiraz Univ Med Sci, Thorac & Vasc Surg Res Ctr, Shiraz, Iran
[2] Shiraz Univ Med Sci, Student Res Comm, Sch Med, Shiraz, Iran
[3] Shiraz Univ Med Sci, Shiraz Transplant Res Ctr STRC, Shiraz, Iran
[4] Shiraz Univ Med Sci, Dept Pathol, Shiraz, Iran
关键词
Galactosemia; Infant; Neonatal Screening; ROC Curve; CLASSICAL GALACTOSEMIA;
D O I
10.5812/ijp-142691
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: The current newborn screening for Classic Galactosemia (CG) presents significant challenges, including a low positive rate and a high false-positive rate. Objectives: In this study, we aimed to establish new cut-off values (COVs) for CG screening and introduce a novel approach. Methods: Total galactose (TGAL: The sum of galactose (Gal) and galactose-1-phosphate (G-1-P)) levels of all newborns born in Fars, Iran, from August 2006 to December 2020, were reviewed to establish cut-off ranges. A receiver operating characteristic (ROC) curve analysis was performed to define an optimal COV. Results: Out of 1,187,436 newborns, 4,893 (0.41%) were recalled for further evaluation due to an initial TGAL >= 4 mg/dI. from a positive screening test, with 160 (3.26%) confirmed to have CG. In the initial negative screening results, nine infants were missed as false negatives. An area under the curve of 0.868 suggested that TGAL is a reliable indicator for distinguishing galactosemia from normal subjects. Receiver operating characteristic curve analysis indicated that a cut-off value (COV) of 5.2 mg/dI. provided a sensitivity and specificity of 80.0% and 81.3%, respectively, making it an optimal conservative value for deciding on further recall in the Iranian setting. Additionally, a COV of 735 mg/dI. demonstrated a sensitivity of 71.3% and specificity of 95.7%, making it a suitable cut-off for immediate referral. Conclusions: We proposed a novel protocol for newborn screening in Iran, establishing a TGAL level of 5.2 mg/dL as a conservative cut-off for CG screening, showing excellent sensitivity while ensuring specificity for recalling suspicious cases. Furthermore, a cut-off of 735 mg/dL was identified for prompt consideration of urgent treatment.
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页数:9
相关论文
共 22 条
[1]   Galactosemia: When is it a newborn screening emergency? [J].
Berry, Gerard T. .
MOLECULAR GENETICS AND METABOLISM, 2012, 106 (01) :7-11
[2]   Classical galactosaemia revisited [J].
Bosch, Annet M. .
JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 (04) :516-525
[3]  
Bosch Annet M, 2005, Hum Mutat, V25, P502, DOI 10.1002/humu.9330
[4]   Developmental Outcomes in Duarte Galactosemia [J].
Carlock, Grace ;
Fischer, S. Taylor ;
Lynch, Mary Ellen ;
Potter, Nancy L. ;
Coles, Claire D. ;
Epstein, Michael P. ;
Mulle, Jennifer G. ;
Kable, Julie A. ;
Barrett, Catherine E. ;
Edwards, Shannan M. ;
Wilson, Elizabeth ;
Fridovich-Keil, Judith L. .
PEDIATRICS, 2019, 143 (01)
[5]  
Chen Y.-T., 2001, METABOLIC MOL BASIS, VI, P1521
[6]   The ability of an LC-MS/MS-based erythrocyte GALT enzyme assay to predict the phenotype in subjects with GALT deficiency [J].
Demirbas, Didem ;
Huang, Xiaoping ;
Daesety, Vikram ;
Feenstra, Susan ;
Haskovic, Minela ;
Qi, Wanshu ;
Gubbels, Cynthia S. ;
Hecht, Leah ;
Levy, Harvey L. ;
Waisbren, Susan E. ;
Berry, Gerard T. .
MOLECULAR GENETICS AND METABOLISM, 2019, 126 (04) :368-376
[7]  
Elsas LJ, 1998, GENET MED, V1, P40
[8]   Newborn Screening for Galactosemia: A Review of 5 Years of Data and Audit of a Revised Reporting Approach [J].
Freer, Dennis E. ;
Ficicioglu, Can ;
Finegold, David .
CLINICAL CHEMISTRY, 2010, 56 (03) :437-444
[9]   Developmental outcomes of children with Duarte galactosemia: exploring the bases of an apparent contradiction in the literature [J].
Fridovich-Keil, Judith L. ;
Carlock, Grace ;
Coles, Claire D. ;
Lynch, Mary Ellen ;
Millians, Molly N. ;
Potter, Nancy L. ;
Powell, Kimberly ;
Richards, Peter ;
Singh, Rani ;
Wittenauer, Angela .
GENETICS IN MEDICINE, 2019, 21 (12) :2683-2685
[10]  
Fujimoto A, 2000, CLIN CHEM, V46, P806