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Newborn Screening Alone Cannot Prevent Most Cases of Severe Vitamin B12 Deficiency in the First Year of Life
Christina Kaufman1, Julian Margreitter2, Marion Herle3
1Division of Metabolism and Children's Research Center, University Children's Hospital of Zurich, University of Zurich, 8008 Zurich, Switzerland.
Insights
Infant vitamin B12 deficiency (B12D) causes severe neurological issues. Newborn screening (NBS) has a low detection rate for symptomatic B12D, but maternal screening is recommended for prevention.
Area of Science:
- Biochemistry
- Pediatrics
- Genetics
Background:
- Vitamin B12 (B12) is crucial for metabolic pathways, and its deficiency (B12D) in infants can cause irreversible neurological damage.
- Maternal B12 status directly impacts infant B12 levels, highlighting the importance of maternal nutrition during pregnancy and breastfeeding.
- B12D is a target condition in some newborn screening (NBS) programs, aiming to detect and treat affected infants early.
Purpose of the Study:
- To retrospectively assess the efficacy of the Austrian NBS algorithm in detecting infants diagnosed with symptomatic B12D within their first year of life.
- To evaluate the correlation between clinical symptoms, NBS data, biochemical markers, and maternal health history in infants with B12D.
- To analyze the impact of B12-related NBS implementation on the incidence of symptomatic infant B12D.
Main Methods:
- Retrospective collection of data from infants diagnosed with B12D in Austria (NBS implemented) and Switzerland (NBS not implemented) between 2012-2022.
- Retrospective analysis of NBS data and correlation with clinical information obtained via survey.
- Analysis of biochemical parameters (B12, total homocysteine, methylmalonic acid) and maternal medical history.
Main Results:
- The Austrian NBS algorithm retrospectively detected only 4.3-9.3% of infants with symptomatic B12D.
- Neurological and hematological symptoms correlated with low B12 and elevated total homocysteine (tHcy) and methylmalonic acid levels.
- Fewer infants with symptomatic B12D were observed post-implementation of B12-related NBS in Austria, suggesting a potential preventive effect.
Conclusions:
- Symptomatic infant B12D leads to severe clinical manifestations, with NBS showing limited retrospective detection capabilities.
- Maternal B12D poses a significant risk for infant B12D and other pregnancy complications.
- Screening pregnant women for B12D is recommended to enhance prevention, ensure healthy pregnancies, and reduce NBS recalls.
Background/Objectives:
Vitamin B12 (B12) is essential for the provision of methyl groups for numerous essential pathways. Infant B12 deficiency (B12D) can lead to severe, even irreversible neurological abnormalities. Maternal B12 status in pregnancy and during the breastfeeding period correlates significantly with the child's B12 status. B12D is a target disease in some newborn screening (NBS) programs. This study investigates whether infants that were clinically symptomatic and diagnosed with B12D in their first year of life could be retrospectively detected by the Austrian NBS algorithm.
Methods:
Data from infants with clinically diagnosed B12D in their first year of life between 2012 and 2022 were retrospectively collected in Austria (B12-related NBS implemented in 2018) and Switzerland (B12-related NBS not implemented). NBS data were retrospectively analysed, and clinical information was collected by a survey. Correlations between clinical symptoms, NBS data, biochemical parameters at diagnosis, maternal medical history and B12 status were analysed.
Results:
Four/forty-eight cases were retrospectively detected by the first-tier NBS parameters. From two children material for second-tier testing was available and B12D was confirmed by elevated total homocysteine (tHcy), resulting in a detection rate between 4.3 and 9.3%. The numbers of neurological and haematological symptoms correlated with low B12 and elevated levels of tHcy and methylmalonic acid. Although the detection rate of symptomatic B12D by NBS was low, fewer infants with symptomatic B12D were observed in the period after implementation of B12-related NBS (Austria). A history of B12D-relevant maternal disease such as pernicious anaemia was reported in 12 cases.
Conclusions:
B12D causes severe clinical symptoms in infants. NBS has a very limited retrospective detection rate of infants with severe B12D but seems to correlate with a reduction in cases due to not yet precisely quantified mechanisms. The workup triggered by NBS recalls is costly and often challenging for families. Maternal B12D increases the risk of infant B12D but also of other pregnancy-related health risks. To increase the efficacy of the prevention of infant B12D, to promote a healthy pregnancy and breastfeeding period, and to reduce the frequency of NBS recalls, pregnant women should be screened for B12D to be counselled and treated.
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