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Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Parental Depression and Anxiety Associated with Newborn Bloodspot Screening for Rare and Variable-Onset Disorders
Natalie A Boychuk1, Niamh S Mulrooney1, Nicole R Kelly1
1Department of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
Insights
Parents of children diagnosed with lysosomal storage disorders (LSDs) or X-linked adrenoleukodystrophy (X-ALD) clinically showed higher odds of depression compared to those diagnosed via newborn bloodspot screening (NBS). This impacts understanding psychosocial outcomes in expanded NBS.
Area of Science:
- Genetics and Genomics
- Pediatrics
- Psychology
Background:
- Expanded newborn bloodspot screening (NBS) enables detection of more rare disorders, including those with variable phenotypes.
- This raises concerns about the psychosocial impact on parents, particularly for complex conditions like lysosomal storage disorders (LSDs) and X-linked adrenoleukodystrophy (X-ALD).
Purpose of the Study:
- To compare the psychological outcomes of parents based on their child's rare disorder and diagnostic pathway (clinical diagnosis vs. NBS).
- To investigate the relationship between diagnostic experience and parental stress and depression.
Main Methods:
- An online cross-sectional survey was administered to 174 parents of children born between 2013-2018.
- Parents were grouped by their child's disorder (LSDs, X-ALD) and diagnosis method (clinical vs. NBS).
- Logistic regression models assessed depression and stress, controlling for demographic variables.
Main Results:
- Parents whose children received a clinical diagnosis for LSDs or X-ALD had significantly higher odds of depression compared to those diagnosed through NBS (OR: 6.06).
- A similar trend for increased parental stress was observed in the clinically diagnosed group, though it did not reach statistical significance (OR: 2.85).
Conclusions:
- Early detection through NBS may be psychologically reassuring for parents of children with complex disorders like LSDs and X-ALD, compared to clinical diagnosis.
- These findings are preliminary and warrant further investigation in larger, diverse populations as NBS and genomic sequencing expand.
Abstract:
The ability to screen newborns for a larger number of disorders, including many with variable phenotypes, is prompting debate regarding the psychosocial impact of expanded newborn bloodspot screening (NBS) on parents. This study compares psychological outcomes of parents of children with a range of NBS/diagnostic experiences, with a particular focus on lysosomal storage disorders (LSDs) and X-linked adrenoleukodystrophy (X-ALD) as representative disorders with complex presentations. An online cross-sectional survey with six domains was completed in 2019 by a volunteer sample of parents with at least one child born between 2013 and 2018. Parents were classified in the analysis stage into four groups based on their child's rare disorder and means of diagnosis. Stress and depression were estimated using dichotomous measures of the depression subscale of the Hospital Anxiety and Depression Scale and the Parental Stress Scale. Logistic regression models were estimated for the relationship between the parent group and stress/depression, controlling for demographic variables (region of the US, income, education, major life events, relationship to the child, number of children, parent age, and race/ethnicity). One hundred seventy-four parents were included in this analysis. Parents of children with an LSD or X-ALD diagnosis clinically may have higher odds of depression (OR: 6.06, 95% CI: 1.64-24.96) compared to parents of children with the same disorders identified through NBS, controlling for covariates. Although a similar pattern was observed for parental stress (OR: 2.85, 95% CI: 0.82-10.37), this did not reach statistical significance. Ethically expanding NBS and genome sequencing require an understanding of the impacts of early detection for complex disorders on families. These initial findings are reassuring, and may have implications as NBS expands. Given our small sample size, it is difficult to generalize these findings to all families. These preliminary trends warrant further investigation in larger and more diverse populations.
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