Related Experiment Video
Updated: May 13, 2026

High Content Screening in Neurodegenerative Diseases
Published on: January 6, 2012
Impact of new screening technologies: should we screen and does phenotype influence this decision?
1Department of Clinical Chemistry, Sheffield Children's NHS Foundation Trust, Sheffield, S10 2TH, UK. Jim.bonham@sch.nhs.uk
Insights
Newborn screening programs for inherited metabolic disorders show benefits, but international practices vary widely. Re-evaluating screening criteria and addressing challenges like false positives are crucial for optimizing patient care.
Area of Science:
- Medical Genetics
- Biochemistry
- Public Health
Background:
- Newborn screening for phenylketonuria highlights the success of organized programs for inherited metabolic disorders.
- Despite advances like electrospray MS/MS, significant international variation in expanded newborn screening practices persists, unrelated to economic factors.
Purpose of the Study:
- To analyze the reasons for international variation in newborn screening practices.
- To identify key challenges and propose solutions for optimizing newborn screening programs as they expand to include more conditions.
Main Methods:
- Review of current newborn screening practices and criteria for disorder suitability.
- Analysis of national policy-making differences and their impact on screening strategies.
- Identification of issues related to outcome studies, parental information, false positives, and mild/atypical cases.
Main Results:
- Existing criteria for assessing disorder suitability for screening may need re-appraisal for rare disorders.
- National policy differences influence screening strategies, necessitating closer scrutiny.
- Increasingly broad screening programs face challenges including the need for standardized outcome studies, improved parental support, managing false positives, and developing proportionate treatments for mild cases.
Conclusions:
- Optimizing newborn screening requires a comprehensive understanding of genetic, biochemical, and clinical features of screened conditions.
- Effective international outcome studies are essential for refining both screening and treatment strategies.
- Addressing practice variations and specific challenges is critical for the continued success of expanded newborn screening programs.
Abstract:
The early detection offered by newborn screening for phenylketonuria clearly demonstrates the benefits for patients with inherited metabolic disorders of well organised screening programmes. It is therefore perhaps surprising that 20 years after the introduction of electrospray MS/MS methods to support expanded newborn screening that considerable international variation in practice, not linked to economic factors, exists. It is likely that the commonly used criteria to assess the suitability of a disorder for screening need to be re-appraised as they apply to rare disorders. In addition, national differences in the pattern of policy making may influence the strategy adopted and these different approaches need to be scrutinised more closely. Despite this contextual variation a number of real issues do need to be addressed as the range of conditions included in screening programmes continues to increase. These include the need for well organised outcome studies based upon agreed case definitions and comparable treatment regimens; the need for appropriate information for parents to support them before and during the screening odyssey; an improved understanding of the impact of false positive results and in particular a clearer understanding of the way in which some of the problems resulting from false positive results can be avoided or ameliorated; the challenge offered by mild or atypical screen positive cases and the consequent design of proportionate treatment options. A thorough understanding of the genetic, biochemical and clinical features of screen positive cases supported by effective international outcome studies is required to optimise both screening and treatment strategies.
Related Concept Videos
Genetic Screens
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which result in visible changes...
Pharmacogenomics: Identification of New Drug Targets
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Background and Environment Affect Phenotype
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
Pharmacogenetics and Pharmacogenomics: Overview
Pharmacogenetics of Phase I Enzymes: Cytochrome P450 Isozymes
