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Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meeting
Martin Lindner1, Georg F Hoffmann, Dietrich Matern
1University Children's Hospital, Heidelberg, Germany. Martin.lindner@med.uni-heidelberg.de
Insights
New-born screening (NBS) for fatty-acid oxidation disorders (FAOD) shows a combined incidence of approximately 1:9,300. Expanding NBS programs to include all FAOD, particularly with tandem mass spectrometry, is recommended if laboratory performance is ensured.
Area of Science:
- Biochemistry
- Genetics
- Public Health
Background:
- New-born screening (NBS) for fatty-acid oxidation disorders (FAOD) is expanding globally.
- FAOD spectrum and incidence vary significantly across ethnic groups.
- Current NBS programs demonstrate clear benefits for medium-chain acyl-CoA dehydrogenase deficiency (MCAD) in Caucasian populations.
Framework:
- International collaboration is crucial for evaluating long-term benefits of NBS for rare FAOD.
- Standardized confirmatory diagnostic procedures are needed for international data comparability.
- The inclusion of conditions with uncertain clinical significance, like short-chain acyl-CoA dehydrogenase deficiency (SCAD), can yield valuable knowledge.
Implementation:
- Tandem mass spectrometry (MS/MS) is a key technology for FAOD screening.
- High laboratory performance standards are essential for reliable NBS results.
- Ethnic variations in FAOD prevalence necessitate tailored screening approaches.
Implications:
- Expanding NBS to include all FAOD is supported by accumulated evidence.
- MS/MS-based NBS programs offer a viable strategy for comprehensive FAOD detection.
- Further research and international cooperation are vital for optimizing FAOD screening protocols and understanding disease impact.
Abstract:
Experience with new-born screening (NBS) for disorders of fatty-acid oxidation (FAOD) is now becoming available from an increasing number of programs worldwide. The spectrum of FAOD differs widely between ethnic groups. Incidence calculations from reports from Australia, Germany, and the USA of a total of 5,256,999 newborns give a combined incidence of all FAOD of approximately 1:9,300. However, it appears to be much lower in Asians. Consequently, a significant prevalence and evidence for a clear benefit of NBS is proven for medium-chain acyl-CoA dehydrogenase deficiency (MCAD) only in countries with a high percentage of Caucasians, with very-long-chain acyl-CoA dehydrogenase deficiency (VLCAD) and long-chain 3-hydroxy acyl-CoA dehydrogenase deficiency (LCHAD) being additional candidates. The long-term benefit for many disorders has still to be evaluated and will require international collaboration, especially for the rarest disorders. Short-chain acyl-CoA dehydrogenase deficiency (SCAD) [as well as Systemic carnitine transporter deficiency (CTD) and dienoyl-CoA reductase deficiency (DE-RED)] are conditions of uncertain clinical significance, but most FAOD have a spectrum of clinical presentations (healthy-death). Confirmatory diagnostic procedures should be agreed upon to ensure international comparability of results and evidence-based modifications. The case of short-chain acyl-CoA dehydrogenase deficiency (SCAD) deficiency shows that even inclusion of conditions without a clearly known natural course may prove useful with respect to gain of knowledge and consecutive exclusion of a biochemical abnormality without clinical significance, although this line of argument implies the existence of structured follow-up programs and bears ethical controversies. As a final conclusion, the accumulated evidence suggests all FAOD should to be included into tandem mass spectrometry (MS/MS)-based NBS programs provided sufficient laboratory performance is guaranteed.
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