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Reference materials for clinical analysis

The measurement of biomarkers, mainly in blood, is performed in many thousands of hospital laboratories.  The results are used to monitor health status, screen for disease, support diagnosis, and monitor the effect of therapies for diseases.

However, measuring biomarkers reliably is not straightforward. The results can be influenced by the calibration of the instrument, chemical instability, the selectivity of a particular method and eventually by the patient's genotype. A lack of harmonisation makes it impossible to compare test results obtained at different hospitals or even the same hospital over a period of time – a situation which is exacerbated by increased levels of population migration and mobility.

Making laboratory results comparable requires standardisation, using reference materials and methods. The need for standardisation and traceability is taken up in the EU Directive on in Vitro Diagnostic Medical Devices (IVD-MD). In Vitro Diagnostics manufacturers can make use of JRC’s standardisation tools in order comply with the requirements of the directive.

/jrc/en/video/ingrid-zegers-blood-tests-reference-standardsIngrid Zegers, Blood Tests Reference Standards

Measurement standards accepted worldwide

The JRC has the expertise to develop reference materials, but also coordinates the input from the clinical chemistry profession, the In Vitro Diagnostics industry and hospital clinicians. The close collaboration with specialists in the field ensures that the reference materials produced are the best suitable for clinical practice and patient outcome. Standardisation is both a scientific and a consensus process. Therefore the independent position of the JRC helps in developing reference systems that are generally accepted.

Support to the development of legislation and guidance documents

The need for standardisation and traceability is taken up in EU legislation. The the EU Directive on In Vitro Diagnostic Medical Devices (IVD-MD) (Directive 98/79/EC) is currently under revision, and the JRC contributed to the drafting of a proposal for a new regulation on in-vitro medical devices. The proposed regulation aims to ensure the smooth functioning of the internal market and a high level of protection of human health and safety.

It is also in this context that the JRC contributes to documentary standards and guidance developed by international initiatives like the International Standards Organisation (ISO), the International federation for Clinical Chemistry and Laboratory Medicine (IFCC) and the Joint Committee for the Traceability of Laboratory Medicine (JCTLM).

Building on a long tradition for the standardisation of the measurement of plasma proteins and enzymes

A major breakthrough in standardising plasma protein measurements was made in the 1990s when the European Commission's Bureau Communautaire de Références (BCR), in collaboration with the International Federation for Clinical Chemistry and Laboratory Medicine (IFCC), released the stable and reliable reference material BCR-470, later re-named ERM-DA470/IFCC, certified for 15 proteins. Since then, the JRC has developed and released a range of clinical reference materials for proteins like C-reactive protein and cystatin C – markers for inflammation and for the functioning of the kidney, respectively. A reference material for 12 protein markers (called ERM-DA470k/IFCC) has been produced to ensure continuity in the measurement of the main plasma proteins like albumin and the antibodies IgG and IgM.

Supporting the early diagnosis and monitoring of major chronic diseases

Chronic diseases like autoimmune diseases, diabetes and Alzheimer disease are not only devastating for the patients and their families, but also have a major societal cost.  The early diagnosis of such diseases is important for the development and implementation of treatments. However, many of these diseases are difficult to diagnose, particularly in early stages. Reliable biomarker measurements could make a big difference. JRC coordinates, together with the International Federation for Clinical Chemistry and Laboratory Medicine, the research required for the standardisation of the relevant biomarkers. Reference materials are being developed for biomarkers for diabetes (HbA1c) autoimmune diseases like vasculitis, rheumatoid arthritis and lupus, as well as for Alzheimer disease.

The JRC approach for the standardisation of complex biomarkers is described in the article Standardisation of protein biomarker measurements: Is it feasible?

/jrc/en/file/179647A global reference tool to fight Alzheimer's


Developing the bioanalysis methods that form the basis for stable reference systems

The reference methods and reference materials developed by the JRC form the basis for reliable and stable clinical measurements. Therefore these need to be developed at a level of quality well beyond what is required in routine analysis. This requires research into the processes underlying the measurements, and the rigorous validation of methods developed. This may seem a slow process, but this is one of the fields where time is required in order to achieve the necessary quality. An example is a method for the quantification of protein calibrants by amino acid analysis. JRC participates in ring trials with metrology institutes from all over the world in order to study how these methods can still be further improved.

Worldwide first certified reference materials for monitoring of leukaemia - ERM-AD623

Chronic myelogenous leukaemia (CML) is a cancer of the white blood cells. In the EU about 6200 new patients per year are diagnosed and CML mainly affects adults. CML can currently not be cured, but kept under control with specific enzyme inhibitors. Regular monitoring of the CML patient is needed to ensure optimal treatment of the patient.