Precise measurement of concentrations of the H6D variant of GDF15 using different assays

Study code
CBR222 - Measuring the H6D variant of GDF15

Lead researcher
Professor Sir Stephen O'Rahilly

Study type
Online

Institution or company
University of Cambridge (Institute of Metabolic Science)

Researcher type
Academic

Speciality area
Cancer, Metabolic and Endocrine Disorders

Recruitment Site
Not applicable (samples only)

Summary

Protein Growth-Differentiation Factor 15 (GDF15) is a newly discovered hormone that can be produced and released into the bloodstream by any cell in the body that is undergoing stress. It acts on the brain to activate hormonal pathways that assist in survival under severe stress; it also seems to play an important role in inducing “illness behaviour” such as lying down and not feeling like eating, which probably helped humans to overcome a range of threats to our survival during our evolution. Today, its major medical significance is in a condition called cancer cachexia, where people with certain cancers lose their appetite and also develop muscle wasting. Many cancers are associated with high circulating GDF15 levels and blocking the action of GDF15 is showing early promise in clinical trials.

Clearly, accurate and precise measurement of GDF15 is critical, as this treatment will only be useful in cases where GDF15 levels are high. We have found that a common genetic variant in GDF155 (H6D) seriously interferes with its measurement by some widely used assays. We have been working with a small diagnostics company that has produced a new assay that is likely not to be interfered with by this genetic variant and in this study we wish to test whether this is the case. We will do so by using the range of available assays to measure GDF15 in 173 stored plasma samples from participants in the Cambridge BioResource whose genetic status of the DNA encoding GDF15 is already known. Having an accurate and affordable means of measuring GDF15 will help advance the development of treatments for cancer cachexia and other conditions (i.e. appetite suppression in obesity).

Publication arising:

Karusheva Y, Ratcliff M, Mörseburg A, Barker P, Melvin A, Sattar N, Burling K, Backmark A, Roth R, Jermutus L, Guiu-Jurado E, Blüher M, Welsh P, Hyvönen M, O'Rahilly S. (2020) 'The Common H202D Variant in GDF-15 Does Not Affect Its Bioactivity but Can Significantly Interfere with Measurement of Its Circulating Levels.' J Appl Lab Med. 7(6):1388-1400 (link)

Conclusion:

The measurement of the protein Growth Differentiation Factor 15 (GDF15) is expanding from scientific research to the clinical arena, with GDF15 levels related to prognosis in several chronic diseases. We undertook studies to determine whether a common variant (H6D, present in 15-30% of people worldwide) of this protein interfered with GDF15’s detection by three of the most commonly used commercially available immunoassays. Our results reveal that this common isoform of GDF15 substantially affects its measurement by one or more widely used assays with implications for the interpretation of studies employing such assays in a clinical setting.