New Radiotracer Improves Differential Diagnosis of Parkinson’s Disease

Metabolism studies in mice revealed that the radiometabolite can penetrate the blood-brain barrier (BBB). It also performed well in dosimetry and radiation protection studies, carried out in cooperation with the Clinic of Nuclear Medicine at the University of Leipzig (Germany), as well as in a toxicity study.

When adenosine attaches to certain receptors, it causes the nerve cells to work more slowly, including those that are significant for PD. The areas of the brain where increased radioactivity is detected must therefore have a particularly high number of receptors, which can be imaged using super-sensitive PET imaging. The study, by an interdisciplinary team from the HZDR Institute of Radiopharmaceutical Cancer Research, won the HZDR third Innovation Contest. The researchers are now preparing for clinical studies to test whether the new substance also proves its value in everyday medical practice.

“No objective criteria for the differential diagnosis of Parkinson’s disease previously existed to detect at early stage whether a patient is sensitive to the side effects, meaning that it was also impossible to develop personalized therapies,” said lead researcher Thu Hang Lai, PhD. “The new radiopharmaceutical means a great benefit for the patients, but can also reduce the treatment costs of health insurance companies.”

¹⁸F is a fluorine radioisotope that decays by positron emission 97% of the time, and electron capture 3% of the time; both modes of decay yield stable oxygen-18 (¹⁸O). ¹⁸F is an important radioisotope as a result of both its short half-life and the emission of positrons when decaying. It is primarily synthesized into fluorodeoxyglucose (FDG) for use in PET scans.

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Helmholtz-Zentrum Dresden-Rossendorf
University of Leipzig