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The Mutation Matters: CSF Profiles of GCase , Sphingolipids, α‐Synuclein in PD GBA

2021; Wiley; Volume: 36; Issue: 5 Linguagem: Inglês

10.1002/mds.28472

1531-8257

Stefanie Lerche, Claudia Schulte, Isabel Wurster, Gerrit Machetanz, Benjamin Röeben, Milan Zimmermann, Christian Deuschle, Ann‐Kathrin Hauser, Judith Böhringer, Ingeborg Krägeloh‐Mann, Katharina Waniek, Ingolf Lachmann, Xuan-Mai Petterson, Ruby W. Chiang, Hye Jung Park, Bing Wang, Inga Liepelt‐Scarfone, Walter Maetzler, Douglas Galasko, Clemens R. Scherzer, Thomas Gasser, Michelle M. Mielke, Samantha J. Hutten, Brit Mollenhauer, S. Pablo Sardi, Daniela Berg, Kathrin Brockmann,

Cellular transport and secretion

ABSTRACT Background With pathway‐specific trials in PD associated with variants in the glucocerebrosidase gene (PD GBA ) under way, we need markers that confirm the impact of genetic variants in patient‐derived biofluids in order to allow patient stratification merely based on genetics and that might serve as biochemical read‐out for target engagement. Objective To explore GBA‐pathway‐specific biomarker profiles cross‐sectionally (TUEPAC‐MIGAP, PPMI) and longitudinally (PPMI). Methods We measured enzyme activity of the lysosomal glucocerebrosidase, CSF levels of glucosylceramides (upstream substrate of glucocerebrosidase), CSF levels of ceramides (downstream product of glucocerebrosidase), lactosylceramides, sphingosines, sphingomyelin (by‐products) and CSF levels of total α‐synuclein in PD GBA patients compared to PD GBA_wildtype patients. Results Cross‐sectionally in both cohorts and longitudinally in PPMI: (1) glucocerebrosidase activity was significantly lower in PD GBA compared to PD GBA_wildtype . (2) CSF levels of upstream substrates (glucosylceramides species) were higher in PD GBA compared to PD GBA_wildtype . (3) CSF levels of total α‐synuclein were lower in PD GBA compared to PD GBA_wildtype . All of these findings were most pronounced in PD GBA with severe mutations (PD GBA_severe ). Cross‐sectionally in TUEPAC‐MIGAP and longitudinally in PPMI, CSF levels of downstream‐products (ceramides) were higher in PD GBA_severe . Cross‐sectionally in TUEPAC‐MIGAP by‐products sphinganine and sphingosine‐1‐phosphate and longitudinally in PPMI species of by‐products lactosylceramides and sphingomyelin were higher in PD GBA_severe . Interpretation These findings confirm that GBA mutations have a relevant functional impact on biomarker profiles in patients. Bridging the gap between genetics and biochemical profiles now allows patient stratification for clinical trials merely based on mutation status. Importantly, all findings were most prominent in PD GBA with severe variants. © 2021 International Parkinson and Movement Disorder Society