期刊
NEUROIMAGE-CLINICAL
卷 36, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2022.103191
关键词
MDMA; Neurotoxicity; Axonal neuropathology; White matter; DTI; Neurofilament light chain
类别
资金
- Swiss National Science Foundation [320030L_179450, 189136]
- Deutsche Forschungsgemeinschaft [BE4045/34-1]
- Swiss National Science Foundation (SNF) [320030L_179450] Funding Source: Swiss National Science Foundation (SNF)
This study used diffusion tensor imaging and neurofilament light chain analysis to investigate white matter alterations in chronic MDMA users. The results showed increased fractional anisotropy in several white matter tracts, but no significant differences in neurofilament light chain levels. Therefore, this human study did not observe the axonal degradation demonstrated in animal models of MDMA use.
3,4-Methylenedioxymethamphetamine (MDMA, Ecstasy) is a serotonin- and noradrenaline-releasing substance, currently among the most widely used illicit substances worldwide. In animal studies, repeated exposure to MDMA has been associated with dendritic but also axonal degeneration in the brain. However, translation of the axonal findings, specifically, to humans has been repeatedly questioned and the few existing studies investigating white matter alterations in human chronic MDMA users have yielded conflicting findings. In this study, we combined whole-brain diffusion tensor imaging and neurofilament light chain (NfL) analysis in blood to reveal potential MDMA-induced axonal neuropathology. To this end, we assessed 39 chronic MDMA users and 39 matched MDMA-naive healthy controls. MDMA users showed increased fractional anisotropy in several white matter tracts, most prominently in the corpus callosum as well as corticospinal tracts, with these findings partly related to MDMA use intensity. However, the NfL levels of MDMA users were not significantly different from those of controls. We conclude that MDMA use is not associated with significant white matter lesions due to the absence of reduced fractional anisotropy and increased NfL levels commonly observed in conditions associated with white matter lesions, including stimulant and ketamine use disorders. Hence, the MDMA-induced axonal degradation demonstrated in animal models was not observed in this human study of chronic MDMA users.
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