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5 and 6) may be irrelevant to the mechanism of action for NMN treatment, and future work should aim to narrow the window of when NMN treatment offers its protection, to help identify when these molecular changes might be relevant to this phenotype

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The field requires urgent Phase I/II human trials before any clinical recommendations can be made

Structurally, TST enzymes exhibit either a single rhodanese domain, such as human TSTD1 and bacterial GlpE and PspE, or a tandem repeat of rhodanese domains, as observed in human TST (hTST), Bos taurus (Rhobov), and Azotobacter vinelandii (RhdA) [12,15]