“…By integrating results from metabolomics and neuroimaging data, Rispoli et al showed a significant reduction in arginine plasma concentration in RRMS and a higher concentration of indolepyruvate in SPMS compared to RRMS. Also, a higher concentration of myelin basic protein, macrophage-derived chemokine, and 5.6-dihydroxyprostaglandin was highlighted in worse disease progression of SPMS [ 1 ]. In a similar approach, in Monaco et al’s article, focusing on the intrathecal inflammation in PMS, neuropathology and molecular and MRI methodologies were integrated, showing molecules connected to a higher meningeal inflammation and grey matter demyelination, namely IFNγ, TNF, IL2, IL22, CXCL13, CXCL10, LTα, IL6, and IL10 [ 5 ].…”