<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(4)</volume><submitter>Lam MA</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>We aimed to investigate the role of oxidative stress in the progression of multiple sclerosis (MS).&lt;h4>Methods&lt;/h4>We determined by liquid chromatography-tandem mass spectrometry nonenzymatic (F2-isoprostanes) and enzymatic oxidation products of arachidonic acid (prostaglandin F2α [PGF2α]) in plasma and CSF of 45 controls (other neurologic disease [OND] with no signs of inflammation) and 62 patients with MS. Oxidation products were correlated with disease severity and validated biomarkers of inflammation (chemokine ligand 13; matrix metalloproteinase-9; osteopontin) and axonal damage (neurofilament light protein).&lt;h4>Results&lt;/h4>Compared with OND controls, plasma concentrations of F2-isoprostanes and PGF2α were significantly lower in patients with progressive disease, and</pubmed_abstract><journal>Neurology(R) neuroimmunology &amp; neuroinflammation</journal><pagination>e256</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4929888</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Absence of systemic oxidative stress and increased CSF prostaglandin F2α in progressive MS.</pubmed_title><pmcid>PMC4929888</pmcid><pubmed_authors>Sellebjerg FT</pubmed_authors><pubmed_authors>Ratzer R</pubmed_authors><pubmed_authors>Olsson T</pubmed_authors><pubmed_authors>Khademi M</pubmed_authors><pubmed_authors>Lam MA</pubmed_authors><pubmed_authors>Romme Christensen J</pubmed_authors><pubmed_authors>Piehl F</pubmed_authors><pubmed_authors>Stocker R</pubmed_authors><pubmed_authors>Maghzal GJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Absence of systemic oxidative stress and increased CSF prostaglandin F2α in progressive MS.</name><description>&lt;h4>Objective&lt;/h4>We aimed to investigate the role of oxidative stress in the progression of multiple sclerosis (MS).&lt;h4>Methods&lt;/h4>We determined by liquid chromatography-tandem mass spectrometry nonenzymatic (F2-isoprostanes) and enzymatic oxidation products of arachidonic acid (prostaglandin F2α [PGF2α]) in plasma and CSF of 45 controls (other neurologic disease [OND] with no signs of inflammation) and 62 patients with MS. Oxidation products were correlated with disease severity and validated biomarkers of inflammation (chemokine ligand 13; matrix metalloproteinase-9; osteopontin) and axonal damage (neurofilament light protein).&lt;h4>Results&lt;/h4>Compared with OND controls, plasma concentrations of F2-isoprostanes and PGF2α were significantly lower in patients with progressive disease, and</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Aug</publication><modification>2025-04-18T19:45:36.38Z</modification><creation>2019-03-27T02:17:21Z</creation></dates><accession>S-EPMC4929888</accession><cross_references><pubmed>27386506</pubmed><doi>10.1212/NXI.0000000000000256</doi></cross_references></HashMap>