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Sökning: onr:"swepub:oai:DiVA.org:uu-375564" > Biochemical Differe...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003712naa a2200445 4500
001oai:DiVA.org:uu-375564
003SwePub
008190131s2019 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3755642 URI
024a https://doi.org/10.3390/cells80200842 DOI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Herman, Stephanieu Uppsala universitet,Klinisk kemi,Institutionen för farmaceutisk biovetenskap,Science for Life Laboratory, SciLifeLab,Spjuth group4 aut0 (Swepub:uu)stehe524
2451 0a Biochemical Differences in Cerebrospinal Fluid between Secondary Progressive and Relapsing-Remitting Multiple Sclerosis
264 c 2019-01-24
264 1b MDPI AG,c 2019
338 a electronic2 rdacarrier
520 a To better understand the pathophysiological differences between secondary progressive multiple sclerosis (SPMS) and relapsing-remitting multiple sclerosis (RRMS), and to identify potential biomarkers of disease progression, we applied high-resolution mass spectrometry (HRMS) to investigate the metabolome of cerebrospinal fluid (CSF). The biochemical differences were determined using partial least squares discriminant analysis (PLS-DA) and connected to biochemical pathways as well as associated to clinical and radiological measures. Tryptophan metabolism was significantly altered, with perturbed levels of kynurenate, 5-hydroxytryptophan, 5-hydroxyindoleacetate, and N-acetylserotonin in SPMS patients compared with RRMS and controls. SPMS patients had altered kynurenine compared with RRMS patients, and altered indole-3-acetate compared with controls. Regarding the pyrimidine metabolism, SPMS patients had altered levels of uridine and deoxyuridine compared with RRMS and controls, and altered thymine and glutamine compared with RRMS patients. Metabolites from the pyrimidine metabolism were significantly associated with disability, disease activity and brain atrophy, making them of particular interest for understanding the disease mechanisms and as markers of disease progression. Overall, these findings are of importance for the characterization of the molecular pathogenesis of SPMS and support the hypothesis that the CSF metabolome may be used to explore changes that occur in the transition between the RRMS and SPMS pathologies.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicin0 (SwePub)3022 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicine0 (SwePub)3022 hsv//eng
653 a cerebrospinal fluid
653 a mass spectrometry
653 a metabolomics
653 a multiple sclerosis
653 a pyrimidine
653 a tryptophan
700a Åkerfeldt, Torbjörnu Uppsala universitet,Klinisk kemi4 aut0 (Swepub:uu)tak20812
700a Spjuth, Ola,c Docent,d 1977-u Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Science for Life Laboratory, SciLifeLab4 aut0 (Swepub:uu)olspj499
700a Burman, Joachim,d 1974-u Uppsala universitet,Neurologi4 aut0 (Swepub:uu)joabu293
700a Kultima, Kimu Uppsala universitet,Klinisk kemi4 aut0 (Swepub:uu)kikul535
710a Uppsala universitetb Klinisk kemi4 org
773t Cellsd : MDPI AGg 8:2q 8:2x 2073-4409
856u https://doi.org/10.3390/cells8020084y Fulltext
856u https://uu.diva-portal.org/smash/get/diva2:1284187/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
856u https://www.mdpi.com/2073-4409/8/2/84/pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-375564
8564 8u https://doi.org/10.3390/cells8020084

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