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Serum albumin level is associated with the severity of neurological dysfunction of NMOSD patients
•Serum albumin (SA) negatively correlated with EDSS in acute phase of NMOSD.•A low SA level was an independent factor of severe disability in acute attacks.•Serum albumin negatively associated with IL-33 in acute phase of NMOSD.•SA may play a protective role in NMOSD partly through its interaction w...
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Published in: | Multiple sclerosis and related disorders 2020-08, Vol.43, p.102130-102130, Article 102130 |
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container_title | Multiple sclerosis and related disorders |
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creator | Yao, Xiao-Ying Wu, Yi-Fan Gao, Mei-Chun Hong, Rong-Hua Ding, Jie Hao, Yong Zhang, Ying Guan, Yang-Tai |
description | •Serum albumin (SA) negatively correlated with EDSS in acute phase of NMOSD.•A low SA level was an independent factor of severe disability in acute attacks.•Serum albumin negatively associated with IL-33 in acute phase of NMOSD.•SA may play a protective role in NMOSD partly through its interaction with IL-33.
Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory autoimmune disease of the central nervous system. Serum albumin (SA) has antioxidant, immunomodulatory and anti-inflammatory effects. However, the roles of SA in NMOSD have not been studied. The current study aimed to clarify the association of SA with disease severity and prognosis in NMOSD patients.
Serum levels of albumin were measured by Bromcresol Green method. Serum level measurements of interleukins were performed using enzyme-linked immunoassay (ELISA) method.
Of all the 130 NMOSD patients, 96 patients were in the acute phase while 34 patients were in the remission phase of disease at the time of sampling. SA concentration was significantly correlated with EDSS score in patients in the acute phase but not in remission phase (r = - 0.388, p |
doi_str_mv | 10.1016/j.msard.2020.102130 |
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Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory autoimmune disease of the central nervous system. Serum albumin (SA) has antioxidant, immunomodulatory and anti-inflammatory effects. However, the roles of SA in NMOSD have not been studied. The current study aimed to clarify the association of SA with disease severity and prognosis in NMOSD patients.
Serum levels of albumin were measured by Bromcresol Green method. Serum level measurements of interleukins were performed using enzyme-linked immunoassay (ELISA) method.
Of all the 130 NMOSD patients, 96 patients were in the acute phase while 34 patients were in the remission phase of disease at the time of sampling. SA concentration was significantly correlated with EDSS score in patients in the acute phase but not in remission phase (r = - 0.388, p < 0.001 and r = - 0.467, p = 0.809, respectively). Logistic analysis revealed that SA was the only significant factor to predict severe NMOSD (EDSS 8.0–9.5) OR = 0.698, 95%CI 0.563–0.865, p = 0.001) after adjustment of other confounding factors. Furthermore, SA was negatively correlated with the serum level of IL-33 (r = -0.438, p = 0.016) in the acute phase of NMOSD patients.
The current study found that low level of SA was an independent indicator of more severe neurological deficit in patients in acute phase of NMOSD. SA concentration was negatively correlated with the serum level of IL-33 in the acute phase of the disease, which implies that SA might participate in the immunopathology of NMOSD partly through its interaction with IL-33.</description><identifier>ISSN: 2211-0348</identifier><identifier>EISSN: 2211-0356</identifier><identifier>DOI: 10.1016/j.msard.2020.102130</identifier><identifier>PMID: 32417662</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Cytokines ; Humans ; Interleukin -33 ; Interleukins ; Neuromyelitis Optica - blood ; Neuromyelitis Optica - physiopathology ; Neuromyelitis optica spectrum disorders ; Prognosis ; Serum Albumin ; Severity of Illness Index</subject><ispartof>Multiple sclerosis and related disorders, 2020-08, Vol.43, p.102130-102130, Article 102130</ispartof><rights>2020</rights><rights>Copyright © 2020. Published by Elsevier B.V.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-a0397307cebe52bee23c7ccfae6b9b058bd3ffef061dd644acb4019a778a7cda3</citedby><cites>FETCH-LOGICAL-c359t-a0397307cebe52bee23c7ccfae6b9b058bd3ffef061dd644acb4019a778a7cda3</cites><orcidid>0000-0002-9921-9760 ; 0000-0001-7366-0796</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32417662$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yao, Xiao-Ying</creatorcontrib><creatorcontrib>Wu, Yi-Fan</creatorcontrib><creatorcontrib>Gao, Mei-Chun</creatorcontrib><creatorcontrib>Hong, Rong-Hua</creatorcontrib><creatorcontrib>Ding, Jie</creatorcontrib><creatorcontrib>Hao, Yong</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Guan, Yang-Tai</creatorcontrib><title>Serum albumin level is associated with the severity of neurological dysfunction of NMOSD patients</title><title>Multiple sclerosis and related disorders</title><addtitle>Mult Scler Relat Disord</addtitle><description>•Serum albumin (SA) negatively correlated with EDSS in acute phase of NMOSD.•A low SA level was an independent factor of severe disability in acute attacks.•Serum albumin negatively associated with IL-33 in acute phase of NMOSD.•SA may play a protective role in NMOSD partly through its interaction with IL-33.
Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory autoimmune disease of the central nervous system. Serum albumin (SA) has antioxidant, immunomodulatory and anti-inflammatory effects. However, the roles of SA in NMOSD have not been studied. The current study aimed to clarify the association of SA with disease severity and prognosis in NMOSD patients.
Serum levels of albumin were measured by Bromcresol Green method. Serum level measurements of interleukins were performed using enzyme-linked immunoassay (ELISA) method.
Of all the 130 NMOSD patients, 96 patients were in the acute phase while 34 patients were in the remission phase of disease at the time of sampling. SA concentration was significantly correlated with EDSS score in patients in the acute phase but not in remission phase (r = - 0.388, p < 0.001 and r = - 0.467, p = 0.809, respectively). Logistic analysis revealed that SA was the only significant factor to predict severe NMOSD (EDSS 8.0–9.5) OR = 0.698, 95%CI 0.563–0.865, p = 0.001) after adjustment of other confounding factors. Furthermore, SA was negatively correlated with the serum level of IL-33 (r = -0.438, p = 0.016) in the acute phase of NMOSD patients.
The current study found that low level of SA was an independent indicator of more severe neurological deficit in patients in acute phase of NMOSD. SA concentration was negatively correlated with the serum level of IL-33 in the acute phase of the disease, which implies that SA might participate in the immunopathology of NMOSD partly through its interaction with IL-33.</description><subject>Cytokines</subject><subject>Humans</subject><subject>Interleukin -33</subject><subject>Interleukins</subject><subject>Neuromyelitis Optica - blood</subject><subject>Neuromyelitis Optica - physiopathology</subject><subject>Neuromyelitis optica spectrum disorders</subject><subject>Prognosis</subject><subject>Serum Albumin</subject><subject>Severity of Illness Index</subject><issn>2211-0348</issn><issn>2211-0356</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE1PwzAMhiMEYmjsFyChHLls5Ktpd-CAxqcE7DA4R2niskxtM5IUtH9PxwZHfLFlv_YrPwidUTKhhMrL1aSJOtgJI2zbYZSTA3TCGKVjwjN5-FeLYoBGMa5IHzKjQtJjNOBM0FxKdoL0AkLXYF2XXeNaXMMn1NhFrGP0xukEFn-5tMRpCTj2w-DSBvsKt9AFX_t3Z3SN7SZWXWuS8-129vI8X9zgtU4O2hRP0VGl6wijfR6it7vb19nD-Gl-_zi7fhobnk3TWBM-zTnJDZSQsRKAcZMbU2mQ5bQkWVFaXlVQEUmtlUJoUwpCpzrPC50bq_kQXezuroP_6CAm1bhooK51C76LigkieMELIXop30lN8DEGqNQ6uEaHjaJEbfGqlfrBq7Z41Q5vv3W-N-jKBuzfzi_MXnC1E0D_5qeDoKLpERiwLoBJynr3r8E3WkeN-A</recordid><startdate>202008</startdate><enddate>202008</enddate><creator>Yao, Xiao-Ying</creator><creator>Wu, Yi-Fan</creator><creator>Gao, Mei-Chun</creator><creator>Hong, Rong-Hua</creator><creator>Ding, Jie</creator><creator>Hao, Yong</creator><creator>Zhang, Ying</creator><creator>Guan, Yang-Tai</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9921-9760</orcidid><orcidid>https://orcid.org/0000-0001-7366-0796</orcidid></search><sort><creationdate>202008</creationdate><title>Serum albumin level is associated with the severity of neurological dysfunction of NMOSD patients</title><author>Yao, Xiao-Ying ; Wu, Yi-Fan ; Gao, Mei-Chun ; Hong, Rong-Hua ; Ding, Jie ; Hao, Yong ; Zhang, Ying ; Guan, Yang-Tai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-a0397307cebe52bee23c7ccfae6b9b058bd3ffef061dd644acb4019a778a7cda3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cytokines</topic><topic>Humans</topic><topic>Interleukin -33</topic><topic>Interleukins</topic><topic>Neuromyelitis Optica - blood</topic><topic>Neuromyelitis Optica - physiopathology</topic><topic>Neuromyelitis optica spectrum disorders</topic><topic>Prognosis</topic><topic>Serum Albumin</topic><topic>Severity of Illness Index</topic><toplevel>online_resources</toplevel><creatorcontrib>Yao, Xiao-Ying</creatorcontrib><creatorcontrib>Wu, Yi-Fan</creatorcontrib><creatorcontrib>Gao, Mei-Chun</creatorcontrib><creatorcontrib>Hong, Rong-Hua</creatorcontrib><creatorcontrib>Ding, Jie</creatorcontrib><creatorcontrib>Hao, Yong</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Guan, Yang-Tai</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Multiple sclerosis and related disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yao, Xiao-Ying</au><au>Wu, Yi-Fan</au><au>Gao, Mei-Chun</au><au>Hong, Rong-Hua</au><au>Ding, Jie</au><au>Hao, Yong</au><au>Zhang, Ying</au><au>Guan, Yang-Tai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum albumin level is associated with the severity of neurological dysfunction of NMOSD patients</atitle><jtitle>Multiple sclerosis and related disorders</jtitle><addtitle>Mult Scler Relat Disord</addtitle><date>2020-08</date><risdate>2020</risdate><volume>43</volume><spage>102130</spage><epage>102130</epage><pages>102130-102130</pages><artnum>102130</artnum><issn>2211-0348</issn><eissn>2211-0356</eissn><abstract>•Serum albumin (SA) negatively correlated with EDSS in acute phase of NMOSD.•A low SA level was an independent factor of severe disability in acute attacks.•Serum albumin negatively associated with IL-33 in acute phase of NMOSD.•SA may play a protective role in NMOSD partly through its interaction with IL-33.
Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory autoimmune disease of the central nervous system. Serum albumin (SA) has antioxidant, immunomodulatory and anti-inflammatory effects. However, the roles of SA in NMOSD have not been studied. The current study aimed to clarify the association of SA with disease severity and prognosis in NMOSD patients.
Serum levels of albumin were measured by Bromcresol Green method. Serum level measurements of interleukins were performed using enzyme-linked immunoassay (ELISA) method.
Of all the 130 NMOSD patients, 96 patients were in the acute phase while 34 patients were in the remission phase of disease at the time of sampling. SA concentration was significantly correlated with EDSS score in patients in the acute phase but not in remission phase (r = - 0.388, p < 0.001 and r = - 0.467, p = 0.809, respectively). Logistic analysis revealed that SA was the only significant factor to predict severe NMOSD (EDSS 8.0–9.5) OR = 0.698, 95%CI 0.563–0.865, p = 0.001) after adjustment of other confounding factors. Furthermore, SA was negatively correlated with the serum level of IL-33 (r = -0.438, p = 0.016) in the acute phase of NMOSD patients.
The current study found that low level of SA was an independent indicator of more severe neurological deficit in patients in acute phase of NMOSD. SA concentration was negatively correlated with the serum level of IL-33 in the acute phase of the disease, which implies that SA might participate in the immunopathology of NMOSD partly through its interaction with IL-33.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32417662</pmid><doi>10.1016/j.msard.2020.102130</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9921-9760</orcidid><orcidid>https://orcid.org/0000-0001-7366-0796</orcidid></addata></record> |
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subjects | Cytokines Humans Interleukin -33 Interleukins Neuromyelitis Optica - blood Neuromyelitis Optica - physiopathology Neuromyelitis optica spectrum disorders Prognosis Serum Albumin Severity of Illness Index |
title | Serum albumin level is associated with the severity of neurological dysfunction of NMOSD patients |
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