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We are analyzing https://link.springer.com/article/10.1186/ar2892.

Title:
Immunoglobulin G galactosylation and sialylation are associated with pregnancy-induced improvement of rheumatoid arthritis and the postpartum flare: results from a large prospective cohort study | Arthritis Research & Therapy
Description:
Introduction Improvement of rheumatoid arthritis (RA) during pregnancy has been causatively associated with increased galactosylation of immunoglobulin G (IgG) N-glycans. Since previous studies were small, did not include the postpartum flare and did not study sialylation, these issues were addressed in the present study. Methods Serum from 148 RA cases and 32 healthy controls was collected at several time points before, during and after pregnancy. Improvement during pregnancy and postpartum flare were determined according to the European League Against Rheumatism (EULAR) response criteria. Galactosylation and sialylation of Immunoglobulin G (IgG) and the presence of bisecting N-acetylglucosamine (GlcNAc) were analyzed by matrix-assisted laser desorption/ionization - time of flight - mass spectrometry (MALDI-TOF-MS). Results IgG1 and IgG2 galactosylation of the cases and controls increased during pregnancy with a maximum in the third trimester. Galactosylation decreased directly postpartum. IgG galactosylation of controls was at a higher level than cases (P < 0.001 at all time points) and a similar pattern was observed for sialylation. Moreover, there was a good association between galactosylation and sialylation. The increase in galactosylation was significantly more pronounced for cases with improvement than cases without improvement during pregnancy. The reverse was true for deteriorators and non-deteriorators postpartum. The presence of bisecting GlcNAc was not significantly influenced by pregnancy or postpartum for cases and controls. Conclusions This large cohort study demonstrates the association of changes in galactosylation with both pregnancy-induced improvement and postpartum flare in RA-patients, suggesting a role for changes in glycosylation in the pregnancy-induced improvement of RA.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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Keywords {🔍}

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Topics {✒️}

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Schema {🗺️}

WebPage:
      mainEntity:
         headline:Immunoglobulin G galactosylation and sialylation are associated with pregnancy-induced improvement of rheumatoid arthritis and the postpartum flare: results from a large prospective cohort study
         description:Improvement of rheumatoid arthritis (RA) during pregnancy has been causatively associated with increased galactosylation of immunoglobulin G (IgG) N-glycans. Since previous studies were small, did not include the postpartum flare and did not study sialylation, these issues were addressed in the present study. Serum from 148 RA cases and 32 healthy controls was collected at several time points before, during and after pregnancy. Improvement during pregnancy and postpartum flare were determined according to the European League Against Rheumatism (EULAR) response criteria. Galactosylation and sialylation of Immunoglobulin G (IgG) and the presence of bisecting N-acetylglucosamine (GlcNAc) were analyzed by matrix-assisted laser desorption/ionization - time of flight - mass spectrometry (MALDI-TOF-MS). IgG1 and IgG2 galactosylation of the cases and controls increased during pregnancy with a maximum in the third trimester. Galactosylation decreased directly postpartum. IgG galactosylation of controls was at a higher level than cases (P &lt; 0.001 at all time points) and a similar pattern was observed for sialylation. Moreover, there was a good association between galactosylation and sialylation. The increase in galactosylation was significantly more pronounced for cases with improvement than cases without improvement during pregnancy. The reverse was true for deteriorators and non-deteriorators postpartum. The presence of bisecting GlcNAc was not significantly influenced by pregnancy or postpartum for cases and controls. This large cohort study demonstrates the association of changes in galactosylation with both pregnancy-induced improvement and postpartum flare in RA-patients, suggesting a role for changes in glycosylation in the pregnancy-induced improvement of RA.
         datePublished:2009-12-16T00:00:00Z
         dateModified:2009-12-16T00:00:00Z
         pageStart:1
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         license:http://creativecommons.org/licenses/by/2.0/
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            Sialic Acid
            GlcNAc
            Glycopeptide
            Signal Height
            EULAR Criterion
            Rheumatology
            Orthopedics
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      headline:Immunoglobulin G galactosylation and sialylation are associated with pregnancy-induced improvement of rheumatoid arthritis and the postpartum flare: results from a large prospective cohort study
      description:Improvement of rheumatoid arthritis (RA) during pregnancy has been causatively associated with increased galactosylation of immunoglobulin G (IgG) N-glycans. Since previous studies were small, did not include the postpartum flare and did not study sialylation, these issues were addressed in the present study. Serum from 148 RA cases and 32 healthy controls was collected at several time points before, during and after pregnancy. Improvement during pregnancy and postpartum flare were determined according to the European League Against Rheumatism (EULAR) response criteria. Galactosylation and sialylation of Immunoglobulin G (IgG) and the presence of bisecting N-acetylglucosamine (GlcNAc) were analyzed by matrix-assisted laser desorption/ionization - time of flight - mass spectrometry (MALDI-TOF-MS). IgG1 and IgG2 galactosylation of the cases and controls increased during pregnancy with a maximum in the third trimester. Galactosylation decreased directly postpartum. IgG galactosylation of controls was at a higher level than cases (P &lt; 0.001 at all time points) and a similar pattern was observed for sialylation. Moreover, there was a good association between galactosylation and sialylation. The increase in galactosylation was significantly more pronounced for cases with improvement than cases without improvement during pregnancy. The reverse was true for deteriorators and non-deteriorators postpartum. The presence of bisecting GlcNAc was not significantly influenced by pregnancy or postpartum for cases and controls. This large cohort study demonstrates the association of changes in galactosylation with both pregnancy-induced improvement and postpartum flare in RA-patients, suggesting a role for changes in glycosylation in the pregnancy-induced improvement of RA.
      datePublished:2009-12-16T00:00:00Z
      dateModified:2009-12-16T00:00:00Z
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      pageEnd:10
      license:http://creativecommons.org/licenses/by/2.0/
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         Sialic Acid
         GlcNAc
         Glycopeptide
         Signal Height
         EULAR Criterion
         Rheumatology
         Orthopedics
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            address:
               name:Department of Rheumatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
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      name:Yaël A de Man
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            name:Erasmus MC University Medical Center Rotterdam
            address:
               name:Department of Rheumatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
               type:PostalAddress
            type:Organization
      name:André M Deelder
      affiliation:
            name:Leiden University Medical Center
            address:
               name:Biomolecular Mass Spectrometry Unit, Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands
               type:PostalAddress
            type:Organization
      name:Johanna MW Hazes
      affiliation:
            name:Erasmus MC University Medical Center Rotterdam
            address:
               name:Department of Rheumatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
               type:PostalAddress
            type:Organization
      name:Radboud JEM Dolhain
      affiliation:
            name:Erasmus MC University Medical Center Rotterdam
            address:
               name:Department of Rheumatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Rheumatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
      name:Biomolecular Mass Spectrometry Unit, Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands
      name:Biomolecular Mass Spectrometry Unit, Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands
      name:Department of Biostatistics, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
      name:Department of Rheumatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
      name:Biomolecular Mass Spectrometry Unit, Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands
      name:Department of Rheumatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
      name:Department of Rheumatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands

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