Malondialdehyde‐Acetaldehyde Adducts and Anti–Malondialdehyde‐Acetaldehyde Antibodies in Rheumatoid Arthritis
Objective Malondialdehyde‐acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was undertaken to investigate the presence of MAA adducts and circulating anti‐MAA antibodies in patients with rheumatoid arthritis (RA). Method...
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Published in | Arthritis & rheumatology (Hoboken, N.J.) Vol. 67; no. 3; pp. 645 - 655 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.03.2015
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Abstract | Objective
Malondialdehyde‐acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was undertaken to investigate the presence of MAA adducts and circulating anti‐MAA antibodies in patients with rheumatoid arthritis (RA).
Methods
Synovial tissue from patients with RA and patients with osteoarthritis (OA) were examined for the presence of MAA‐modified and citrullinated proteins. Anti‐MAA antibody isotypes were measured in RA patients (n = 1,720) and healthy controls (n = 80) by enzyme‐linked immunosorbent assay. Antigen‐specific anti–citrullinated protein antibodies (ACPAs) were measured in RA patients using a multiplex antigen array. Anti‐MAA isotype concentrations were compared in a subset of RA patients (n = 80) and matched healthy controls (n = 80). Associations of anti‐MAA antibody isotypes with disease characteristics, including ACPA positivity, were examined in all RA patients.
Results
Expression of MAA adducts was increased in RA synovial tissue compared to OA synovial tissue, and colocalization with citrullinated proteins was found. Increased levels of anti‐MAA antibody isotypes were observed in RA patients compared to controls (P < 0.001). Among RA patients, anti‐MAA antibody isotypes were associated with seropositivity for ACPAs and rheumatoid factor (P < 0.001) in addition to select measures of disease activity. Higher anti‐MAA antibody concentrations were associated with a greater number of positive antigen‐specific ACPA analytes (expressed at high titer) (P < 0.001) and a higher ACPA score (P < 0.001), independent of other covariates.
Conclusion
MAA adduct formation is increased in RA and appears to result in robust antibody responses that are strongly associated with ACPAs. These results support speculation that MAA formation may be a cofactor that drives tolerance loss, resulting in the autoimmune responses characteristic of RA. |
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AbstractList | Objective
Malondialdehyde‐acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was undertaken to investigate the presence of MAA adducts and circulating anti‐MAA antibodies in patients with rheumatoid arthritis (RA).
Methods
Synovial tissue from patients with RA and patients with osteoarthritis (OA) were examined for the presence of MAA‐modified and citrullinated proteins. Anti‐MAA antibody isotypes were measured in RA patients (n = 1,720) and healthy controls (n = 80) by enzyme‐linked immunosorbent assay. Antigen‐specific anti–citrullinated protein antibodies (ACPAs) were measured in RA patients using a multiplex antigen array. Anti‐MAA isotype concentrations were compared in a subset of RA patients (n = 80) and matched healthy controls (n = 80). Associations of anti‐MAA antibody isotypes with disease characteristics, including ACPA positivity, were examined in all RA patients.
Results
Expression of MAA adducts was increased in RA synovial tissue compared to OA synovial tissue, and colocalization with citrullinated proteins was found. Increased levels of anti‐MAA antibody isotypes were observed in RA patients compared to controls (P < 0.001). Among RA patients, anti‐MAA antibody isotypes were associated with seropositivity for ACPAs and rheumatoid factor (P < 0.001) in addition to select measures of disease activity. Higher anti‐MAA antibody concentrations were associated with a greater number of positive antigen‐specific ACPA analytes (expressed at high titer) (P < 0.001) and a higher ACPA score (P < 0.001), independent of other covariates.
Conclusion
MAA adduct formation is increased in RA and appears to result in robust antibody responses that are strongly associated with ACPAs. These results support speculation that MAA formation may be a cofactor that drives tolerance loss, resulting in the autoimmune responses characteristic of RA. OBJECTIVEMalondialdehyde-acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was undertaken to investigate the presence of MAA adducts and circulating anti-MAA antibodies in patients with rheumatoid arthritis (RA).METHODSSynovial tissue from patients with RA and patients with osteoarthritis (OA) were examined for the presence of MAA-modified and citrullinated proteins. Anti-MAA antibody isotypes were measured in RA patients (n = 1,720) and healthy controls (n = 80) by enzyme-linked immunosorbent assay. Antigen-specific anti-citrullinated protein antibodies (ACPAs) were measured in RA patients using a multiplex antigen array. Anti-MAA isotype concentrations were compared in a subset of RA patients (n = 80) and matched healthy controls (n = 80). Associations of anti-MAA antibody isotypes with disease characteristics, including ACPA positivity, were examined in all RA patients.RESULTSExpression of MAA adducts was increased in RA synovial tissue compared to OA synovial tissue, and colocalization with citrullinated proteins was found. Increased levels of anti-MAA antibody isotypes were observed in RA patients compared to controls (P < 0.001). Among RA patients, anti-MAA antibody isotypes were associated with seropositivity for ACPAs and rheumatoid factor (P < 0.001) in addition to select measures of disease activity. Higher anti-MAA antibody concentrations were associated with a greater number of positive antigen-specific ACPA analytes (expressed at high titer) (P < 0.001) and a higher ACPA score (P < 0.001), independent of other covariates.CONCLUSIONMAA adduct formation is increased in RA and appears to result in robust antibody responses that are strongly associated with ACPAs. These results support speculation that MAA formation may be a cofactor that drives tolerance loss, resulting in the autoimmune responses characteristic of RA. Malondialdehyde-acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was undertaken to investigate the presence of MAA adducts and circulating anti-MAA antibodies in patients with rheumatoid arthritis (RA). Synovial tissue from patients with RA and patients with osteoarthritis (OA) were examined for the presence of MAA-modified and citrullinated proteins. Anti-MAA antibody isotypes were measured in RA patients (n = 1,720) and healthy controls (n = 80) by enzyme-linked immunosorbent assay. Antigen-specific anti-citrullinated protein antibodies (ACPAs) were measured in RA patients using a multiplex antigen array. Anti-MAA isotype concentrations were compared in a subset of RA patients (n = 80) and matched healthy controls (n = 80). Associations of anti-MAA antibody isotypes with disease characteristics, including ACPA positivity, were examined in all RA patients. Expression of MAA adducts was increased in RA synovial tissue compared to OA synovial tissue, and colocalization with citrullinated proteins was found. Increased levels of anti-MAA antibody isotypes were observed in RA patients compared to controls (P < 0.001). Among RA patients, anti-MAA antibody isotypes were associated with seropositivity for ACPAs and rheumatoid factor (P < 0.001) in addition to select measures of disease activity. Higher anti-MAA antibody concentrations were associated with a greater number of positive antigen-specific ACPA analytes (expressed at high titer) (P < 0.001) and a higher ACPA score (P < 0.001), independent of other covariates. MAA adduct formation is increased in RA and appears to result in robust antibody responses that are strongly associated with ACPAs. These results support speculation that MAA formation may be a cofactor that drives tolerance loss, resulting in the autoimmune responses characteristic of RA. Objective Malondialdehyde-acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was undertaken to investigate the presence of MAA adducts and circulating anti-MAA antibodies in patients with rheumatoid arthritis (RA). Methods Synovial tissue from patients with RA and patients with osteoarthritis (OA) were examined for the presence of MAA-modified and citrullinated proteins. Anti-MAA antibody isotypes were measured in RA patients (n = 1,720) and healthy controls (n = 80) by enzyme-linked immunosorbent assay. Antigen-specific anti-citrullinated protein antibodies (ACPAs) were measured in RA patients using a multiplex antigen array. Anti-MAA isotype concentrations were compared in a subset of RA patients (n = 80) and matched healthy controls (n = 80). Associations of anti-MAA antibody isotypes with disease characteristics, including ACPA positivity, were examined in all RA patients. Results Expression of MAA adducts was increased in RA synovial tissue compared to OA synovial tissue, and colocalization with citrullinated proteins was found. Increased levels of anti-MAA antibody isotypes were observed in RA patients compared to controls (P < 0.001). Among RA patients, anti-MAA antibody isotypes were associated with seropositivity for ACPAs and rheumatoid factor (P < 0.001) in addition to select measures of disease activity. Higher anti-MAA antibody concentrations were associated with a greater number of positive antigen-specific ACPA analytes (expressed at high titer) (P < 0.001) and a higher ACPA score (P < 0.001), independent of other covariates. Conclusion MAA adduct formation is increased in RA and appears to result in robust antibody responses that are strongly associated with ACPAs. These results support speculation that MAA formation may be a cofactor that drives tolerance loss, resulting in the autoimmune responses characteristic of RA. |
Author | Duryee, Michael J. Benissan‐Messan, Dathe Hunter, Carlos D. Young, Kathleen A. Mikuls, Ted R. Thiele, Geoffrey M. Sokolove, Jeremy Mohring, Stephen M. Robinson, William H. Anderson, Daniel R. Nicholas, Anthony P. O'Dell, James R. Tuma, Dean J. Dusad, Anand Klassen, Lynell W. Sayles, Harlan |
Author_xml | – sequence: 1 givenname: Geoffrey M. surname: Thiele fullname: Thiele, Geoffrey M. organization: VA Nebraska–Western Iowa Health Care System, Omaha, Nebraska, and University of Nebraska Medical Center – sequence: 2 givenname: Michael J. surname: Duryee fullname: Duryee, Michael J. organization: VA Nebraska–Western Iowa Health Care System, Omaha, Nebraska, and University of Nebraska Medical Center – sequence: 3 givenname: Daniel R. surname: Anderson fullname: Anderson, Daniel R. organization: University of Nebraska Medical Center – sequence: 4 givenname: Lynell W. surname: Klassen fullname: Klassen, Lynell W. organization: VA Nebraska–Western Iowa Health Care System, Omaha, Nebraska, and University of Nebraska Medical Center – sequence: 5 givenname: Stephen M. surname: Mohring fullname: Mohring, Stephen M. organization: University of Nebraska Medical Center – sequence: 6 givenname: Kathleen A. surname: Young fullname: Young, Kathleen A. organization: University of Nebraska Medical Center – sequence: 7 givenname: Dathe surname: Benissan‐Messan fullname: Benissan‐Messan, Dathe organization: University of Nebraska Medical Center – sequence: 8 givenname: Harlan surname: Sayles fullname: Sayles, Harlan organization: University of Nebraska Medical Center – sequence: 9 givenname: Anand surname: Dusad fullname: Dusad, Anand organization: University of Nebraska Medical Center – sequence: 10 givenname: Carlos D. surname: Hunter fullname: Hunter, Carlos D. organization: University of Nebraska Medical Center – sequence: 11 givenname: Jeremy surname: Sokolove fullname: Sokolove, Jeremy organization: VA Palo Alto Health Care System and Stanford University – sequence: 12 givenname: William H. surname: Robinson fullname: Robinson, William H. organization: VA Palo Alto Health Care System and Stanford University – sequence: 13 givenname: James R. surname: O'Dell fullname: O'Dell, James R. organization: VA Nebraska–Western Iowa Health Care System, Omaha, Nebraska, and University of Nebraska Medical Center – sequence: 14 givenname: Anthony P. surname: Nicholas fullname: Nicholas, Anthony P. organization: University of Alabama at Birmingham – sequence: 15 givenname: Dean J. surname: Tuma fullname: Tuma, Dean J. organization: VA Nebraska–Western Iowa Health Care System – sequence: 16 givenname: Ted R. surname: Mikuls fullname: Mikuls, Ted R. organization: VA Nebraska–Western Iowa Health Care System, Omaha, Nebraska, and University of Nebraska Medical Center |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25417811$$D View this record in MEDLINE/PubMed |
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Malondialdehyde‐acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was... Malondialdehyde-acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was... Objective Malondialdehyde-acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was... OBJECTIVEMalondialdehyde-acetaldehyde (MAA) adducts are a product of oxidative stress associated with tolerance loss in several disease states. This study was... |
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SubjectTerms | Acetaldehyde - immunology Adult Aged Antigens Arthritis, Rheumatoid - immunology Autoantibodies - blood Cross Reactions Drug therapy Enzyme-Linked Immunosorbent Assay Female Humans Immunohistochemistry Male Malondialdehyde - immunology Middle Aged Osteoarthritis - immunology Peptides, Cyclic - immunology Rheumatism Rheumatoid arthritis Synovial Membrane - immunology |
Title | Malondialdehyde‐Acetaldehyde Adducts and Anti–Malondialdehyde‐Acetaldehyde Antibodies in Rheumatoid Arthritis |
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