Presence of Autoantibodies in Males and Females With Rheumatoid Arthritis: A Systematic Review and Metaanalysis
Rheumatoid arthritis (RA) is more common in females, and although the cause of RA is unknown, it is characterized by the production of autoantibodies. The aims of this study were to determine whether RA-associated autoantibodies are more often found in females than males and to identify factors that...
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Published in | Journal of rheumatology |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Canada
01.07.2022
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Online Access | Get more information |
ISSN | 0315-162X |
DOI | 10.3899/jrheum.211020 |
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Abstract | Rheumatoid arthritis (RA) is more common in females, and although the cause of RA is unknown, it is characterized by the production of autoantibodies. The aims of this study were to determine whether RA-associated autoantibodies are more often found in females than males and to identify factors that influence the relationship between sex and seropositivity.
Databases were searched and studies of RA (N ≥ 100) were included if they reported proportion of seropositive patients with RA by sex. Metaanalyses and metaregression were conducted using the random-effects model. Covariates regressed were smoking, age, BMI, Health Assessment Questionnaire-Disability Index (HAQ-DI), and the Disease Activity Score in 28 joints (DAS28).
Eighty-four studies with a total of 141,381 subjects with rheumatoid factor (RF) seropositivity and 95,749 subjects with anticitrullinated protein antibody (ACPA) seropositivity met inclusion criteria. The mean age of participants ranged from 37 to 68 years and the proportion of female subjects ranged from 9% to 92%. Results indicated that females were less likely than males to be seropositive: odds ratio (OR) 0.84 [95% CI 0.77-0.91] for RF and OR 0.88 [95% CI 0.81-0.95] for ACPA. BMI, smoking, mean age, DAS28, and HAQ-DI did not affect the relationship between sex and seropositivity.
Although studies report that females have higher RA disease activity than males and that seropositivity predicts worse outcomes, females were less likely to be seropositive than males. |
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AbstractList | Rheumatoid arthritis (RA) is more common in females, and although the cause of RA is unknown, it is characterized by the production of autoantibodies. The aims of this study were to determine whether RA-associated autoantibodies are more often found in females than males and to identify factors that influence the relationship between sex and seropositivity.
Databases were searched and studies of RA (N ≥ 100) were included if they reported proportion of seropositive patients with RA by sex. Metaanalyses and metaregression were conducted using the random-effects model. Covariates regressed were smoking, age, BMI, Health Assessment Questionnaire-Disability Index (HAQ-DI), and the Disease Activity Score in 28 joints (DAS28).
Eighty-four studies with a total of 141,381 subjects with rheumatoid factor (RF) seropositivity and 95,749 subjects with anticitrullinated protein antibody (ACPA) seropositivity met inclusion criteria. The mean age of participants ranged from 37 to 68 years and the proportion of female subjects ranged from 9% to 92%. Results indicated that females were less likely than males to be seropositive: odds ratio (OR) 0.84 [95% CI 0.77-0.91] for RF and OR 0.88 [95% CI 0.81-0.95] for ACPA. BMI, smoking, mean age, DAS28, and HAQ-DI did not affect the relationship between sex and seropositivity.
Although studies report that females have higher RA disease activity than males and that seropositivity predicts worse outcomes, females were less likely to be seropositive than males. |
Author | Hadwen, Brook Cairns, Ewa Yu, Richard Barra, Lillian |
Author_xml | – sequence: 1 givenname: Brook orcidid: 0000-0001-5921-9697 surname: Hadwen fullname: Hadwen, Brook email: lillian.barra@sjhc.london.on.ca organization: B. Hadwen, BMSc, Department of Epidemiology and Biostatistics, Western University; R. Yu, MD, Department of Medicine, Division of Rheumatology, Western University; E. Cairns, PhD, Department of Medicine, Division of Rheumatology, and Department of Microbiology and Immunology, Western University; L. Barra, MD, Department of Epidemiology and Biostatistics, Department of Medicine, Division of Rheumatology, and Department of Microbiology and Immunology, Western University, London, Ontario, Canada. The authors declare no conflicts of interest relevant to this article. Address correspondence to Dr. L. Barra, 268 Grosvenor St, Suite D2-160, London, ON N6H 4Z1, Canada. Email: lillian.barra@sjhc.london.on.ca. Accepted for publication March 8, 2022 – sequence: 2 givenname: Richard orcidid: 0000-0002-8915-9514 surname: Yu fullname: Yu, Richard email: lillian.barra@sjhc.london.on.ca organization: B. Hadwen, BMSc, Department of Epidemiology and Biostatistics, Western University; R. Yu, MD, Department of Medicine, Division of Rheumatology, Western University; E. Cairns, PhD, Department of Medicine, Division of Rheumatology, and Department of Microbiology and Immunology, Western University; L. Barra, MD, Department of Epidemiology and Biostatistics, Department of Medicine, Division of Rheumatology, and Department of Microbiology and Immunology, Western University, London, Ontario, Canada. The authors declare no conflicts of interest relevant to this article. Address correspondence to Dr. L. Barra, 268 Grosvenor St, Suite D2-160, London, ON N6H 4Z1, Canada. Email: lillian.barra@sjhc.london.on.ca. Accepted for publication March 8, 2022 – sequence: 3 givenname: Ewa orcidid: 0000-0003-2748-3076 surname: Cairns fullname: Cairns, Ewa email: lillian.barra@sjhc.london.on.ca organization: B. Hadwen, BMSc, Department of Epidemiology and Biostatistics, Western University; R. Yu, MD, Department of Medicine, Division of Rheumatology, Western University; E. Cairns, PhD, Department of Medicine, Division of Rheumatology, and Department of Microbiology and Immunology, Western University; L. Barra, MD, Department of Epidemiology and Biostatistics, Department of Medicine, Division of Rheumatology, and Department of Microbiology and Immunology, Western University, London, Ontario, Canada. The authors declare no conflicts of interest relevant to this article. Address correspondence to Dr. L. Barra, 268 Grosvenor St, Suite D2-160, London, ON N6H 4Z1, Canada. Email: lillian.barra@sjhc.london.on.ca. Accepted for publication March 8, 2022 – sequence: 4 givenname: Lillian orcidid: 0000-0001-8614-6972 surname: Barra fullname: Barra, Lillian email: lillian.barra@sjhc.london.on.ca organization: B. Hadwen, BMSc, Department of Epidemiology and Biostatistics, Western University; R. Yu, MD, Department of Medicine, Division of Rheumatology, Western University; E. Cairns, PhD, Department of Medicine, Division of Rheumatology, and Department of Microbiology and Immunology, Western University; L. Barra, MD, Department of Epidemiology and Biostatistics, Department of Medicine, Division of Rheumatology, and Department of Microbiology and Immunology, Western University, London, Ontario, Canada. The authors declare no conflicts of interest relevant to this article. Address correspondence to Dr. L. Barra, 268 Grosvenor St, Suite D2-160, London, ON N6H 4Z1, Canada. Email: lillian.barra@sjhc.london.on.ca. Accepted for publication March 8, 2022 |
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