Complement activation in patients with primary antiphospholipid syndrome

Objective:To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).Methods:Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analyse...

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Published inAnnals of the rheumatic diseases Vol. 68; no. 6; pp. 1030 - 1035
Main Authors Oku, K, Atsumi, T, Bohgaki, M, Amengual, O, Kataoka, H, Horita, T, Yasuda, S, Koike, T
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd and European League Against Rheumatism 01.06.2009
BMJ Publishing Group
Elsevier Limited
Subjects
Online AccessGet full text
ISSN0003-4967
1468-2060
1468-2060
DOI10.1136/ard.2008.090670

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Abstract Objective:To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).Methods:Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH50) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time.Results:Serum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH50: 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity.Conclusion:Hypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation.
AbstractList To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS). Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH(50)) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time. Serum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH(50): 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity. Hypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation.
Objective: To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS). Methods: Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH50) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time. Results: Serum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH50: 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity. Conclusion: Hypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation.
To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).OBJECTIVETo investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH(50)) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time.METHODSThirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH(50)) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time.Serum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH(50): 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity.RESULTSSerum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH(50): 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity.Hypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation.CONCLUSIONHypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation.
Author Horita, T
Atsumi, T
Kataoka, H
Amengual, O
Oku, K
Yasuda, S
Bohgaki, M
Koike, T
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  fullname: Atsumi, T
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  surname: Amengual
  fullname: Amengual, O
  email: at3tat@med.hokudai.ac.jp
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  surname: Kataoka
  fullname: Kataoka, H
  email: at3tat@med.hokudai.ac.jp
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  surname: Horita
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  fullname: Koike, T
  email: at3tat@med.hokudai.ac.jp
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ContentType Journal Article
Copyright 2009 BMJ Publishing Group and European League Against Rheumatism
2009 INIST-CNRS
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Issue 6
Keywords Vascular disease
Human
Immunopathology
Platelet
Antiphospholipid antibody syndrome
Rheumatology
Autoimmune disease
Cardiovascular disease
Hemopathy
Activation
Language English
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Snippet Objective:To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).Methods:Thirty-six patients with...
Objective: To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS). Methods: Thirty-six patients with...
To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS). Thirty-six patients with primary APS, 42...
To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).OBJECTIVETo investigate the significance of...
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StartPage 1030
SubjectTerms Adolescent
Adult
Aged
Anticoagulants
Antigen-Antibody Complex - analysis
Antiphospholipid Syndrome - blood
Antiphospholipid Syndrome - immunology
Biological and medical sciences
Blood Coagulation
Blood platelets
Case-Control Studies
Complement Activation - immunology
Complement C3 - analysis
Complement C3a - analysis
Complement C4 - analysis
Complement C4a - analysis
Connective Tissue Diseases - immunology
Cross-Sectional Studies
Disease
Diseases of the osteoarticular system
Female
Humans
Hypotheses
Immunoglobulins
Lupus
Male
Medical imaging
Medical sciences
Middle Aged
NMR
Nuclear magnetic resonance
Plasma
Pregnancy
Retrospective Studies
Statistics, Nonparametric
Thrombosis
Tumor Necrosis Factor-alpha - blood
Tumor necrosis factor-TNF
Young Adult
Title Complement activation in patients with primary antiphospholipid syndrome
URI http://ard.bmj.com/content/68/6/1030.full
https://api.istex.fr/ark:/67375/NVC-8F5PQZSL-C/fulltext.pdf
https://www.ncbi.nlm.nih.gov/pubmed/18625630
https://www.proquest.com/docview/1777857926
https://www.proquest.com/docview/67226673
Volume 68
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