Correlation between the levels of antinuclear antibodies, anti-DNA antibodies, and complement in systemic lupus erythematosus. 1988

C P Nguyen, and V V Cao, and J Fehér, and P Gergely
Second Department of Medicine, Semmelweis University, Budapest.

Antinuclear antibody (ANA) titres, anti-native DNA levels, serum haemolytic complement (CH50), and complement components C3 and C4 were determined in 550 serum samples taken from patients with active (311 samples) or inactive (239) systemic lupus erythematosus (SLE). Increased anti-DNA levels were shown in 82% of the samples from patients with active and in 57.8% of those from inactive, disease. Decreased levels of CH50, and C3, C4 were found in 37, 50, and 80% of the samples taken from active and in 22, 29, and 67% of those from inactive, disease, respectively. Positive ANA test was found in 94.7% of the patients with active and 87.9% of those with inactive, disease. Significant differences were found between the two groups for all parameters. The correlations were close between the values of anti-DNA antibodies and CH50, as well as between the levels of CH50 and C3. Relationship between anti-DNA antibodies and C3 levels, as well as between CH50 and C4 levels was also demonstrated. Six subgroups for expressing the positivity of five parameters, 32 patterns of positive parameters were found and their possible application were suggested. In combining these parameters and using appropriate patterns, their determination may be helpful not only for the diagnosis but also for the assessment of disease activity.

UI MeSH Term Description Entries
D008180 Lupus Erythematosus, Systemic A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. Libman-Sacks Disease,Lupus Erythematosus Disseminatus,Systemic Lupus Erythematosus,Disease, Libman-Sacks,Libman Sacks Disease
D003176 Complement C3 A glycoprotein that is central in both the classical and the alternative pathway of COMPLEMENT ACTIVATION. C3 can be cleaved into COMPLEMENT C3A and COMPLEMENT C3B, spontaneously at low level or by C3 CONVERTASE at high level. The smaller fragment C3a is an ANAPHYLATOXIN and mediator of local inflammatory process. The larger fragment C3b binds with C3 convertase to form C5 convertase. C3 Complement,C3 Precursor,Complement 3,Complement C3 Precursor,Complement Component 3,Precursor-Complement 3,Pro-C3,Pro-Complement 3,C3 Precursor, Complement,C3, Complement,Complement, C3,Component 3, Complement,Precursor Complement 3,Precursor, C3,Precursor, Complement C3,Pro C3,Pro Complement 3
D003181 Complement C4 A glycoprotein that is important in the activation of CLASSICAL COMPLEMENT PATHWAY. C4 is cleaved by the activated COMPLEMENT C1S into COMPLEMENT C4A and COMPLEMENT C4B. C4 Complement,C4 Complement Component,Complement 4,Complement C4, Precursor,Complement Component 4,Pro-C4,Pro-complement 4,C4, Complement,Complement Component, C4,Complement, C4,Component 4, Complement,Component, C4 Complement,Pro C4,Pro complement 4
D004247 DNA A deoxyribonucleotide polymer that is the primary genetic material of all cells. Eukaryotic and prokaryotic organisms normally contain DNA in a double-stranded state, yet several important biological processes transiently involve single-stranded regions. DNA, which consists of a polysugar-phosphate backbone possessing projections of purines (adenine and guanine) and pyrimidines (thymine and cytosine), forms a double helix that is held together by hydrogen bonds between these purines and pyrimidines (adenine to thymine and guanine to cytosine). DNA, Double-Stranded,Deoxyribonucleic Acid,ds-DNA,DNA, Double Stranded,Double-Stranded DNA,ds DNA
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000974 Antibodies, Antinuclear Autoantibodies directed against various nuclear antigens including DNA, RNA, histones, acidic nuclear proteins, or complexes of these molecular elements. Antinuclear antibodies are found in systemic autoimmune diseases including systemic lupus erythematosus, Sjogren's syndrome, scleroderma, polymyositis, and mixed connective tissue disease. Anti-DNA Antibodies,Antibodies, Anti-DNA,Antinuclear Antibodies,Antinuclear Autoantibodies,Antinuclear Autoantibody,Antinuclear Factors,Antinuclear Antibody,Antinuclear Factor,Anti DNA Antibodies,Antibody, Antinuclear,Autoantibody, Antinuclear,Factor, Antinuclear

Related Publications

C P Nguyen, and V V Cao, and J Fehér, and P Gergely
May 1965, Saishin igaku. Modern medicine,
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
January 1989, Immunology series,
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
October 1959, Arthritis and rheumatism,
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
June 1989, The Medical journal of Malaysia,
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
November 1965, Acta pathologica japonica,
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
May 1977, Clinical and experimental immunology,
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
June 1985, Polski tygodnik lekarski (Warsaw, Poland : 1960),
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
December 1984, Medicina clinica,
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
February 1985, Recenti progressi in medicina,
C P Nguyen, and V V Cao, and J Fehér, and P Gergely
May 1992, Rheumatic diseases clinics of North America,
Copied contents to your clipboard!