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1.
Int J Rheum Dis ; 13(3): 273-9, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20704626

ABSTRACT

AIM: The purpose of the study is to measure serum and synovial fluid levels of activin A and inhibin A in patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE) and osteoarthritis (OA) and correlate them with disease activity parameters. SUBJECTS AND METHODS: This study included 60 patients with various rheumatic diseases (20 with RA, 20 with SLE and 20 with OA), as well as 10 healthy controls. All of them were subjected to complete history-taking, examination and estimation of disease activity index. The following investigations were done for all subjects: serum and synovial activin A, inhibin A, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), anti-dsDNA and complements 3 and 4. RESULTS: Serum levels of activin A were significantly higher in RA, SLE and OA than controls and in RA and SLE versus OA The mean values of serum inhibin A were significantly higher in all studied groups than controls. Synovial activin A and inhibin A were significantly higher in RA than OA. Positive correlations were found between serum activin A and disease activity parameters of RA. In SLE, positive correlations were found between serum activin A and inhibin A with ESR and SLE Disease Activity Index. CONCLUSIONS: Serum activin A and inhibin A were significantly higher in RA and SLE. Serum levels correlated positively with disease activity parameters of RA and SLE. However, synovial levels were significantly higher in RA than OA but showed no correlation or negative correlation with disease activity. We recommend further studies to detect the exact role of activin A and inhibin A in these conditions.


Subject(s)
Arthritis, Rheumatoid/metabolism , Inhibin-beta Subunits/metabolism , Inhibins/metabolism , Lupus Erythematosus, Systemic/metabolism , Osteoarthritis, Knee/metabolism , Synovial Fluid/metabolism , Adult , Antibodies, Antinuclear/blood , Arthritis, Rheumatoid/blood , Arthritis, Rheumatoid/immunology , Biomarkers/blood , Biomarkers/metabolism , Blood Sedimentation , C-Reactive Protein/metabolism , Complement C3/metabolism , Complement C4/metabolism , DNA/immunology , Egypt , Female , Humans , Inhibin-beta Subunits/blood , Inhibins/blood , Lupus Erythematosus, Systemic/blood , Lupus Erythematosus, Systemic/immunology , Male , Middle Aged , Osteoarthritis, Knee/blood , Osteoarthritis, Knee/immunology , Severity of Illness Index
2.
J Egypt Soc Parasitol ; 32(3): 907-21, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12512823

ABSTRACT

Ninety individuals (76 males and 14 females) were classified into four groups. G1 (Control) included 20 healthy individuals. G2 (Chronic hepatitis) included 20 patients, G3 (Liver cirrhosis group) included 30 patients, and G4 (HCC) included 20 patients with HCC. All groups were subjected to clinical examination, abdominal ultrasonography, complete blood picture, HCV antibodies, HBs Ag, and function tests (total and direct bilirubin, total plasma proteins and albumin, prothrombin time and concentration, and liver enzymes AST, ALT and ALP). Patients of G3 & 4 were classified according to Child-Pugh classification into A. B and C. Upper endoscopic examination was done for 36/50 patients with chronic hepatitis or HCC. Circulating VEGF levels were determined by ELISA. There was a statistically high significant levels of circulating VEGF in G1, 2 & 3 than in the controls. A statistically significant higher level of circulating VEGF in G4 than in G3 & G4, and a statistically negative significant between VEGF levels and platelet count in G2. No significant correlation between VEGF and the grade of esophageal varices in G3 & G4. and no significant correlation between VEGF and upper GIT bleeding or spider naevi (vascular skin changes) in G2. A statistically significant was in correlation between VEGF and degree of hepatic dysfunction.


Subject(s)
Endothelial Growth Factors/blood , Intercellular Signaling Peptides and Proteins/blood , Liver Diseases/blood , Lymphokines/blood , Adult , Carcinoma, Hepatocellular/blood , Chronic Disease , Endothelium, Vascular , Female , Hepatitis/blood , Humans , Liver Cirrhosis/blood , Liver Neoplasms/blood , Male , Middle Aged , Vascular Endothelial Growth Factor A , Vascular Endothelial Growth Factors
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