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1.
Ter Arkh ; 64(5): 75-7, 1992.
Article in Russian | MEDLINE | ID: mdl-1333648

ABSTRACT

Patients with systemic lupus erythematosus (SLE), systemic scleroderma (SSD) and donors were examined for the blood levels of adrenocorticotropic hormone, hydrocortisone, follicle-stimulating hormone, luteinizing hormone, prolactin, estradiol, testosterone, progesterone, thyroid-stimulating hormone, triiodothyronine, thyroxin, and insulin. The corticotropin load test was carried out in 38 SLE patients, 32 SSD patients and 24 donors. The prednisolone test was made in 15 SSD patients and 27 donors. The studies were made with the aid of RIA. The patients with SLE manifested a decline of the basal level of hydrocortisone as well as a reduction of the reserve potentialities of the pituitary-adrenal system. The patients with SSD demonstrated a negligible decrease of the basal level of hydrocortisone with an evident lowering of the reserves of the same system. The treatment of SLE and SSD patients with glucocorticoids was followed by marked hyperinsulinemia.


Subject(s)
Adrenocorticotropic Hormone , Hormones/blood , Lupus Erythematosus, Systemic/blood , Prednisolone , Scleroderma, Systemic/blood , Female , Humans , Male , Sex Characteristics , Time Factors
3.
Ter Arkh ; 59(5): 27-31, 1987.
Article in Russian | MEDLINE | ID: mdl-3497464

ABSTRACT

The time course of immunopathological symptoms of lupus erythematosus was studied in 117 patients over a period of 5 years. It was established that routine multimodality therapy while resulting in a positive time course of clinical and clinico-biochemical indices, did not ensure the normalization of immunological parameters, particularly of the T-system of immunity. Courses of theophylline and splenin therapy were added to multimodality therapy to raise therapeutic efficacy and to return to normal the status of the immune system. A regular follow-up made it possible to stabilize the disease in 82.1% of the LE patients and to preserve working capacity in 50.4% of them.


Subject(s)
Ambulatory Care , Lupus Erythematosus, Systemic/immunology , Adult , Combined Modality Therapy , Complement System Proteins/analysis , Drug Therapy, Combination , Female , Follow-Up Studies , HLA Antigens/analysis , Humans , Immunoglobulins/analysis , Lupus Erythematosus, Systemic/therapy , Male , T-Lymphocytes/immunology , Time Factors
5.
Ter Arkh ; 56(10): 40-4, 1984.
Article in Russian | MEDLINE | ID: mdl-6596770

ABSTRACT

A study was made of the rate of HLA system antigens in 75 patients with different clinical versions and immuno-pathological manifestations of systemic lupus erythematosus (SLE). A total of 350 normal subjects comprised the control group. During SLE, a high rate of DNW3, B8 and AI antigens was revealed. Associative relations were established between individual clinical syndromes of SLE and immuno-pathological manifestations of the disease and definite antigens of the HLA system. The results of typing HLA system antigens can be used as additional criteria of SLE diagnosis, disease prediction, and choice of adequate therapy schemes.


Subject(s)
HLA Antigens/analysis , Lupus Erythematosus, Systemic/immunology , Adolescent , Adult , Antibody Formation , Female , HLA-A Antigens , HLA-B Antigens , Histocompatibility Antigens Class II/analysis , Humans , Immunity, Cellular , Lupus Erythematosus, Systemic/diagnosis , Male , Middle Aged , Serologic Tests
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