ДДД. С. Дильманова

Д. С. Дильманова

*This is an algorithmically generated author record based on publicly available information.

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Д. С. Дильманова has a total of 19 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Vasculitis mimics. Part 2. Large and medium vessel vasculitis mimickers: genetic vasculopathies. Mimickers of small vessel vasculitis

    by G. M. Tarasova, O. N. Egorova, T. M. Reshetnyak, B. G. Issayeva, Д. С. Дильманова, N. M. Maripkhan

    Genetic vasculopathies can mimic large and medium vessel vasculitis, while occlusive non-vasculitic vasculopathies and infections are often mimickers of small and medium vessel vasculitis. Most of these conditions are as severe as systemic vasculitides but require fundamentally different, and often urgent treatment approaches.

  • Open Access

    Steroid-sparing strategy for the treatment of vasculitis associated with antineutrophil cytoplasmic antibodies

    by O. N. Egorova, G. M. Tarasova, A. V. Datsina, B. G. Issayeva, Д. С. Дильманова, S. M Issayeva, A. M. Lila, С. М. Исаева

    Glucocorticoids (GC) and immunosuppressants (IS) are traditional treatments for vasculitis associated with antineutrophil cytoplasmic antibodies (ANCA), often resulting in the development of infections, diabetes mellitus and other adverse events (AEs). The development of a steroid-sparing strategy using biologic disease-modifying antirheumatic drugs (bDMARDs, including rituximab, etc.) and synthetic targeted drugs (avacopan) has radically improved the course of the disease. Currently, there are increasing number of basic and clinical trials of numerous bDMARDs that effectively reduce the number of AEs associated with GC and IS. The steroid-sparing therapeutic strategy not only shows considerable efficacy, but also opens up new perspectives for the treatment of patients with ANCA-associated systemic vasculitis.

  • Open Access

    Efficacy and safety of the biosimilar etanercept in the treatment of patients with rheumatoid arthritis and spondyloarthritis

    by B. G. Issayeva, Д. С. Дильманова, A. S. Amanzholova, S. M. Issayeva, A. B. Kanapina, A. E. Turtaeva, G. Sh. Trimova

    Objective: to evaluate the efficacy and safety of the biosimilar etanercept (ETC, Altebrel) in patients with rheumatoid arthritis (RA) and spondyloarthritis (SpA) in clinical practice.Material and methods. The study included 20 patients with a confirmed diagnosis of RA and 8 with SpA: 5 with axial SpA with radiological signs of sacroiliitis (r-axSpA), 3 with peripheral psoriatic arthritis (PsA). The mean age of the patients with RA was 47.7±12.3 years, and the mean age of SpA patients was 40.4±15.9 years. Patients with RA had moderate or high disease activity: mean DAS28-ESR index 5.2±1.0, median CDAI – 22.5 [15.5; 35.0], SDAI – 31.9 [24.4; 38.6], CRP level – 11 [0.9; 32.5] mg/L. Patients with r-axSpA had high activity and functional impairment, the median BASDAI was 5.5 [3.5; 8.0], BASFI – 6 [4; 6], CRP level – 17.5 [12.5; 27] mg/L. In PsA, the average DAS28 was 6.25±0.71. All patients were prescribed Altebrel at a dose of 50 mg subcutaneously weekly against a background of disease-modifying antirheumatic drugs. Patients were examined at baseline and then after 3 and 6 months of treatment.Results and discussion. During treatment with the biosimilar ETC, all patients with RA showed a decrease in inflammatory activity markers: after 3 and 6 months of therapy, the mean DAS28-ESR value decreased to 3.5±1.2 and 2.3±0.7 (p Conclusion. The results of the study demonstrate the high efficacy of Altebrel in rheumatic diseases, including RA and SpA.

  • Open Access

    On the problem of differential diagnosis in the detection of antineutrophil cytoplasmic antibodies

    by O. N. Egorova, G. M. Tarasova, B. G. Issaeva, A. V. Datsina, Д. С. Дильманова, S. M. Issaeva, M. G. Nogaeva, A. G. Issaeva, A. S. Amanzholova, M. M. Saparbayeva, et al.

    Vasculitides associated with antineutrophil cytoplasmic antibodies (ANCA) are a group of systemic autoimmune diseases characterized by necrotizing lesions of the walls of predominantly small vessels and the presence of ANCA against proteinase 3 or myeloperoxidase. However, an increase in ANCA levels can also be observed in other diseases, including autoimmune, malignant and infectious diseases, which complicates the interpretation of clinical and laboratory data and requires a differential diagnosis.