Д. С. Дильманова
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Д. С. Дильманова has a total of 19 co-authors. Here are the top co-authors by number of shared publications:
- Bakytsholpan G. Issayeva
Kazakh National Medical University named after S.D. Asfendiyarov
3 shared publications - Olga N. Egorova
V.A. Nasonova Research Institute of Rheumatology
3 shared publications - Samal M. Issayeva
Kazakh National Medical University named after S.D. Asfendiyarov
3 shared publications - A. B. Kanapina
JSC «Scientific Center of Pediatrics and Pediatric Surgery», Kazakhstan, Almaty
2 shared publications - A. S. Amanzholova
Kazakh National Medical University named after S.D. Asfendiyarov
2 shared publications - A. V. Datsina
V.A. Nasonova Research Institute of Rheumatology
2 shared publications
Latest Publications
- Open Access
- 24 June 2025
- Published by IMA Press, LLC in Modern Rheumatology Journal
- Vol. 19 (3) , 19-26
Vasculitis mimics. Part 2. Large and medium vessel vasculitis mimickers: genetic vasculopathies. Mimickers of small vessel vasculitis
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.
- 24 June 2025
- Published by IMA Press, LLC in Modern Rheumatology Journal
- Vol. 19 (3) , 19-26
Open AccessVasculitis mimics. Part 2. Large and medium vessel vasculitis mimickers: genetic vasculopathies. Mimickers of small vessel vasculitis
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
- 20 October 2024
- Published by IMA Press, LLC in Modern Rheumatology Journal
- Vol. 18 (5) , 107-115
Steroid-sparing strategy for the treatment of vasculitis associated with antineutrophil cytoplasmic antibodies
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.
- 20 October 2024
- Published by IMA Press, LLC in Modern Rheumatology Journal
- Vol. 18 (5) , 107-115
Open AccessSteroid-sparing strategy for the treatment of vasculitis associated with antineutrophil cytoplasmic antibodies
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
- 20 October 2024
- Published by IMA Press, LLC in Modern Rheumatology Journal
- Vol. 18 (5) , 65-74
Efficacy and safety of the biosimilar etanercept in the treatment of patients with rheumatoid arthritis and spondyloarthritis
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.
- 20 October 2024
- Published by IMA Press, LLC in Modern Rheumatology Journal
- Vol. 18 (5) , 65-74
Open AccessEfficacy and safety of the biosimilar etanercept in the treatment of patients with rheumatoid arthritis and spondyloarthritis
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
- 19 April 2024
- Published by IMA Press, LLC in Modern Rheumatology Journal
- Vol. 18 (2) , 7–15
On the problem of differential diagnosis in the detection of antineutrophil cytoplasmic antibodies
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.
- 19 April 2024
- Published by IMA Press, LLC in Modern Rheumatology Journal
- Vol. 18 (2) , 7–15
Open AccessOn the problem of differential diagnosis in the detection of antineutrophil cytoplasmic antibodies
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.