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Somatic mutations and the risk of undifferentiated autoinflammatory disease in MDS [Elektronski vir] : an under-recognized but prognostically important complicationWatad, Abdulla ...Objectives: We theorized that myelodysplastic syndrome (MDS) with somatic mutations and karyotype abnormalities are associated with autoinflammation, and that the presence of autoinflammatory disease ... affected prognosis in MDS. Methods: One hundred thirty-four MDS patients were assessed for the prevalence of autoinflammatory complications and its link with karyotypes and somaticmutation status. Autoinflammatory complications were described either as well-defined autoinflammatory diseases (AD) or undifferentiated "autoinflammatory disease" (UAD) (defined as CRP over 10.0 mg/L on five consecutive occasions, taken at separate times and not explained by infection). Several patient characteristics including demographic, clinical, laboratory, cytogenetics charts, and outcomes, were compared between different groups. Results: Sixty-two (46.3%) patients had an autoinflammatory complication manifesting as arthralgia (43.5% vs. 23.6%, p = 0.0146), arthritis (30.6% vs. 15.3%, p = 0.0340), skin rash (27.4% vs. 12.5%, p = 0.0301), pleuritis (14.5% vs. 4.2%, p = 0.0371) and unexplained fever (27.4% vs. 0%, p < 0.0001). AD were found in 7.4% of MDS patients (with polymyalgia rheumatic being the most frequently one). Classical autoimmune diseases were found only in 4 MDS patients (3.0%). Transcription factor pathway mutations (RUNX1, BCOR, WTI, TP53) (OR 2.20 [95%CI 1.02-4.75], p = 0.0451) and abnormal karyotypes (OR 2.76 [95%CI 1.22-6.26], p = 0.0153) were associated with autoinflammatory complications. Acute leukaemic transformation was more frequent in MDS patients with autoinflammatory features than those without (27.4% vs. 9.7%, p = 0.0080). Conclusions: Autoinflammatory complications are common inMDS. Somatic mutations of transcription factor pathways and abnormal karyotypes are associated with greater risk of autoinflammatory complications, which are themselves linked to malignant transformation and a worse prognosis.Source: Frontiers in immunology. - ISSN 1664-3224 ([Vol.] 12, 19 Feb. 2021, str. 1-12)Type of material - e-article ; adult, seriousPublish date - 2021Language - englishCOBISS.SI-ID - 57751555
Author
Watad, Abdulla |
Kačar, Mark |
Bragazzi, Nicola Luigi |
Zhou, Qiao |
Jassam, Miriam |
Taylor, Jan |
Roman, Eve |
Smith, Alexandra, (medicina) |
Jones, Richard A. |
Amital, Howard
Topics
Myelodysplastic syndromes |
Genetics |
Mielodisplastični sindrom |
Genetika |
avtovnetne bolezni |
nediferencirana avtovnetna bolezen |
molekularna karakterizacija |
somatske mutacije |
autoinflammation |
undifferentiated autoinflammatory disease |
molecular characterization |
somatic mutations
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Watad, Abdulla | ![]() |
Kačar, Mark | 55248 |
Bragazzi, Nicola Luigi | ![]() |
Zhou, Qiao | ![]() |
Jassam, Miriam | ![]() |
Taylor, Jan | ![]() |
Roman, Eve | ![]() |
Smith, Alexandra, (medicina) | ![]() |
Jones, Richard A. | ![]() |
Amital, Howard | ![]() |
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