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Objective: The aim of this meta-analysis is to investigate the relationship between interleukin (IL)-10 levels and its polymorphism and Takayasu arteritis (TAK).
Methods: Five databases including PubMed, Web of Science, Ovid, Sinomed and China National Knowledge Infrastructure (CNKI) were gone through from inception to March 31, 2022. Studies were screened according to the inclusion and exclusion criteria. Newcastle-Ottawa Scale (NOS) was applied to assess study quality. Strengths of association were evaluated by odds ratio (OR) and 95% CI. The T v. t (allele contrast), TT v. tt (homozygous contrast), Tt vs tt (heterozygous contrast), TT + Tt vs tt (dominant contrast) and TT vs Tt + tt (recessive contrast) models were adopted.
Results: Seven studies were included. No significant relationship between IL-10 and TAK was detected in the included patients (P > 0.05). The levels of IL-10 were lower in the active group than those in the stable group, which was -0.47 (95% CI: -0.93, 0.00) (P = 0.05). No significant relationships between IL-10 and TAK were found under all contrasts for polymorphisms rs1800871, rs1800872 and rs1800896 (P > 0.05).
Conclusions: There was no significant difference in IL-10 levels between TAK patients and control subjects. The levels of IL-10 were lower in TAK patients in the active stage. There was no significant association between IL-10 gene polymorphisms and TAK. Further well-designed studies with larger sample sizes in patients with different stages are needed.
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http://dx.doi.org/10.1111/1756-185X.14717 | DOI Listing |
Rev Clin Esp (Barc)
September 2025
Servicio de Medicina Interna, Unidad de Ecografía Clínica, Hospital San Carlos, San Fernando, Cádiz, Spain. Electronic address:
BMJ Case Rep
September 2025
Department of Nephrology, Christian Medical College, Vellore, Tamil Nadu, India
Renal involvement in Takayasu arteritis (TA) has been reported, but glomerular lesions causing nephrotic syndrome (NS) are rare. This is a case report of TA presenting with NS due to secondary amyloidosis.A woman in her late 40s was diagnosed as TA at the age of 15 years presented with nephrotic range proteinuria.
View Article and Find Full Text PDFJACC Case Rep
August 2025
Department of Radiology, Hospital México, San José, Costa Rica.
Case Summary: A 20-year-old woman presented with acute coronary syndrome. Invasive coronary angiography revealed complete occlusion of the left main coronary artery. Subsequent computed tomography angiography demonstrated occlusion of the left subclavian, left vertebral, and superior mesenteric arteries, along with circumferential thickening of the abdominal aorta, consistent with Takayasu arteritis.
View Article and Find Full Text PDFJACC Case Rep
August 2025
Paediatric Cardiothoracic Department, Alder Hey Children's Hospital, Liverpool, United Kingdom. Electronic address:
Background: Takayasu arteritis (TA) is a large-vessel vasculitis that primarily affects the aorta and the pulmonary and coronary arteries.
Case Summary: A 4-year-old boy was diagnosed in 2022 with pyoderma gangrenosum (PG) and required prolonged multidisciplinary care, including aggressive medical immunosuppression for severe skin lesions. In October 2024, after a period of clinical stability, he presented with a seizure and right-sided weakness.
Autoimmun Rev
August 2025
Departments of Medicine and Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Canada; Population Health Research Institute, Hamilton Health Sciences / McMaster University, Hamilton, Canada. Electronic address:
The fragility of randomized controlled trials (RCTs) of large vessel vasculitis (LVV) - defined as the minimum number of outcome events that would need to change to reverse the trial's conclusions - has not been comprehensively studied. We identified relevant RCTs with a systematic literature review till April 2025. The fragility index (FI)/ reverse fragility index (RFI) and fragility quotient (FQ, i.
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