Araştırma Makalesi

Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis

Cilt: 16 Sayı: 3 30 Eylül 2025
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Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis

Öz

Aim: Antineutrophil cytoplasmic antibodies (ANCA) autoantibodies target neutrophil and monocyte lysosomal granules. The objective of the study is to investigate patients with a positive ANCA test for autoimmune disorders and vasculitis. Materials and Methods: This 4-year retrospective cohort research analyzed 9.480 Turkish tertiary hospital serum samples. The baseline evaluation included 218 eligible ANCA-positive patients with vasculitis (AAV) and other autoimmune and non-autoimmune diseases. Results: The other two groups have less pulmonary, renal, ear nose and throat (ENT), ophthalmic, and neurologic involvement than AAV individuals. AAV and autoimmune disease patients have higher joint and skin involvement than non-autoimmune disease patients. Hypertension and chronic renal failure are more common in AAV and non-autoimmune individuals than autoimmune ones. Chronic obstructive pulmonary disease (COPD) and proteinuria are higher in AAV patients than autoimmune disease patients. AAV patients have more hematuria than the other two. For non-autoimmune disease, myeloperoxidase (MPO) titer and erythrocyte sedimentation rate (ESR) are higher than for autoimmune disease. High proteinase 3 (PR3) titers are associated with AAV and autoimmune disorders. AAV patients have higher CRP and complement 3(C3) than the other two groups. In AAV, C4 and rheumatoid factor (RF) are higher than in non-autoimmune disease. Patients with autoimmune disease had higher initial GFR than the other two groups. Conclusion: We concluded that ANCA may be positive in numerous AAV-like diseases. A tertiary hospital found a strong correlation between ANCA titers, particularly PR3, and AAV clinical diagnosis. ANCA titre and organ system extent may be clinical AAV diagnostic indicators.

Anahtar Kelimeler

Destekleyen Kurum

Destekleyen kurum yoktur.

Etik Beyan

Etik kurul tarafından çalışma onaylanmıştır.E2-23-4480 nolu etik kurul örneğidir.

Kaynakça

  1. Tsukui D, Kimura Y, Kono H. Pathogenesis and pathology of anti-neutrophil cytoplasmic antibody(ANCA - associated vasculitis. J Transl Autoimmun 2021; 4:1 00094.
  2. de Groot K, Csernok E, van der Woude D. History of antineutrophil cytoplasmic autoantibodies: Milestones in rheumatology. Z Rheumatol 2025; 84: 219-224.
  3. Savige J, Trevisin M, Pollock W. Testing and reporting antineutrophil cytoplasmic antibodies (ANCA) in treated vasculitis and non-vasculitic disease. J Immunol Methods. 2018; 458: 1-7.
  4. Folci M, Ramponi G, Solitano V, Brunetta E. Serum ANCA as Disease Biomarkers: Clinical Implications Beyond Vasculitis. Clin Rev Allergy Immunol 2022; 63: 107-123.
  5. Qi F, Hao J, Wei W. Impact of different ANCA serotypes on the long-term outcome of ANCA-associated vasculitis patients. Ann Med 2023; 55: 2289614.
  6. Jiang C, Liu J, Wang H, Liu H, Fu Z, Li M et al. Anti-neutrophil cytoplasmic antibody patterns can predict clinical relapse in ANCA-associated vasculitis: overall population and subgroups. Clin Exp Rheumatol 2023; 41: 848-55.
  7. Walulik A, Łysak K, Błaszkiewicz M, Górecki I, Gomułka K. The Role of Neutrophils in ANCA-Associated Vasculitis: The Pathogenic Role and Diagnostic Utility of Autoantibodies. Int J Mol Sci 2023 7; 24: 17217.
  8. Sun XJ, Li ZY, Chen M. Pathogenesis of anti-neutrophil cytoplasmic antibody-associated vasculitis. Rheumatol Immunol Res 2023; 4: 11-21.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Otoimmünite, İmmünoloji (Diğer), Klinik Mikrobiyoloji

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

30 Eylül 2025

Gönderilme Tarihi

18 Nisan 2025

Kabul Tarihi

14 Ağustos 2025

Yayımlandığı Sayı

Yıl 2025 Cilt: 16 Sayı: 3

Kaynak Göster

APA
Salman, E., & Toyran, A. (2025). Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis. Turkish Journal of Clinics and Laboratory, 16(3), 486-492. https://doi.org/10.18663/tjcl.1679367
AMA
1.Salman E, Toyran A. Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis. TJCL. 2025;16(3):486-492. doi:10.18663/tjcl.1679367
Chicago
Salman, Emrah, ve Alparslan Toyran. 2025. “Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis”. Turkish Journal of Clinics and Laboratory 16 (3): 486-92. https://doi.org/10.18663/tjcl.1679367.
EndNote
Salman E, Toyran A (01 Eylül 2025) Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis. Turkish Journal of Clinics and Laboratory 16 3 486–492.
IEEE
[1]E. Salman ve A. Toyran, “Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis”, TJCL, c. 16, sy 3, ss. 486–492, Eyl. 2025, doi: 10.18663/tjcl.1679367.
ISNAD
Salman, Emrah - Toyran, Alparslan. “Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis”. Turkish Journal of Clinics and Laboratory 16/3 (01 Eylül 2025): 486-492. https://doi.org/10.18663/tjcl.1679367.
JAMA
1.Salman E, Toyran A. Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis. TJCL. 2025;16:486–492.
MLA
Salman, Emrah, ve Alparslan Toyran. “Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis”. Turkish Journal of Clinics and Laboratory, c. 16, sy 3, Eylül 2025, ss. 486-92, doi:10.18663/tjcl.1679367.
Vancouver
1.Emrah Salman, Alparslan Toyran. Clinical investigation of patients with positive antineutrophil cytoplasmic antibodies (ANCA) test for autoimmunity and vasculitis. TJCL. 01 Eylül 2025;16(3):486-92. doi:10.18663/tjcl.1679367


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