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Makale detayı · 2025 · article

Exploring the genetic interaction between ERAP1 / ERAP2 and HLA-B*52:01 in Takayasu arteritis

Dergi Rheumatology
ISSN1462-0324
YÖKSİS OpenAlex Açık erişim · green
Yıl2025
Atıf0OpenAlex
Yüzdelik%34,1
FWCI0,01,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q1

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıRheumatology
  • Katalog eşleşmesi (ISSN)Rheumatology
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

OBJECTIVES: Takayasu arteritis is a rare vasculitis characterized by inflammation of large arteries. Given the robust genetic association with HLA-B*52:01, it was recently proposed to classify Takayasu arteritis within the spectrum of MHC-I-opathies. Although genetic associations in ERAP1 and ERAP2 have been described in several MHC-I-opathies, their role in Takayasu arteritis remains unclear. This study investigated the genetic interaction between ERAP1/ERAP2 and HLA-B*52:01 in Takayasu arteritis. METHODS: Using data from a large multi-ancestral GWAS, we examined the genetic association between ERAP1 and ERAP2 polymorphisms with Takayasu arteritis. Next, we conducted genetic interaction analyses between ERAP1/ERAP2 polymorphisms and HLA-B*52:01, followed by a meta-analysis across populations. In addition, we conducted a genetic association test for ERAP1/ERAP2 polymorphisms restricted to HLA-B*52:01-positive individuals. RESULTS: Our analyses suggested no significant genetic interactions between ERAP1 or ERAP2 and HLA-B*52:01 in Takayasu arteritis, which contrasts with the findings observed in other MHC-I-opathies. In addition, no significant associations between ERAP1/ERAP2 and Takayasu arteritis were detected, including analyses under dominant or recessive models, or after stratifying by HLA-B*52:01 status. CONCLUSION: These results suggest that the genetic profile of Takayasu arteritis differs from other MHC-I-opathies, supporting its classification as a distinct subtype within this group of immune-mediated diseases. These finding are hypothesis-generating, and validation in larger cohorts is warranted.

Konular

Atıflar

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Yazarlar

10
  1. Casares-Marfil D 1
  2. GÜHER SARUHAN DİRESKENELİ 2
  3. Grayson P.C 3
  4. Enrico Tombetti 4
  5. Jiang L 5
  6. Merkel P.A 6
  7. Vasculitis Clinical Research Consortium . 7
  8. Turkish Takayasu Study Group . 8
  9. Sawalha AH 9
  10. AŞKIN ATEŞ ANKARA ÜNİVERSİTESİ 10