Identification of novel genetic susceptibility loci in African American lupus patients in a candidate gene association study.

نویسندگان

  • Elena Sánchez
  • Mary E Comeau
  • Barry I Freedman
  • Jennifer A Kelly
  • Kenneth M Kaufman
  • Carl D Langefeld
  • Elizabeth E Brown
  • Graciela S Alarcón
  • Robert P Kimberly
  • Jeffrey C Edberg
  • Rosalind Ramsey-Goldman
  • Michelle Petri
  • John D Reveille
  • Luis M Vilá
  • Joan T Merrill
  • Betty P Tsao
  • Diane L Kamen
  • Gary S Gilkeson
  • Judith A James
  • Timothy J Vyse
  • Patrick M Gaffney
  • Chaim O Jacob
  • Timothy B Niewold
  • Bruce C Richardson
  • John B Harley
  • Marta E Alarcón-Riquelme
  • Amr H Sawalha
چکیده

OBJECTIVE Candidate gene and genome-wide association studies have identified several disease susceptibility loci in lupus patients. These studies have largely been performed in lupus patients who are Asian or of European ancestry. This study was undertaken to examine whether some of these same susceptibility loci increase lupus risk in African American individuals. METHODS Single-nucleotide polymorphisms tagging 15 independent lupus susceptibility loci were genotyped in a set of 1,724 lupus patients and 2,024 healthy controls of African American descent. The loci examined included PTPN22, FCGR2A, TNFSF4, STAT4, CTLA4, PDCD1, PXK, BANK1, MSH5 (HLA region), CFB (HLA region), C8orf13-BLK region, MBL2, KIAA1542, ITGAM, and MECP2/IRAK1. RESULTS We found the first evidence of genetic association between lupus in African American patients and 5 susceptibility loci (C8orf13-BLK, BANK1, TNFSF4, KIAA1542, and CTLA4; P = 8.0 × 10⁻⁶, P = 1.9 × 10⁻⁵, P = 5.7 × 10⁻⁵, P = 0.00099, and P = 0.0045, respectively). Further, we confirmed the genetic association between lupus and 5 additional lupus susceptibility loci (ITGAM, MSH5, CFB, STAT4, and FCGR2A; P = 7.5 × 10⁻¹¹, P = 5.2 × 10⁻⁸, P = 8.7 × 10⁻⁷ , P = 0.0058, and P = 0.0070, respectively), and provided evidence, for the first time, of genome-wide significance for the association between lupus in African American patients and ITGAM and MSH5 (HLA region). CONCLUSION These findings provide evidence of novel genetic susceptibility loci for lupus in African Americans and demonstrate that the majority of lupus susceptibility loci examined confer lupus risk across multiple ethnicities.

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عنوان ژورنال:
  • Arthritis and rheumatism

دوره 63 11  شماره 

صفحات  -

تاریخ انتشار 2011