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Brief Report: The Genetic Profile of Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis.
Hinks, Anne; Marion, Miranda C; Cobb, Joanna; Comeau, Mary E; Sudman, Marc; Ainsworth, Hannah C; Bowes, John; Becker, Mara L; Bohnsack, John F; Haas, Johannes-Peter; Lovell, Daniel J; Mellins, Elizabeth D; Nelson, J Lee; Nordal, Ellen; Punaro, Marilynn; Reed, Ann M; Rose, Carlos D; Rosenberg, Alan M; Rygg, Marite; Smith, Samantha L; Stevens, Anne M; Videm, Vibeke; Wallace, Carol A; Wedderburn, Lucy R; Yarwood, Annie; Yeung, Rae S M; Langefeld, Carl D; Thompson, Susan D; Thomson, Wendy; Prahalad, Sampath.
Afiliação
  • Hinks A; University of Manchester, Manchester, UK.
  • Marion MC; Wake Forest University School of Medicine, Winston-Salem, North Carolina.
  • Cobb J; University of Manchester and Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
  • Comeau ME; Wake Forest University School of Medicine, Winston-Salem, North Carolina.
  • Sudman M; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Ainsworth HC; Wake Forest University School of Medicine, Winston-Salem, North Carolina.
  • Bowes J; University of Manchester, Manchester, UK.
  • Becker ML; Children's Mercy Kansas City, Kansas City, Missouri.
  • Bohnsack JF; University of Utah, Salt Lake City.
  • Haas JP; German Centre for Pediatric and Adolescent Rheumatology, Garmisch-Partenkirchen, Germany.
  • Lovell DJ; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Mellins ED; Stanford University, Stanford, California.
  • Nelson JL; Fred Hutchinson Cancer Research Center and University of Washington, Seattle.
  • Nordal E; University Hospital of North Norway and UIT The Arctic University of Norway, Tromsø, Norway.
  • Punaro M; Arthritis Clinic Texas Scottish Rite Hospital for Children and University of Texas Southwestern Medical Center, Dallas.
  • Reed AM; Duke University School of Medicine, Durham, North Carolina.
  • Rose CD; DuPont Children's Hospital, Wilmington, Delaware.
  • Rosenberg AM; University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
  • Rygg M; Norwegian University of Science and Technology and St. Olav's University Hospital, Trondheim, Norway.
  • Smith SL; University of Manchester, Manchester, UK.
  • Stevens AM; Seattle Children's Research Institute and University of Washington, Seattle.
  • Videm V; Norwegian University of Science and Technology and St. Olav's University Hospital, Trondheim, Norway.
  • Wallace CA; Seattle Children's Hospital and Research Institute, Seattle, Washington.
  • Wedderburn LR; University College London and NIHR Great Ormond Street Hospital Biomedical Research Centre, London, UK.
  • Yarwood A; University of Manchester, Manchester, UK.
  • Yeung RSM; The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada.
  • Langefeld CD; Wake Forest University School of Medicine, Winston-Salem, North Carolina.
  • Thompson SD; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Thomson W; University of Manchester and Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
  • Prahalad S; Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, Georgia.
Arthritis Rheumatol ; 70(6): 957-962, 2018 06.
Article em En | MEDLINE | ID: mdl-29426059
ABSTRACT

OBJECTIVE:

Juvenile idiopathic arthritis (JIA) comprises 7 heterogeneous categories of chronic childhood arthritides. Approximately 5% of children with JIA have rheumatoid factor (RF)-positive arthritis, which phenotypically resembles adult rheumatoid arthritis (RA). Our objective was to compare and contrast the genetics of RF-positive polyarticular JIA with those of RA and selected other JIA categories, to more fully understand the pathophysiologic relationships of inflammatory arthropathies.

METHODS:

Patients with RF-positive polyarticular JIA (n = 340) and controls (n = 14,412) were genotyped using the Immunochip array. Single-nucleotide polymorphisms were tested for association using a logistic regression model adjusting for admixture proportions. We calculated weighted genetic risk scores (wGRS) of reported RA and JIA risk loci, and we compared the ability of these wGRS to predict RF-positive polyarticular JIA.

RESULTS:

As expected, the HLA region was strongly associated with RF-positive polyarticular JIA (P = 5.51 × 10-31 ). Nineteen of 44 RA risk loci and 6 of 27 oligoarticular/RF-negative polyarticular JIA risk loci were associated with RF-positive polyarticular JIA (P < 0.05). The RA wGRS predicted RF-positive polyarticular JIA (area under the curve [AUC] 0.71) better than did the oligoarticular/RF-negative polyarticular JIA wGRS (AUC 0.59). The genetic profile of patients with RF-positive polyarticular JIA was more similar to that of RA patients with age at onset 16-29 years than to that of RA patients with age at onset ≥70 years.

CONCLUSION:

RF-positive polyarticular JIA is genetically more similar to adult RA than to the most common JIA categories and thus appears to be a childhood-onset presentation of autoantibody-positive RA. These findings suggest common disease mechanisms, which could lead to novel therapeutic targets and shared treatment strategies.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite Juvenil / Artrite Reumatoide / Fator Reumatoide / Autoanticorpos / Perfil Genético Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite Juvenil / Artrite Reumatoide / Fator Reumatoide / Autoanticorpos / Perfil Genético Idioma: En Ano de publicação: 2018 Tipo de documento: Article