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HLA-B27 predicts a more extended disease with increasing age at onset in boys with juvenile idiopathic arthritis

Berntson, Lillemor, 1957- (författare)
Uppsala universitet,Institutionen för kvinnors och barns hälsa,Pediatrisk inflammationsforskning/Nevéus
Damgård, M. (författare)
Department of Pediatrics, Falun Hospital
Andersson-Gäre, Boel (författare)
Jönköping University,HHJ. Kvalitetsförbättringar, innovationer och ledarskap inom vård och socialt arbete,Department of Pediatrics, Ryhov County Hospital
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Herlin, T. (författare)
Århus University Hospital
Nielsen, S. (författare)
University Clinic of Pediatrics II, Rigshospitalet
Nordal, E. (författare)
Institute of Clinical Medicine/Institute of Community Medicine, University of Tromsø
Rygg, M. (författare)
Department of Laboratory Medicine, Children’s and Women’s Health, Faculty of Medicine, Norwegian University of Science and Technology
Zak, M. (författare)
University Clinic of Pediatrics II, Rigshospitalet
Fasth, Anders, 1945 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,Department of Pediatrics, Göteborg University
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 (creator_code:org_t)
2008
2008
Engelska.
Ingår i: British Journal of Rheumatology. - 0263-7103 .- 1460-2172 .- 0315-162X .- 1499-2752. ; 35:10, s. 2055-2061
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • OBJECTIVE: Juvenile idiopathic arthritis (JIA) is a heterogeneous condition with very few clinical and laboratory signs that can help predict the course and severity of the disease in the individual patient. The cell-surface antigen HLA-B27 is well known to be associated with spondyloarthropathies, reactive arthritis, and enthesitis. HLA-B27 plays an important role in the classification of JIA, since evidence of sacroiliitis most often evolves after years of arthritis in other joints. We investigated the associations of HLA-B27 and the clinical manifestations of JIA using a method as close to a population-based study as possible.METHODS: We studied an incidence-based cohort of 305 patients collected prospectively in 3 Nordic countries (Sweden, Norway, Denmark). Clinical and serological data of the first 3 years of the disease were collected.RESULTS: HLA-B27 was found to be positive in 25.5% of the patients, and we found a higher proportion of HLA-B27-positive boys with older age at disease onset (p=0.034). Regression analysis showed a correlation of 0.7 in the HLA-B27-positive boys, pointing to a higher risk of more joint involvement with older age at disease onset. By Fisher's exact test, involvement of small joints in the lower extremities was associated with HLA-B27 in boys (p=0.011), but not in girls (p=0.687). HLA-B27 was associated with inflammatory back pain in both sexes (p=0.041 in boys, p=0.042 in girls), but with enthesitis only in boys (p<0.001 in boys, p=0.708 in girls).CONCLUSION: HLA-B27 is of increasing importance with older age at disease onset in boys with JIA, predicting more active joints within the first 3 years of disease, and also involving small joints in the lower extremity to a greater degree than in HLA-B27-negative boys. During the first 3 years of disease the occurrence of HLA-B27 is associated with inflammatory back pain in both sexes, but with enthesitis only in boys. Our data present new challenges for the ILAR classification of JIA.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)

Nyckelord

Adolescent
Age of Onset
Arthritis
Juvenile Rheumatoid/genetics
Child
Child
Preschool
Denmark
Disease Progression
Female
Genetic Predisposition to Disease/genetics
HLA-B27 Antigen/genetics
Humans
Longitudinal Studies
Male
Norway
Sex Factors
Sweden
MEDICINE

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