Journal
JOURNAL OF RHEUMATOLOGY
Volume 47, Issue 2, Pages 204-210Publisher
J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.181209
Keywords
ANKYLOSING SPONDYLITIS; GENETIC POLYMORPHISMS; EPIDEMIOLOGY
Categories
Funding
- Liaison Committee [5056/46051000]
- Research Council of Norway [249944]
- National Health and Medical Research Council Senior Principal Research Fellowship [APP1024879]
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Objective. The genetic component of ankylosing spondylitis (AS) development is similar to 90%. Of the known heritability, similar to 20% is explained by HLA-B27, and 113 identified AS-associated single-nucleotide polymorphisms (SNP) account for similar to 7.4%. The objectives were to construct a weighted genetic risk score (wGRS) using currently known genome-wide susceptibility SNP, and to evaluate its predictive ability for AS in the Norwegian population-based Nord-Trondelag Health Study (HUNT). Methods. AS cases (n = 164) and controls (n = 49,032) were from the second (1995-1997) and third (2006-2008) waves of the HUNT study, to which the entire adult population of the northern region of Trondelag was invited. A wGRS based on 110 SNP weighted by published OR for AS was constructed, representing each person's carriage of all risk variants. Logistic regression models including the wGRS alone or in combination with HLA-B27 carrier state and other adjustment variables (sex, age, smoking, body mass index, and hypertension) were developed. Discrimination among models was compared using area under the curve (AUC). Results. The wGRS was associated with AS (OR 1.7, 95% CI 1.4-2.1), but showed low discrimination (AUC 0.62, 95% CI 0.58-0.67). HLA-B27 was significantly associated with AS (OR 50, 95% CI 32-81), showing high discrimination (AUC 0.88, 95% CI 0.85-0.90). Combining the wGRS and HLA-B27 improved prediction (AUC 0.90, 95% CI 0.87-0.92; p < 0.001 vs wGRS alone, p < 0.01 vs HLA-B27 alone). Further inclusion of adjustment variables gave a small improvement (AUC 0.91, 95% CI 0.89-0.94; p = 0.03). Conclusion. Prediction in a population-based setting based on all currently known AS susceptibility SNP was better than HLA-B27 carrier state alone, although the improvement was small and of uncertain clinical value.
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