Brophy Sinead, Hickey Sarah, Menon Ajit, Taylor Gordon, Bradbury Linda, Hamersma Jasmin, Calin Andrei
Epidemiology Department, Royal National Hospital for Rheumatic Diseases, Upper Borough Walls, Bath, UK.
J Rheumatol. 2004 Sep;31(9):1775-8.
The heritability of disease activity and function in ankylosing spondylitis (AS) have been estimated at 0.51 and 0.63 (i.e., 51% and 63%), respectively. We examined the concordance of disease severity among family members in terms of disease activity, function, radiological change, prevalence of iritis, and juvenile onset.
Disease activity and functional impairment due to AS were studied using the Bath AS Disease Activity Index (BASDAI) and Functional Index (BASFI) self-administered questionnaires; radiographic involvement was measured using the Bath AS Radiology Index (BASRI) scale. Familial correlation of BASDAI and BASFI was assessed in 406 families with 2 or more cases, using the program PAP. Parent-child and sibling-sibling concordance for iritis and juvenile AS were also studied in these families. Heritability of radiological disease severity based on the BASRI was assessed in 29 families containing 60 affected individuals using the program SOLAR.
Correlations between parent-child pairs for disease activity and function were 0.07 for both. Correlations between sibling pairs for disease activity and function were 0.27 and 0.36, respectively. The children of AS parents with iritis were more likely to develop iritis [27/71 (38%)] than children of non-iritis AS parents [13/70 (19%)] (p = 0.01). Parents with JAS were more likely to have children with JAS [17/30 (57%) compared to non-JAS parents 34/111 (30%)] (p = 0.002). The heritability of radiological disease severity based on the BASRI was 0.62.
While correlation in severity between parent and child is poor, siblings do resemble each other in terms of severity, supporting the findings of segregation studies indicating significant genetic dominance in the heritable component of disease activity. Significant parent-child concordance for iritis and juvenile disease onset suggest that there are genetic risk factors for these traits independent of those determining the risk of AS itself. The finding of significant heritability of radiological change (BASRI) provides support using an objective measure for the observed heritability of the questionnaire-assessed disease severity scores, BASDAI and BASFI.
强直性脊柱炎(AS)疾病活动度和功能的遗传度估计分别为0.51和0.63(即51%和63%)。我们从疾病活动度、功能、放射学改变、虹膜炎患病率和青少年发病情况方面研究了家庭成员间疾病严重程度的一致性。
使用巴斯强直性脊柱炎疾病活动指数(BASDAI)和功能指数(BASFI)自评问卷研究AS导致的疾病活动度和功能损害;使用巴斯强直性脊柱炎放射学指数(BASRI)量表测量放射学受累情况。使用PAP程序在406个有2例及以上病例的家庭中评估BASDAI和BASFI的家族相关性。在这些家庭中还研究了亲子及同胞间虹膜炎和青少年AS的一致性。使用SOLAR程序在29个包含60名受累个体的家庭中评估基于BASRI的放射学疾病严重程度的遗传度。
亲子对之间疾病活动度和功能的相关性均为0.07。同胞对之间疾病活动度和功能的相关性分别为0.27和0.36。患有虹膜炎的AS患者的子女比未患虹膜炎的AS患者的子女更易患虹膜炎[27/71(38%)比13/70(19%)](p = 0.01)。患有青少年型AS(JAS)的父母比未患JAS的父母更易生育患有JAS的子女[17/30(57%)比34/111(30%)](p = 0.002)。基于BASRI的放射学疾病严重程度的遗传度为0.62。
虽然亲子间严重程度的相关性较差,但同胞间在严重程度方面确实相似,这支持了分离研究的结果,表明在疾病活动度的遗传成分中存在显著的遗传显性。虹膜炎和青少年疾病发病的亲子间显著一致性表明,这些特征存在独立于决定AS本身风险的遗传危险因素。放射学改变(BASRI)显著遗传度的发现,为通过客观测量支持问卷评估的疾病严重程度评分(BASDAI和BASFI)的观察到的遗传度提供了依据。