McDermott E, Khan M A, Deighton C
Rheumatology Unit, City Hospital, Nottingham, United Kingdom.
Ann Rheum Dis. 1996 Jul;55(7):475-7. doi: 10.1136/ard.55.7.475.
To determine whether preliminary evidence supporting features of genetic anticipation in familial rheumatoid arthritis (RA) could be replicated in independent and larger samples.
Data were obtained from records of 59 multicase families from the Arthritis and Rheumatism Council (ARC) National Repository in Manchester, 65 multicase families from Cleveland, Ohio, USA, and 253 consecutive patients with RA attending clinics in Nottingham.
Mean ages of disease onset in the parents affected with RA were consistently greater than those in the probands. In the ARC data, the mean age difference in disease onset between the affected mother and proband pairs was 16.0 years (95% confidence interval (CI) 7.2 to 24.8 years, n = 11); in the Cleveland data it was 7.8 years (95% CI 0.9 to 14.7 years, n = 24), and in the Nottingham data it was 10.4 years (95% CI 2.8 to 18.0 years, n = 28). Similar results were found in the limited number of father-proband pairs. Unlike the findings of earlier work, there was no correlation between proband age at disease onset and age of the parent at conception of the proband.
In independent and larger familial RA data sets, features of genetic anticipation were replicated. Our findings support the case for further research at a molecular level into genetic anticipation in those families with two successive generations affected by RA.
确定支持家族性类风湿关节炎(RA)遗传早现特征的初步证据能否在独立且更大的样本中得到重复验证。
数据取自曼彻斯特关节炎与风湿病理事会(ARC)国家资料库中59个多病例家庭的记录、美国俄亥俄州克利夫兰市65个多病例家庭的记录以及诺丁汉诊所连续就诊的253例RA患者的记录。
患RA的父母的疾病平均发病年龄始终大于先证者的发病年龄。在ARC的数据中,患病母亲与先证者对之间的疾病发病平均年龄差为16.0岁(95%置信区间(CI)7.2至24.8岁,n = 11);在克利夫兰的数据中为7.8岁(95%CI 0.9至14.7岁,n = 24),在诺丁汉的数据中为10.4岁(95%CI 2.8至18.0岁,n = 28)。在数量有限的父亲-先证者对中也发现了类似结果。与早期研究结果不同的是,先证者疾病发病年龄与先证者受孕时父母年龄之间没有相关性。
在独立且更大的家族性RA数据集中,遗传早现特征得到了重复验证。我们的研究结果支持在分子水平上对两代连续受RA影响的家庭中的遗传早现进行进一步研究。