Deighton C, Heslop P, McDonagh J, Walker D, Thomson G
Department of Integrative Biology, University of California at Berkeley 94720.
Ann Rheum Dis. 1994 Dec;53(12):833-5. doi: 10.1136/ard.53.12.833.
To determine if there is evidence for genetic anticipation in rheumatoid arthritis (RA) by analysing the possibility that parental disease status and age at proband conception influence the age of onset and disease severity of the proband.
RA outpatients were identified and data were also taken from Newcastle multicase RA pedigrees. Comparisons of age of onset and parental age at proband conception were made for pedigrees grouped according to the disease status of the parents. Correlation coefficients and linear regression models were calculated for the age of RA onset in the probands. Measures of disease severity were compared in RA mother-proband pairs.
The results were similar in both the outpatient (n = 153) and multicase pedigree (n = 15) samples. Significant results were confined to pedigrees in which the mother had RA (20 of the outpatient probands and seven of the multicase group). Probands in these sibships had a younger age of RA onset than their affected mothers (38.3 years (95% confidence interval (CI) 33.8 to 42.8) versus 53.7 (47.3 to 60.0) (p = 0.002) in the outpatient sample; 32.4 years (25.3 to 39.6) versus 43.4 years (29.0 to 57.9) (p = 0.1) in the multicase pedigrees). In the maternal RA group, both the maternal and paternal age at proband conception showed significant negative correlations (r = -0.65, p = 0.002 and r = -0.60, p = 0.005, respectively in the outpatient sample) and linear regression coefficients with age of proband disease onset. In seven affected mother-proband pairs, the probands had a tendency to more severe disease, despite shorter disease duration and younger age.
This preliminary analysis has suggested that within pedigrees in which the mother has RA, the features of genetic anticipation and observations consistent with premutation models may prevail.
通过分析先证者受孕时父母的疾病状态和年龄对先证者发病年龄及疾病严重程度的影响,确定类风湿关节炎(RA)中是否存在遗传早现的证据。
确定RA门诊患者,并从纽卡斯尔多病例RA家系中获取数据。根据父母的疾病状态对家系进行分组,比较先证者的发病年龄和受孕时父母的年龄。计算先证者RA发病年龄的相关系数和线性回归模型。比较RA母亲-先证者对中的疾病严重程度指标。
门诊患者(n = 153)和多病例家系(n = 15)样本的结果相似。显著结果仅限于母亲患有RA的家系(门诊先证者中有20例,多病例组中有7例)。这些同胞关系中的先证者RA发病年龄比其患病母亲年轻(门诊样本中分别为38.3岁(95%置信区间(CI)33.8至42.8)和53.7岁(47.3至60.0)(p = 0.002);多病例家系中分别为32.4岁(25.3至39.6)和43.4岁(29.0至57.9)(p = 0.1))。在母亲患RA的组中,先证者受孕时母亲和父亲的年龄均与先证者疾病发病年龄呈显著负相关(门诊样本中r分别为-0.65,p = 0.002和r = -0.60,p = 0.005),并与线性回归系数相关。在7对患病母亲-先证者对中,尽管病程较短且年龄较小,但先证者有疾病更严重的倾向。
这项初步分析表明,在母亲患有RA的家系中,遗传早现的特征以及与前突变模型一致的观察结果可能占主导。