Toussirot E, Tiberghien P, Balblanc J C, Kremer P, Despaux J, Dupond J L, Wendling D
Department of Rheumatology, University Hospital J. Minjoz, Besançon, France.
Rheumatol Int. 1998;17(6):233-6. doi: 10.1007/s002960050040.
Rheumatoid nodulosis (RN) is a rare condition associating rheumatoid nodules, episodes of arthritis, cystic bone lesions and, generally, positive rheumatoid factors (RF). It is considered a benign variant of rheumatoid arthritis (RA). In this study, we determined the HLA DRB1* alleles of our RN patients and compared the distribution of these alleles to those of 74 healthy controls and 104 RA patients with and without nodules. Four RN patients were observed. All had subcutaneous nodules and RF were negative in three patients. Of the 104 RA patients, 18 had nodules (nodRA). Systemic manifestation (including vasculitis, peripheral neuropathy or lung involvement) were found in seven of these nodRA cases (33.8%) and most had positive RF and erosive changes on X-rays. Only one RN patient had a RA-associated allele (DRB10101). The frequencies of the HLA DRB1 alleles encompassing the "rheumatoid" shared epitope were similar to those of other RA series: *0101, 34.6% (P = 0.03 compared with controls); *0401, 26.9% (P < 0.0001); *0404, 12.5% (P = 0.04); *0405, 4.8% (P = 0.8); *1001, 8.6% (P = 0.5). Of the nodRA and seronegative RA patients, 77.7% and 53.3%, respectively, presented the shared epitope. Thus, there was a tendency to decreased expression of the RA-associated alleles in RN (25%) compared with nodRA and seronegative RA patients. This study is restricted by the small number of tested RN patients, but the results suggest that the RA-associated alleles are poorly expressed in RN.
类风湿结节病(RN)是一种罕见病症,伴有类风湿结节、关节炎发作、囊性骨病变,且通常类风湿因子(RF)呈阳性。它被认为是类风湿关节炎(RA)的一种良性变体。在本研究中,我们测定了RN患者的HLA DRB1等位基因,并将这些等位基因的分布与74名健康对照者以及104名有或无结节的RA患者的等位基因分布进行比较。观察到4例RN患者。所有患者均有皮下结节,3例患者RF呈阴性。在104例RA患者中,18例有结节(结节性RA)。这些结节性RA病例中有7例(33.8%)出现全身表现(包括血管炎、周围神经病变或肺部受累),且大多数患者RF呈阳性,X线有侵蚀性改变。只有1例RN患者具有与RA相关的等位基因(DRB10101)。包含“类风湿”共享表位的HLA DRB1*等位基因频率与其他RA系列相似:*01⁰¹,34.6%(与对照相比,P = 0.03);*04⁰¹,26.9%(P < 0.0001);*04⁰⁴,12.5%(P = 0.04);*04⁰⁵,4.8%(P = 0.8);*10⁰¹,8.6%(P = 0.5)。在结节性RA和血清阴性RA患者中,分别有77.7%和53.3%呈现共享表位。因此,与结节性RA和血清阴性RA患者相比,RN中与RA相关等位基因的表达有降低趋势(25%)。本研究受限于检测的RN患者数量较少,但结果表明与RA相关的等位基因在RN中表达不佳。