Maharaj B, Hammond M G, Appadoo B, Leary W P, Pudifin D J
Circulation. 1987 Aug;76(2):259-61. doi: 10.1161/01.cir.76.2.259.
To determine whether genetic factors could be involved in the pathogenesis of rheumatic heart disease, we performed HLA-A and HLA-B typing in 120 black patients with severe chronic rheumatic heart disease requiring cardiac surgery, and HLA-DR and HLA-DQ typing in 103 and 97 of these patients, respectively. The HLA typing was done by a standard microlymphocytotoxicity method. Patients were 12 to 60 years old (mean 27.6 +/- 14.5). No differences in HLA-A, HLA-B, and HLA-DQ frequencies between patients and controls were noted. HLA-DR 1 antigen was present in 12.6% of patients compared with 2.7% of normal control subjects (corrected p less than .045; relative risk = 5.2) and the HLA-DRw6 antigen was present in 31.1% of patients compared with 15% of control subjects (corrected p less than .045; relative risk = 2.6). These findings suggest that genetically determined immune-response factors may play a role in the pathogenesis of severe chronic rheumatic heart disease.
为了确定遗传因素是否可能参与风湿性心脏病的发病机制,我们对120例需要心脏手术的重度慢性风湿性心脏病黑人患者进行了HLA - A和HLA - B分型,对其中103例和97例患者分别进行了HLA - DR和HLA - DQ分型。HLA分型采用标准的微量淋巴细胞毒性方法。患者年龄在12至60岁之间(平均27.6 +/- 14.5)。未发现患者与对照组之间HLA - A、HLA - B和HLA - DQ频率存在差异。12.6%的患者存在HLA - DR 1抗原,而正常对照受试者中这一比例为2.7%(校正p值小于0.045;相对风险 = 5.2);31.1%的患者存在HLA - DRw6抗原,而对照受试者中这一比例为15%(校正p值小于0.045;相对风险 = 2.6)。这些发现表明,基因决定的免疫反应因素可能在重度慢性风湿性心脏病的发病机制中起作用。