Kobayashi Y, Chen X M, Hiki Y, Fujii K, Kashiwagi N
Kidney Int. 1985 Aug;28(2):193-7. doi: 10.1038/ki.1985.140.
The HLA systems of forty Japanese patients with adult-onset nephrotic syndrome and biopsy-proven minimal change were investigated. HLA-DRw8 was found in 35% of the patients and HLA-DQw3 in 95%, compared to 12.6 and 63.1% of the control, respectively (DRw8: and Pc less than 0.01, RR = 3.74; DQw3: Pc less than 0.02, RR = 11.1). The phenotype frequencies of all but one HLA-DR antigens, DR4, DR5, DRw8, and DRw9 associating with DQw3, were observed to increase (patient vs. control: DR4, 65 vs. 41.4%; DR5, 10 vs. 4.3%; DRw9, 20 vs. 23%). These results suggest that HLA-DQw3 may be a primary genetic marker associated with a major susceptibility gene to adult-onset minimal change nephrotic syndrome in the Japanese population.
对40例经活检证实为微小病变的日本成年肾病综合征患者的HLA系统进行了研究。在35%的患者中发现了HLA-DRw8,在95%的患者中发现了HLA-DQw3,而对照组的这一比例分别为12.6%和63.1%(DRw8:Pc小于0.01,RR = 3.74;DQw3:Pc小于0.02,RR = 11.1)。观察到除一种HLA-DR抗原(与DQw3相关的DR4、DR5、DRw8和DRw9)外,所有其他HLA-DR抗原的表型频率均升高(患者与对照组相比:DR4,65%对41.4%;DR5,10%对4.3%;DRw9,20%对23%)。这些结果表明,HLA-DQw3可能是与日本人群成年起病微小病变肾病综合征主要易感基因相关的主要遗传标记。