Danzé P M, Colombel J F, Jacquot S, Loste M N, Heresbach D, Ategbo S, Khamassi S, Périchon B, Semana G, Charron D, Cézard J P
Laboratoire de Biochimie, Hôpital B., CH et U Lille, France.
Gut. 1996 Jul;39(1):69-72. doi: 10.1136/gut.39.1.69.
Published studies on the association between HLA class II genes and inflammatory bowel disease are contradictory perhaps because of the limited size and ethnic heterogeneity of the populations studied.
To compare the frequencies of HLA class II genes in a large number of French patients with Crohn's disease and in an ethnically matched control group.
344 patients (196 F, 148 M, mean age 23.6 years) with Crohn's disease were molecularly genotyped for the HLA-DQB1 and DRB1 alleles. The results were compared with those for an ethnically matched control population of 488 white adults.
There were two significant variations of alleles at the DQB1 locus: an increase in DQB10501 allele frequency (chi 2 = 10.6, corrected p value (pc) = 0.01, odds ratio (OR) = 1.61) and a decrease in DQB10602/0603 allele frequencies (chi 2 = 8.43, pc = 0.037, OR = 0.66). DRB1 analysis showed associations with three allelic variations: an increase in the frequencies of DRB101 (chi 2 = 12.86, pc = 0.003, OR = 1.75) and DRB107 alleles (chi 2 = 11.18, pc = 0.008, OR = 1.58) and a very significant decrease in that of the DRB1*03 allele (chi 2 = 19.7, pc = 9.10(-5), OR = 0.46).
The alleles DRB101 and DRB107 are associated with susceptibility to Crohn's disease. The strong negative association between the DRB103 allele and Crohn's disease suggests that the HLA-DRB103 allele mediates 'resistance' to Crohn's disease.
已发表的关于人类白细胞抗原(HLA)Ⅱ类基因与炎症性肠病之间关联的研究结果相互矛盾,这可能是由于所研究人群规模有限以及种族异质性所致。
比较大量法国克罗恩病患者与种族匹配的对照组中HLAⅡ类基因的频率。
对344例克罗恩病患者(196例女性,148例男性,平均年龄23.6岁)进行HLA - DQB1和DRB1等位基因的分子基因分型。将结果与488名白人成年人的种族匹配对照人群的结果进行比较。
DQB1位点存在两个显著的等位基因变异:DQB10501等位基因频率增加(卡方值=10.6,校正P值(pc)=0.01,优势比(OR)=1.61),DQB10602/0603等位基因频率降低(卡方值=8.43,pc =0.037, OR =0.66)。DRB1分析显示与三个等位基因变异有关联:DRB101(卡方值=12.86,pc =0.003,OR =1.75)和DRB107等位基因频率增加(卡方值=11.18,pc =0.008,OR =1.58),DRB1*03等位基因频率非常显著降低(卡方值=19.7,pc =9.10(-5),OR =0,46)。
DRB01和DRB107等位基因与克罗恩病易感性相关。DRB103等位基因与克罗恩病之间的强负相关表明HLA - DRB103等位基因介导对克罗恩病的“抵抗”。