Venkateshwari A, Vidyasagar A, Prasad R, Pratap B, Pratibha N
Department of Genetics, Osmania University, Hyderabad, India.
Hum Genet. 1997 Dec;101(2):201-4. doi: 10.1007/s004390050614.
To date, there have been few studies on pepsinogen polymorphism. The present study examines the polymorphism of pepsinogen by PAGE in 155 duodenal ulcer cases and 92 control subjects. The Indian population presents a higher frequency of the B phenotype (associated with absence of the pg 5 fraction) and the C haplotype compared to other populations. Heterozygotes, in particular AC phenotypic individuals, are found to be associated significantly with the disease compared to control subjects. All the genes of the multigene complex controlling pepsinogen polymorphism seem to be interacting, thereby leading to such an association. Thus, studies at the gene level may be helpful in explaining the genetic etiology and heterogeneity of duodenal ulcer disease.
迄今为止,关于胃蛋白酶原多态性的研究很少。本研究通过聚丙烯酰胺凝胶电泳(PAGE)检测了155例十二指肠溃疡患者和92例对照者的胃蛋白酶原多态性。与其他人群相比,印度人群中B表型(与缺乏pg 5组分相关)和C单倍型的频率较高。与对照者相比,杂合子,特别是AC表型个体,与该疾病显著相关。控制胃蛋白酶原多态性的多基因复合体的所有基因似乎都在相互作用,从而导致了这种关联。因此,基因水平的研究可能有助于解释十二指肠溃疡疾病的遗传病因和异质性。