predisposition to crohn disease (CD) seems to be genetically determined bur, though several reports on the matter, the association between HLA antigens and the disease is still controversial. PCR-SSP high resolution typing in 107 CD patients, and in subgroups selected according to clinical features, showed a positive association with the rare haplotype DRB1*07, DQB1*0303 both in the overall patients (p = 0.002; pc = ns) and in the subgroup of nonfistulized patients (p = 0.0008; pc = 0.032). moreover, the protective role of the haplotype DRB1*03, DQB1*0201 (p = 0.029) was confirmed also in Italian patients, whereas no strong association with HLA class I alleles has been found. In addition, variability of the HLA alleles frequency in CD subgroups was observed, supporting the hypothesis of a genetic heterogeneity of thr disease and suggesting that HLA alleles distribution in selected groups may allow to identify patients with probably different prognosis or associated complications. (C) american society for histocompatibility and Immunogenetics, 2001.
Lombardi, M.l., Pirozzi, G., Luongo, V., Mercuro, O., Pace, E., Del Vecchio Blanco, G., et al. (2001). Crohn disease: Susceptibility and disease heterogeneity revealed by HLA genotyping. HUMAN IMMUNOLOGY, 62(7), 701-704 [10.1016/S0198-8859(01)00259-2].
Crohn disease: Susceptibility and disease heterogeneity revealed by HLA genotyping
Del Vecchio Blanco, G.;
2001-01-01
Abstract
predisposition to crohn disease (CD) seems to be genetically determined bur, though several reports on the matter, the association between HLA antigens and the disease is still controversial. PCR-SSP high resolution typing in 107 CD patients, and in subgroups selected according to clinical features, showed a positive association with the rare haplotype DRB1*07, DQB1*0303 both in the overall patients (p = 0.002; pc = ns) and in the subgroup of nonfistulized patients (p = 0.0008; pc = 0.032). moreover, the protective role of the haplotype DRB1*03, DQB1*0201 (p = 0.029) was confirmed also in Italian patients, whereas no strong association with HLA class I alleles has been found. In addition, variability of the HLA alleles frequency in CD subgroups was observed, supporting the hypothesis of a genetic heterogeneity of thr disease and suggesting that HLA alleles distribution in selected groups may allow to identify patients with probably different prognosis or associated complications. (C) american society for histocompatibility and Immunogenetics, 2001.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
