2007
DOI: 10.1111/j.1399-0039.2007.00904.x
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HLA class I and class II frequencies in patients with sarcoidosis from Croatia: role of HLA‐B8, −DRB1*0301, and −DQB1*0201 haplotype in clinical variations of the disease

Abstract: Sarcoidosis is an immune-mediated, multiorgan, granulomatous disease triggered by a combination of environmental and genetic factors. Numerous studies have reported about an association of human leukocyte antigen (HLA) alleles with sarcoidosis, with variation of alleles in different ethnic groups. Therefore, we investigated 142 Croatian sarcoidosis patients treated at the University Hospital for Lung Diseases Jordanovac, Zagreb, Croatia. Diagnosis was based on the presence of typical clinical features, chest X… Show more

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Cited by 18 publications
(13 citation statements)
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“…Previously, in various Caucasian populations, DRB1*15 and the haplotype HLA-DRB1*15:01-DQB1*06:02 have been demonstrated to be associated with the persistent form of sarcoidosis [11,15,[17][18][19]36,37]. In this study the persistent subgroup exhibited only nominal association with the DRB1*15:01 allele.…”
Section: Discussionmentioning
confidence: 53%
“…Previously, in various Caucasian populations, DRB1*15 and the haplotype HLA-DRB1*15:01-DQB1*06:02 have been demonstrated to be associated with the persistent form of sarcoidosis [11,15,[17][18][19]36,37]. In this study the persistent subgroup exhibited only nominal association with the DRB1*15:01 allele.…”
Section: Discussionmentioning
confidence: 53%
“…In sarcoidosis, there are reports about associations to both HLA class I and II genes as well as to non‐HLA genes . The role of linkage disequilibrium (LD), defined as the tendency for genetic variants located close to each to be associated within a population more often than if they were unlinked, has been discussed in sarcoidosis as well as in other diseases.…”
Section: Discussionmentioning
confidence: 99%
“…Some results have been demonstrated across studies and different racial and ethnic groups. For example, HLA-DRB1*03 has been consistently associated with spontaneous resolution and mild disease as demonstrated in Swedish [56], Polish [73], Croatian [74], Czech [75], and Finish populations [76]. A striking influence of DRB1*03 on the disease course has been shown in a distinct subgroup of sarcoidosis patients, with Löfgren's syndrome [18].…”
Section: Geneticsmentioning
confidence: 99%