TY - JOUR
T1 - Analysis of IL6 and IL1A gene polymorphisms in UK and Dutch patients with sarcoidosis
AU - Grutters, Jan C.
AU - Sato, Hiroe
AU - Pantelidis, Panagiotis
AU - Ruven, Henk J.T.
AU - McGrath, Deirdre S.
AU - Wells, Athol U.
AU - Van den Bosch, Jules M.M.
AU - Welsh, Kenneth I.
AU - Du Bois, Roland M.
PY - 2003/3
Y1 - 2003/3
N2 - Background: Proinflammatory cytokines are a major determinant in the inflammatory events leading to sarcoidosis. Genetic variations in the genes encoding these cytokines might contribute to sarcoidosis susceptibility, disease severity and outcome. Methods: In the present study we genotyped two clinically well-defined cohorts of Caucasian sarcoidosis patients from different European countries (each with their own controls) for the following polymorphisms using SSP-PCR: IL6-174(G/C), IL6 intron 4(A/G) and IL1A-889(C/T). In total, 516 individuals were studied (147 UK + 102 Dutch patients, 101 UK + 166 Dutch controls). Disease severity data at presentation included chest radiographic stage, FVC, DLCO, and extrapulmonary manifestations. Disease progression was evaluated on follow-up chest radiographs and sequential lung function measurements (2, 4 years). Results: No differences in genotype, carriage and allele frequencies of the investigated polymorphisms were found in either of the populations. Analysis of genotype data in relation to disease severity data, however, showed a slightly increased carrier frequency of the rarer -174C allele in patients with Stage IV sarcoidosis (p = 0.03, pc = 0.09). Pulmonary function progression analysis did not reveal significant associations. Conclusions: Although the investigated polymorphisms are unlikely to contribute to sarcoidosis susceptibility, the IL6-174C allele might have a role in the genetics underlying sarcoidosis severity or the progression towards pulmonary fibrosis in a particular subgroup.
AB - Background: Proinflammatory cytokines are a major determinant in the inflammatory events leading to sarcoidosis. Genetic variations in the genes encoding these cytokines might contribute to sarcoidosis susceptibility, disease severity and outcome. Methods: In the present study we genotyped two clinically well-defined cohorts of Caucasian sarcoidosis patients from different European countries (each with their own controls) for the following polymorphisms using SSP-PCR: IL6-174(G/C), IL6 intron 4(A/G) and IL1A-889(C/T). In total, 516 individuals were studied (147 UK + 102 Dutch patients, 101 UK + 166 Dutch controls). Disease severity data at presentation included chest radiographic stage, FVC, DLCO, and extrapulmonary manifestations. Disease progression was evaluated on follow-up chest radiographs and sequential lung function measurements (2, 4 years). Results: No differences in genotype, carriage and allele frequencies of the investigated polymorphisms were found in either of the populations. Analysis of genotype data in relation to disease severity data, however, showed a slightly increased carrier frequency of the rarer -174C allele in patients with Stage IV sarcoidosis (p = 0.03, pc = 0.09). Pulmonary function progression analysis did not reveal significant associations. Conclusions: Although the investigated polymorphisms are unlikely to contribute to sarcoidosis susceptibility, the IL6-174C allele might have a role in the genetics underlying sarcoidosis severity or the progression towards pulmonary fibrosis in a particular subgroup.
KW - IL-1
KW - IL-6
KW - Polymorphism (genetics)
KW - Prognosis
KW - Sarcoidosis
UR - http://www.scopus.com/inward/record.url?scp=0037540060&partnerID=8YFLogxK
M3 - Article
C2 - 12737276
AN - SCOPUS:0037540060
SN - 1124-0490
VL - 20
SP - 20
EP - 27
JO - Sarcoidosis Vasculitis and Diffuse Lung Diseases
JF - Sarcoidosis Vasculitis and Diffuse Lung Diseases
IS - 1
ER -