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Early prediction of sarcoidosis prognosis with HLA typing: a 5 year follow-up study

机译:HLA分型对结节病预后的早期预测:一项为期5年的随访研究

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摘要

A wide range of HLA-DR alleles have been associated with sarcoidosis either in terms of disease phenotype or extra pulmonary involvement, however the effect on non-resolution in different ethnic groups is not fully understood. The aim of this study was to investigate whether disease characterics and HLA-DRB1 alleles may early reflect non resolution in sarcoidosis. 91 patients who were diagnosed in Cukurova University Faculty of Medicine Department of Chest Diseases between 1993-2012 and were followed up until June 2017 were included in the study. All patients underwent HLA analysis by the Sequence Specific Oligonucleotide Prob (SSOP) method. Fifteen of them were excluded from the study group due to lost of follow-up (n=6) and not yet passed 5 years since diagnosis (n=9). Complete resolution at 5 year was defined according to the predefined standard criteria (ACCESS). The resolution rate was 51.3%. The HLA-DRB1*14 allele was significantly higher in patients without resolution (11.8 vs 1.3%)(p=0.006). According to multivariate logistic regression analysis the independent risk factors of non resolution were female gender (OR: 12.6; 95%CI: 2.1-74.9, p=0.005), HLA DRB1*14 allele (OR:51.9; 95%CI: 3.6-735.8, p=0.000), baseline TLCO<75%(predicted) (OR:3.8; 95%CI: 1.1-13.7, p=0.028), extra-pulmonary involvement (OR:3.7; 95%CI: 1.0-13.1, p=0.038) and advanced stage at baseline (OR: 8.3; 95%CI: 1.9-35.4, p=0.001). HLA-DRB1*14 alleles, lower baseline TLCO, advanced stage, female gender or the presence of extra-pulmonary involvement could predict long term non-resolution in sarcoidosis. Early prediction of long term prognosis may affect treatment decisions and avoid further deterioration in these patient groups.
机译:就疾病表型或肺外受累而言,广泛的HLA-DR等位基因已与结节病相关,但是对不同种族对非分辨力的影响尚不完全清楚。这项研究的目的是调查疾病特征和HLA-DRB1等位基因是否可能早期反映结节病的不消退。该研究纳入了1993年至2012年之间在库库洛娃大学医学院胸部疾病系诊断并随访至2017年6月的91例患者。所有患者均通过序列特异性寡核苷酸概率(SSOP)方法进行了HLA分析。其中有15例由于失访而被排除在研究组之外(n = 6),并且自诊断以来还没有通过5年(n = 9)。根据预定义的标准标准(ACCESS)定义了5年时的完全分辨率。分辨率为51.3%。在没有分辨力的患者中,HLA-DRB1 * 14等位基因显着更高(11.8 vs 1.3%)(p = 0.006)。根据多因素logistic回归分析,无法解决的独立危险因素是女性(OR:12.6; 95%CI:2.1-74.9,p = 0.005),HLA DRB1 * 14等位基因(OR:51.9; 95%CI:3.6- 735.8,p = 0.000),基线TLCO <75%(预测)(OR:3.8; 95%CI:1.1-13.7,p = 0.028),肺外受累(OR:3.7; 95%CI:1.0-13.1, p = 0.038)和基线晚期(OR:8.3; 95%CI:1.9-35.4,p = 0.001)。 HLA-DRB1 * 14等位基因,基线TLCO较低,晚期,女性或肺外受累可预测结节病的长期不消退。长期预后的早期预测可能会影响治疗决策,并避免这些患者组进一步恶化。

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