Ozyilmaz Ezgi, Ozturk Ozlem Goruroglu, Durmaz Ali, Othman Hasan Orhan, Guzelbaba Bugra, Seydaoglu Gulsah, Kuleci Sedat, Hanta Ismail, Erken Eren, Kocabas Ali
Cukurova University Faculty of Medicine, Department of Pulmonary Disease, Adana, Turkey.
Cukurova University Faculty of Medicine, Department of Medical Biochemistry, Adana, Turkey.
Sarcoidosis Vasc Diffuse Lung Dis. 2018;35(3):184-191. doi: 10.36141/svdld.v35i3.6781. Epub 2018 Apr 28.
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-DRB114 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 DRB114 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. .
多种HLA - DR等位基因已被证明与结节病的疾病表型或肺外受累有关,然而,其对不同种族群体中疾病不缓解的影响尚未完全明确。本研究的目的是调查疾病特征和HLA - DRB1等位基因是否可以早期反映结节病的不缓解情况。本研究纳入了1993年至2012年间在库库洛瓦大学医学院胸科疾病科确诊并随访至2017年6月的91例患者。所有患者均采用序列特异性寡核苷酸探针(SSOP)法进行HLA分析。其中15例因失访(n = 6)和诊断后未满5年(n = 9)被排除在研究组之外。5年时的完全缓解根据预先定义的标准标准(ACCESS)进行定义。缓解率为51.3%。未缓解患者的HLA - DRB114等位基因显著更高(11.8%对1.3%)(p = 0.006)。根据多因素逻辑回归分析,不缓解的独立危险因素为女性(OR:12.6;95%CI:2.1 - 74.9,p = 0.005)、HLA DRB114等位基因(OR:51.9;95%CI:3.6 - 735.8,p = 0.000)、基线TLCO<75%(预测值)(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)和基线时晚期(OR:8.3;95%CI:1.9 - 35.4,p = 0.001)。HLA - DRB1*14等位基因、较低的基线TLCO、晚期、女性性别或肺外受累的存在可预测结节病的长期不缓解。长期预后的早期预测可能会影响治疗决策,并避免这些患者群体的进一步恶化。