期刊论文详细信息
American journal of clinical and experimental immunology
Association of HSP90B1 genetic polymorphisms with efficacy of glucocorticoids and improvement of HRQoL in systemic lupus erythematosus patients from Anhui Province
Shuang Liu1  Sheng-Xiu Liu2  Sheng-Qian Xu3  Xiu-Xiu Sun4  Su-Su Li5  Fa-Ming Pan6  Yuan-Yuan Gu7  Qiao-Mei Xie8  Jin-Hui Tao9  Jian-Hua Xu1,10  Man Zhang1,11 
[1] Department of Biochemistry and Molecular Biology, School of Basic Medicine, Anhui Medical University, Hefei 230032, Anhui, China;Department of Clinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui, China;Department of Clinical Laboratory, The Second Affiliated Hospital of Anhui Medical University, Hefei 230601, Anhui, China;Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei 230032, Anhui, China;Department of Laboratory Medicine, School of Public Health, Anhui Medical University, Hefei 230032, Anhui, China;Department of Nephrology, The Second Affiliated Hospital of Anhui Medical University, Hefei 230601, Anhui, China;Department of Rheumatology and Immunology, Anhui Medical University Affiliated Provincial Hospital, Hefei 230001, Anhui, China;Department of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui, China;Department of Rheumatology and Immunology, The Second Affiliated Hospital of Anhui Medical University, Hefei 230601, Anhui, China;Institute of Dermatology and Department of Dermatology, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui, China;The Key Laboratory of Major Autoimmune Diseases, Hefei 230032, Anhui, China
关键词: Systemic lupus erythematosus;    HSP90B1;    polymorphism;    glucocorticoids;    health-related quality of life;   
DOI  :  
学科分类:过敏症与临床免疫学
来源: e-Century Publishing Corporation
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【 摘 要 】

Objective: The aim of this study was to investigate the associations between HSP90B1 gene polymorphisms and the efficacy of glucocorticoids (GCs) and the improvement of health-related quality of life (HRQoL) in Anhui patients with systemic lupus erythematosus (SLE). Method: A total of 305 patients with SLE were recruited to the study. These patients were treated with GCs for 12 weeks and classified into two groups (sensitivity and insensitivity) according to the response to GCs measured by the scores on SLE disease activity index (SLEDAI). The HRQoL of SLE patients were evaluated by 36-item Short Form Health Survey (SF-36) at baseline and 12 weeks respectively. HapMap database and Haploview software were used to select HSP90B1 gene tag single nucleotide polymorphisms (SNPs). Benjamini & Hochberg (BH) method based on false discovery rate (FDR) was used for multiple testing correction. Results: A total of 291 patients were included in final data analysis with 14 patients excluded due to loss to follow-up. Among these patients, 160 patients were sensitive to GCs and 131 patients were insensitive to GCs. Twelve tag SNPs of HSP90B1 gene were selected. The rs12426382 polymorphism was associated with the efficacy of GCs (dominant model: crude OR=0.514, 95% CI=0.321-0.824, P=0.006; adjusted OR=0.513, 95% CI=0.317-0.831, P=0.007). After BH correction, there was no association between rs12426382 polymorphism and efficacy of GCs (PBH=0.084). In haplotype analysis, the haplotype CCCGAACATCCC (OR=2.273, 95% CI=1.248-4.139, P=0.006) and CTGGGACGTTC (OR=0.436, 95% CI=0.208-0.916, P=0.025) showed significant associations with the efficacy of GCs. After corrected by BH method, CCCGAACATCCC was still associated with the efficacy of GCs (PBH=0.048). The rs3794241, rs1165681, rs2722188, rs3794240 and rs10861147 polymorphisms were associated with the improvement of HRQoL among SLE patients (P < 0.05). But no association existed after the correction of BH method (P > 0.05). Conclusions: The results of this study demonstrated that HSP90B1 genetic polymorphisms might be associated with the efficacy of GCs, but not associated with the improvement of HRQoL in Anhui population with SLE.

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