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Copy number variations and polymorphisms in HSP90AB1 and risk of systemic lupus erythematosus and efficacy of glucocorticoids

Identifieur interne : 000928 ( Main/Exploration ); précédent : 000927; suivant : 000929

Copy number variations and polymorphisms in HSP90AB1 and risk of systemic lupus erythematosus and efficacy of glucocorticoids

Auteurs : Man Zhang ; Yuanyuan Gu ; Shunwei Huang ; Qiuyue Lou ; Qiaomei Xie ; Zhiwei Xu ; Yangfan Chen ; Faming Pan ; Shengqian Xu ; Shengxiu Liu ; Jinhui Tao ; Shuang Liu ; Jing Cai ; Peiling Chen ; Long Qian ; Chunhuai Wang ; Chunmei Liang ; Hailiang Huang ; Haifeng Pan ; Hong Su ; Jian Cheng ; Yuzhou Zhang ; Wenbiao Hu ; Yanfeng Zou

Source :

RBID : PMC:6653051

Abstract

Abstract

The aim of our study was to assess the associations of HSP90AB1 copy number variations (CNVs) with systemic lupus erythematosus (SLE) risk and glucocorticoids (GCs) efficacy, as well as the relationship between HSP90AB1 single‐nucleotide polymorphisms (SNPs) and GCs efficacy. HSP90AB1 CNVs and SLE risk were analysed in 519 patients and 538 controls. Patients treated with GCs were followed up for 12 weeks and were divided into sensitive and insensitive groups to investigate the effects of CNVs (419 patients) and SNPs (457 patients) on the efficacy of GCs. Health‐related quality of life (HRQoL) was also measured by SF‐36 at baseline and week 12 to explore the relationship between CNVs/SNPs and HRQoL improvements in Chinese SLE patients. Our results indicated a statistically significant association between HSP90AB1 CNVs and SLE (PBH = 0.039), and this association was more pronounced in the female subgroup (PBH = 0.039). However, we did not detect association of HSP90AB1 CNVs/SNPs with efficacy of GCs. But we found a marginal association between SNP rs13296 and improvement in Role‐emotional, while this association was not strong enough to survive in the multiple testing corrections. Collectively, our findings suggest that the copy number of HSP90AB1 is associated with SLE susceptibility. But copy number and polymorphisms of HSP90AB1 may not be associated with efficacy of GCs.


Url:
DOI: 10.1111/jcmm.14410
PubMed: 31124601
PubMed Central: 6653051


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<title>Abstract</title>
<p>The aim of our study was to assess the associations of HSP90AB1 copy number variations (CNVs) with systemic lupus erythematosus (SLE) risk and glucocorticoids (GCs) efficacy, as well as the relationship between HSP90AB1 single‐nucleotide polymorphisms (SNPs) and GCs efficacy. HSP90AB1 CNVs and SLE risk were analysed in 519 patients and 538 controls. Patients treated with GCs were followed up for 12 weeks and were divided into sensitive and insensitive groups to investigate the effects of CNVs (419 patients) and SNPs (457 patients) on the efficacy of GCs. Health‐related quality of life (HRQoL) was also measured by SF‐36 at baseline and week 12 to explore the relationship between CNVs/SNPs and HRQoL improvements in Chinese SLE patients. Our results indicated a statistically significant association between HSP90AB1 CNVs and SLE (
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<name sortKey="Zhang, Man" sort="Zhang, Man" uniqKey="Zhang M" first="Man" last="Zhang">Man Zhang</name>
<name sortKey="Zhang, Yuzhou" sort="Zhang, Yuzhou" uniqKey="Zhang Y" first="Yuzhou" last="Zhang">Yuzhou Zhang</name>
<name sortKey="Zou, Yanfeng" sort="Zou, Yanfeng" uniqKey="Zou Y" first="Yanfeng" last="Zou">Yanfeng Zou</name>
</noCountry>
</tree>
</affiliations>
</record>

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