TRAF1-C5影响原发性胆汁性肝硬化患者的生活质量。

Clinical & Developmental Immunology Pub Date : 2013-01-01 Epub Date: 2013-04-28 DOI:10.1155/2013/510547
Joanna Raszeja-Wyszomirska, Ewa Wunsch, Agnieszka Kempinska-Podhorodecka, Daniel S Smyk, Dimitrios P Bogdanos, Malgorzata Milkiewicz, Piotr Milkiewicz
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引用次数: 9

摘要

背景:先前的研究报道了非hla免疫调节基因的特定等位基因与原发性胆汁性肝硬化(PBC)患者较高的疲劳评分之间的关联。目的:研究肿瘤坏死因子受体家族成员TRAF1-C5单核苷酸多态性与健康相关生活质量(HRQoL)变量的关系。患者和方法:分析120例白种人pbc中TRAF1-C5基因多态性rs2900180和rs3761847。采用SF-36、PBC-40和PBC-27问卷评估HRQoL。结果:rs2900180 TT基因型与SF-36结构域活力(P < 0.05)、心理健康(P < 0.05)、心理成分综合评分(P < 0.05)呈负相关。rs3761847 GG纯合子活力(P < 0.05)、心理健康(P < 0.05)、心理成分综合评分(P < 0.05)和社会功能障碍(P < 0.01)较低。等位基因分析表明,rs2900180的T等位基因和rs3761847的G等位基因分别与SF-36的活力(P < 0.05和P < 0.01)、社会功能(P < 0.05和P < 0.05)、心理健康(P < 0.01和P < 0.05)和心理成分综合评分(P < 0.01和P < 0.05)相关。基因分型和等位基因分析未发现与PBC-40和PBC-27结构域相关。结论:rs2900180和rs3761847多态性与HRQoL变量的关联表明TRAF1参与了PBC患者QoL受损的诱导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TRAF1-C5 affects quality of life in patients with primary biliary cirrhosis.

Background: Previous studies reported associations between specific alleles of non-HLA immunoregulatory genes and higher fatigue scores in patients with primary biliary cirrhosis (PBC).

Aim: To study the relationship between variables of health-related quality of life (HRQoL) and single nucleotide polymorphisms of TRAF1-C5, a member of the tumor necrosis factor receptor family.

Patients and methods: TRAF1-C5 gene polymorphisms, rs2900180 and rs3761847, were analysed in 120 Caucasian PBCs. The HRQoL was assessed with SF-36, PBC-40, and PBC-27 questionnaires.

Results: We found a negative association between TT genotype of rs2900180 and SF-36's domains vitality (P < 0.05), mental health (P < 0.05), and mental component summary score (P < 0.05). GG homozygotes of rs3761847 had lower vitality (P < 0.05), mental health (P < 0.05), mental component summary score (P < 0.05) and impairment of social functioning (P < 0.01). Allelic analysis has shown that T allele of rs2900180 and G allele of rs3761847 related to SF-36's vitality (P < 0.05 and P < 0.01), social functioning (P < 0.05 and P < 0.05), mental health (P < 0.01 and P < 0.05), and mental component summary score (P < 0.01 and P < 0.05), respectively. Genotyping and allelic analysis did not reveal correlation with PBC-40 and PBC-27 domains.

Conclusion: The association between rs2900180 and rs3761847 polymorphisms and HRQoL variables indicates that TRAF1 is involved in the induction of impaired QoL in PBC.

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