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Genetic predictors of systemic sclerosis-associated interstitial lung disease: a review of recent literature

机译:全身硬化相关间质肺病遗传预测因子:近期文学综述

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摘要

The interplay between genetic and environmental factors is likely involved in the pathogenesis of systemic sclerosis (SSc). Interstitial lung disease associated in the context of SSc (SSc-ILD)is associated with significant morbidity, and is the leading cause of death in SSc. The spectrum of SSc-ILD severity is wide, ranging from patients with only limited and inherently stable pulmonary involvement, to those with extensive and progressive pulmonary fibrosis. In order to provide accurate prognostic information for patients, and to initiate appropriate monitoring and treatment regimens, the ability to identify patients at risk of developing severe ILD early in the disease course is crucial. Identification of genetic variants involved in disease pathogenesis can not only potentially provide diagnostic/prognostic markers, but can also highlight dysregulated molecular pathways for therapeutic targeting. A number of genetic associations have been established for susceptibility to SSc, but far fewer studies have investigated genetic susceptibility to SSc-ILD specifically. In this review we present a summary of the studies assessing genetic associations with SSc-ILD.
机译:遗传和环境因素之间的相互作用可能参与全身硬化症(SSC)的发病机制。在SSC(SSC-ILD)背景下相关的间质肺病与显着的发病率有关,是SSC中死亡的主要原因。 SSC-ILD严重程度的频谱宽,患者仅限于仅限有限和本质上稳定的肺部受累,对具有广泛和逐渐进行的肺纤维化的患者。为了为患者提供准确的预后信息,并开始适当的监测和治疗方案,鉴定疾病过程早期患者患有严重ILD风险的能力至关重要。鉴定疾病发病机制涉及的遗传变异不能仅潜在提供诊断/预后标志物,但也可以突出用于治疗性靶向的失调分子途径。已经建立了许多遗传关联对SSC的易感性,但研究更少,研究了对SSC-ILD的遗传易感性。在本报告中,我们展示了评估与SSC-ILD的遗传关联的研究摘要。

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