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Use of biomarkers in the management of children with lupus

机译:使用生物标志物治疗狼疮患儿

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摘要

Childhood systemic lupus erythematosus (SLE) is known to have a worse prognosis than adult-onset disease, and monitoring and treatment of the disease are still a challenge. Thus, there is an urgent need for highly reliable, noninvasive biomarkers for early detection of relapses, to avoid long-term complications and to optimize the management of children with LN. Recent studies of pediatric patients have yielded novel specific biomarkers for SLE diagnosis which can be used for monitoring disease activity and response to treatment. The most promising biomarkers in juvenile-onset SLE include cell-bound complement activation products, some genomic profiles, and urinary proteins such as neutrophil gelatinase-associated lipocalin, monocyte chemoattractant protein-1, and alpha-1-acid glycoprotein. None of these might be suitable for use as a single SLE-biomarker. More likely a combination of novel biomarkers with traditionally used data, including autoantibodies and complement, might help to enhance sensitivity and specificity for early diagnosis, disease monitoring, and prediction of relapses.cp.
机译:已知儿童系统性红斑狼疮(SLE)的预后要比成人发病的疾病差,对疾病的监测和治疗仍然是一个挑战。因此,迫切需要高度可靠的非侵入性生物标志物,以及早发现复发,避免长期并发症并优化LN儿童的治疗。儿科患者的最新研究已经产生了用于SLE诊断的新型特异性生物标志物,可用于监测疾病活动和对治疗的反应。少年期SLE中最有前途的生物标志物包括细胞结合的补体激活产物,一些基因组图谱和尿蛋白,例如中性粒细胞明胶酶相关的脂蛋白,单核细胞趋化蛋白1和α-1酸性糖蛋白。这些都不适合用作单个SLE生物标记。新型生物标志物与包括自身抗体和补体在内的传统数据结合使用,可能有助于提高早期诊断,疾病监测和复发预测的敏感性和特异性。

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