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Method of predicting rapid progression of fibrosis and therapy and reagents therefor

机译:预测纤维化和治疗迅速进展的方法及其试剂

摘要

This invention relates to molecular diagnostics and, more specifically DNA-based tests for the prognosis and/or monitoring of fibrotic disease progression in humans, and processes for stratifying patients based on their likely rates of fibrotic disease progression. The invention also relates to the field of therapy for fibrotic disease, based on such prognoses, monitoring and stratification results, such as in monitoring and/or stratifying and/or treating patients having a higher likelihood of rapid fibrotic disease progression.
机译:本发明涉及分子诊断,更具体地进行DNA的试验,用于对人类的预后和/或监测纤维化疾病进展的预后和/或监测,以及基于其可能的纤维化疾病进展的分层患者的方法。本发明还涉及纤维化疾病的治疗领域,基于这种预期,监测和分层结果,例如在监测和/或分层和/或治疗具有较高纤维化疾病进展的可能性患者的患者。

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