Marzin Pauline, Cormier-Daire Valérie
Clinical Genetics, INSERM UMR 1163, Paris Descartes-Sorbonne Paris Cité University, IMAGINE Institute, Necker Enfants Malades Hospital, Paris, France.
Clinical Genetics, INSERM UMR 1163, Paris Descartes-Sorbonne Paris Cité University, IMAGINE Institute, Necker Enfants Malades Hospital, 149 rue de sevres, Paris, 75015, France.
Ther Adv Endocrinol Metab. 2020 Mar 3;11:2042018820904016. doi: 10.1177/2042018820904016. eCollection 2020.
The last few decades have been marked by the identification of numerous genes implicated in genetic disorders, helping in the elucidation of the underlying pathophysiology of these conditions. This has allowed new therapeutic approaches to emerge such as cellular therapy, gene therapy, or pharmacological therapy for various conditions. Skeletal dysplasias are good models to illustrate these scientific advances. Indeed, several therapeutic strategies are currently being investigated in osteogenesis imperfecta; there are ongoing clinical trials based on pharmacological approaches, targeting signaling pathways in achondroplasia and fibrodysplasia ossificans progressiva or the endoplasmic reticulum stress in metaphyseal dysplasia type Schmid or pseudoachondroplasia. Moreover, the treatment of hypophosphatasia or Morquio A disease illustrates the efficacy of enzyme drug replacement. To provide a highly specialized multidisciplinary approach, these treatments are managed by reference centers. The emergence of treatments in skeletal dysplasia provides new perspectives on the prognosis of these severe conditions and may change prenatal counseling in these diseases over the coming years.
过去几十年的特点是发现了许多与遗传疾病相关的基因,这有助于阐明这些疾病的潜在病理生理学。这使得针对各种病症的新治疗方法得以出现,如细胞治疗、基因治疗或药物治疗。骨骼发育异常是说明这些科学进展的良好模型。事实上,目前正在成骨不全症中研究几种治疗策略;基于药物方法的临床试验正在进行,这些试验针对软骨发育不全、进行性骨化性纤维发育不良中的信号通路,或施密德型干骺端发育异常或假性软骨发育不全中的内质网应激。此外,低磷血症或莫尔基奥A病的治疗说明了酶替代药物的疗效。为了提供高度专业化的多学科方法,这些治疗由参考中心管理。骨骼发育异常治疗方法的出现为这些严重病症的预后提供了新的视角,并可能在未来几年改变这些疾病的产前咨询。