囊性纤维化调节剂疗法。

IF 15.1 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Shijing Jia, Jennifer L Taylor-Cousar
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引用次数: 10

摘要

囊性纤维化(CF)是一种遗传性多系统疾病,可导致进行性支气管扩张、胰腺内分泌和外分泌功能不全、远端肠梗阻综合征、肝功能障碍等疾病。传统的治疗方法侧重于治疗或预防对每个器官系统的损害,如肺部的雾化药物,糖尿病的胰岛素和补充胰酶。然而,针对由个体基因突变引起的特异性囊性纤维化跨膜传导调节蛋白畸形的高效调节疗法的出现改变了CF患者的生活和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cystic Fibrosis Modulator Therapies.

Cystic fibrosis (CF) is an inherited multisystemic disease that can cause progressive bronchiectasis, pancreatic endocrine and exocrine insufficiency, distal intestinal obstruction syndrome, liver dysfunction, and other disorders. Traditional therapies focused on the treatment or prevention of damage to each organ system with incremental modalities such as nebulized medications for the lungs, insulin for diabetes, and supplementation with pancreatic enzymes. However, the advent of highly effective modulator therapies that target specific cystic fibrosis transmembrane conductance regulator protein malformations resulting from individual genetic mutations has transformed the lives and prognosis for persons with CF.

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来源期刊
Annual review of medicine
Annual review of medicine 医学-医学:内科
CiteScore
24.90
自引率
0.00%
发文量
58
期刊介绍: The Annual Review of Medicine, which has been published since 1950, focuses on important advancements in diverse areas of medicine. These include AIDS/HIV, cardiology, clinical pharmacology, dermatology, endocrinology/metabolism, gastroenterology, genetics, immunology, infectious disease, neurology, oncology/hematology, pediatrics, psychiatry, pulmonology, reproductive medicine, and surgery. The journal's current volume has transitioned from a gated access model to an open access model through the Annual Reviews' Subscribe to Open program. All articles published in the journal are now available under a CC BY license.
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