Marelich G P, Cross C E
Dept of Internal Medicine, UC Davis School of Medicine, Sacramento, 95817, USA.
West J Med. 1996 Apr;164(4):321-34.
The Cystic Fibrosis Foundation currently tracks about 20,000 Americans with cystic fibrosis, an autosomal recessive genetic disease that leads to multisystem complications. With the institution of better therapeutic regimens over the past 2 decades, more patients with this disease are surviving to adulthood. Within the past decade, both clinical and basic science research in the field of cystic fibrosis has progressed at a rapid rate. The intent of this review is to introduce readers to the molecular, cellular, and systemic disorders of this disease. We discuss treatment strategies involving antibiotics, nutrition, immune-response mediators, chest physiotherapy, and sputum-active agents with respect to the airway dysfunction of cystic fibrosis. Other common complications, recent developments, transplantation, and gene therapy are also reviewed.
囊性纤维化基金会目前追踪着约2万名患有囊性纤维化的美国人,这是一种常染色体隐性遗传病,可导致多系统并发症。在过去20年中,随着更好治疗方案的实施,更多患有这种疾病的患者存活至成年。在过去十年中,囊性纤维化领域的临床和基础科学研究都取得了快速进展。本综述旨在向读者介绍这种疾病的分子、细胞和全身紊乱情况。我们针对囊性纤维化的气道功能障碍,讨论了涉及抗生素、营养、免疫反应介质、胸部物理治疗和痰液活性剂的治疗策略。其他常见并发症、最新进展、移植和基因治疗也在本文中进行了综述。