Divisions of Pediatric Endocrinology, University of Minnesota, Minneapolis, Minnesota, USA.
Curr Opin Endocrinol Diabetes Obes. 2010 Aug;17(4):335-41. doi: 10.1097/MED.0b013e32833a780d.
To provide an updated literature review highlighting important aspects of cystic fibrosis-related diabetes (CFRD) including epidemiology, pathogenesis, complications, screening, and management.
Although CFRD continues to be associated with increased rates of mortality in the cystic fibrosis (CF) population, this has improved over the past several years, and the previous sex difference is no longer present. Recent studies support that CFRD is primarily caused by insulin deficiency due to loss of beta cells, which may occur via a number of mechanisms including oxidative stress. Aggressive screening programs with oral-glucose tolerance testing and early treatment with insulin for patients with CFRD with or without fasting hyperglycemia have led to improvements in nutritional states and lung function. Oral agents do not appear to be effective in CFRD.
CFRD is the most common comorbidity in the CF population and is associated with microvascular complications and protein catabolism leading to worse health outcomes. Recognition of glycemic abnormalities through aggressive screening has led to improvements in nutritional status, pulmonary function, and mortality rates.
提供囊性纤维化相关糖尿病(CFRD)的重要方面的最新文献综述,包括流行病学、发病机制、并发症、筛查和管理。
尽管 CFRD 仍与囊性纤维化(CF)人群的死亡率增加相关,但近年来有所改善,并且以前的性别差异不再存在。最近的研究支持 CFRD 主要是由于β细胞丧失导致的胰岛素缺乏引起的,这可能通过多种机制发生,包括氧化应激。通过口服葡萄糖耐量试验进行积极的筛查计划,并对有或没有空腹高血糖的 CFRD 患者早期使用胰岛素治疗,导致营养状况和肺功能得到改善。口服药物似乎对 CFRD 无效。
CFRD 是 CF 人群中最常见的合并症,与微血管并发症和蛋白质分解代谢有关,导致健康状况恶化。通过积极筛查发现血糖异常,可改善营养状况、肺功能和死亡率。