Clinical and psychosocial changes over late childhood and adolescence and early life determinants of long term clinical outcomes in cystic fibrosis

童年晚期和青春期的临床和社会心理变化以及囊性纤维化长期临床结果的早期生活决定因素

• 批准号: nhmrc : 1044829
• 负责人: A/Pr Richard Massie
• 金额: $ 78.41万
• 依托单位: The University of Queensland
• 依托单位国家: 澳大利亚
• 项目类别: Project Grants
• 财政年份: 2013
• 资助国家: 澳大利亚
• 起止时间: 2013-01-01 至 2017-12-31
• 项目状态: 已结题
• 来源: https://researchdata.edu.au/clinical-psychosocial-changes-cystic-fibrosis/111692
• 关键词: Clinical; psychosocial; changes; over; late

Cystic fibrosis is the most common life shortening inherited disease in Caucasians. Lung damage starts in infancy and lung function falls most rapidly in adolescence although why and how this happens and early life determinants are not known. This study takes advantage of a previous study that monitored young children from 3 months to 5 years of life and follows them closely through early adolescence to investigate the protective and risk factors for falling lung function.

囊性纤维化是高加索人最常见的缩短寿命的遗传性疾病。肺损伤开始于婴儿期，肺功能福尔斯下降最快的是在青春期，虽然为什么和如何发生这种情况和早期生活的决定因素尚不清楚。这项研究利用了以前的一项研究，该研究监测了3个月至5岁的幼儿，并密切跟踪他们到青春期早期，以调查肺功能下降的保护和风险因素。