Guilbert Theresa, Krawiec Marzena
Division of Pediatric Pulmonary Medicine, Arizona Respiratory Center, University of Arizona, 1501 N. Campbell Avenue, Tucson, AZ 85724, USA.
Pediatr Clin North Am. 2003 Jun;50(3):523-38. doi: 10.1016/s0031-3955(03)00044-0.
For some children, asthma is a disease whose symptoms seem to remit with time. Numerous children, however, develop disease that is persistent throughout their lifetimes and is associated with more severe symptoms, increased airway reactivity, and loss of lung function. These children typically have a family history of asthma and demonstrate increased airways reactivity and atopy in childhood. A clearer picture of the natural history of asthma in the developing child has been derived from the results of several longitudinal studies. Although some questions have been clarified, several questions still remain. Now that the incidence and severity of asthma seem to be increasing, children born in the last 10 years may experience more severe disease or a different pathophysiology than those born 30 to 40 years ago. New cohort studies are needed to assess this possibility. Additional investigations into the genetics of asthma causation will help elucidate the different phenotypic expressions of this complex disease. Once these different phenotypic groups can be identified early in life, further studies can be performed to explore the impact of therapeutic intervention on the severity of asthma symptoms and loss of lung function.
对于一些儿童来说,哮喘是一种症状似乎会随时间缓解的疾病。然而,许多儿童会患上在其一生中持续存在的疾病,这种疾病与更严重的症状、气道反应性增加以及肺功能丧失有关。这些儿童通常有哮喘家族史,并且在儿童期表现出气道反应性增加和特应性。通过几项纵向研究的结果,对发育中儿童哮喘的自然史有了更清晰的认识。虽然一些问题已经得到澄清,但仍有几个问题存在。鉴于哮喘的发病率和严重程度似乎在增加,过去10年出生的儿童可能比30至40年前出生的儿童经历更严重的疾病或不同的病理生理学。需要新的队列研究来评估这种可能性。对哮喘病因遗传学的进一步研究将有助于阐明这种复杂疾病的不同表型表达。一旦这些不同的表型组能够在生命早期被识别出来,就可以进行进一步的研究,以探索治疗干预对哮喘症状严重程度和肺功能丧失的影响。