Association of cystic fibrosis transmembrane conductance regulator gene variants with acute lung injury in African American children with pneumonia*.

Association of cystic fibrosis transmembrane conductance regulator gene variants with acute lung injury in African American children with pneumonia*.
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囊性纤维化跨膜电导调节基因变异与非裔美国肺炎儿童急性肺损伤的关联*。

DOI:
10.1097/ccm.0b013e31825d8f73
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发表时间:
2012
影响因子:
8.8
通讯作者:
Dahmer,MaryK
Dahmer,MaryK
中科院分区:
医学1区
文献类型:
--
作者:
Baughn,JulieM;Quasney,MichaelW;Simpson,Pippa;Merchant,Daniel;Li,Shun-Hwa;Levy,Hara;Dahmer,MaryK

文献摘要

相似文献

Objectives:The cystic fibrosis transmembrane conductance regulator regulates fluid balance in alveolar epithelial cells and appears to modulate the inflammatory response. To determine whether more severe lung injury in children who develop community-acquired pneumonia is associated with variations known to affect function in the gene coding for cystic fibrosis transmembrane conductance regulator.Design:A prospective cohort genetic association study of lung injury in children with community-acquired pneumonia.Setting:Three major tertiary care children’s hospitals.Subjects:Caucasian and African American children with community-acquired pneumonia either evaluated in the emergency department or admitted to the hospital.Interventions:None.Measurements and Main Results:Caucasian and African American children with pneumonia were genotyped for the most common variants reported to affect cystic fibrosis transmembrane conductance regulator function, the p. 508del mutation, the (TG) m T n variable repeat region, and the M470V polymorphism in the cystic fibrosis transmembrane conductance regulator gene. Genotypes and haplotypes were determined, and the association of high-risk alleles or high-risk haplotypes (defined as the presence of at least one variant known to decrease the level of functional cystic fibrosis transmembrane conductance regulator) with the need for mechanical ventilation or the development of acute lung injury was evaluated. Forty-two children in the Caucasian cohort (n= 304) required mechanical ventilation; 32 developed acute lung injury. Forty-three children in the African American cohort (n= 474) required mechanical ventilation; 29 developed acute lung injury. In African American children, high-risk (TG) m T n alleles known to result in decreased levels of functional cystic fibrosis transmembrane conductance regulator were associated with the need for mechanical ventilation (p=. 0013) and the development of acute lung injury (p=. 0061). Multivariable analysis demonstrated that high-risk (TG) m T n alleles were independently associated with mechanical ventilation (odds ratios= 3.19; 95% confidence interval, 1.63–6.26) and acute lung injury (odds ratios= 3.36; 95% confidence interval, 1.50–7.53) in African American children.Conclusion:Genetic variation in cystic fibrosis transmembrane conductance regulator is associated with acute lung injury in African American children with community-acquired pneumonia.