Entzian P, Müller E, Boysen A, Artlich A, Schwinger E, Schlaak M
Medizinische Klinik, Forschungsinstitut Borstel, Germany.
Scand J Clin Lab Invest. 1995 May;55(3):263-6. doi: 10.3109/00365519509089622.
It has been suggested that the delta F508 deletion, the most common mutation in the cystic fibrosis (CF) gene, might be linked to chronic bronchial hypersecretion. We investigated whether such an association could be found in chronic bronchitis, since chronic bronchial hypersecretion is an important and specific element of chronic bronchitis. We screened 100 patients hospitalized for chronic bronchitis with six of the most frequently occurring CF gene mutations: delta F508, R553X, G542X, G551D, N1303K, and 621-1G-->T. Only one patient affected by chronic bronchitis and diffuse bronchiectasis was heterozygous for the deletion delta F508; no other mutations were found. This is not significantly different from the expected frequency of CF carriers in northern Europe, which is 1 in 25. Thus, no association between the most commonly occurring cystic fibrosis genes and chronic bronchitis is likely to exist and routine screening of patients without further signs of cystic fibrosis would seem to be of no benefit in northern Europe.
有人提出,囊性纤维化(CF)基因中最常见的突变——ΔF508缺失,可能与慢性支气管分泌亢进有关。鉴于慢性支气管分泌亢进是慢性支气管炎的一个重要且特异的要素,我们研究了在慢性支气管炎中是否能发现这种关联。我们用CF基因最常出现的六种突变对100名因慢性支气管炎住院的患者进行了筛查:ΔF508、R553X、G542X、G551D、N1303K和621-1G→T。只有一名患慢性支气管炎和弥漫性支气管扩张的患者为ΔF508缺失杂合子;未发现其他突变。这与北欧CF携带者的预期频率(1/25)无显著差异。因此,在北欧,最常见的囊性纤维化基因与慢性支气管炎之间不太可能存在关联,对无囊性纤维化进一步体征的患者进行常规筛查似乎并无益处。