Casola L, Di Matteo G, Romano M, Rutigliano B, Mastella G
Clin Chim Acta. 1979 May 16;94(1):83-8. doi: 10.1016/0009-8981(79)90188-8.
In a study of eight glycosidases in serum samples from 72 cystic fibrosis patients, 85 cystic fibrosis parents and 34 healthy and diseased controls, significant elevations of mean alpha-glucosidase levels were found in cystic fibrosis patients. All other glycosidases did not show any significant change. Mean alpha-glucosidase levels in obligate heterozygotes were the same as in control individuals. Moreover, alpha-glucosidase levels in cystic fibrosis patients correlated with the degree of clinical impairment as measured by the Schwachman score.
在一项针对72名囊性纤维化患者、85名囊性纤维化患者的父母以及34名健康对照者和患病对照者血清样本中的8种糖苷酶的研究中,发现囊性纤维化患者的平均α-葡萄糖苷酶水平显著升高。所有其他糖苷酶均未显示出任何显著变化。 obligate杂合子中的平均α-葡萄糖苷酶水平与对照个体相同。此外,囊性纤维化患者的α-葡萄糖苷酶水平与通过施瓦克曼评分衡量的临床损伤程度相关。