Objectives: To utilize radiosensitivity testing to improve early diagnosis of patients with ataxia-telangiectasia (A-T). Study design: We established normal ranges for the colony survival assay (CSA) by testing cells from 104 patients with typical A-T, 29 phenotypic normal patients, and 19 A-T heterozygotes, We also analyzed 61 samples from patients suspected of having A-T and 25 patients with related disorders to compare the CSA with other criteria in the diagnosis of A-T. Results: When cells were irradiated with 1.0 Gy, the mean survival fraction (muSF +/- 1 SD) for patients with A-T was 13.1% +/- 7.2% compared with 50.1% 13.5% for healthy control patients. These data served to define a diagnostic range for the CSA (ie, <21%), a normal range (>36%), and a nondiagnostic intermediate range of 21% to 36%. The mutations of patients with A-T with intermediate radiosensitivity tended to cluster around the functional domains of the ATM gene. Conclusions:The CSA is a useful adjunctive test for confirming an early clinical diagnosis of A-T However, CSA is also abnormal in other chromosomal instability and immunodeficiency disorders.
Early diagnosis of ataxia-telangiectasia using radiosensitivity testing / Xia, Sun; Sara G., Becker Catania; Helen H., Chun; Mee Jeong, Hwang; Yong, Huo; Zhijun, Wang; Midori, Mitui; Ozden, Sanal; Chessa, Luciana; Barbara, Crandall; Richard A., Gatti. - In: THE JOURNAL OF PEDIATRICS. - ISSN 0022-3476. - 140:6(2002), pp. 724-731. [10.1067/mpd.2002.123879]
Early diagnosis of ataxia-telangiectasia using radiosensitivity testing
CHESSA, Luciana;
2002
Abstract
Objectives: To utilize radiosensitivity testing to improve early diagnosis of patients with ataxia-telangiectasia (A-T). Study design: We established normal ranges for the colony survival assay (CSA) by testing cells from 104 patients with typical A-T, 29 phenotypic normal patients, and 19 A-T heterozygotes, We also analyzed 61 samples from patients suspected of having A-T and 25 patients with related disorders to compare the CSA with other criteria in the diagnosis of A-T. Results: When cells were irradiated with 1.0 Gy, the mean survival fraction (muSF +/- 1 SD) for patients with A-T was 13.1% +/- 7.2% compared with 50.1% 13.5% for healthy control patients. These data served to define a diagnostic range for the CSA (ie, <21%), a normal range (>36%), and a nondiagnostic intermediate range of 21% to 36%. The mutations of patients with A-T with intermediate radiosensitivity tended to cluster around the functional domains of the ATM gene. Conclusions:The CSA is a useful adjunctive test for confirming an early clinical diagnosis of A-T However, CSA is also abnormal in other chromosomal instability and immunodeficiency disorders.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


