Agjm. Hanselaar et al., DNA-CYTOMETRY OF PROGRESSIVE AND REGRESSIVE CERVICAL INTRAEPITHELIAL NEOPLASIA, Analytical cellular pathology, 16(1), 1998, pp. 11-27
A retrospective analysis was performed on archival cervical smears fro
m a group of 56 women with cervical intraepithelial neoplasia (CIN), w
ho had received follow-up by cytology only. Automated image cytometry
of Feulgen stained DNA was used to determine the differences between p
rogressive and regressive lesions. The first group of 30 smears was fr
om women who had developed cancer after initial smears with dysplastic
changes (progressive group). The second group of 26 smears with dyspl
astic changes had shown regression to normal (regressive group). The g
oal of the study was to determine if differences in cytometric feature
s existed between the progressive and regressive groups. CIN categorie
s I, II and III were represented in both groups, and measurements were
pooled across diagnostic categories. Images of up to 700 intermediate
cells were obtained from each slide, and cells were scanned exhaustiv
ely for the detection of diagnostic cells. Discriminant function analy
sis was performed for both intermediate and diagnostic cells. The most
significant differences between the groups were found for diagnostic
cells, with a cell classification accuracy of 82%. Intermediate cells
could be classified with 60% accuracy. Cytometric features which affor
ded the best discrimination were characteristic of the chromatin organ
ization in diagnostic cells (nuclear texture). Slide classification wa
s performed by thresholding the number of cells which exhibited progre
ssion associated changes (PAC) in chromatin configuration, with an acc
uracy of 93 and 73% for diagnostic and intermediate cells, respectivel
y. These results indicate that regardless of the extent of nuclear aty
pia as reflected in the CIN category, features of chromatin organizati
on can potentially be used to predict the malignant or progressive pot
ential of CIN lesions.