Abstract #3: Converting from CIS to Definite Multiple Sclerosis: An Imaging Based Predictive Model
详细信息    查看全文
文摘

Objective

To quantitatively assess brain parenchymal fraction (BPF), gray matter (GM) atrophy, and white matter (WM) lesion load and to determine their association with the likelihood of CIS patients to convert to definite multiple sclerosis (MS) over time.

Background

Patients with clinically isolated syndromes (CIS) are those presenting a first neurologic episode suggestive of MS. A better understanding of the different biomarkers of brain damage in the early stages of MS and their association to clinical progression are essential so that treatments designed to limit or delay tissue damage may be initiated.

Methods

This is a retrospective study of baseline MRI examinations obtained from 12 CIS patients. Eight out of the 12 patients converted to definite MS within 5 years. Demographic characteristics of the patients who converted and did not convert (mean ± SD) were: age converters = 31.3 ± 8.6 and age non-converters = 27.7 ± 5.2. Brain MR images were processed by an experienced observer using both semi-automated and manual techniques in order to estimate BPF, thalamus, putamen, caudate, and globus pallidus volumes, as well as PD/T2-weighted, T1-weighted, and Gd-T1w lesion volumes. Comparisons between converters and non-converters were based on a Wilcoxon rank sum test. The predictive value of each variable was investigated using a logistic regression.

Results

In those patients who converted, BPF was significantly lower than in those who did not convert (0.761 ± 0.034 vs. 0.812 ± 0.016; p = 0.008). BPF was a perfect discriminator between converters and non-converters. All patients with a BPF > 0.795 did not convert and all patients with a BPF < 0.795 converted. We continue to accumulate additional patients for analysis to extend and confirm these findings.

Conclusions

In this preliminary study we found an association between BPF and the likelihood of CIS patients to convert to definite MS. These finding implicate brain atrophy present in the early stages of the disease as playing a role in further disease progression.

Support

This study was supported by research grants from the National Institutes of Health (1R01NS055083-01) and the National Multiple Sclerosis Society (RG4032A1/1, RG3705A1; RG3798A2).

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700