Test characteristics of the ankle-brachial index and ankle-brachial difference for medial arterial calcification on X-ray in type 1 diabetes
详细信息    查看全文
文摘
| Figures/TablesFigures/Tables | ReferencesReferences

Objective

Medial arterial calcification (MAC) is common in diabetes, has a characteristic appearance on X-ray imaging, and has been linked with peripheral arterial stiffness and cardiovascular disease. However, few studies have measured X-ray MAC. It has been suggested that an ankle-brachial index (ABI) >1.30 or an ankle-brachial difference (ABD) >75 mm Hg may identify X-ray MAC, but test characteristics are unknown. We hypothesized that an ABI >1.30 and ABD >75 mm Hg would have high specificity but low sensitivity for MAC on X-ray imaging.

Methods

This was a cross-sectional study of 185 community-living individuals with type 1 diabetes. The ABI and the ABD were assessed. The outcome was linear ¡°tram-track¡± calcifications in the lower limbs characteristic of MAC.

Results

Mean age was 32 ¡À 6 years, and mean diabetes duration was 23 ¡À7 years. X-ray MAC was noted in 97 individuals (57 % ), 15 (8 % ) had ABI >1.30, and 14 (8 % ) had ABD >75 mm Hg. As assessed by the ABI, the area under the receiver operating characteristic curve for MAC was modest (0.65) and was slightly higher for the ABD (0.75). An ABI >1.30 had high specificity (99 % ) and positive predictive value (93 % ) but poor sensitivity (14 % ) and an overall accuracy of 55 % for MAC. An ABD >50 mm Hg remained highly specific (98 % ) but had higher sensitivity (30 % ) and overall accuracy (62 % ).

Conclusions

Individuals with type 1 diabetes and an ABI >1.30 or ABD >50 mm Hg are very likely to have MAC on X-ray imaging, yet many with MAC will not have an ABI or ABD above these thresholds. Given the high specificity, evaluating high ABI or ABD may be useful to understand correlates of MAC but may underestimate MAC prevalence.

© 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