4.3 Article

Predictive Value of the Ankle-Brachial Index for All-Cause and Cardio-Cerebrovascular Mortality

期刊

ANGIOLOGY
卷 74, 期 7, 页码 649-656

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/00033197221121016

关键词

ankle-brachial index; all-cause mortality; cardio-cerebrovascular mortality; peripheral arterial disease; arterial calcification

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The present study investigated the association between ankle-brachial index (ABI) and all-cause or cardio-cerebrovascular mortality. The findings revealed that ABI below 1.06 was associated with the highest risk of all-cause, cardio-cerebrovascular, and cancer mortality. However, after adjusting for potential confounders, ABI between 1.06 and 1.12 was associated with the lowest risk of all-cause mortality.
The present study explored the relationship between the ankle-brachial index (ABI) (>.9) and all-cause or cardio-cerebrovascular mortality. Participant details were obtained from the National Health and Nutrition Examination Survey 1999-2004. The association between baseline ABI and the risk of mortality was evaluated by a priori defined quartile categories and on a continuous scale (per .1-unit change) with Cox regression models adjusted for demographic and traditional risk factors. A total of 7087 individuals (age: 59.6 +/- 12.8 years) were included; 3612 (51.0%) were male. After an average follow-up of 12.2 years, 1926 deaths occurred. Kaplan-Meier analysis showed that the lowest ABI quartile (<1.06) was associated with the highest risk of all-cause, cardio-cerebrovascular and cancer mortality (all P < .001). However, after adjusting for potential confounders, ABI ranging between 1.06 and 1.12 was associated with the lowest risk of all-cause mortality (hazard ratio .88, 95% confidence interval .78-1.00, P < .05) compared with the reference group (<1.06). Besides, splines showed the relationship was nonlinear (P < .05) and the inflection point was 1.11. In conclusion, the level of ABI associated with the lowest risk of all-cause mortality was 1.11, under which a lower ABI was independently associated with an increased risk of all-cause mortality.

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