Dietary intake and cardiovascular outcomes in patients with chronic vascular disease: insights from the COMPASS trial cohort

医学 队列 疾病 队列研究 指南针 动脉粥样硬化性心血管疾病 内科学 地图学 地理
作者
Darryl Wan,Mahshid Dehghan,Russell J. de Souza,Chinthanie Ramasundarahettige,John W. Eikelboom,Jackie Bosch,Aldo P. Maggioni,Deepak L. Bhatt,Salim Yusuf,Sonia S. Anand
出处
期刊:European Journal of Preventive Cardiology [Oxford University Press]
卷期号:30 (8): 709-718 被引量:3
标识
DOI:10.1093/eurjpc/zwad062
摘要

Abstract Aims Patients with coronary artery disease (CAD) and patients with peripheral artery disease (PAD) are at risk for major adverse cardiovascular events (MACE) and major adverse limb events (MALE). There are limited data regarding dietary patterns and the risk of recurrent MACE and MALE in CAD and PAD patients. We aimed to identify dietary patterns associated with MACE and MALE in patients with CAD and/or PAD. Methods and results We analysed data collected from patients enrolled into the Cardiovascular Outcomes for People Using Anticoagulation Strategies (COMPASS) trial, in which diet was assessed by a short food frequency questionnaire (FFQ) at baseline. Two dietary pattern scores, the modified Alternate Healthy Eating Index (mAHEI) and Mediterranean Diet Score (mMDS), were calculated. We tested the association between mAHEI and mMDS and the incidence of MACE and/or MALE. The mean mAHEI score was 23.0 ± 7.7 (out of 70) overall and was similar comparing CAD and PAD patients. The incidence of MACE or MALE was 6.3% in the lowest diet quality quartile (as assessed by mAHEI) compared with 4.2% in the highest quartile over 30 months. In the fully adjusted model, the hazard ratio of a low diet quality (Quartile 1) compared with the highest (Quartile 4) for MACE or MALE was 1.27 (95% CI: 1.08–1.49; P = 0.004, Q1 vs. Q4). This excess hazard was primarily driven by higher MACE in both the CAD and PAD cohorts. Conclusions Poor diet quality as assessed by the mAHEI is independently associated with a higher risk of recurrent MACE and MALE in patients with chronic CAD and/or PAD.
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