在一项多民族伊朗病例对照研究中,含糖饮料消费与过早冠状动脉疾病的风险

IF 4.1 2区 医学 Q2 NUTRITION & DIETETICS
Noushin Mohammadifard, Negar Ostadsharif, Ghazaleh Bahrami, Motahare Bateni, Ehsan Zarepur, Fatemeh Nouri, Fereidoon Nouhi, Nahid Azdaki, Nahid Salehi, Masoud Lotfizadeh, Samad Ghaffari, Arsalan Salari, Mostafa Dehghani, Mostafa Cheraghi, Ahmadreza Assareh, Hassan Alikhasi, Fahimeh Haghighatdoost, Nizal Sarrafzadegan
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引用次数: 0

摘要

背景:含糖饮料(SSBs)与冠状动脉疾病(CAD)的关联在亚洲尚未得到证实,在亚洲,SSBs是主要的超加工食品。目的:我们旨在研究伊朗成年人SSBs与早发CAD (PCAD)之间的关系。设计:病例对照。参与者:伊朗人多中心研究,包括2006年PCAD和1131名健康个体作为对照组。主要结果测量:使用经过验证的食物频率问卷(FFQ)评估膳食摄入量。ssb由人造果汁和含糖饮料组成。根据血管造影结果和血管闭塞率确定PCAD。统计分析:采用二元逻辑回归评估SSBs四分位数中PCAD的几率。结果:参与者的平均(SD)年龄和SSB摄入量分别为51.5岁和46.9 g/d。在完全调整模型中,与第一个四分位数的参与者相比,第四个四分位数的参与者患PCAD的风险更高(OR = 1.50, 95% CI: 1.12, 2.00; P趋势= 0.044)。一致地,SSB消费与pad的严重程度直接相关。SSB摄入量越高,发生重度PCAD的风险越大(OR Q4 vs. Q1 = 1.34, 95% CI: 1.06, 1.68; P)结论:本研究表明SSB摄入量高可能与PCAD的高风险相关。然而,需要更多的前瞻性队列研究来证实这种关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sugar-sweetened beverage consumption and risk of premature coronary artery disease in a multi-ethnic Iranian case-control study.

Background: The association of sugar sweetened beverages (SSBs) and coronary artery disease (CAD) has not been well-established in Asians, where SSBs are the leading ultra-processed food product.

Objective: We aim to examine the association between SSBs and premature CAD (PCAD) in Iranian adults.

Design: Case-control.

Participants: A multi-centric study of Iranians including 2006 PCAD and 1131 healthy individuals as control group.

Main outcome measures: Dietary intakes were assessed using a validated food frequency questionnaire (FFQ). SSBs consist of artificial juice and sugar -sweetened drinks. The PCAD was determined based on the results of angiography and the occlusion percent of vessels.

Statistical analysis: The odds of PCAD across the quartiles of SSBs were assessed by binary logistic regression.

Results: The mean (SD) age of participants and SSB consumption was 51.5 years and 46.9 g/d, respectively. In the fully-adjusted model, compared with participants in the first quartile, those in the fourth quartile had higher risk of PCAD (OR = 1.50, 95% CI: 1.12, 2.00; P trend = 0.044). Consistently, SSB consumption was directly associated with the severity of PCAD. The higher SSB consumption, the greater risk for the severe PCAD (OR Q4 vs. Q1 = 1.34, 95% CI: 1.06, 1.68; P < 0.001).

Conclusion: This study demonstrated that higher consumption of SSB might be associated with higher risk of PCAD. However, more prospective cohort studies are necessary to confirm this association.

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来源期刊
Nutrition & Metabolism
Nutrition & Metabolism 医学-营养学
CiteScore
8.40
自引率
0.00%
发文量
78
审稿时长
4-8 weeks
期刊介绍: Nutrition & Metabolism publishes studies with a clear focus on nutrition and metabolism with applications ranging from nutrition needs, exercise physiology, clinical and population studies, as well as the underlying mechanisms in these aspects. The areas of interest for Nutrition & Metabolism encompass studies in molecular nutrition in the context of obesity, diabetes, lipedemias, metabolic syndrome and exercise physiology. Manuscripts related to molecular, cellular and human metabolism, nutrient sensing and nutrient–gene interactions are also in interest, as are submissions that have employed new and innovative strategies like metabolomics/lipidomics or other omic-based biomarkers to predict nutritional status and metabolic diseases. Key areas we wish to encourage submissions from include: -how diet and specific nutrients interact with genes, proteins or metabolites to influence metabolic phenotypes and disease outcomes; -the role of epigenetic factors and the microbiome in the pathogenesis of metabolic diseases and their influence on metabolic responses to diet and food components; -how diet and other environmental factors affect epigenetics and microbiota; the extent to which genetic and nongenetic factors modify personal metabolic responses to diet and food compositions and the mechanisms involved; -how specific biologic networks and nutrient sensing mechanisms attribute to metabolic variability.
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