Center for Lipid Metabolomics, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Division of Preventive Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
JAMA Netw Open. 2024 May 1;7(5):e2414322. doi: 10.1001/jamanetworkopen.2024.14322.
Higher adherence to the Mediterranean diet has been associated with reduced risk of all-cause mortality, but data on underlying molecular mechanisms over long follow-up are limited.
To investigate Mediterranean diet adherence and risk of all-cause mortality and to examine the relative contribution of cardiometabolic factors to this risk reduction.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study included initially healthy women from the Women's Health Study, who had provided blood samples, biomarker measurements, and dietary information. Baseline data included self-reported demographics and a validated food-frequency questionnaire. The data collection period was from April 1993 to January 1996, and data analysis took place from June 2018 to November 2023.
Mediterranean diet score (range, 0-9) was computed based on 9 dietary components.
Thirty-three blood biomarkers, including traditional and novel lipid, lipoprotein, apolipoprotein, inflammation, insulin resistance, and metabolism measurements, were evaluated at baseline using standard assays and nuclear magnetic resonance spectroscopy. Mortality and cause of death were determined from medical and death records. Cox proportional hazards regression was used to calculate hazard ratios (HRs) for Mediterranean diet adherence and mortality risk, and mediation analyses were used to calculate the mediated effect of different biomarkers in understanding this association.
Among 25 315 participants, the mean (SD) baseline age was 54.6 (7.1) years, with 329 (1.3%) Asian women, 406 (1.6%) Black women, 240 (0.9%) Hispanic women, 24 036 (94.9%) White women, and 95 (0.4%) women with other race and ethnicity; the median (IQR) Mediterranean diet adherence score was 4.0 (3.0-5.0). Over a mean (SD) of 24.7 (4.8) years of follow-up, 3879 deaths occurred. Compared with low Mediterranean diet adherence (score 0-3), adjusted risk reductions were observed for middle (score 4-5) and upper (score 6-9) groups, with HRs of 0.84 (95% CI, 0.78-0.90) and 0.77 (95% CI, 0.70-0.84), respectively (P for trend < .001). Further adjusting for lifestyle factors attenuated the risk reductions, but they remained statistically significant (middle adherence group: HR, 0.92 [95% CI, 0.85-0.99]; upper adherence group: HR, 0.89 [95% CI, 0.82-0.98]; P for trend = .001). Of the biomarkers examined, small molecule metabolites and inflammatory biomarkers contributed most to the lower mortality risk (explaining 14.8% and 13.0%, respectively, of the association), followed by triglyceride-rich lipoproteins (10.2%), body mass index (10.2%), and insulin resistance (7.4%). Other pathways, including branched-chain amino acids, high-density lipoproteins, low-density lipoproteins, glycemic measures, and hypertension, had smaller contributions (<3%).
In this cohort study, higher adherence to the Mediterranean diet was associated with 23% lower risk of all-cause mortality. This inverse association was partially explained by multiple cardiometabolic factors.
较高的地中海饮食依从性与全因死亡率降低相关,但关于长期随访中潜在分子机制的数据有限。
调查地中海饮食依从性与全因死亡率的关系,并研究心脏代谢因素对这种风险降低的相对贡献。
设计、设置和参与者:本队列研究纳入了来自妇女健康研究的最初健康女性,她们提供了血液样本、生物标志物测量和饮食信息。基线数据包括自我报告的人口统计学信息和经过验证的食物频率问卷。数据收集期为 1993 年 4 月至 1996 年 1 月,数据分析于 2018 年 6 月至 2023 年 11 月进行。
根据 9 种饮食成分计算地中海饮食评分(范围 0-9)。
使用标准测定法和核磁共振光谱法,在基线时评估了 33 种血液生物标志物,包括传统和新型脂质、脂蛋白、载脂蛋白、炎症、胰岛素抵抗和代谢测量。通过医疗和死亡记录确定死亡率和死亡原因。使用 Cox 比例风险回归计算地中海饮食依从性和死亡率风险的危险比(HR),并进行中介分析以计算不同生物标志物在理解这种关联中的中介作用。
在 25315 名参与者中,平均(SD)基线年龄为 54.6(7.1)岁,329 名(1.3%)为亚洲女性,406 名(1.6%)为黑人女性,240 名(0.9%)为西班牙裔女性,24036 名(94.9%)为白人女性,95 名(0.4%)为其他种族和民族的女性;中位数(IQR)地中海饮食依从性评分为 4.0(3.0-5.0)。在平均(SD)24.7(4.8)年的随访期间,发生了 3879 例死亡。与低地中海饮食依从性(评分 0-3)相比,中(评分 4-5)和高(评分 6-9)组的调整后风险降低,HR 分别为 0.84(95%CI,0.78-0.90)和 0.77(95%CI,0.70-0.84)(趋势 P<0.001)。进一步调整生活方式因素减弱了风险降低,但仍具有统计学意义(中等依从性组:HR,0.92[95%CI,0.85-0.99];高依从性组:HR,0.89[95%CI,0.82-0.98];趋势 P=0.001)。在所检查的生物标志物中,小分子代谢物和炎症生物标志物对降低死亡率的风险贡献最大(分别解释了关联的 14.8%和 13.0%),其次是甘油三酯丰富的脂蛋白(10.2%)、体重指数(10.2%)和胰岛素抵抗(7.4%)。其他途径,包括支链氨基酸、高密度脂蛋白、低密度脂蛋白、血糖测量和高血压,贡献较小(<3%)。
在这项队列研究中,较高的地中海饮食依从性与全因死亡率降低 23%相关。这种负相关部分是由多种心脏代谢因素解释的。