Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA30322, USA.
Department of Biostatistics, School of Public Health, University of Alabama, Birmingham, AL, USA.
Br J Nutr. 2023 Feb 14;129(3):523-534. doi: 10.1017/S0007114522001349. Epub 2022 May 10.
One potential mechanism by which diet and lifestyle may affect chronic disease risk and subsequent mortality is through chronic systemic inflammation. In this study, we investigated whether the inflammatory potentials of diet and lifestyle, separately and combined, were associated with all-cause, all-CVD and all-cancer mortality risk. We analysed data on 18 484 (of whom 4103 died during follow-up) Black and White men and women aged ≥45 years from the prospective REasons for Geographic and Racial Differences in Stroke study. Using baseline (2003-2007) Block 98 FFQ and lifestyle questionnaire data, we constructed the previously validated inflammation biomarker panel-weighted, 19-component dietary inflammation score (DIS) and 4-component lifestyle inflammation score (LIS) to reflect the overall inflammatory potential of diet and lifestyle. From multivariable Cox proportional hazards models, the hazards ratios (HR) and their 95 % CI for the DIS-all-cause mortality and LIS-all-cause mortality risk associations were 1·32 (95 % CI (1·18, 1·47); < 0·01) and 1·25 (95 % CI (1·12, 1·38); < 0·01), respectively, among those in the highest relative to the lowest quintiles. The findings were similar by sex and race and for all-cancer mortality, but weaker for all-CVD mortality. The joint HR for all-cause mortality among those in the highest relative to the lowest quintiles of both the DIS and LIS was 1·91 (95 % CI 1·57, 2·33) ( < 0·01). Diet and lifestyle, via their contributions to systemic inflammation, separately, but perhaps especially jointly, may be associated with higher mortality risk among men and women.
饮食和生活方式可能通过慢性系统性炎症影响慢性病风险和随后的死亡率,这是一个潜在机制。在这项研究中,我们调查了饮食和生活方式的炎症潜力,分别和联合,是否与全因、全心血管疾病和全癌症死亡率风险相关。我们分析了来自前瞻性地理和种族差异中风研究(REasons for Geographic and Racial Differences in Stroke study)的 18484 名年龄≥45 岁的黑人和白人男性和女性的数据(其中 4103 人在随访期间死亡)。使用基线(2003-2007 年)Block 98 FFQ 和生活方式问卷数据,我们构建了先前验证的炎症生物标志物加权、19 成分饮食炎症评分(DIS)和 4 成分生活方式炎症评分(LIS),以反映饮食和生活方式的整体炎症潜力。从多变量 Cox 比例风险模型中,DIS-全因死亡率和 LIS-全因死亡率风险关联的危险比(HR)及其 95%CI 分别为 1.32(95%CI(1.18,1.47);<0.01)和 1.25(95%CI(1.12,1.38);<0.01),在最高五分位数与最低五分位数之间。这些发现在性别和种族之间以及全癌症死亡率方面相似,但全心血管疾病死亡率方面较弱。在 DIS 和 LIS 最高五分位数与最低五分位数之间的所有原因死亡率的联合 HR 为 1.91(95%CI 1.57,2.33)(<0.01)。饮食和生活方式通过其对系统性炎症的贡献,分别但也许特别是联合,可能与男性和女性更高的死亡率风险相关。