Uncovering the possible link between dietary advanced glycation end products and mortality risk: A systematic review and meta-analysis

被引:0
作者
Ahmadirad, Hamid [1 ]
Farhadnejad, Hossein [1 ]
Norouzzadeh, Mostafa [1 ]
Jahromi, Mitra Kazemi [2 ]
Mokhtari, Ebrahim [1 ,3 ]
Omrani, Morteza [4 ]
Teymoori, Farshad [4 ,5 ]
Sadeghi, Reza [4 ,5 ]
Mirmiran, Parvin [1 ]
Bagherian, Maryam [6 ]
机构
[1] Shahid Beheshti Univ Med Sci, Res Inst Endocrine Disorders, Res Inst Endocrine Sci, Nutr & Endocrine Res Ctr, Tehran, Iran
[2] Hormozgan Univ Med Sci, Endocrinol & Metab Res Ctr, Bandar Abbas, Iran
[3] Shiraz Univ Med Sci, Sch Nutr & Food Sci, Dept Community Nutr, Shiraz, Iran
[4] Iran Univ Med Sci, Sch Publ Hlth, Dept Nutr, Tehran, Iran
[5] Iran Univ Med Sci, Nutr Sci Res Ctr, Tehran, Iran
[6] Iran Univ Med Sci, Firoozgar Hosp, Sch Med, Dept Hematol & Oncol & Stem Cell Transplantat, Tehran, Iran
关键词
Advanced glycation end products; Mortality; Meta-analysis; BREAST-CANCER; ENDPRODUCTS; HEALTH; GLYCOTOXINS; FAILURE;
D O I
10.1016/j.canep.2025.102807
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Recently, observational studies have focused on dietary advanced glycation end products (dAGEs) as predictive risk factors for chronic diseases and their related mortality. The current systematic review and meta- analysis aimed to synthesize the available evidence and quantify the possible association of dAGEs and risk of all- cause or cause-specific mortality. Methods: A comprehensive and systematic search was conducted in online literature databases, including PubMed, Scopus and Web of Science until January 2025 without any language limitation. The hazard ratio (HR) with 95 % confidence interval (CI) for the included studies were extracted and converted into log HR. Also, we used a random-effects model with inverse variance weighting method to compute the pooled effect size. Results: Six eligible studies (including 18 reports) were included in the current meta-analysis. 111,543 participants, aged 45.6-79 years old, participated in these observational studies, and the duration of follow-up varied from 3.8 to 16 years. According to the pooled results of our analysis, no significant association was observed between dAGEs and its components with the risk of all-cause mortality (HR=1.02; 95 %CI=0.92, 1.13; I2= 73.2 %), cancer mortality (HR=1.00; 95 %CI=0.88, 1.13; I2= 41.0 %) and CVDs mortality (HR=1.16; 95 % CI=0.86, 1.55; I2=86.1 %). Sex, target population, dAGEs components, region, dAGEs assessment method, and dietary data collection methods were the sources of heterogeneity. Conclusions: In conclusion, our study suggested that there was no significant association between dAGEs intake and all-cause or cause-specific mortality.
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页数:14
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