Physical Examination Center, Gusu School, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Nanjing Medical University, 242 Guangji Road, Suzhou, 215008, China.
Department of Nutrition and Food Hygiene, School of Public Health, Soochow University, 199 Ren'ai Road, Suzhou, 215123, China.
Eur J Nutr. 2024 Feb;63(1):173-183. doi: 10.1007/s00394-023-03253-2. Epub 2023 Oct 2.
Large population-based studies for the associations between dietary advanced glycation end products (dAGEs) intake and liver steatosis remain lacking. It is necessary to clarify the relationship of dAGEsintake with liver steatosis through the National Health and Nutrition Survey (NHANES).
A total of 5856 participants in the NHANES 2017-2018 were included. The dietary AGEs intake, including ε-(carboxymethyl)lysine(CML), Nε-(1-carboxyethyl)lysine (CEL), and Nδ-(5-hydro-5-methyl-4-imidazolon-2-yl)-ornithine (MG-H1) were estimated using the combination of ultra-performance LC-tandem MS dietary AGEs database and two 24-h dietary recall interviews. Liver steatosis was assessed by controlled attenuation parameter via transient elastography. Logistic regression model was adopted to explore the relationships between dAGEs intake and hepatic steatosis.
Compared with individuals of total dAGEs, CML, MG-H1 in the lowest tertile, those in the highest tertile had highest risk of hepatic steatosis, and the corresponding odds radios(ORs) (95% confidence interval(CI)) were 1.37 (1.01, 1.84), 1.36 (1.04,1.78) and 1.40 (1.06, 1.85), respectively. Subgroups analysis found that the positive association between dAGEs, CML, CEL and MG-H1 and hepatic steatosis appeared stronger in subjects with obesity and those with abnormal waist circumference (WC).
There was a positive correlation between dAGEs, CML, MG-H1, and hepatic steatosis, and this association mainly existed in subjects with obesity and those with abnormal WC. Dietary AGEs restriction might be of high priority for subjects with obesity for the prevention of fatty liver disease. Further longitudinal studies are required to confirm the causal associations and explore the potential mechanisms.
目前缺乏关于饮食晚期糖基化终产物(dAGEs)摄入与肝脂肪变性之间关联的大型基于人群的研究。有必要通过国家健康和营养调查(NHANES)阐明 dAGEs 摄入与肝脂肪变性的关系。
共纳入 NHANES 2017-2018 年的 5856 名参与者。采用超高效 LC-串联 MS 饮食 AGEs 数据库和两次 24 小时饮食回顾访谈相结合的方法,估算饮食 AGEs 摄入,包括 ε-(羧甲基)赖氨酸(CML)、Nε-(1-羧乙基)赖氨酸(CEL)和 Nδ-(5-氢-5-甲基-4-咪唑烷-2-基)-鸟氨酸(MG-H1)。通过瞬态弹性成像评估肝脂肪变性。采用 logistic 回归模型探讨 dAGEs 摄入与肝脂肪变性的关系。
与总 dAGEs 个体相比,CML、MG-H1 最低三分位者和最高三分位者肝脂肪变性的风险最高,相应的比值比(ORs)(95%置信区间(CI))分别为 1.37(1.01,1.84)、1.36(1.04,1.78)和 1.40(1.06,1.85)。亚组分析发现,dAGEs、CML、CEL 和 MG-H1 与肝脂肪变性之间的正相关关系在肥胖和腰围异常的受试者中更为明显。
dAGEs、CML、MG-H1 与肝脂肪变性呈正相关,这种相关性主要存在于肥胖和腰围异常的受试者中。对于肥胖者,限制饮食 AGEs 可能是预防脂肪肝疾病的首要任务。需要进一步的纵向研究来确认因果关系并探讨潜在机制。