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Relative Protein Intake and Physical Function in Older Adults: A Systematic Review and Meta-Analysis of Observational Studies.相对蛋白质摄入量与老年人身体功能:观察性研究的系统评价和荟萃分析。
Nutrients. 2018 Sep 19;10(9):1330. doi: 10.3390/nu10091330.
2
Is there any evidence that AGE/sRAGE is a universal biomarker/risk marker for diseases?AGE/sRAGE 是否是疾病的通用生物标志物/风险标志物?有相关证据吗?
Mol Cell Biochem. 2019 Jan;451(1-2):139-144. doi: 10.1007/s11010-018-3400-2. Epub 2018 Jun 30.
3
Dietary Approaches in the Management of Diabetic Patients with Kidney Disease.糖尿病肾病患者管理中的饮食方法
Nutrients. 2017 Jul 31;9(8):824. doi: 10.3390/nu9080824.
4
Effects of Two Different Dietary Patterns on Inflammatory Markers, Advanced Glycation End Products and Lipids in Subjects without Type 2 Diabetes: A Randomised Crossover Study.两种不同饮食模式对非2型糖尿病受试者炎症标志物、晚期糖基化终产物和脂质的影响:一项随机交叉研究
Nutrients. 2017 Mar 29;9(4):336. doi: 10.3390/nu9040336.
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Contribution of dietary advanced glycation end products (AGE) to circulating AGE: role of dietary fat.膳食晚期糖基化终产物(AGE)对循环中AGE的贡献:膳食脂肪的作用。
Br J Nutr. 2015 Dec 14;114(11):1797-806. doi: 10.1017/S0007114515003487. Epub 2015 Sep 22.
6
Protein Requirements and Recommendations for Older People: A Review.老年人的蛋白质需求与建议:综述
Nutrients. 2015 Aug 14;7(8):6874-99. doi: 10.3390/nu7085311.
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Evaluating the effects of preanalytical variables on the stability of the human plasma proteome.评估分析前变量对人血浆蛋白质组稳定性的影响。
Anal Biochem. 2015 Jun 1;478:14-22. doi: 10.1016/j.ab.2015.03.003. Epub 2015 Mar 10.
8
Ratio of serum levels of AGEs to soluble form of RAGE is a predictor of endothelial function.血清 AGEs 与可溶性 RAGE 比值是内皮功能的预测指标。
Diabetes Care. 2015 Jan;38(1):119-25. doi: 10.2337/dc14-1435. Epub 2014 Oct 21.
9
Dietary intake of advanced glycation end products did not affect endothelial function and inflammation in healthy adults in a randomized controlled trial.在一项随机对照试验中,健康成年人的晚期糖基化终产物饮食摄入量并未影响内皮功能和炎症。
J Nutr. 2014 Jul;144(7):1037-42. doi: 10.3945/jn.113.189480. Epub 2014 Apr 17.
10
Low levels of serum soluble receptors for advanced glycation end products, biomarkers for disease state: myth or reality.晚期糖基化终产物血清可溶性受体水平低下,作为疾病状态的生物标志物:是神话还是现实。
Int J Angiol. 2014 Mar;23(1):11-6. doi: 10.1055/s-0033-1363423.

健康、衰老和身体成分研究中的膳食蛋白质摄入量与循环晚期糖基化终产物/晚期糖基化终产物受体浓度。

Dietary protein intake and circulating advanced glycation end product/receptor for advanced glycation end product concentrations in the Health, Aging, and Body Composition Study.

机构信息

Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Am J Clin Nutr. 2020 Dec 10;112(6):1558-1565. doi: 10.1093/ajcn/nqaa241.

DOI:10.1093/ajcn/nqaa241
PMID:33301008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7727487/
Abstract

BACKGROUND

Advanced glycation end products (AGEs) promote adverse health effects and may contribute to the multi-system functional decline observed in aging. Diet is a major source of AGEs, and foods high in protein may increase circulating AGE concentrations. However, epidemiological evidence that high-protein diets increase AGEs is lacking.

OBJECTIVES

We examined whether dietary protein intake was associated with serum concentrations of the major AGE carboxymethyl-lysine (CML) and the soluble receptor for AGEs (sRAGE) in 2439 participants from the Health, Aging, and Body Composition study (mean age, 73.6 ± 2.9 y; 52% female; 37% black).

METHODS

CML and sRAGE were measured by ELISA, and the CML/sRAGE ratio was calculated. Protein intake was estimated using an interviewer-administered FFQ and categorized based on current recommendations for older adults: <0.8 g/kg/d (n = 1077), 0.8 to <1.2 g/kg/d (n = 922), and ≥1.2 g/kg/d (n = 440). Associations between protein intake and AGE-RAGE biomarkers were examined using linear regression models adjusted for demographics, height, lifestyle behaviors, prevalent disease, cognitive function, inflammation, and other dietary factors.

RESULTS

CML concentrations were higher in individuals with higher total protein intake (adjusted least squares mean ± SE: <0.8 g/kg/d, 829 ± 17 ng/ml; 0.8 to <1.2 g/kg/d, 860 ± 15 ng/ml; ≥1.2 g/kg/d, 919 ± 23 ng/ml; P for trend = 0.001), as were sRAGE concentrations (<0.8 g/kg/d, 1412 ± 34 pg/ml; 0.8 to <1.2 g/kg/d, 1479 ± 31 pg/ml; ≥1.2 g/kg/d, 1574 ± 47 pg/ml; P for trend < 0.0001). Every 0.1 g/kg/d increment in total protein intake was associated with a 13.3 ± 3.0 ng/ml increment in CML and a 22.1 ± 6.0 pg/ml increment in sRAGE (P < 0.0001 for both). Higher CML and sRAGE concentrations were also associated with higher intakes of both animal and vegetable protein (all P values ≤ 0.01). There were no significant associations with the CML/sRAGE ratio.

CONCLUSIONS

Higher dietary protein intake was associated with higher CML and sRAGE concentrations in older adults; however, the CML/sRAGE ratio remained similar across groups.

摘要

背景

晚期糖基化终产物(AGEs)会对健康产生不良影响,并可能导致衰老过程中观察到的多系统功能下降。饮食是 AGEs 的主要来源,高蛋白食物可能会增加循环 AGE 浓度。然而,尚无高蛋白质饮食会增加 AGEs 的流行病学证据。

目的

我们研究了 2439 名来自健康、衰老和身体成分研究(平均年龄 73.6±2.9 岁;52%为女性;37%为黑人)参与者的膳食蛋白质摄入量与血清中主要 AGE 羧甲基赖氨酸(CML)和可溶性 AGE 受体(sRAGE)浓度之间的关系。

方法

通过 ELISA 测定 CML 和 sRAGE,并计算 CML/sRAGE 比值。通过访谈者管理的 FFQ 估计蛋白质摄入量,并根据老年人的现行建议进行分类:<0.8 g/kg/d(n=1077)、0.8 至<1.2 g/kg/d(n=922)和≥1.2 g/kg/d(n=440)。使用线性回归模型调整人口统计学、身高、生活方式行为、现患疾病、认知功能、炎症和其他饮食因素后,研究蛋白质摄入量与 AGE-RAGE 生物标志物之间的关联。

结果

总蛋白摄入量较高的个体 CML 浓度较高(调整后的最小二乘均数±SE:<0.8 g/kg/d,829±17 ng/ml;0.8 至<1.2 g/kg/d,860±15 ng/ml;≥1.2 g/kg/d,919±23 ng/ml;P 趋势=0.001),sRAGE 浓度也较高(<0.8 g/kg/d,1412±34 pg/ml;0.8 至<1.2 g/kg/d,1479±31 pg/ml;≥1.2 g/kg/d,1574±47 pg/ml;P 趋势<0.0001)。总蛋白摄入量每增加 0.1 g/kg/d,CML 增加 13.3±3.0 ng/ml,sRAGE 增加 22.1±6.0 pg/ml(均 P<0.0001)。较高的 CML 和 sRAGE 浓度也与动物蛋白和植物蛋白的摄入量较高有关(所有 P 值均≤0.01)。CML/sRAGE 比值与蛋白质摄入量之间没有显著关联。

结论

较高的膳食蛋白质摄入量与老年人的 CML 和 sRAGE 浓度较高有关;然而,各组之间的 CML/sRAGE 比值相似。