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炎症标志物、犬尿氨酸途径和 B 族维生素与年龄和死亡率的关联,以及炎症老化的特征。

Association of Markers of Inflammation, the Kynurenine Pathway and B Vitamins with Age and Mortality, and a Signature of Inflammaging.

机构信息

Precision Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia.

Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Australia.

出版信息

J Gerontol A Biol Sci Med Sci. 2022 Apr 1;77(4):826-836. doi: 10.1093/gerona/glab163.

Abstract

BACKGROUND

Inflammation is a key feature of aging. We aimed to (i) investigate the association of 34 blood markers potentially involved in inflammatory processes with age and mortality and (ii) develop a signature of "inflammaging."

METHODS

Thirty-four blood markers relating to inflammation, B vitamin status, and the kynurenine pathway were measured in 976 participants in the Melbourne Collaborative Cohort Study at baseline (median age = 59 years) and follow-up (median age = 70 years). Associations with age and mortality were assessed using linear and Cox regression, respectively. A parsimonious signature of inflammaging was developed and its association with mortality was compared with 2 marker scores calculated across all markers associated with age and mortality, respectively.

RESULTS

The majority of markers (30/34) were associated with age, with stronger associations observed for neopterin, cystatin C, interleukin (IL)-6, tumor necrosis factor alpha (TNF-α), several markers of the kynurenine pathway and derived indices KTR (kynurenine/tryptophan ratio), PAr index (ratio of 4-pyridoxic acid and the sum of pyridoxal 5'-phosphate and pyridoxal), and HK:XA (3-hydroxykynurenine/xanthurenic acid ratio). Many markers (17/34) showed an association with mortality, in particular IL-6, neopterin, C-reactive protein, quinolinic acid, PAr index, and KTR. The inflammaging signature included 10 markers and was strongly associated with mortality (hazard ratio [HR] per SD = 1.40, 95% CI: 1.24-1.57, p = 2 × 10-8), similar to scores based on all age-associated (HR = 1.38, 95% CI: 1.23-1.55, p = 4 × 10-8) and mortality-associated markers (HR = 1.43, 95% CI: 1.28-1.60, p = 1 × 10-10), respectively. Strong evidence of replication of the inflammaging signature association with mortality was found in the Hordaland Health Study.

CONCLUSION

Our study highlights the key role of the kynurenine pathway and vitamin B6 catabolism in aging, along with other well-established inflammation-related markers. A signature of inflammaging based on 10 markers was strongly associated with mortality.

摘要

背景

炎症是衰老的一个关键特征。我们的目的是:(i)研究 34 种可能与炎症过程有关的血液标志物与年龄和死亡率的关系;(ii)构建“炎症衰老”的特征。

方法

在基线(中位年龄=59 岁)和随访(中位年龄=70 岁)时,对墨尔本合作队列研究中的 976 名参与者测量了 34 种与炎症、B 族维生素状态和犬尿酸途径有关的血液标志物。使用线性和 Cox 回归分别评估与年龄和死亡率的相关性。构建了一个简单的炎症衰老特征,并将其与死亡率的相关性与分别基于所有与年龄和死亡率相关的标志物计算的 2 个标志物评分进行比较。

结果

大多数标志物(30/34)与年龄相关,其中神经氨酸、半胱氨酸蛋白酶抑制剂 C、白细胞介素(IL)-6、肿瘤坏死因子-α(TNF-α)、犬尿酸途径的几种标志物及其衍生指数 KTR(犬尿酸/色氨酸比)、PAr 指数(4-吡啶羧酸与吡哆醛 5'-磷酸和吡哆醛之和的比值)和 HK:XA(3-羟基犬尿酸/黄尿酸比)的相关性更强。许多标志物(17/34)与死亡率相关,特别是 IL-6、神经氨酸、C 反应蛋白、喹啉酸、PAr 指数和 KTR。炎症衰老特征包括 10 种标志物,与死亡率密切相关(每标准差的危险比[HR]为 1.40,95%CI:1.24-1.57,p=2×10-8),与基于所有与年龄相关的标志物(HR=1.38,95%CI:1.23-1.55,p=4×10-8)和与死亡率相关的标志物(HR=1.43,95%CI:1.28-1.60,p=1×10-10)的评分相似。在霍达兰健康研究中,也发现了炎症衰老特征与死亡率之间相关性的有力证据。

结论

我们的研究强调了犬尿酸途径和维生素 B6 分解代谢在衰老过程中以及其他已确立的炎症相关标志物中的关键作用。基于 10 种标志物的炎症衰老特征与死亡率密切相关。

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