Pre-diagnostic plasma advanced glycation end-products and soluble receptor for advanced glycation end-products and mortality in colorectal cancer patients.

IF 5.7 2区 医学 Q1 ONCOLOGY International Journal of Cancer Pub Date : 2024-12-01 Epub Date: 2024-07-26 DOI:10.1002/ijc.35114
Jinze Li, Jacqueline Roshelli Baker, Elom K Aglago, Zhiwei Zhao, Li Jiao, Heinz Freisling, David J Hughes, Anne Kirstine Eriksen, Anne Tjønneland, Gianluca Severi, Verena Katzke, Rudolf Kaaks, Matthias B Schulze, Giovanna Masala, Valeria Pala, Fabrizio Pasanisi, Rosario Tumino, Lisa Padroni, Roel C H Vermeulen, Inger T Gram, Tonje Braaten, Paula Gabriela Jakszyn, Maria-José Sánchez, Jesús-Humberto Gómez-Gómez, Conchi Moreno-Iribas, Pilar Amiano, Keren Papier, Elisabete Weiderpass, Inge Huybrechts, Alicia K Heath, Casper Schalkwijk, Mazda Jenab, Veronika Fedirko
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引用次数: 0

Abstract

Advanced glycation end-products (AGEs), formed endogenously or obtained exogenously from diet, may contribute to chronic inflammation, intracellular signaling alterations, and pathogenesis of several chronic diseases including colorectal cancer (CRC). However, the role of AGEs in CRC survival is less known. The associations of pre-diagnostic circulating AGEs and their soluble receptor (sRAGE) with CRC-specific and overall mortality were estimated using multivariable-adjusted Cox proportional hazards regression among 1369 CRC cases in the European Prospective Investigation into Cancer and Nutrition (EPIC) study. Concentrations of major plasma AGEs, Nε-[carboxy-methyl]lysine (CML), Nε-[carboxy-ethyl]lysine (CEL) and Nδ-[5-hydro-5-methyl-4-imidazolon-2-yl]-ornithine (MG-H1), were measured using ultra-performance liquid chromatography mass-spectrometry. sRAGE was assessed by enzyme-linked immunosorbent assay. Over a mean follow-up period of 96 months, 693 deaths occurred of which 541 were due to CRC. Individual and combined AGEs were not statistically significantly associated with CRC-specific or overall mortality. However, there was a possible interaction by sex for CEL (Pinteraction = .05). Participants with higher sRAGE had a higher risk of dying from CRC (HRQ5vs.Q1 = 1.67, 95% CI: 1.21-2.30, Ptrend = .02) or any cause (HRQ5vs.Q1 = 1.38, 95% CI: 1.05-1.83, Ptrend = .09). These associations tended to be stronger among cases with diabetes (Pinteraction = .03) and pre-diabetes (Pinteraction <.01) before CRC diagnosis. Pre-diagnostic AGEs were not associated with CRC-specific and overall mortality in individuals with CRC. However, a positive association was observed for sRAGE. Our findings may stimulate further research on the role of AGEs and sRAGE in survival among cancer patients with special emphasis on potential effect modifications by sex and diabetes.

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诊断前血浆高级糖化终产物和高级糖化终产物可溶性受体与结直肠癌患者的死亡率。
高级糖化终产物(AGEs)由内源性形成或从饮食中外源性获得,可能会导致慢性炎症、细胞内信号改变以及包括结直肠癌(CRC)在内的多种慢性疾病的发病机制。然而,AGEs 在 CRC 生存中的作用却鲜为人知。在欧洲癌症与营养前瞻性调查(EPIC)研究的 1369 例 CRC 病例中,采用多变量调整 Cox 比例危险回归法估算了诊断前循环 AGEs 及其可溶性受体(sRAGE)与 CRC 特异性死亡率和总死亡率的关系。使用超高效液相色谱质谱法测量了血浆中主要 AGE 的浓度,包括 Nε-[羧甲基]赖氨酸(CML)、Nε-[羧乙基]赖氨酸(CEL)和 Nδ-[5-氢-5-甲基-4-咪唑啉-2-基]-鸟氨酸(MG-H1)。在平均 96 个月的随访期间,共有 693 人死亡,其中 541 人死于 CRC。从统计学角度看,单个 AGEs 和组合 AGEs 与 CRC 特异性死亡率或总死亡率无显著相关性。不过,CEL可能与性别存在交互作用(Pinteraction = .05)。sRAGE 较高的参与者死于 CRC(HRQ5vs.Q1 = 1.67,95% CI:1.21-2.30,Ptrend = .02)或任何原因(HRQ5vs.Q1 = 1.38,95% CI:1.05-1.83,Ptrend = .09)的风险较高。这些关联在糖尿病(Pinteraction = .03)和糖尿病前期(Pinteraction
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来源期刊
CiteScore
13.40
自引率
3.10%
发文量
460
审稿时长
2 months
期刊介绍: The International Journal of Cancer (IJC) is the official journal of the Union for International Cancer Control—UICC; it appears twice a month. IJC invites submission of manuscripts under a broad scope of topics relevant to experimental and clinical cancer research and publishes original Research Articles and Short Reports under the following categories: -Cancer Epidemiology- Cancer Genetics and Epigenetics- Infectious Causes of Cancer- Innovative Tools and Methods- Molecular Cancer Biology- Tumor Immunology and Microenvironment- Tumor Markers and Signatures- Cancer Therapy and Prevention
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