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微量营养素和血清代谢物在椎间盘退变中的作用:孟德尔随机化研究与中介分析的见解

The role of micronutrients and serum metabolites in intervertebral disk degeneration: insights from a Mendelian randomization study and mediation analysis.

作者信息

Jiang Nizhou, Wang Quanxiang, Jiang Jian, Li Lei

机构信息

Department of Spine Surgery, Central Hospital of Dalian University of Technology, Dalian, China.

Department of Spine Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

出版信息

Front Nutr. 2024 Oct 21;11:1428403. doi: 10.3389/fnut.2024.1428403. eCollection 2024.

DOI:10.3389/fnut.2024.1428403
PMID:39498405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11532028/
Abstract

BACKGROUND

Intervertebral disk degeneration (IVDD) is a complex degenerative skeletal condition, potentially influenced by micronutrients and serum metabolites in its etiology. However, the exact causal relationship between these factors and IVDD remains ambiguous.

METHODS

The research employed a Two-Sample Mendelian Randomization (2SMR) analysis to thoroughly evaluate the causal relationship between 15 micronutrients (consisting of 7 minerals and 8 vitamins) as exposure variables, 1,091 blood metabolites, and 309 metabolite ratios as intermediary factors, and IVDD as the outcome. Additionally, reverse MR analysis and mediation analysis were carried out to validate the reliability of the results and explore the underlying mechanism by which micronutrients influence the risk of IVDD by regulating metabolites.

RESULTS

Among the micronutrients examined, vitamin B12 exhibited a noteworthy negative correlation with the incidence of IVDD (OR: 0.752, 95% [CI]: 0.573-0.987,  = 0.040), indicating a potential reduction in IVDD risk with increased vitamin B12 consumption. Of the 1,091 blood metabolites and 309 metabolite ratios analyzed, 52 metabolites displayed significant associations with IVDD, primarily linked to amino acid, fatty acid, nucleotide, and sphingolipid metabolic pathways. Mediation analysis identified 4-acetaminophen sulfate as a potential mediator in the protective effect of vitamin B12 against IVDD.

CONCLUSION

This study has shown that vitamin B12 may reduce the risk of IVDD and has identified 52 serum metabolites that are associated with IVDD. Furthermore, it proposes that 4-acetaminophen sulfate could serve as a potential mechanism by which vitamin B12 exerts its inhibitory effects on IVDD.

摘要

背景

椎间盘退变(IVDD)是一种复杂的退行性骨骼疾病,其病因可能受微量营养素和血清代谢物的影响。然而,这些因素与IVDD之间的确切因果关系仍不明确。

方法

本研究采用两样本孟德尔随机化(2SMR)分析,全面评估15种微量营养素(包括7种矿物质和8种维生素)作为暴露变量、1091种血液代谢物和309种代谢物比值作为中介因素与IVDD作为结局之间的因果关系。此外,进行了反向MR分析和中介分析,以验证结果的可靠性,并探讨微量营养素通过调节代谢物影响IVDD风险的潜在机制。

结果

在所检测的微量营养素中,维生素B12与IVDD的发病率呈显著负相关(OR:0.752,95%[CI]:0.573 - 0.987,P = 0.040),表明随着维生素B12摄入量的增加,IVDD风险可能降低。在分析的1091种血液代谢物和309种代谢物比值中,52种代谢物与IVDD显示出显著关联,主要与氨基酸、脂肪酸、核苷酸和鞘脂代谢途径有关。中介分析确定对乙酰氨基酚硫酸盐是维生素B12对IVDD保护作用的潜在中介物。

结论

本研究表明维生素B12可能降低IVDD的风险,并确定了52种与IVDD相关的血清代谢物。此外,研究提出对乙酰氨基酚硫酸盐可能是维生素B12对IVDD发挥抑制作用的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/dc7dcc606b58/fnut-11-1428403-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/830e3f59abc6/fnut-11-1428403-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/b922fa62e41e/fnut-11-1428403-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/d1c21fdb460b/fnut-11-1428403-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/dc7dcc606b58/fnut-11-1428403-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/830e3f59abc6/fnut-11-1428403-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/a41a3a05f958/fnut-11-1428403-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/b922fa62e41e/fnut-11-1428403-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/d1c21fdb460b/fnut-11-1428403-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/11532028/dc7dcc606b58/fnut-11-1428403-g005.jpg

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Selenium-SelK-GPX4 axis protects nucleus pulposus cells against mechanical overloading-induced ferroptosis and attenuates senescence of intervertebral disc.硒- SelK-GPX4 轴保护髓核细胞免受机械超负荷诱导的铁死亡,并减轻椎间盘衰老。
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Lactic acid promotes nucleus pulposus cell senescence and corresponding intervertebral disc degeneration via interacting with Akt.
乳酸通过与 Akt 相互作用促进髓核细胞衰老和相应的椎间盘退变。
Cell Mol Life Sci. 2024 Jan 12;81(1):24. doi: 10.1007/s00018-023-05094-y.
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SEPHS1 attenuates intervertebral disc degeneration by delaying nucleus pulposus cell senescence through the Hippo-Yap/Taz pathway.SEPHS1 通过 Hippo-Yap/Taz 通路延缓髓核细胞衰老来减轻椎间盘退变。
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