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特应性皮炎的昼夜代谢组学。

The circadian metabolome of atopic dermatitis.

机构信息

Epithelial Therapeutics Unit, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, Md.

Departments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.

出版信息

J Allergy Clin Immunol. 2024 Apr;153(4):1148-1154. doi: 10.1016/j.jaci.2023.11.926. Epub 2024 Jan 21.


DOI:10.1016/j.jaci.2023.11.926
PMID:38262502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10999347/
Abstract

BACKGROUND: Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by dry, pruritic skin. Several studies have described nocturnal increases in itching behavior, suggesting a role for the circadian rhythm in modulating symptom severity. However, the circadian rhythm of metabolites in the skin and serum of patients with AD is yet to be described. OBJECTIVE: We sought to assess circadian patterns of skin and serum metabolism in patients with AD. METHODS: Twelve patients with moderate to severe AD and 5 healthy volunteers were monitored for 28 hours in a controlled environment. Serum was collected every 2 hours and tape strips every 4 hours from both lesional and nonlesional skin in participants with AD and location-, sex-, and age-matched healthy skin of controls. We then performed an untargeted metabolomics analysis, examining the circadian peaks of metabolism in patients with AD. RESULTS: Distinct metabolic profiles were observed in AD versus control samples. When accounting for time of collection, the greatest differences in serum metabolic pathways were observed in arachidonic acid, steroid biosynthesis, and terpenoid backbone biosynthesis. We identified 42 circadian peaks in AD or control serum and 17 in the skin. Pathway enrichment and serum-skin metabolite correlation varied throughout the day. Differences were most evident in the late morning and immediately after sleep onset. CONCLUSIONS: Although limited by a small sample size and observational design, our findings suggest that accounting for sample collection time could improve biomarker detection studies in AD and highlight that metabolic changes may be associated with nocturnal differences in symptom severity.

摘要

背景:特应性皮炎(AD)是一种慢性炎症性皮肤病,其特征为皮肤干燥、瘙痒。有几项研究描述了夜间瘙痒行为增加,表明昼夜节律在调节症状严重程度方面发挥作用。然而,AD 患者皮肤和血清中的代谢物昼夜节律尚未被描述。

目的:我们旨在评估 AD 患者皮肤和血清代谢的昼夜节律模式。

方法:12 名中重度 AD 患者和 5 名健康志愿者在受控环境中监测 28 小时。每隔 2 小时采集血清,每隔 4 小时从 AD 患者的皮损和非皮损皮肤以及性别和年龄匹配的健康志愿者的皮肤采集胶带条。然后,我们进行了非靶向代谢组学分析,以检查 AD 患者代谢的昼夜节律峰值。

结果:与对照样本相比,AD 样本中观察到不同的代谢特征。当考虑到采集时间时,AD 患者血清代谢途径的最大差异在于花生四烯酸、类固醇生物合成和萜烯骨架生物合成。我们在 AD 或对照血清中鉴定出 42 个昼夜节律峰值,在皮肤中鉴定出 17 个昼夜节律峰值。途径富集和血清-皮肤代谢物相关性随时间变化。差异在上午晚些时候和睡眠开始后最明显。

结论:尽管样本量小且设计为观察性研究,但我们的发现表明,考虑样本采集时间可以提高 AD 中的生物标志物检测研究,并强调代谢变化可能与夜间症状严重程度的差异有关。

相似文献

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[2]
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[3]
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[4]
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[2]
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[3]
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[4]
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本文引用的文献

[1]
Diisocyanates influence models of atopic dermatitis through direct activation of TRPA1.

PLoS One. 2023

[2]
Stratum corneum lipid and cytokine biomarkers at age 2 months predict the future onset of atopic dermatitis.

J Allergy Clin Immunol. 2023-5

[3]
Skin biomarkers predict development of atopic dermatitis in infancy.

Allergy. 2023-3

[4]
Impact of Skin Tissue Collection Method on Downstream MALDI-Imaging.

Metabolites. 2022-5-30

[5]
Using MetaboAnalyst 5.0 for LC-HRMS spectra processing, multi-omics integration and covariate adjustment of global metabolomics data.

Nat Protoc. 2022-8

[6]
Mitochondrial Activity Is Upregulated in Nonlesional Atopic Dermatitis and Amenable to Therapeutic Intervention.

J Invest Dermatol. 2022-10

[7]
Peroxisomal Fatty Acid Oxidation and Glycolysis Are Triggered in Mouse Models of Lesional Atopic Dermatitis.

JID Innov. 2021-6-15

[8]
The circadian clock and diseases of the skin.

FEBS Lett. 2021-10

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MetaboAnalyst 5.0: narrowing the gap between raw spectra and functional insights.

Nucleic Acids Res. 2021-7-2

[10]
Skin as a window to body-clock time.

Proc Natl Acad Sci U S A. 2018-11-27

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