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本文引用的文献

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TwinsUK: The UK Adult Twin Registry Update.英国双胞胎登记库(TwinsUK):英国成人双胞胎登记库更新
Twin Res Hum Genet. 2019 Dec;22(6):523-529. doi: 10.1017/thg.2019.65. Epub 2019 Sep 17.
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The Short-Chain Fatty Acid Acetate in Body Weight Control and Insulin Sensitivity.短链脂肪酸乙酸在体重控制和胰岛素敏感性中的作用。
Nutrients. 2019 Aug 18;11(8):1943. doi: 10.3390/nu11081943.
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Gut microbiome and serum metabolome analyses identify molecular biomarkers and altered glutamate metabolism in fibromyalgia.肠道微生物组和血清代谢组分析鉴定出纤维肌痛的分子生物标志物和谷氨酸代谢改变。
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Pain. 2019 Nov;160(11):2589-2602. doi: 10.1097/j.pain.0000000000001640.
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Species-level functional profiling of metagenomes and metatranscriptomes.宏基因组和宏转录组的物种水平功能分析。
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Multi-OMICS analyses of frailty and chronic widespread musculoskeletal pain suggest involvement of shared neurological pathways.多组学分析衰弱和慢性广泛性肌肉骨骼疼痛表明存在共同的神经通路参与。
Pain. 2018 Dec;159(12):2565-2572. doi: 10.1097/j.pain.0000000000001364.
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Use of dietary indices to control for diet in human gut microbiota studies.使用膳食指数来控制人体肠道微生物群研究中的饮食。
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Current understanding of the human microbiome.人类微生物组的现有认识。
Nat Med. 2018 Apr 10;24(4):392-400. doi: 10.1038/nm.4517.
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Environment dominates over host genetics in shaping human gut microbiota.环境在塑造人类肠道微生物群方面优于宿主遗传学。
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Functional Genomics of Host-Microbiome Interactions in Humans.人类宿主-微生物组相互作用的功能基因组学。
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慢性广泛性疼痛与肠道微生物组之间的关联。

An association between chronic widespread pain and the gut microbiome.

机构信息

Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London, UK.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Rheumatology (Oxford). 2021 Aug 2;60(8):3727-3737. doi: 10.1093/rheumatology/keaa847.

DOI:10.1093/rheumatology/keaa847
PMID:33331911
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8328510/
Abstract

OBJECTIVES

Chronic widespread musculoskeletal pain (CWP) is a characteristic symptom of fibromyalgia, which has been shown to be associated with an altered gut microbiome. Microbiome studies to date have not examined the milder CWP phenotype specifically nor have they explored the role of raised BMI. The aim of this study was to investigate whether the microbiome is abnormal in CWP.

METHODS

CWP was assessed using a standardized screening questionnaire in female volunteers from the TwinsUK cohort including 113 CWP cases and 1623 controls. The stool microbiome was characterized using 16S rRNA amplicon sequencing and amplicon sequence variants, and associations with CWP examined using linear mixed-effects models adjusting for BMI, age, diet, family relatedness and technical factors.

RESULTS

Alpha diversity was significantly lower in CWP cases than controls (Mann-Whitney test, P-values 2.3e-04 and 1.2e-02, for Shannon and Simpson indices respectively). The species Coprococcus comes was significantly depleted in CWP cases (Padj = 3.04e-03). A genome-wide association study (GWAS) performed for C. comes in TwinsUK followed by meta-analysis with three Dutch cohorts (total n = 3521) resulted in nine suggestive regions, with the most convincing on chromosome 4 near the TRAM1L1 gene (rs76957229, P = 7.4e-8). A Mendelian randomization study based on the results of the GWAS did not support a causal role for C. comes on the development of CWP.

CONCLUSIONS

We have demonstrated reduced diversity in the microbiome in CWP, indicating an involvement of the gut microbiota in CWP; prospectively the microbiome may offer therapeutic opportunities for this condition.

摘要

目的

慢性广泛性肌肉骨骼疼痛(CWP)是纤维肌痛的特征性症状,现已证实其与肠道微生物组的改变有关。迄今为止,微生物组研究尚未专门检查较轻的 CWP 表型,也未探讨 BMI 升高的作用。本研究旨在调查 CWP 患者的微生物组是否异常。

方法

使用来自 TwinsUK 队列的女性志愿者的标准化筛查问卷评估 CWP,该问卷包括 113 例 CWP 病例和 1623 例对照。使用 16S rRNA 扩增子测序和扩增子序列变异来描述肠道微生物组,并使用线性混合效应模型调整 BMI、年龄、饮食、家族相关性和技术因素来检查与 CWP 的关联。

结果

CWP 病例的 alpha 多样性明显低于对照组(Mann-Whitney 检验,Shannon 和 Simpson 指数的 P 值分别为 2.3e-04 和 1.2e-02)。Coprococcus comes 物种在 CWP 病例中明显减少(Padj = 3.04e-03)。在 TwinsUK 中对 C. comes 进行全基因组关联研究(GWAS),然后在三个荷兰队列(总 n = 3521)中进行荟萃分析,结果得到了 9 个提示区域,最有说服力的是染色体 4 上靠近 TRAM1L1 基因的区域(rs76957229,P = 7.4e-8)。基于 GWAS 结果的孟德尔随机化研究不支持 C. comes 对 CWP 发展的因果作用。

结论

我们已经证明 CWP 中微生物组的多样性降低,表明肠道微生物组参与了 CWP;前瞻性地,微生物组可能为这种疾病提供治疗机会。