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代谢组学揭示阿片类使用障碍的生物标志物。

Metabolomics reveals biomarkers of opioid use disorder.

机构信息

Department of Nutrition, Nutrition Research Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Digestive Oncology Research Center, Digestive Diseases Research Institute, Tehran University of Medical Science, Tehran, Iran.

出版信息

Transl Psychiatry. 2021 Feb 4;11(1):103. doi: 10.1038/s41398-021-01228-7.

DOI:10.1038/s41398-021-01228-7
PMID:33542199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7862627/
Abstract

Opioid use disorder (OUD) is diagnosed using the qualitative criteria defined by the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5). Diagnostic biomarkers for OUD do not currently exist. Our study focused on developing objective biological markers to differentiate chronic opiate users with OUD from chronic opiate users without OUD. Using biospecimens from the Golestan Cohort Study, we compared the metabolomics profiles of high opium users who were diagnosed as OUD positive with high opium users who were diagnosed as OUD negative. High opium use was defined as maximum weekly opium usage greater than or equal to the median usage (2.4 g per week), and OUD was defined as having 2 or more DSM-5 criteria in any 12-month period. Among the 218 high opium users in this study, 80 were diagnosed as OUD negative, while 138 were diagnosed as OUD positive. Seven hundred and twelve peaks differentiated high opium users diagnosed as OUD positive from high opium users diagnosed as OUD negative. Stepwise logistic regression modeling of subject characteristics data together with the 712 differentiating peaks revealed a signature that is 95% predictive of an OUD positive diagnosis, a significant (p < 0.0001) improvement over a 63% accurate prediction based on subject characteristic data for these samples. These results suggest that a metabolic profile can be used to predict an OUD positive diagnosis.

摘要

阿片类使用障碍(OUD)是使用《精神障碍诊断与统计手册》第五版(DSM-5)定义的定性标准诊断的。目前还没有 OUD 的诊断生物标志物。我们的研究重点是开发客观的生物标志物,以区分患有 OUD 的慢性阿片类使用者和没有 OUD 的慢性阿片类使用者。我们使用来自戈勒斯坦队列研究的生物标本,比较了被诊断为 OUD 阳性的高鸦片使用者和被诊断为 OUD 阴性的高鸦片使用者的代谢组学特征。高鸦片使用定义为每周鸦片使用量最大大于或等于中位数(每周 2.4 克),OUD 定义为在任何 12 个月期间有 2 个或更多 DSM-5 标准。在这项研究的 218 名高鸦片使用者中,80 名被诊断为 OUD 阴性,138 名被诊断为 OUD 阳性。712 个峰区分了被诊断为 OUD 阳性的高鸦片使用者和被诊断为 OUD 阴性的高鸦片使用者。对受试者特征数据和 712 个区分峰进行逐步逻辑回归建模,揭示了一个对 OUD 阳性诊断有 95%预测能力的特征,这比基于这些样本的受试者特征数据进行的 63%准确预测有显著提高(p<0.0001)。这些结果表明,代谢谱可用于预测 OUD 阳性诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/7862627/dc971cd243b3/41398_2021_1228_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/7862627/97e4f5f0db87/41398_2021_1228_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/7862627/dc971cd243b3/41398_2021_1228_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/7862627/97e4f5f0db87/41398_2021_1228_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/7862627/dc971cd243b3/41398_2021_1228_Fig2_HTML.jpg

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2
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Arch Iran Med. 2019 Oct 1;22(10):541-545.
3
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Nutrients. 2024 Sep 26;16(19):3250. doi: 10.3390/nu16193250.
4
Untargeted metabolomics reveal signatures of a healthy lifestyle.非靶向代谢组学揭示健康生活方式的特征。
Sci Rep. 2024 Jun 13;14(1):13630. doi: 10.1038/s41598-024-64561-z.
5
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6
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7
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Gut Microbes. 2023 Dec;15(2):2246184. doi: 10.1080/19490976.2023.2246184.
8
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Nat Commun. 2023 May 30;14(1):3120. doi: 10.1038/s41467-023-38710-3.
9
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Biol Psychiatry. 2020 Jan 1;87(1):54-63. doi: 10.1016/j.biopsych.2019.07.027. Epub 2019 Aug 6.
4
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J Hum Genet. 2019 Feb;64(2):73-85. doi: 10.1038/s10038-018-0527-7. Epub 2018 Nov 6.
6
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9
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Trends Mol Med. 2018 Feb;24(2):109-120. doi: 10.1016/j.molmed.2017.12.009. Epub 2018 Jan 25.
10
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Neuroscience. 2018 Apr 15;376:188-203. doi: 10.1016/j.neuroscience.2018.01.027. Epub 2018 Jan 31.