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本文引用的文献

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Plasma Tryptophan-Kynurenine Metabolites Are Altered in Human Immunodeficiency Virus Infection and Associated With Progression of Carotid Artery Atherosclerosis.血浆色氨酸-犬尿氨酸代谢物在人类免疫缺陷病毒感染中发生改变,并与颈动脉粥样硬化的进展相关。
Clin Infect Dis. 2018 Jul 2;67(2):235-242. doi: 10.1093/cid/ciy053.
2
Choline and its metabolites are differently associated with cardiometabolic risk factors, history of cardiovascular disease, and MRI-documented cerebrovascular disease in older adults.胆碱及其代谢产物与老年人的心脏代谢危险因素、心血管疾病史以及磁共振成像记录的脑血管疾病存在不同程度的关联。
Am J Clin Nutr. 2017 Jun;105(6):1283-1290. doi: 10.3945/ajcn.116.137158. Epub 2017 Mar 29.
3
Association of Macrophage Inflammation Biomarkers With Progression of Subclinical Carotid Artery Atherosclerosis in HIV-Infected Women and Men.巨噬细胞炎症生物标志物与HIV感染女性和男性亚临床颈动脉粥样硬化进展的关联。
J Infect Dis. 2017 May 1;215(9):1352-1361. doi: 10.1093/infdis/jix082.
4
Brief Report: Intestinal Microbiota-Produced Trimethylamine-N-Oxide and Its Association With Coronary Stenosis and HIV Serostatus.简短报告:肠道微生物群产生的氧化三甲胺及其与冠状动脉狭窄和HIV血清学状态的关联。
J Acquir Immune Defic Syndr. 2016 May 1;72(1):114-8. doi: 10.1097/QAI.0000000000000937.
5
Microbiota-Dependent Marker TMAO Is Elevated in Silent Ischemia but Is Not Associated With First-Time Myocardial Infarction in HIV Infection.微生物群依赖标志物氧化三甲胺(TMAO)在无症状性缺血中升高,但与HIV感染患者首次心肌梗死无关。
J Acquir Immune Defic Syndr. 2016 Feb 1;71(2):130-6. doi: 10.1097/QAI.0000000000000843.
6
HIV Infection Is Associated With Progression of Subclinical Carotid Atherosclerosis.HIV感染与亚临床颈动脉粥样硬化的进展相关。
Clin Infect Dis. 2015 Aug 15;61(4):640-50. doi: 10.1093/cid/civ325. Epub 2015 Apr 22.
7
Plaque burden in HIV-infected patients is associated with serum intestinal microbiota-generated trimethylamine.HIV感染患者的斑块负荷与血清中肠道微生物群产生的三甲胺有关。
AIDS. 2015 Feb 20;29(4):443-52. doi: 10.1097/QAD.0000000000000565.
8
HIV-induced alteration in gut microbiota: driving factors, consequences, and effects of antiretroviral therapy.HIV 诱导的肠道菌群改变:驱动因素、后果和抗逆转录病毒治疗的影响。
Gut Microbes. 2014 Jul 1;5(4):562-70. doi: 10.4161/gmic.32132. Epub 2014 Jul 31.
9
Intestinal microbial metabolism of phosphatidylcholine and cardiovascular risk.肠道微生物对磷脂酰胆碱的代谢与心血管风险
N Engl J Med. 2013 Apr 25;368(17):1575-84. doi: 10.1056/NEJMoa1109400.
10
HIV status, burden of comorbid disease, and biomarkers of inflammation, altered coagulation, and monocyte activation.HIV 状态、合并症负担以及炎症、凝血功能改变和单核细胞激活的生物标志物。
Clin Infect Dis. 2012 Jul;55(1):126-36. doi: 10.1093/cid/cis406. Epub 2012 Apr 24.

肠道微生物相关胆碱代谢物三甲胺 N-氧化物与 HIV 感染患者颈动脉粥样硬化进展相关。

Gut Microbial-Related Choline Metabolite Trimethylamine-N-Oxide Is Associated With Progression of Carotid Artery Atherosclerosis in HIV Infection.

机构信息

Department of Nutrition and Food Hygiene, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

出版信息

J Infect Dis. 2018 Sep 22;218(9):1474-1479. doi: 10.1093/infdis/jiy356.

DOI:10.1093/infdis/jiy356
PMID:29912352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6151074/
Abstract

We examined associations of 5 plasma choline metabolites with carotid plaque among 520 HIV-infected and 217 HIV-uninfected participants (112 incident plaque cases) over 7 years. After multivariable adjustment, higher gut microbiota-related metabolite trimethylamine-N-oxide (TMAO) was associated with an increased risk of carotid plaque in HIV-infected participants (risk ratio = 1.25 per standard deviation increment; 95% confidence interval, 1.05-1.50; P = .01). TMAO was positively correlated with biomarkers of monocyte activation and inflammation (sCD14, sCD163). Further adjustment for these biomarkers attenuated the association between TMAO and carotid plaque (P = .08). Among HIV-infected individuals, plasma TMAO was associated with carotid atherosclerosis progression, partially through immune activation and inflammation.

摘要

我们在 7 年内研究了 520 名 HIV 感染者和 217 名 HIV 未感染者(112 名新发病例)中 5 种血浆胆碱代谢物与颈动脉斑块之间的关联。经过多变量调整后,与肠道微生物群相关的代谢物三甲胺 N-氧化物(TMAO)较高与 HIV 感染者颈动脉斑块风险增加相关(风险比=每标准偏差增加 1.25;95%置信区间,1.05-1.50;P =.01)。TMAO 与单核细胞活化和炎症的生物标志物(sCD14、sCD163)呈正相关。进一步调整这些生物标志物减弱了 TMAO 与颈动脉斑块之间的关联(P =.08)。在 HIV 感染者中,血浆 TMAO 与颈动脉粥样硬化进展有关,部分通过免疫激活和炎症。