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Reduced trunk fat and triglycerides after strength training are associated with reduced LPS levels in HIV-infected individuals.力量训练后躯干脂肪和甘油三酯减少与HIV感染者LPS水平降低有关。
J Acquir Immune Defic Syndr. 2014 Jun 1;66(2):e52-4. doi: 10.1097/QAI.0000000000000132.
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Plasma lipopolysaccharide and triglycerides are independently associated and both markers correlate with the development of metabolic syndrome in HIV infection.
J Acquir Immune Defic Syndr. 2014 Apr 1;65(4):e158-61. doi: 10.1097/QAI.0000000000000055.
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HIV and the heart: the impact of antiretroviral therapy: a global perspective.HIV 与心脏:抗逆转录病毒疗法的影响:全球视角。
Eur Heart J. 2013 Dec;34(46):3538-46. doi: 10.1093/eurheartj/eht388. Epub 2013 Oct 14.
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Assessing the human gut microbiota in metabolic diseases.评估代谢疾病中的人类肠道微生物群。
Diabetes. 2013 Oct;62(10):3341-9. doi: 10.2337/db13-0844.
5
Microbial translocation and metabolic and body composition measures in treated and untreated HIV infection.接受治疗和未接受治疗的HIV感染中的微生物易位、代谢及身体成分指标
AIDS Res Hum Retroviruses. 2014 Mar;30(3):272-7. doi: 10.1089/AID.2013.0162. Epub 2013 Oct 8.
6
Urinary excretion of kynurenine and tryptophan, cardiovascular events, and mortality after elective coronary angiography.色氨酸和犬尿氨酸尿液排泄与择期冠状动脉造影后的心血管事件和死亡率。
Eur Heart J. 2013 Sep;34(34):2689-96. doi: 10.1093/eurheartj/eht264. Epub 2013 Jul 25.
7
Dysbiosis of the gut microbiota is associated with HIV disease progression and tryptophan catabolism.肠道微生物群落失调与 HIV 疾病进展和色氨酸分解代谢有关。
Sci Transl Med. 2013 Jul 10;5(193):193ra91. doi: 10.1126/scitranslmed.3006438.
8
Discrepant coagulation profile in HIV infection: elevated D-dimer but impaired platelet aggregation and clot initiation.HIV 感染患者的凝血功能异常:D-二聚体升高,但血小板聚集和凝血起始功能受损。
AIDS. 2013 Nov 13;27(17):2749-58. doi: 10.1097/01.aids.0000432462.21723.ed.
9
Plasma lipopolysaccharide is closely associated with glycemic control and abdominal obesity: evidence from bariatric surgery.血浆脂多糖与血糖控制及腹型肥胖密切相关:来自减肥手术的证据。
Diabetes Care. 2013 Nov;36(11):3627-32. doi: 10.2337/dc13-0451. Epub 2013 Jul 8.
10
Microbial translocation in HIV infection is associated with dyslipidemia, insulin resistance, and risk of myocardial infarction.HIV 感染中的微生物易位与血脂异常、胰岛素抵抗和心肌梗死风险有关。
J Acquir Immune Defic Syndr. 2013 Dec 15;64(5):425-33. doi: 10.1097/QAI.0b013e31829f919d.

HIV感染中的微生物易位与心脏代谢危险因素

Microbial translocation and cardiometabolic risk factors in HIV infection.

作者信息

Trøseid Marius, Manner Ingjerd W, Pedersen Karin K, Haissman Judith M, Kvale Dag, Nielsen Susanne D

机构信息

1 Department of Infectious Diseases, Oslo University Hospital , Oslo, Norway .

出版信息

AIDS Res Hum Retroviruses. 2014 Jun;30(6):514-22. doi: 10.1089/aid.2013.0280. Epub 2014 Mar 25.

DOI:10.1089/aid.2013.0280
PMID:24521167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4046217/
Abstract

The widespread access to antiretroviral treatment during the past decades has transformed HIV infection from a lethal disease to a chronic condition, in which the relative burden of non-AIDS-related chronic disorders such as cardiovascular disease, malignancy, renal, liver, and bone disease has increased. The adjusted relative risk for myocardial infarction is reported to be around 2-fold compared to that of the general population, which over time is likely to translate into increased absolute risk in an aging population. Thus, delineating potentially HIV-specific pathogenetic mechanisms is crucial in order to tailor novel strategies for prophylaxis and treatment. This review will focus on advances in the field that possibly link HIV-induced alterations of the gut mucosa and consequent microbial translocation to cardiometabolic risk factors in HIV infection. Recent work suggests that markers of microbial translocation are closely associated with several cardiovascular risk factors such as dyslipidemia, insulin resistance, hypertension, coagulation abnormalities, endothelial dysfunction, and carotid atherosclerosis. Future studies should investigate whether associations between microbial translocation and cardiovascular risk factors will translate into increased risk of acute events, and whether strategies to target gut microbiota and microbial translocation might reduce such a risk.

摘要

在过去几十年中,抗逆转录病毒治疗的广泛应用已将艾滋病毒感染从一种致命疾病转变为一种慢性疾病,在此过程中,心血管疾病、恶性肿瘤、肾脏、肝脏和骨骼疾病等非艾滋病相关慢性疾病的相对负担有所增加。据报道,与普通人群相比,心肌梗死的校正相对风险约为2倍,随着时间的推移,这可能会导致老年人群中绝对风险的增加。因此,明确潜在的艾滋病毒特异性致病机制对于制定新的预防和治疗策略至关重要。本综述将聚焦于该领域的进展,这些进展可能将艾滋病毒引起的肠道黏膜改变以及随之而来的微生物易位与艾滋病毒感染中的心脏代谢危险因素联系起来。最近的研究表明,微生物易位标志物与血脂异常、胰岛素抵抗、高血压、凝血异常、内皮功能障碍和颈动脉粥样硬化等多种心血管危险因素密切相关。未来的研究应调查微生物易位与心血管危险因素之间的关联是否会转化为急性事件风险的增加,以及针对肠道微生物群和微生物易位的策略是否可能降低这种风险。