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横断面单中心研究:使用电子烟的健康年轻人群循环免疫细胞中细胞氧化应激升高:对未来心血管风险的影响。

Elevated Cellular Oxidative Stress in Circulating Immune Cells in Otherwise Healthy Young People Who Use Electronic Cigarettes in a Cross-Sectional Single-Center Study: Implications for Future Cardiovascular Risk.

机构信息

Division of Infectious Disease Department of Medicine David Geffen School of Medicine at UCLA Los Angeles CA.

Division of Cardiology Department of Medicine David Geffen School of Medicine at UCLA Los Angeles CA.

出版信息

J Am Heart Assoc. 2020 Sep 15;9(18):e016983. doi: 10.1161/JAHA.120.016983. Epub 2020 Sep 8.

DOI:10.1161/JAHA.120.016983
PMID:32896211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7726977/
Abstract

Background Tobacco cigarettes (TCs) increase oxidative stress and inflammation, both instigators of atherosclerotic cardiac disease. It is unknown if electronic cigarettes (ECs) also increase immune cell oxidative stress. We hypothesized an ordered, "dose-response" relationship, with tobacco-product type as "dose" (lowest in nonsmokers, intermediate in EC vapers, and highest in TC smokers), and the "response" being cellular oxidative stress (COS) in immune cell subtypes, in otherwise, healthy young people. Methods and Results Using flow cytometry and fluorescent probes, COS was determined in immune cell subtypes in 33 otherwise healthy young people: nonsmokers (n=12), EC vapers (n=12), and TC smokers (n=9). Study groups had similar baseline characteristics, including age, sex, race, and education level. A dose-response increase in proinflammatory monocytes and lymphocytes, and their COS content among the 3 study groups was found: lowest in nonsmokers, intermediate in EC vapers, and highest in TC smokers. These findings were most striking in CD14CD16 and CD14CD16 proinflammatory monocytes and were reproduced with 2 independent fluorescent probes of COS. Conclusions These findings portend the development of premature cardiovascular disease in otherwise healthy young people who chronically vape ECs. On the other hand, that the COS is lower in EC vapers compared with TC smokers warrants additional investigation to determine if switching to ECs may form part of a harm-reduction strategy. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT03823885.

摘要

背景

香烟会增加氧化应激和炎症,这两者都是动脉粥样硬化性心脏病的诱因。目前尚不清楚电子烟是否也会增加免疫细胞的氧化应激。我们假设存在一种有序的“剂量-反应”关系,其中烟草产品类型为“剂量”(从不吸烟的人最低,电子烟使用者处于中间,而吸烟的人最高),而“反应”则是免疫细胞亚群中的细胞氧化应激(COS),这在其他方面健康的年轻人中是如此。

方法和结果

我们使用流式细胞术和荧光探针,在 33 名其他方面健康的年轻人的免疫细胞亚群中确定了细胞氧化应激(COS):从不吸烟的人(n=12)、电子烟使用者(n=12)和吸烟的人(n=9)。研究组具有相似的基线特征,包括年龄、性别、种族和教育水平。在 3 个研究组中,发现促炎单核细胞和淋巴细胞以及它们的 COS 含量呈剂量依赖性增加:从不吸烟的人最低,电子烟使用者处于中间,而吸烟的人最高。这些发现,在 CD14CD16 和 CD14CD16 促炎单核细胞中最为明显,并且用 2 种独立的 COS 荧光探针得到了重现。

结论

这些发现预示着在其他方面健康的年轻人中,长期使用电子烟会导致过早发生心血管疾病。另一方面,与吸烟的人相比,电子烟使用者的 COS 较低,这需要进一步调查,以确定是否将电子烟作为减少危害的策略的一部分。

注册网址

https://www.clinicaltrials.gov;唯一标识符:NCT03823885。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/7726977/6cf8dc0d58d0/JAH3-9-e016983-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/7726977/4b6fd2a9d523/JAH3-9-e016983-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/7726977/6cf8dc0d58d0/JAH3-9-e016983-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/7726977/4b6fd2a9d523/JAH3-9-e016983-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/7726977/6cf8dc0d58d0/JAH3-9-e016983-g005.jpg

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