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Age alters expression and inducibility of heme oxygenase isozymes in mice.年龄会改变小鼠体内血红素加氧酶同工酶的表达及诱导性。
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Dual pathways of carbon monoxide-mediated vasoregulation: modulation by redox mechanisms.一氧化碳介导的血管调节的双重途径:氧化还原机制的调节
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Bench-to-bedside review: Carbon monoxide--from mitochondrial poisoning to therapeutic use.从线粒体中毒到治疗用途的综述:一氧化碳。
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Heme oxygenase-1 and carbon monoxide in vascular pathobiology: focus on angiogenesis.血红素加氧酶-1与一氧化碳在血管病理生物学中的作用:聚焦于血管生成
Circulation. 2008 Jan 15;117(2):231-41. doi: 10.1161/CIRCULATIONAHA.107.698316.
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Genome-wide association with select biomarker traits in the Framingham Heart Study.弗雷明汉心脏研究中与特定生物标志物特征的全基因组关联研究。
BMC Med Genet. 2007 Sep 19;8 Suppl 1(Suppl 1):S11. doi: 10.1186/1471-2350-8-S1-S11.
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End-expiratory carbon monoxide levels in healthy subjects living in a densely populated urban environment.生活在人口密集城市环境中的健康受试者的呼气末一氧化碳水平。
Sci Total Environ. 2006 Feb 1;354(2-3):150-6. doi: 10.1016/j.scitotenv.2005.02.018. Epub 2005 Apr 7.
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Carbon monoxide: endogenous production, physiological functions, and pharmacological applications.一氧化碳:内源性生成、生理功能及药理学应用。
Pharmacol Rev. 2005 Dec;57(4):585-630. doi: 10.1124/pr.57.4.3.
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Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement.代谢综合征的诊断与管理:美国心脏协会/美国国立心肺血液研究所科学声明
Circulation. 2005 Oct 25;112(17):2735-52. doi: 10.1161/CIRCULATIONAHA.105.169404. Epub 2005 Sep 12.
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Heterogeneity of cardiovascular risk among smokers is related to degree of carbon monoxide exposure.吸烟者心血管风险的异质性与一氧化碳暴露程度有关。
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Metabolic syndrome and vascular disease: is nature or nurture leading the new epidemic of cardiovascular disease?代谢综合征与血管疾病:是先天因素还是后天因素导致了心血管疾病的新流行?
Circulation. 2004 Jan 6;109(1):2-4. doi: 10.1161/01.CIR.0000110642.73995.BF.

社区中呼出的一氧化碳与代谢综合征和心血管疾病的风险。

Exhaled carbon monoxide and risk of metabolic syndrome and cardiovascular disease in the community.

机构信息

The Framingham Heart Study, 73 Mount Wayte Ave, Ste 2, Framingham, MA 01702-5803, USA.

出版信息

Circulation. 2010 Oct 12;122(15):1470-7. doi: 10.1161/CIRCULATIONAHA.110.941013. Epub 2010 Sep 27.

DOI:10.1161/CIRCULATIONAHA.110.941013
PMID:20876437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2975571/
Abstract

BACKGROUND

Endogenous carbon monoxide (CO) at physiological concentrations is cytoprotective, whereas excess levels reflect underlying oxidative stress, inflammation, and vascular pathology and portend adverse clinical sequelae. However, the relation of exhaled CO to metabolic/vascular risk in the community is unknown.

METHODS AND RESULTS

We related exhaled CO, a surrogate measure of blood CO concentration, to the risk of developing new-onset metabolic syndrome and incident cardiovascular disease following 14 943 routine examinations (4139 unique participants; mean age, 46 years, 53% women) in the Framingham Heart Study. Baseline exhaled CO was associated with the presence of cardiometabolic risk factors (including smoking) and prevalent metabolic syndrome (odds ratio, 1.09 per log CO; 95% confidence interval, 1.02 to 1.17; P=0.01). During up to 4 years of follow-up, 1458 participants developed new-onset metabolic syndrome, and 416 experienced a first cardiovascular disease event. Compared with individuals in the lowest quartile of exhaled CO, those in the highest quartile were more likely to develop metabolic syndrome (odds ratio, 1.48; 95% confidence interval, 1.25 to 1.76; P<0.0001) and cardiovascular disease events (hazard ratio, 1.66; 95% confidence interval, 1.14 to 2.40; P=0.008) in multivariable analyses that included adjustment for smoking status.

CONCLUSION

In our community-based sample, higher exhaled CO levels predicted the development of metabolic syndrome and future cardiovascular disease events, underscoring the importance of this endogenous second messenger in the pathogenesis of metabolic and vascular risk.

摘要

背景

生理浓度的内源性一氧化碳(CO)具有细胞保护作用,而过量的 CO 则反映了潜在的氧化应激、炎症和血管病理,并预示着不良的临床后果。然而,社区人群呼出气 CO 与代谢/血管风险的关系尚不清楚。

方法和结果

我们将呼出气 CO(血液 CO 浓度的替代测量指标)与Framingham 心脏研究中 14943 次常规检查(4139 名独特参与者;平均年龄 46 岁,53%为女性)中发生新发代谢综合征和心血管疾病事件的风险相关联。基线呼出气 CO 与心血管代谢危险因素(包括吸烟)和现患代谢综合征相关(比值比,每 log CO 增加 1.09;95%置信区间,1.02 至 1.17;P=0.01)。在最多 4 年的随访期间,1458 名参与者发生新发代谢综合征,416 名参与者发生首次心血管疾病事件。与呼出气 CO 最低四分位数的个体相比,呼出气 CO 最高四分位数的个体更有可能发生代谢综合征(比值比,1.48;95%置信区间,1.25 至 1.76;P<0.0001)和心血管疾病事件(风险比,1.66;95%置信区间,1.14 至 2.40;P=0.008),多变量分析包括对吸烟状况的调整。

结论

在我们的基于社区的样本中,较高的呼出气 CO 水平预测了代谢综合征和未来心血管疾病事件的发生,这突显了这种内源性第二信使在代谢和血管风险发病机制中的重要性。