[血浆酰基肉碱和胆汁酸水平与中国成人冠心病发病率的关系]。

Z Y Wu, S Y Song, C Q Yu, D J Y Sun, P Pei, H D Du, J S Chen, Z M Chen, J Lyu, L M Li, Y J Pang
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引用次数: 0

摘要

目的:探讨血浆酰基肉碱和胆汁酸水平与中国成年人冠心病发病风险的关系。方法:2004-2008年在全国10个地区进行中国嘉道里生物库基线调查,2008年7 - 10月进行第一次调查,收集问卷、体检和血样等数据。目前的研究基于第一次CKB调查中2,159名个体的靶向质谱代谢组学测量。采用Cox比例风险回归模型评估酰基肉碱和胆汁酸与冠心病的关系。构建未加权代谢物评分来评估酰基肉碱和胆汁酸对冠心病发生的总体影响。用受试者工作特征(ROC)曲线下面积(AUC)评价代谢物对冠心病预测模型性能的影响。对冠心病发病率的随访于2018年12月31日进行审查。结果:参与者平均年龄(53.1±9.8)岁,男性754人(34.9%)。在(10.5±0.1)年的随访中,记录了140例冠心病。酰基肉碱C3-OH、C5:1、C5:1- dc和去氧胆酸(DCA) 4种代谢物与冠心病发病率相关,危险度(95%CI)分别为1.474(1.230 ~ 1.767)、0.761(0.637 ~ 0.909)、0.773(0.650 ~ 0.918)和1.309(1.113 ~ 1.539)[错误发现率(FDR)0.05]。所有代谢物评分,包括短链、中链、长链酰基肉碱、原发性和继发性胆汁酸评分均与冠心病风险相关(FDR0.05)。与传统模型相比,DCA或4种关键代谢物的添加使预测模型的AUC分别从0.803(0.761-0.845)提高至0.812(0.772-0.852)和0.817(0.778-0.857)(均P0.05)。结论:酰基肉碱和胆汁酸水平与冠心病发生风险相关,DCA或4种关键代谢物可提高对冠心病发病的预测能力。
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[Associations of plasma acylcarnitine and bile acid levels with incidence of coronary heart disease in Chinese adults].

Objective: To explore the associations of plasma acylcarnitine and bile acid levels with the risk of incident coronary heart disease (CHD) in Chinese adults. Methods: The baseline survey of China Kadoorie Biobank (CKB) took place in 10 areas across China during 2004-2008, and the first resurvey took place from July to October 2008, with collection of data via questionnaire, physical examination and blood samples. The current study was based on 2 159 individuals with targeted mass spectrometry metabolomic measurements from the first resurvey of CKB. The associations of acylcarnitines and bile acids with incident CHD were assessed using Cox proportional hazards regression models. Unweighted metabolites scores were constructed to assess the overall effect of acylcarnitines and bile acids on incident CHD. The impact of metabolites on the performance of CHD prediction model was evaluated with the receiver operating characteristic (ROC) area under the curve (AUC). Follow-up for CHD incidence was censored on December 31, 2018. Results: The mean age of the participants was (53.1±9.8) years and 754 were males (34.9%). During (10.5±0.1) years of follow-up, 140 cases of CHD were recorded. Four metabolites including acylcarnitines C3-OH, C5:1, C5:1-DC, and deoxycholic acid (DCA) showed associations with CHD incidence and the HR (95%CI) were 1.474 (1.230-1.767), 0.761 (0.637-0.909), 0.773 (0.650-0.918), and 1.309 (1.113-1.539), respectively [false discovery rate (FDR)0.05]. All metabolite scores, including short-chain, medium-chain, long-chain acylcarnitines, primary and secondary bile acids scores were associated with the risk of CHD (FDR0.05). Compared to the traditional models, the addition of DCA or 4 key metabolites increased the AUC of the predictive model from 0.803 (0.761-0.845) to 0.812 (0.772-0.852) and 0.817 (0.778-0.857), respectively (all P0.05). Conclusions: Acylcarnitine and bile acid levels are associated with the risk of CHD, and DCA or 4 key metabolites can improve the predictive ability for CHD incidence.

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Zhonghua yi xue za zhi
Zhonghua yi xue za zhi Medicine-Medicine (all)
CiteScore
0.80
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0.00%
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400
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