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同型半胱氨酸及尿酸水平与社区人群中国动脉粥样硬化性心血管疾病风险预测关系的研究
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作者 王露 聂颖 +3 位作者 马丽华 薛丽佳 公维红 刘红军 《心肺血管病杂志》 CAS 2024年第2期103-109,共7页
目的:基于中国动脉粥样硬化性心血管疾病风险预测[prediction for atherosclerotic cardio-vascular disease(ASCVD)risk in China,China-PAR]模型,探讨血同型半胱氨酸(homocysteine,HCY)及UA水平与社区人群心血管病10年风险的关系。方... 目的:基于中国动脉粥样硬化性心血管疾病风险预测[prediction for atherosclerotic cardio-vascular disease(ASCVD)risk in China,China-PAR]模型,探讨血同型半胱氨酸(homocysteine,HCY)及UA水平与社区人群心血管病10年风险的关系。方法:以2023年3月至5月,在我中心体检的1699例50~85岁参检者作为对象,收集年龄、性别等基本临床特征,检测HCY、UA等生化指标,采用China-PAR模型进行心血管10年风险评分。按照血HCY及UA是否升高,分为四组:HCY及UA正常组,单纯高HCY组,单纯高UA组,HCY及UA升高组,比较四组间China-PAR评分的差异。结果:HCY及UA正常组,单纯高HCY组,单纯高UA组,HCY及UA升高组的心血管10年风险值中位数分别为:7.6%,11.1%,9.5%,12.9%;各组心血管10年风险高危分布情况分别为:484例(37.8%),78例(54.9%),97例(45.8%),39例(60.0%)。HCY及UA升高组心血管10年风险值中位数、高危占比显著高于前三组(P<0.01)。单因素二元Logistic回归分析显示:BMI、TG、肌酐、FBG、HbAlc、HCY、UA与心血管10年风险高危相关(P<0.01),相关系数分别为:0.158、0.258、0.009、0.715、0.986、0.059、0.003;多因素二元Logistic回归显示:BMI,FBG、HbAlc、HCY对心血管10年风险高危有显著的正向影响关系(P<0.01),相关系数分别为:0.108、0.468、0.433、0.044,UA对心血管10年风险高危无相关(P>0.05)。结论:血HCY及UA水平与社区人群China-PAR心血管10年风险高危正相关,且血HCY的相关性强于血UA。 展开更多
关键词 中国动脉粥样硬化性心血管疾病风险预测 高同型半胱氨酸 高尿酸血症
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持续气道正压通气对严重阻塞性睡眠呼吸暂停综合征患者心血管疾病风险的影响 被引量:4
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作者 许娟 嵇友林 姜永前 《实用临床医药杂志》 CAS 2014年第24期25-29,共5页
目的初步探讨持续气道正压通气(CPAP)治疗对严重阻塞性睡眠呼吸暂停综合征(OSAS)患者炎症因子水平和心血管疾病(CVD)风险的影响。方法选取经多导睡眠图(PSG)确诊的严重OSAS患者[睡眠呼吸暂停低通气指数(AHI)≥30次/h]50例。分别记录CPA... 目的初步探讨持续气道正压通气(CPAP)治疗对严重阻塞性睡眠呼吸暂停综合征(OSAS)患者炎症因子水平和心血管疾病(CVD)风险的影响。方法选取经多导睡眠图(PSG)确诊的严重OSAS患者[睡眠呼吸暂停低通气指数(AHI)≥30次/h]50例。分别记录CPAP治疗前及治疗10周后受试者的ESS评分、血压、呼吸暂停低通气指数(AHI)及脉搏血氧饱和度(Sp O2)、空腹血糖、血清胰岛素、胆固醇、甘油三酯、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇、纤维蛋白原及TNF-α、SCD40L水平。以稳态模式评估胰岛素抵抗(HOMA-IR)。心血管疾病风险评估根据性别特异的多变量的风险因素算法计算。CPAP治疗1 0周后根据CPAP治疗时间分为2组:依从性好组(≥4 h/晚)及依从性差组(<4 h/晚)。结果在使用CPAP≥4 h/晚(n=33)的患者可以发现收缩压、舒张压、总胆固醇、甘油三酯、空腹血糖、空腹胰岛素、HOMA-IR、TNF-α、SCD40L水平在治疗后下降,与心血管疾病风险下降相关。而在CPAP治疗<4 h/晚组患者中未发现上述改变。总体的依从性与心血管疾病风险及系统炎症的降低呈直线相关。BMI和面罩漏气可能是预测治疗依从性的可靠因素。结论有效的CPAP治疗可以降低严重OSAS患者的血压、血脂、TNF-α、SCD40L水平,提高胰岛素敏感性,降低患心血管疾病的风险。 展开更多
关键词 持续气道正压通气治疗 阻塞性睡眠呼吸暂停综合征 心血管疾病风险预测 依从性
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Nonalcoholic fatty liver disease is a novel predictor of cardiovascular disease 被引量:56
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作者 Masahide Hamaguchi Takao Kojima +10 位作者 Noriyuki Takeda Chisato Nagata Jun Takeda Hiroshi Sarui Yutaka Kawahito Naohisa Yoshida Atsushi Suetsugu Takahiro Kato Junichi Okuda Kazunori Ida Toshikazu Yoshikawa 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第10期1579-1584,共6页
AIM:To clarify whether nonalcoholic fatty liver disease(NAFLD)increases the risk of cardiovascular disease.METHODS:We carried out a prospective observational study with a total of 1637 apparently healthy Japanese men ... AIM:To clarify whether nonalcoholic fatty liver disease(NAFLD)increases the risk of cardiovascular disease.METHODS:We carried out a prospective observational study with a total of 1637 apparently healthy Japanese men and women who were recruited from a health check-up program.NAFLD was diagnosed by abdominal ultrasonography.The metabolic syndrome(MS)was defined according to the modified National Cholesterol Education Program(NCEP)ATP Ⅲ criteria.Five years after the baseline evaluations,the incidence of cardiovascular disease was assessed by a self-administered questionnaire.RESULTS:Among 1221 participants available for outcome analyses,the incidence of cardiovascular disease was higher in 231 subjects with NAFLD at baseline(5 coronary heart disease,6 ischemic stroke,and 1 cerebral hemorrhage)than 990 subjects without NAFLD(3 coronary heart disease,6 ischemic stroke,and 1 cerebral hemorrhage).Multivariate analyses indicated that NAFLD was a predictor of cardiovascular disease independent of conventional risk factors(odds ratio 4.12,95% CI,1.58 to 10.75,P = 0.004).MS was alsoindependently associated with cardiovascular events.But simultaneous inclusion of NAFLD and MS in a multivariate model revealed that NAFLD but not MS retained a statistically significant correlation with cardiovascular disease.CONCLUSION:Although both of them were predictors of cardiovascular disease,NAFLD but not MS retained a statistically significant correlation with cardiovascular disease in a multivariate model.NAFLD is a strong predictor of cardiovascular disease and may play a central role in the cardiovascular risk of MS. 展开更多
关键词 Nonalcoholic fatty liver disease Metabolic syndrome Coronary heart disease Cardiovascular disease Risk factors
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Novel biomarkers for cardiovascular risk prediction 被引量:21
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作者 Juan WANG Guo-Juan TAN +3 位作者 Li-Na HAN Yong-Yi BAI Miao HE Hong-Bin LIU 《Journal of Geriatric Cardiology》 SCIE CAS CSCD 2017年第2期135-150,共16页
Cardiovascular disease (CVD) is the leading cause of death and disability worldwide. The primary prevention of CVD is dependent upon the ability to identify high-risk individuals long before the development of overt... Cardiovascular disease (CVD) is the leading cause of death and disability worldwide. The primary prevention of CVD is dependent upon the ability to identify high-risk individuals long before the development of overt events. This highlights the need for accurate risk strati- fication. An increasing number of novel biomarkers have been identified to predict cardiovascular events. Biomarkers play a critical role in the definition, prognostication, and decision-making regarding the management of cardiovascular events. This review focuses on a variety of promising biomarkers that provide diagnostic and prognostic information. The myocardial tissue-specific biomarker cardiac troponin, high- sensitivity assays for cardiac troponin, and heart-type fatty acid binding proteinall help diagnose myocardial infarction (MI) in the early hours following symptoms. Inflammatory markers such as growth differentiation factor-15, high-sensitivity C-reactive protein, fibrinogen, and uric acid predict MI and death. Pregnancy-associated plasma protein A, myeloperoxidase, and matrix metalloproteinases predict the risk of acute cor- onary syndrome. Lipoprotein-associated phospholipase A2 and secretory phospholipase A2 predict incident and recurrent cardiovascular events. Finally, elevated natriuretic peptides, ST2, endothelin-1, mid-regional-pro-adrenomedullin, copeptin, and galectin-3 have all been well validated to predict death and heart failure following a MI and provide risk stratification information for heart failure. Rapidly develop- ing new areas, such as assessment ofmicro-RNA, are also explored. All the biomarkers reflect different aspects of the development ofather- osclerosis. 展开更多
关键词 BIOMARKER Cardiovascular disease PREDICTION Risk stratification
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Ankle-brachial index as a predictor of all-cause and cardio- vascular disease mortality in 3733 Chinese patients with high cardiovascular risk 被引量:1
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作者 Buaijiaer Hasimu Da-Yi Hu +3 位作者 Wen-Lin Ma Jin-Ming Yu Zhi-Feng Li Jue Li 《Journal of Geriatric Cardiology》 SCIE CAS CSCD 2010年第1期7-10,共4页
Objective To assess the association between 1-year risk of all-cause and cardiovascular disease (CVD) mortality and ankle-brachial index (ABI) in Chinese patients who were at high CVD risk. Methods Totally 3733 pa... Objective To assess the association between 1-year risk of all-cause and cardiovascular disease (CVD) mortality and ankle-brachial index (ABI) in Chinese patients who were at high CVD risk. Methods Totally 3733 patients with high CV risk had bilateral ABI measurements at baseline and were followed up for 1-1.5 years. Patients were divided to four groups: 1) coronary heart disease (CHD); 2) ischemic stroke (IS); 3) diabetes mellitus (DM); 4) very high risk group(VHR), low ABI was defined as 〈0.9. Results A total of 3179 patients were analyzed. The prevalence of low ABI was 28.1%. At 1 year, all-cause mortality was 8.7%, and 27.6% was attributable to CVD; mortality due to CV events was 4.8% and 1.5%. After adjusting other risk factors the hazard ratio of low ABI was 1.623 for all-cause mortality and 2.304 for CVD mortality. Similar in patient with and without low ABI, respectively were found in four groups.Conclusion ABI is a strong and independent predictor ofrnortality. Patients with a low ABI have a substantially increased risk of all-cause mortality and CVD mortality (J Geriatr Cardio12010; 7:17-20). 展开更多
关键词 ankle-brachial index peripheral arterial disease CHINESE MORTALITY
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