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The associations of self-rated health with cardiovascular risk proteins: a proteomics approach

机译:自我评价健康与心血管风险蛋白的关联:蛋白质组学方法

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Though subjective, poor self-rated health (SRH) has consistently been shown to predict cardiovascular disease (CVD). The underlying mechanism is unclear. This study evaluates the associations of SRH with biomarkers for CVD, aiming to explore potential pathways between poor SRH and CVD. Based on the Malm? Diet and Cancer Cardiovascular Cohort study, a targeted proteomics approach was used to assess the associations of SRH with 88 cardiovascular risk proteins, measured in plasma from 4521 participants without CVD. The false discovery rate (FDR) was controlled using the Benjamini and Hochberg method. Covariates taken into consideration were age, sex, traditional CVD risk factors (low-density lipoprotein cholesterol, systolic blood pressure, anti-hypertensive medication, diabetes, body mass index, smoking), comorbidity, life-style and psycho-social factors (education level, living alone, alcohol consumption, low physical activity, psychiatric medication, sleep duration, and unemployment). Age and sex-adjusted associations with SRH was found for 34 plasma proteins. Nine of them remained significant after adjustments for traditional CVD risk factors. After further adjustment for comorbidity, life-style and psycho-social factors, only leptin (β?=???0.035, corrected p?=?0.016) and C–C motif chemokine 20 (CCL20; β?=???0.054, corrected p?=?0.016) were significantly associated with SRH. Poor SRH was associated with raised concentrations of many plasma proteins. However, the relationships were largely attenuated by adjustments for CVD risk factors, comorbidity and psycho-social factors. Leptin and CCL20 were associated with poor SRH in the present study and could potentially be involved in the SRH–CVD link.
机译:虽然主观,差的自评健康(SRH)一直被证明预测心血管疾病(CVD)。潜在的机制尚不清楚。本研究评估了SRH与CVD生物标志物的关联,旨在探讨贫困SRH和CVD之间的潜在途径。基于麦芽?饮食和癌症心血管队列研究,使用目标蛋白质组学方法来评估SRH与88个心血管风险蛋白的关联,从4521名参与者中测量的4521名没有CVD。使用Benjamini和Hochberg方法控制虚假发现率(FDR)。考虑的协变量是年龄,性别,传统CVD危险因素(低密度脂蛋白胆固醇,收缩压,抗高血压药物,糖尿病,体重指数,吸烟),合并症,生活方式和心理社会因素(教育水平,单独生活,酒精消费,低体育活动,精神病药物,睡眠持续时间和失业率)。发现了34个血浆蛋白的年龄和性别调整的关联与SRH。在调整传统CVD危险因素后,它们的九个仍然显着。经过进一步调整合并症,生活方式和心理社会因素,只有瘦素(β?= ??? 0.035,校正P?=β016)和C-C主题趋化因子20(CCL20;β= ??? 0.054 ,矫正p?=Δ016)与SRH显着相关。 SRH可怜的SRH与许多血浆蛋白质的升高浓度有关。然而,通过对CVD危险因素,合并症和心理社会因素的调整来说,这种关系很大程度上减弱了。瘦素和CCL20在本研究中与SRH差有关,可能涉及SRH-CVD链路。

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