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Evaluation of emerging biomarkers in cardiovascular risk stratification of hypertensive patients: A 2-year study

机译:高血压患者心血管危险分层中新兴生物标志物的评估:一项为期两年的研究

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Objective: To evaluate if there is a correlation between some new emerging biomarkers, such as lipoprotein(a) (Lp[a]), apo(a) isoform phenotyping, soluble advanced glycation end products (sRAGE), soluble CD40 ligand (sCD40L), serum myeloperoxidase (MPO), and cardiovascular risk stratification. Research design and methods: Three hundred patients were enrolled in this open-label, casecontrol design trial: 156 hypertensive patients and 144 healthy subjects as control group. Hypertensive patients were treated according to the latest ESH/ESC guidelines, until the desirable goal of systolic blood pressure (SBP) <140mmHg, and diastolic blood pressure (DBP) <90mmHg was reached. We evaluated at baseline and after 6, 12, 18, and 24 months: SBP, DBP, lipid profile, Lp(a), apo(a) isoform phenotyping, sRAGE, sCD40L, and MPO. Results: Hypertensive patients presented higher levels of blood pressure, Lp(a), sCD40L, and MPO and lower levels of sRAGE compared with controls. We observed a decrease of blood pressure, Lp(a), sCD40L, and MPO and an increase of sRAGE after anti-hypertensive treatment. Moreover we observed moderate, but statistically significant, correlations between blood pressure decrease and Lp(a), MPO, and sCD40L decrease and between blood pressure decrease and sRAGE increase. There was also a modest, positive correlation between low molecular weight apo(a) isoforms and hypertension. A limitation of this study is that we cannot exclude a role for lifestyle measures. Furthermore the studied markers seem to improve with blood pressure lowering treatment, but we do not have enough statistical power to definitely state which drug used has a specific action on the various variables measured. Conclusion: Lp(a), sRAGE, MPO, sCD40L, and low molecular weight apo(a) isoforms are associated with hypertension and may represent an increased cardiovascular risk. Longer studies are needed to see if these parameters can be also used to predict specific complications linked to hypertension.
机译:目的:评估一些新出现的生物标志物之间是否存在相关性,例如脂蛋白(a)(Lp [a]),载脂蛋白(a)亚型表型,可溶性高级糖基化终产物(sRAGE),可溶性CD40配体(sCD40L) ,血清髓过氧化物酶(MPO)和心血管疾病危险分层。研究设计和方法:300例患者参加了这项开放性病例对照设计试验:156例高血压患者和144例健康受试者作为对照组。根据最新的ESH / ESC指南对高血压患者进行治疗,直至达到理想的收缩压(SBP)<140mmHg和舒张压(DBP)<90mmHg。我们在基线以及6、12、18和24个月后进行了评估:SBP,DBP,脂质分布,Lp(a),apo(a)亚型表型,sRAGE,sCD40L和MPO。结果:与对照组相比,高血压患者的血压,Lp(a),sCD40L和MPO的水平较高,而sRAGE的水平较低。我们观察到降压治疗后血压,Lp(a),sCD40L和MPO降低以及sRAGE升高。此外,我们观察到血压下降与Lp(a),MPO和sCD40L下降之间以及血压下降与sRAGE上升之间存在中度但具有统计学意义的相关性。低分子量载脂蛋白(a)亚型与高血压之间也存在适度的正相关。该研究的局限性在于我们不能排除生活方式测量的作用。此外,研究的指标似乎随着降血压治疗而改善,但我们没有足够的统计能力来明确说明所用的药物对所测得的各种变量具有特定作用。结论:Lp(a),sRAGE,MPO,sCD40L和低分子量apo(a)亚型与高血压相关,可能代表增加的心血管风险。需要更长的研究来看看这些参数是否也可以用于预测与高血压有关的特定并发症。

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