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Discrepancies Between Physician-Perceived and Calculated Cardiovascular Risk in Primary Prevention: Implications for LDL-C Target Achievement and Appropriate Lipid-Lowering Therapy. 初级预防中医生感知和计算的心血管风险之间的差异:LDL-C目标实现和适当降脂治疗的意义
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-03-01 Epub Date: 2025-02-19 DOI: 10.1007/s40292-025-00705-0
Arturo Cesaro, Vincenzo Acerbo, Francesco Scialla, Enrica Golia, Claudia Concilio, Gianmaria Scherillo, Gianantonio De Michele, Vincenzo de Sio, Antonio Capolongo, Luisa Di Donato, Maria Grazia Monaco, Simona Sperlongano, Alberto Ruggiero, Felice Gragnano, Elisabetta Moscarella, Carmine Riccio, Paolo Calabrò

Introduction: Accurate risk assessment is critical in cardiovascular (CV) prevention, yet physicians often underestimate CV risk, leading to inadequate preventive measures.

Aim: This study evaluates the concordance between physician-perceived CV risk and calculated CV risk in a primary prevention setting.

Methods: This cross-sectional study included primary prevention patients from the Cardiology Outpatient Clinic of Caserta Hospital, Italy. Two independent cardiologists evaluated the physician-perceived risk, and a third resolved discrepancies. CV risk was calculated using SCORE2 for patients with 70 years or less and SCORE2-OP for those with more than 70 years. The concordance between perceived and calculated risks was assessed using Cohen's kappa coefficient. Multivariate logistic regression analysis was performed to examine the influence of risk estimation on achieving low-density lipoprotein cholesterol (LDL-C) targets recommended by the ESC.

Results: 389 patients had complete data for CV risk calculation. Physician-perceived risk categorized 8.7% of patients as low/moderate, 37.8% as high, and 53.5% as very-high risk. In contrast, calculated CV risk according to the SCORE2/SCORE2-OP classified 8% as low/moderate, 5.7% as high, and 86.4% as very-high risk. The concordance between perceived and calculated CV risk was poor (Cohen's kappa 0.208, p < 0.001). Underestimated patients reached LDL-C targets in 16% of cases, well-estimated in 34.5%, and overestimated in 76.9%. Statin use was significantly lower in patients with underestimated CV risk (29.2%) compared to well-estimated (50%) and overestimated (76.9%) groups (p < 0.001). Multivariate analysis showed that patients with overestimated risk were more likely to achieve LDL-C targets (OR 5.33, CI 1.33-21.42, p = 0.018), whereas underestimated patients were 47% less likely (OR 0.53, CI 0.3-0.93, p = 0.027).

Conclusions: A significant discrepancy exists between physician-perceived and calculated CV risk, leading to risk underestimation in over one-third of patients. This underestimation is associated with lower LDL-C target achievement and reduced statin use.

准确的风险评估对心血管疾病的预防至关重要,但医生往往低估了心血管疾病的风险,导致预防措施不足。目的:本研究评估初级预防中医生感知的CV风险和计算的CV风险之间的一致性。方法:这项横断面研究包括来自意大利卡塞塔医院心脏病科门诊的一级预防患者。两位独立的心脏病专家评估了医生认为的风险,第三位专家解决了差异。70岁及以下的患者使用SCORE2计算CV风险,70岁以上的患者使用SCORE2- op计算CV风险。感知风险和计算风险之间的一致性使用Cohen's kappa系数进行评估。采用多因素logistic回归分析来检验风险评估对达到ESC推荐的低密度脂蛋白胆固醇(LDL-C)目标的影响。结果:389例患者有完整的CV风险计算数据。医生感知风险将8.7%的患者分类为低/中度,37.8%为高,53.5%为非常高风险。相比之下,根据SCORE2/SCORE2- op计算的CV风险为8%为低/中度,5.7%为高,86.4%为极高风险。感知和计算的CV风险之间的一致性较差(Cohen’s kappa 0.208, p)。结论:医生感知和计算的CV风险之间存在显著差异,导致超过三分之一的患者存在风险低估。这种低估与较低的LDL-C目标达成和减少他汀类药物的使用有关。
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引用次数: 0
The Relationship Between Blood Pressure and Heart Rate Response During Exercise Testing with Microcirculation Indices. 微循环指标运动试验中血压与心率反应的关系。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-03-01 Epub Date: 2024-12-24 DOI: 10.1007/s40292-024-00695-5
Ioannis Liatakis, Kyriakos Dimitriadis, Eleni Manta, Ioannis Andrikou, Nikolaos Pyrpyris, Fotios Tatakis, Dimitrios Konstantinidis, Konstantinos Thomopoulos, Antonios Manolis, Dimitrios Tousoulis, Konstantinos Tsioufis

Introduction: Hypertension is associated with changes in microcirculation, while increased blood pressure (BP) during exercise stress testing has been correlated with adverse outcomes.

Aim: To evaluate the relationship of microcirculation with exercise BP response in hypertensive individuals.

Methods: 105 hypertensive individuals underwent exercise stress testing and nail-fold videocapillaroscopy assessment, in order to evaluate the relationship of BP response to exercise with capillary density.

Results: A significant negative correlation between diastolic BP at 1-minute recovery and capillary density was revealed (Pearson's r = -0.365, p = 0.043). A significant negative correlation was also observed between capillary density and peak heart rate (HR) (Pearson's r = -0.364, p = 0.024) and HR increase from stage 1 to 2 (Pearson's r = -0.746, p = 0.013).

Conclusion: Capillary rarefaction is associated with an abnormal BP and HR response to exercise, highlighting the role of microcirculation in BP regulation during exercise.

导论:高血压与微循环改变有关,而运动应激试验期间血压升高与不良后果相关。目的:探讨高血压患者微循环与运动血压反应的关系。方法:对105例高血压患者进行运动应激试验和折甲血管镜检查,评价运动后血压反应与毛细血管密度的关系。结果:恢复1分钟时舒张压与毛细血管密度呈显著负相关(Pearson’s r = -0.365, p = 0.043)。毛细血管密度与峰值心率(HR) (Pearson’s r = -0.364, p = 0.024)和心率从1期到2期的增加(Pearson’s r = -0.746, p = 0.013)也呈显著负相关。结论:微循环在运动血压调节中的作用与运动时血压和心率的异常反应有关。
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引用次数: 0
Comparative Efficacy of Continuous Positive Airway Pressure and Antihypertensive Medications in Obstructive Sleep Apnea-Related Hypertension: A Narrative Review. 持续气道正压和降压药物治疗阻塞性睡眠呼吸暂停相关高血压的比较疗效:一项叙述性综述。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-03-01 Epub Date: 2024-12-24 DOI: 10.1007/s40292-024-00691-9
Olumide Damilola Akinmoju, Gbolahan Olatunji, Emmanuel Kokori, Ikponmwosa Jude Ogieuhi, Adetola Emmanuel Babalola, Emeka Stanley Obi, Chidera Stanley Anthony, Odemona Glory Toluwanibukun, Adewunmi Akingbola, Adedoyin Esther Alao, Adenowo Goodness Boluwatife, Aarushi Venkatraman, Areesha Babar, Nicholas Aderinto

Introduction: Obstructive sleep apnea (OSA) presents a significant global health concern, affecting a substantial portion of the population, particularly among young and middle-aged adults.

Aim: This review aims to assess the efficacy of continuous positive airway pressure (CPAP) compared to antihypertensive medications in managing OSA-related hypertension.

Methods: A comprehensive literature search was conducted across multiple databases, yielding studies published from 2000 to March 2024 that investigated CPAP, antihypertensives, or their combination therapy in OSA patients. Six definitive studies were analyzed, including two randomized controlled trials (RCTs), one randomized double-blind placebo-controlled crossover trial, one placebo-controlled trial, one open-label multicenter trial, and one longitudinal cohort study. These studies comprised 939 participants, with intervention durations ranging from four weeks to six months.

Results: Analysis of CPAP monotherapy revealed variable efficacy, with some studies demonstrating significant reductions in 24-hour mean blood pressure and diastolic pressure, while others reported non-significant changes. CPAP therapy combined with antihypertensives showed additive effects, particularly in reducing office blood pressure measurements. Antihypertensive medications, such as valsartan, exhibited superior efficacy in reducing blood pressure compared to CPAP alone. Factors influencing therapy effectiveness included CPAP compliance, patient characteristics, and coexisting comorbidities. Patients with good CPAP adherence experienced greater reductions in blood pressure. The duration of exposure to OSA and the type of hypertension also impacted the therapy response.

Conclusion: While CPAP and antihypertensive medications offer significant benefits in managing hypertension among OSA patients, challenges such as CPAP intolerance and medication side effects exist. Personalized treatment considering individual patient factors is crucial for optimal management.

梗阻性睡眠呼吸暂停(OSA)是一个重要的全球健康问题,影响了相当一部分人口,特别是青壮年。目的:本综述旨在评估持续气道正压通气(CPAP)与降压药物治疗osa相关性高血压的疗效。方法:对多个数据库进行了全面的文献检索,检索了2000年至2024年3月发表的关于OSA患者使用CPAP、抗高血压药物或其联合治疗的研究。我们分析了6项权威性研究,包括2项随机对照试验(rct)、1项随机双盲安慰剂对照交叉试验、1项安慰剂对照试验、1项开放标签多中心试验和1项纵向队列研究。这些研究包括939名参与者,干预时间从四周到六个月不等。结果:CPAP单药治疗的分析显示疗效不一,一些研究显示24小时平均血压和舒张压显著降低,而另一些研究报告无显著变化。CPAP联合抗高血压药物显示出叠加效应,特别是在降低办公室血压测量值方面。降压药物,如缬沙坦,与单独CPAP相比,在降低血压方面表现出优越的疗效。影响治疗效果的因素包括CPAP依从性、患者特征和共存的合并症。良好的CPAP依从性患者血压下降幅度更大。暴露于OSA的持续时间和高血压类型也会影响治疗反应。结论:虽然CPAP和抗高血压药物在控制OSA患者高血压方面有显著的益处,但存在CPAP不耐受和药物副作用等挑战。考虑个体患者因素的个性化治疗对于最佳管理至关重要。
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引用次数: 0
Effect of nebivolol monotherapy or combination therapy on blood pressure levels in patients with hypertension: an updated systematic review and multilevel meta-analysis of 91 randomized controlled trials. 奈必洛尔单药或联合疗法对高血压患者血压水平的影响:91 项随机对照试验的最新系统综述和多层次荟萃分析。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-01-01 Epub Date: 2024-10-29 DOI: 10.1007/s40292-024-00687-5
Athanasios Manolis, Paschalis Karakasis, Dimitrios Patoulias, Michalis Doumas, Manolis Kallistratos, Costas Thomopoulos, Maria Koutsaki, Guido Grassi, Giuseppe Mancia

Aims: To systematically appraise and summarize the available evidence from published randomized controlled trials considering the effect of nebivolol on blood pressure in patients with hypertension.

Methods: Literature search was performed through Medline (via PubMed), Cochrane Library and Scopus until December 15, 2023. Double-independent study selection, data extraction and quality assessment were performed. Evidence was pooled with three-level mixed-effects meta-analysis.

Results: In total, 7,737 participants with hypertension, who were treated with nebivolol, were analyzed across 91 RCTs. Nebivolol was associated with significantly greater reduction in office systolic and diastolic BP compared to placebo (MD = - 6.01 mmHg; 95% CI = [- 7.46, - 4.55] and MD = - 5.01 mmHg; 95% CI = [- 5.91, - 4.11], respectively). Moreover, resulted a similar reduction in systolic BP (MD = - 0.22 mmHg; 95% CI = [- 0.91, 0.46]) and a significantly greater reduction in diastolic BP compared to the active comparator (MD = - 0.71 mmHg; 95% CI = [- 1.27, - 0.16]). When considering the effect of nebivolol on 24-hour ambulatory BP, notable reductions were observed compared to placebo. In contrast, compared to the active comparators, there was no significant difference in systolic BP reduction, but a significant reduction in diastolic BP favoring nebivolol. Based on moderator analyses, the impact of nebivolol on the pooled estimates remained independent of the dose of nebivolol, age, male sex, trial duration, body mass index (BMI), baseline diabetes, heart failure, and baseline systolic and diastolic BP.

Conclusion: Nebivolol, compared to placebo, showed a significant BP reduction and was non-inferior to other active comparators in terms of BP reduction.

目的:系统评估和总结已发表的随机对照试验中有关奈必洛尔对高血压患者血压影响的现有证据:通过 Medline(通过 PubMed)、Cochrane Library 和 Scopus 进行文献检索,直至 2023 年 12 月 15 日。进行了双重独立的研究筛选、数据提取和质量评估。采用三级混合效应荟萃分析对证据进行汇总:91项研究共对7737名接受奈必洛尔治疗的高血压患者进行了分析。与安慰剂相比,奈必洛尔能显著降低办公室收缩压和舒张压(MD = - 6.01 mmHg; 95% CI = [- 7.46, - 4.55] 和 MD = - 5.01 mmHg; 95% CI = [- 5.91, - 4.11])。此外,与活性比较药相比,收缩压降低幅度相似(MD = - 0.22 mmHg; 95% CI = [- 0.91, 0.46]),舒张压降低幅度明显更大(MD = - 0.71 mmHg; 95% CI = [- 1.27, - 0.16])。如果考虑到奈必洛尔对 24 小时非卧床血压的影响,与安慰剂相比,可观察到明显的降压效果。相反,与活性对比药相比,收缩压的降低没有显著差异,但舒张压的显著降低有利于奈必洛尔。根据慢化剂分析,奈必洛尔对汇总估计值的影响与奈必洛尔的剂量、年龄、男性性别、试验持续时间、体重指数(BMI)、基线糖尿病、心力衰竭以及基线收缩压和舒张压无关:结论:与安慰剂相比,奈必洛尔能显著降低血压,且在降低血压方面不劣于其他活性比较药。
{"title":"Effect of nebivolol monotherapy or combination therapy on blood pressure levels in patients with hypertension: an updated systematic review and multilevel meta-analysis of 91 randomized controlled trials.","authors":"Athanasios Manolis, Paschalis Karakasis, Dimitrios Patoulias, Michalis Doumas, Manolis Kallistratos, Costas Thomopoulos, Maria Koutsaki, Guido Grassi, Giuseppe Mancia","doi":"10.1007/s40292-024-00687-5","DOIUrl":"10.1007/s40292-024-00687-5","url":null,"abstract":"<p><strong>Aims: </strong>To systematically appraise and summarize the available evidence from published randomized controlled trials considering the effect of nebivolol on blood pressure in patients with hypertension.</p><p><strong>Methods: </strong>Literature search was performed through Medline (via PubMed), Cochrane Library and Scopus until December 15, 2023. Double-independent study selection, data extraction and quality assessment were performed. Evidence was pooled with three-level mixed-effects meta-analysis.</p><p><strong>Results: </strong>In total, 7,737 participants with hypertension, who were treated with nebivolol, were analyzed across 91 RCTs. Nebivolol was associated with significantly greater reduction in office systolic and diastolic BP compared to placebo (MD = - 6.01 mmHg; 95% CI = [- 7.46, - 4.55] and MD = - 5.01 mmHg; 95% CI = [- 5.91, - 4.11], respectively). Moreover, resulted a similar reduction in systolic BP (MD = - 0.22 mmHg; 95% CI = [- 0.91, 0.46]) and a significantly greater reduction in diastolic BP compared to the active comparator (MD = - 0.71 mmHg; 95% CI = [- 1.27, - 0.16]). When considering the effect of nebivolol on 24-hour ambulatory BP, notable reductions were observed compared to placebo. In contrast, compared to the active comparators, there was no significant difference in systolic BP reduction, but a significant reduction in diastolic BP favoring nebivolol. Based on moderator analyses, the impact of nebivolol on the pooled estimates remained independent of the dose of nebivolol, age, male sex, trial duration, body mass index (BMI), baseline diabetes, heart failure, and baseline systolic and diastolic BP.</p><p><strong>Conclusion: </strong>Nebivolol, compared to placebo, showed a significant BP reduction and was non-inferior to other active comparators in terms of BP reduction.</p>","PeriodicalId":12890,"journal":{"name":"High Blood Pressure & Cardiovascular Prevention","volume":" ","pages":"7-31"},"PeriodicalIF":3.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142521748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Triple Therapy with Telmisartan, Amlodipine, and Rosuvastatin (TAR) Versus Telmisartan/Amlodipine (TA) and Telmisartan/Rosuvastatin (TR) Combinations in Hypertension and Dyslipidemia: A Systematic Review and Meta-analysis. 特米沙坦、氨氯地平和瑞舒伐他汀三联疗法(TAR)与特米沙坦/氨氯地平(TA)和特米沙坦/瑞舒伐他汀组合(TR)治疗高血压和血脂异常:系统综述与元分析》。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-01-01 Epub Date: 2024-11-19 DOI: 10.1007/s40292-024-00689-3
Shady Habboush, Navyamani V Kagita, Ahmed F Gadelmawla, Ahmed Elmoursi, Nooraldin Merza, Ahmed A Abdo, Al Hussein M Zahran, Moustafa Eldeib, Alsayed A Almarghany, Mohamed M Abdelfadil, Mohamed A Abdelkarim, Islam Shawky, Omar M Mohammed, Abdullah Alharran, Mahmoud M Ali, Shereef Elbardisy

Introduction: Hypertension and dyslipidemia are common contributors to cardiovascular disease (CVD), often occurring together. Effectively Managing both is key to reducing mortality and morbidity, but complex regimens reduce adherence.

Aim: This study investigated the comparative efficacy and safety of a three-drug regimen (TAR) containing telmisartan, amlodipine, and rosuvastatin against two-drug combinations (TA and TR) for managing hypertension and dyslipidemia.

Methods: We searched PubMed, Web of Science, Cochrane, Embase, and Scopus databases for relevant articles matching our inclusion criteria. Following the application of inclusion criteria, four studies were selected for qualitative analysis and four studies for meta-analysis.

Results: Our analysis showed TAR [n = 155] significantly reduced mean systolic blood pressure (MSSBP) at week 4 compared to TR (n = 163) (MD = -15.65 mmHg) and TA (MD = -4.63 mmHg). TAR also showed superiority over all groups (TR [n = 163], TA [n = 162]) in MSSBP reduction. For low-density lipoprotein-cholesterol (LDL-C), TAR only showed a significant difference at week 4 compared to TA (MD = -86.41 mg/dL), with no difference between TAR and TR at either week 4 or 8.

Conclusion: Our findings suggest that TAR may be a safe and effective therapeutic option for the concurrent management of hypertension and dyslipidemia. However, there is no significant difference regarding adverse events between both arms.

导言:高血压和血脂异常是心血管疾病(CVD)的常见诱因,通常同时发生。目的:本研究调查了含有替米沙坦、氨氯地平和罗伐他汀的三药治疗方案(TAR)与两药组合(TA和TR)治疗高血压和血脂异常的疗效和安全性比较:我们在 PubMed、Web of Science、Cochrane、Embase 和 Scopus 数据库中搜索符合纳入标准的相关文章。根据纳入标准,我们选择了 4 项研究进行定性分析,4 项研究进行荟萃分析:我们的分析表明,与 TR(n = 163)(MD = -15.65 mmHg)和 TA(MD = -4.63 mmHg)相比,TAR [n = 155]能显著降低第 4 周的平均收缩压(MSSBP)。在降低 MSSBP 方面,TAR 也优于所有组别(TR [n = 163]、TA [n = 162])。在低密度脂蛋白胆固醇(LDL-C)方面,TAR仅在第4周与TA相比有显著差异(MD = -86.41毫克/分升),而在第4周或第8周,TAR与TR均无差异:我们的研究结果表明,TAR 是同时治疗高血压和血脂异常的一种安全有效的治疗方案。但是,两组患者在不良反应方面没有明显差异。
{"title":"Triple Therapy with Telmisartan, Amlodipine, and Rosuvastatin (TAR) Versus Telmisartan/Amlodipine (TA) and Telmisartan/Rosuvastatin (TR) Combinations in Hypertension and Dyslipidemia: A Systematic Review and Meta-analysis.","authors":"Shady Habboush, Navyamani V Kagita, Ahmed F Gadelmawla, Ahmed Elmoursi, Nooraldin Merza, Ahmed A Abdo, Al Hussein M Zahran, Moustafa Eldeib, Alsayed A Almarghany, Mohamed M Abdelfadil, Mohamed A Abdelkarim, Islam Shawky, Omar M Mohammed, Abdullah Alharran, Mahmoud M Ali, Shereef Elbardisy","doi":"10.1007/s40292-024-00689-3","DOIUrl":"10.1007/s40292-024-00689-3","url":null,"abstract":"<p><strong>Introduction: </strong>Hypertension and dyslipidemia are common contributors to cardiovascular disease (CVD), often occurring together. Effectively Managing both is key to reducing mortality and morbidity, but complex regimens reduce adherence.</p><p><strong>Aim: </strong>This study investigated the comparative efficacy and safety of a three-drug regimen (TAR) containing telmisartan, amlodipine, and rosuvastatin against two-drug combinations (TA and TR) for managing hypertension and dyslipidemia.</p><p><strong>Methods: </strong>We searched PubMed, Web of Science, Cochrane, Embase, and Scopus databases for relevant articles matching our inclusion criteria. Following the application of inclusion criteria, four studies were selected for qualitative analysis and four studies for meta-analysis.</p><p><strong>Results: </strong>Our analysis showed TAR [n = 155] significantly reduced mean systolic blood pressure (MSSBP) at week 4 compared to TR (n = 163) (MD = -15.65 mmHg) and TA (MD = -4.63 mmHg). TAR also showed superiority over all groups (TR [n = 163], TA [n = 162]) in MSSBP reduction. For low-density lipoprotein-cholesterol (LDL-C), TAR only showed a significant difference at week 4 compared to TA (MD = -86.41 mg/dL), with no difference between TAR and TR at either week 4 or 8.</p><p><strong>Conclusion: </strong>Our findings suggest that TAR may be a safe and effective therapeutic option for the concurrent management of hypertension and dyslipidemia. However, there is no significant difference regarding adverse events between both arms.</p>","PeriodicalId":12890,"journal":{"name":"High Blood Pressure & Cardiovascular Prevention","volume":" ","pages":"49-60"},"PeriodicalIF":3.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142667636","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Calling for Action: The Need of Large-Scale Cohorts to Uncover the Cardiovascular Risk in Non-Sleepy Obstructive Sleep Apnea. 呼吁行动起来:需要大规模队列研究来揭示非睡眠型阻塞性睡眠呼吸暂停症的心血管风险。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-01-01 Epub Date: 2024-10-12 DOI: 10.1007/s40292-024-00680-y
Giuseppe Maiolino, Miguel Angel Martinez Garcia, Davide Soranna, Antonella Zambon, Roberto Vettor, Gianfranco Parati, David Gozal, Martino F Pengo

Since randomized clinical trials currently do not support continuous positive airway pressure treatment of asymptomatic obstructive sleep apnea (OSA) we proposed the Obesity, Symptoms, and CARdiovascular assessment (OSCAR) algorithm to aid clinicians in the management of asymptomatic low-risk moderate-severe OSA, focusing on weight loss, symptoms and cardiovascular disease (CVD) risk assessment. Exploiting the data of the Sleep Heart Health Study we selected subjects with a body mass index (BMI) < 30 Kg/m2, no history of CVD or sleepiness and compared 552 patients with moderate-severe OSA (OSCAR(-)) to 916 individuals without OSA (No-OSA). After adjusting for age, gender, and BMI, there was no significant difference in the risk of major adverse cardiovascular events (MACE) between OSCAR(-) and No-OSA (1.05; 95%CI 0.81-1.37). The study suggests that low-risk moderate-severe OSA patients may not have a greater risk of MACE compared to those without OSA and highlights the need for further research on this topic.

由于随机临床试验目前并不支持对无症状阻塞性睡眠呼吸暂停(OSA)进行持续气道正压治疗,因此我们提出了肥胖、症状和心血管评估(OSCAR)算法,以帮助临床医生管理无症状低风险中度重度 OSA,重点是减轻体重、症状和心血管疾病(CVD)风险评估。利用睡眠心脏健康研究的数据,我们选择了体重指数(BMI)为2、无心血管疾病或嗜睡病史的受试者,并将552名中重度OSA患者(OSCAR(-))与916名无OSA患者(No-OSA)进行了比较。在对年龄、性别和体重指数进行调整后,OSCAR(-)和No-OSA发生主要不良心血管事件(MACE)的风险没有明显差异(1.05;95%CI 0.81-1.37)。该研究表明,与无 OSA 患者相比,低风险的中度-重度 OSA 患者发生 MACE 的风险可能并不大,并强调了进一步研究该课题的必要性。
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引用次数: 0
Hypertension in the Shadows of Conflict: The Impact of the Sudan War on Blood Pressure Management. 冲突阴影下的高血压:苏丹战争对血压管理的影响。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-01-01 Epub Date: 2024-10-24 DOI: 10.1007/s40292-024-00684-8
Ibrahim Nagmeldin Hassan, Nagmeldin Abuassa, Mohamed Ibrahim

The Sudan conflict has severely impacted hypertension management, exacerbating the condition through chronic stress, disrupted healthcare, and lifestyle changes. Hypertension, a major risk factor for cardiovascular diseases, worsens with war-related stress and limited access to medications due to damaged healthcare infrastructure. Additionally, displacement, economic hardship, and food insecurity contribute to poor diets and reduced physical activity, further complicating blood pressure control. This article highlights the urgent need for adaptive healthcare strategies, such as mobile clinics and international aid, to address these challenges. A concerted effort is required to improve hypertension management and outcomes in conflict-affected populations.

苏丹冲突严重影响了高血压的治疗,长期的压力、中断的医疗保健和生活方式的改变加剧了高血压的病情。高血压是心血管疾病的一个主要风险因素,随着战争带来的压力以及医疗基础设施的损坏导致药物供应受限,高血压病情会进一步恶化。此外,流离失所、经济困难和粮食不安全导致饮食不健康和体育锻炼减少,使血压控制更加复杂。这篇文章强调了适应性医疗策略的迫切需要,如流动诊所和国际援助,以应对这些挑战。需要共同努力改善受冲突影响人群的高血压管理和治疗效果。
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引用次数: 0
Antisense Oligonucleotides in Dyslipidemia Management: A Review of Clinical Trials. 反义寡核苷酸治疗血脂异常:临床试验综述。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-01-01 Epub Date: 2024-10-30 DOI: 10.1007/s40292-024-00682-w
Ikponmwosa Jude Ogieuhi, Kristen Callender, God-Dowell O Odukudu, Emeka Stanley Obi, Kudzaishe Muzofa, Adetola Emmanuel Babalola, Oshomoh Mark-Anthony Ugiomoh, Kenechukwu Hilary Umenzeakor, Adewunmi Akingbola, Charity Onetemizeh Ayoson, Emmanuel Uchenna Agbo, Moses Chukwuebuka Odoeke

Introduction: Elevated serum total cholesterol levels, very low-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides, or a decreased serum high-density lipoprotein cholesterol concentration characterize dyslipidemia. Antisense Oligonucleotide therapy in dyslipidemia targets apolipoprotein B (ApoB), an essential component of low-density lipoprotein (LDL) associated with atherosclerosis development.

Aim: This review aims to critically evaluate the efficacy and safety of this group of medications in mitigating dyslipidemia in at-risk individuals and its potential role in advancing personalized medicine in the management of dyslipidemias.

Methods: A detailed search was conducted from multiple databases adhering to the PRISMA guidelines. Clinical trials and randomized controlled trials on antisense oligonucleotides for management of dyslipidemias were included, excluding non-English studies, case reports and all forms of reviews. Data was screened, with duplicates removed, and key findings were synthesized using a narrative approach.

Results and conclusion: The potential of antisense oligonucleotides (ASOs) to treat dyslipidemia and other disorders has attracted much interest. Several studies and clinical trials have been conducted on the safety and tolerability of ASOs for dyslipidemia. Although statins are the mainstay management of hypercholesterolemia, there is evidence from clinical trials that ASOs can even be more effective with little to no side effects. Novel therapeutic approaches such as antisense oligonucleotides (ASOs) offer tailored therapeutic alternatives. ASOs such as Mipomersen and Volanesorsen provide additional treatment options for patients with inherited lipid abnormalities by lowering certain atherogenic lipoproteins such as apo B and ApoC-III, respectively.

导言:血清总胆固醇、极低密度脂蛋白胆固醇、低密度脂蛋白胆固醇、甘油三酯水平升高或血清高密度脂蛋白胆固醇浓度降低是血脂异常的特征。反义寡核苷酸治疗血脂异常的靶点是载脂蛋白 B(ApoB),它是低密度脂蛋白(LDL)的重要组成部分,与动脉粥样硬化的发展有关。目的:本综述旨在批判性地评估这类药物在缓解高危人群血脂异常方面的疗效和安全性,以及其在推进个性化医疗管理血脂异常方面的潜在作用:方法:按照 PRISMA 指南对多个数据库进行了详细检索。纳入了有关反义寡核苷酸治疗血脂异常的临床试验和随机对照试验,排除了非英语研究、病例报告和各种形式的综述。对数据进行了筛选,删除了重复数据,并采用叙述法对主要研究结果进行了综合:反义寡核苷酸(ASO)治疗血脂异常和其他疾病的潜力引起了广泛关注。目前已就反义寡核苷酸治疗血脂异常的安全性和耐受性开展了多项研究和临床试验。虽然他汀类药物是治疗高胆固醇血症的主要药物,但临床试验的证据表明,ASO 甚至可以更有效,而且几乎没有副作用。反义寡核苷酸(ASO)等新型治疗方法提供了量身定制的替代治疗方案。Mipomersen 和 Volanesorsen 等 ASO 可分别降低某些致动脉粥样硬化脂蛋白(如载脂蛋白 B 和载脂蛋白 C-III),从而为遗传性血脂异常患者提供更多的治疗选择。
{"title":"Antisense Oligonucleotides in Dyslipidemia Management: A Review of Clinical Trials.","authors":"Ikponmwosa Jude Ogieuhi, Kristen Callender, God-Dowell O Odukudu, Emeka Stanley Obi, Kudzaishe Muzofa, Adetola Emmanuel Babalola, Oshomoh Mark-Anthony Ugiomoh, Kenechukwu Hilary Umenzeakor, Adewunmi Akingbola, Charity Onetemizeh Ayoson, Emmanuel Uchenna Agbo, Moses Chukwuebuka Odoeke","doi":"10.1007/s40292-024-00682-w","DOIUrl":"10.1007/s40292-024-00682-w","url":null,"abstract":"<p><strong>Introduction: </strong>Elevated serum total cholesterol levels, very low-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides, or a decreased serum high-density lipoprotein cholesterol concentration characterize dyslipidemia. Antisense Oligonucleotide therapy in dyslipidemia targets apolipoprotein B (ApoB), an essential component of low-density lipoprotein (LDL) associated with atherosclerosis development.</p><p><strong>Aim: </strong>This review aims to critically evaluate the efficacy and safety of this group of medications in mitigating dyslipidemia in at-risk individuals and its potential role in advancing personalized medicine in the management of dyslipidemias.</p><p><strong>Methods: </strong>A detailed search was conducted from multiple databases adhering to the PRISMA guidelines. Clinical trials and randomized controlled trials on antisense oligonucleotides for management of dyslipidemias were included, excluding non-English studies, case reports and all forms of reviews. Data was screened, with duplicates removed, and key findings were synthesized using a narrative approach.</p><p><strong>Results and conclusion: </strong>The potential of antisense oligonucleotides (ASOs) to treat dyslipidemia and other disorders has attracted much interest. Several studies and clinical trials have been conducted on the safety and tolerability of ASOs for dyslipidemia. Although statins are the mainstay management of hypercholesterolemia, there is evidence from clinical trials that ASOs can even be more effective with little to no side effects. Novel therapeutic approaches such as antisense oligonucleotides (ASOs) offer tailored therapeutic alternatives. ASOs such as Mipomersen and Volanesorsen provide additional treatment options for patients with inherited lipid abnormalities by lowering certain atherogenic lipoproteins such as apo B and ApoC-III, respectively.</p>","PeriodicalId":12890,"journal":{"name":"High Blood Pressure & Cardiovascular Prevention","volume":" ","pages":"33-47"},"PeriodicalIF":3.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142545132","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Antihypertensive Medication Category Prescriptions and Blood Pressure Control in African Surinamese and Ghanaian Migrants with Hypertension in Amsterdam, The Netherlands: The HELIUS Study. 荷兰阿姆斯特丹患有高血压的非洲裔苏里南人和加纳人的抗高血压药物类别处方和血压控制情况:HELIUS 研究。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-01-01 Epub Date: 2024-11-02 DOI: 10.1007/s40292-024-00690-w
Joshua A N van Apeldoorn, Luka Jansen, Marieke P Hoevenaar-Blom, Ralf E Harskamp, Henrike Galenkamp, Bert-Jan H van den Born, Charles Agyemang, Edo Richard, Eric P Moll van Charante

West African (WA) migrants in Europe have higher hypertension rates than the host populations. For African migrants, guidelines recommend diuretics and/or calcium channel blockers (CCB) for primary cardiovascular disease prevention, but data on antihypertensive medication (AHM) prescription patterns or related hypertension control rates are lacking. We assessed AHM prescription patterns and its relation to hypertension control among hypertensive WA migrants in the Netherlands compared to the host population. Cross-sectional data from WA or Dutch origin participants from the HELIUS study were used. Participants with treated hypertension and without diabetes, cardiovascular disease, or microalbuminuria were selected. We used logistic and linear regression analyses to assess the association between AHM categories and hypertension control rates (systolic blood pressure (BP) ≤ 140 mmHg and diastolic BP ≤ 90 mmHg) and the systolic BP levels. We compared 999 WA participants and 314 Dutch participants. Hypertension control rates were lower in the WA origin compared to Dutch origin participants (44.3% versus 58.0%, p < 0.001). For WA participants, prescription rates for any AHM category were: CCB (54.8%), diuretics (18.5%) beta-blocking agents (27.3%) and renin-angiotensin system blockers (52.6%). Prescription rates were higher for CCB and similar for diuretics compared to the Dutch participants. Neither CCB nor diuretics were associated with better control rates. Compared to Dutch participants, West African participants had similar diuretic prescriptions but significantly higher prescriptions for CCB. However, neither medications was associated with better hypertension control. Future research should explore physician and patient factors to improve hypertension control.

欧洲的西非(WA)移民的高血压发病率高于东道国人口。对于非洲移民,指南建议使用利尿剂和/或钙通道阻滞剂(CCB)进行心血管疾病的初级预防,但缺乏有关降压药(AHM)处方模式或相关高血压控制率的数据。与东道国人口相比,我们评估了荷兰西澳高血压移民的降压药处方模式及其与高血压控制的关系。我们使用了来自 HELIUS 研究的西澳大利亚或荷兰原籍参与者的横断面数据。研究人员选择了接受过治疗的高血压患者,他们没有糖尿病、心血管疾病或微量白蛋白尿。我们使用逻辑和线性回归分析来评估 AHM 类别与高血压控制率(收缩压 (BP) ≤ 140 mmHg 和舒张压 (BP) ≤ 90 mmHg)和收缩压水平之间的关系。我们对 999 名西澳大利亚参与者和 314 名荷兰参与者进行了比较。与荷兰籍参与者相比,西澳大利亚参与者的高血压控制率较低(44.3% 对 58.0%,P
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引用次数: 0
Echocardiographic Assessment in Patients with Vascular Ehlers-Danlos Syndrome: Insights from an Unexplored Field. 血管性 Ehlers-Danlos 综合征患者的超声心动图评估:未开发领域的启示。
IF 3.1 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-01-01 Epub Date: 2024-11-02 DOI: 10.1007/s40292-024-00692-8
Giacomo Buso, Anna Paini, Claudia Agabiti-Rosei, Fabio Bertacchini, Deborah Stassaldi, Sara Capellini, Carlo Aggiusti, Massimo Salvetti, Carolina De Ciuceis, Marco Ritelli, Marina Venturini, Marina Colombi, Maria Lorenza Muiesan

Introduction: Vascular Ehlers-Danlos syndrome (vEDS) is an inherited connective tissue disorder characterized by arterial fragility. Celiprolol is a β1-adrenoceptor antagonist with partial β2 agonist activity that has been shown to reduce rates of vascular events in this setting, though the underlying mechanisms are not yet fully understood. Moreover, very few echocardiographic data are available in patients with vEDS.

Aim: To perform a comprehensive echocardiographic assessment of a cohort of patients with vEDS with or without celiprolol therapy compared with healthy subjects.

Methods: Twenty patients with genetically confirmed diagnosis of vEDS followed at our Institution (University Hospital of Brescia, Italy) were divided into two groups according to whether or not they were on celiprolol therapy at the maximum recommended dose (400 mg daily) for at least 12 months. Both groups were compared to 10 healthy individuals matched for sex, age, body mass index (BMI), and office blood pressure (BP) values. Each participant underwent transthoracic echocardiography with tissue Doppler analysis (TDI) for a comprehensive evaluation of cardiac structure and function.

Results: Mean age was 35 years and mean BMI was 21.6 kg/m2. Female sex was prevalent (60%). Left ventricular (LV) internal diameter values tended to be lower in patients with untreated vEDS than in healthy controls (4.33 vs 4.74 cm, respectively), though this difference was not statistically significant. Similar data were observed for LV mass index (56.9 vs 68.6 g/m2), stroke volume (56.6 vs 71.6 mL), and E/A ratio (1.26 vs 1.66), whereas an opposite trend was observed for e' lateral (13.2 vs 12.2 cm/s). No statistically significant difference was found between groups in terms of other parameters of LV mass, systolic and diastolic function. A normal LV geometry was found in all the cases. Indices of mechano-energetic efficiency and ventricular-arterial coupling were also similar between groups. No patient presented with aortic root dilation, mitral valve prolapse, valve insufficiency of more than mild degree, or valve stenosis of any degree.

Conclusion: Our study suggests that patients with vEDS have normal cardiac mass and geometry, as well as normal systolic and diastolic function. Celiprolol therapy does not seem to significantly influence such aspects. Compared with vascular imaging, less stringent follow-up with echocardiography seems reasonable in this setting. Future studies with prospective design should confirm these aspects.

简介血管性埃勒斯-丹洛斯综合征(vEDS)是一种以动脉脆性为特征的遗传性结缔组织疾病。塞利洛尔是一种具有部分β2受体激动活性的β1肾上腺素受体拮抗剂,已被证明可降低这种情况下的血管事件发生率,但其潜在机制尚未完全明了。此外,vEDS 患者的超声心动图数据很少。目的:与健康人相比,对接受或不接受塞利洛尔治疗的一组 vEDS 患者进行全面的超声心动图评估:在本院(意大利布雷西亚大学医院)接受随访的 20 名经基因确诊的 vEDS 患者根据是否按最大推荐剂量(每天 400 毫克)使用塞利洛尔治疗至少 12 个月分为两组。两组患者均与 10 名性别、年龄、体重指数 (BMI) 和办公室血压 (BP) 值相匹配的健康人进行了比较。每位参与者都接受了带有组织多普勒分析(TDI)的经胸超声心动图检查,以全面评估心脏结构和功能:平均年龄为 35 岁,平均体重指数为 21.6 kg/m2。女性占多数(60%)。未经治疗的vEDS患者的左心室(LV)内径值往往低于健康对照组(分别为4.33厘米和4.74厘米),但这一差异并无统计学意义。在左心室质量指数(56.9 vs 68.6 g/m2)、每搏量(56.6 vs 71.6 mL)和E/A比值(1.26 vs 1.66)方面也观察到类似的数据,而在e'侧(13.2 vs 12.2 cm/s)方面则观察到相反的趋势。在左心室质量、收缩和舒张功能的其他参数方面,组间差异无统计学意义。所有病例的左心室几何形状均正常。各组之间的机械能效率和心室-动脉耦合指数也相似。没有患者出现主动脉根部扩张、二尖瓣脱垂、轻度以上瓣膜功能不全或任何程度的瓣膜狭窄:我们的研究表明,vEDS 患者的心脏质量和几何形状正常,收缩和舒张功能也正常。塞利洛尔治疗似乎对这些方面没有明显影响。与血管造影相比,在这种情况下对超声心动图的随访不那么严格似乎是合理的。未来采用前瞻性设计的研究应能证实这些方面。
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引用次数: 0
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High Blood Pressure & Cardiovascular Prevention
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