Some patients of heart failure with improved ejection fraction (HFimpEF) have subsequent decline in left ventricular ejection fraction (LVEF) after improvement, and their prognosis is uncertain.
Aims
We aimed to examine the clinical characteristics and long-term prognosis of this sub-population of HFimpEF.
Methods
We examined 399 consecutive patients with HF with reduced ejection fraction (HFrEF, LVEF ≤ 40 %) with LVEF data at both baseline and follow-up in the CHART-2 Study. We classified them as follows; persistent HFrEF group (LVEF ≤ 40 % at 1-year and 2-year follow-up, n = 238), temporary HFimpEF group (≥10 % increase from baseline with LVEF > 40 % at 1-year follow-up but LVEF ≤ 40 % at 2-year follow-up, n = 22), and persistent HFimpEF group (≥10 % increase from baseline with LVEF > 40 % at 1-year follow-up, and LVEF > 40 % at 2-year follow-up, n = 139).
Results
The temporary HFimpEF group (adjusted hazard ratio: 2.95; 95 % CI: 1.55–5.63) and the persistent HFrEF group (2.53; 1.75–3.67) were associated with increased risks for the composite of cardiovascular death and HF hospitalization. The risk factors for decline in LVEF included LVEF (adjusted odds ratio: 0.80; 95 %CI: 0.69–0.90), LV end-diastolic dimension (LVDd) (1.14; 1.05–1.25), B-type natriuretic peptide (BNP) levels (1.04 per 10 pg/mL increase; 1.00–1.08), estimated glomerular filtration rate (eGFR) levels (0.95; 0.92–0.99) and serum sodium levels (0.70; 0.50–0.91) at 1-year follow-up.
Conclusions
These results indicate that patients with HFrecEF account for 23% of those with HFrEF and that 12% of them have subsequent decline in LVEF associated with similar worse prognosis as in those with persistent HFrEF.
{"title":"Prognostic significance of subsequent decline in LVEF in heart failure with improved ejection fraction − A report from the CHART-2 study −","authors":"Takuya Takigahira , Kotaro Nochioka , Satoshi Miyata , Takashi Shiroto , Takumi Inoue , Kai Susukita , Hideka Hayashi , Hiroyuki Takahama , Jun Takahashi , Hiroaki Shimokawa , Satoshi Yasuda","doi":"10.1016/j.ijcha.2026.101877","DOIUrl":"10.1016/j.ijcha.2026.101877","url":null,"abstract":"<div><h3>Background</h3><div>Some patients of heart failure with improved ejection fraction (HFimpEF) have subsequent decline in left ventricular ejection fraction (LVEF) after improvement, and their prognosis is uncertain.</div></div><div><h3>Aims</h3><div>We aimed to examine the clinical characteristics and long-term prognosis of this sub-population of HFimpEF.</div></div><div><h3>Methods</h3><div>We examined 399 consecutive patients with HF with reduced ejection fraction (HFrEF, LVEF ≤ 40 %) with LVEF data at both baseline and follow-up in the CHART-2 Study. We classified them as follows; persistent HFrEF group (LVEF ≤ 40 % at 1-year and 2-year follow-up, n = 238), temporary HFimpEF group (≥10 % increase from baseline with LVEF > 40 % at 1-year follow-up but LVEF ≤ 40 % at 2-year follow-up, n = 22), and persistent HFimpEF group (≥10 % increase from baseline with LVEF > 40 % at 1-year follow-up, and LVEF > 40 % at 2-year follow-up, n = 139).</div></div><div><h3>Results</h3><div>The temporary HFimpEF group (adjusted hazard ratio: 2.95; 95 % CI: 1.55–5.63) and the persistent HFrEF group (2.53; 1.75–3.67) were associated with increased risks for the composite of cardiovascular death and HF hospitalization. The risk factors for decline in LVEF included LVEF (adjusted odds ratio: 0.80; 95 %CI: 0.69–0.90), LV end-diastolic dimension (LVDd) (1.14; 1.05–1.25), B-type natriuretic peptide (BNP) levels (1.04 per 10 pg/mL increase; 1.00–1.08), estimated glomerular filtration rate (eGFR) levels (0.95; 0.92–0.99) and serum sodium levels (0.70; 0.50–0.91) at 1-year follow-up.</div></div><div><h3>Conclusions</h3><div>These results indicate that patients with HFrecEF account for 23% of those with HFrEF and that 12% of them have subsequent decline in LVEF associated with similar worse prognosis as in those with persistent HFrEF.</div></div>","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101877"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146022365","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}
Pub Date : 2026-02-01Epub Date: 2026-01-09DOI: 10.1016/j.ijcha.2025.101862
Sabahat Ul Ain Munir Abbasi , Riya Bhagwan , Aamna Rehman , Neha Malik , Sanya Ashraf Khaskheli , Najaf Ahmed Rajpar , Rayyan Nabi , Ayesha Amir Basra , Shehdev Meghwar , Raheel Ahmed , Kalpana Singh
Background
Anthracyclines (ANT) are widely used in chemotherapy, but their dose-dependent Cardiotoxicity limits long-term use. Carvedilol, a non-selective beta-blocker, has shown potential as a Cardioprotective agent for patients receiving ANT, though its overall effectiveness remains unclear. This systematic review and meta-analysis aimed to assess the impact of carvedilol on cardiac function and survival in patients with anthracycline-induced Cardiotoxicity.
Methods
We performed a comprehensive search of major electronic databases through March 2025 for studies comparing carvedilol with placebo or no treatment in human subjects with ANT-Induced Cardiotoxicity. Primary outcomes included left ventricular ejection fraction (LVEF), left ventricular systolic dysfunction (LVSD), left ventricular systolic and diastolic diameters (LVsD, LVdD), and mortality. Secondary outcomes included echocardiographic and Doppler parameters. Random-effects models were used to calculate standard mean differences (SMDs) and risk ratios (RR) using RevMan 5.4.
Results
A total of fourteen studies were included, thirteen in the meta-analysis and one in the systematic review only, comprising 1,245 participants (carvedilol: 679; control: 566). Carvedilol significantly preserved LVEF (SMD: 0.33, 95% CI: 0.09, 0.58) and reduced the risk of LVSD (RR: 0.26, 95% CI: 0.11, 0.62). It also decreased systolic (SMD: −0.39, 95% CI: −0.53, −0.26) as well as diastolic ventricular diameter (SMD: −0.19, 95% CI: −0.38, −0.00). However, no significant difference in short-term mortality was observed.
Conclusion
Carvedilol appears to protect cardiac function in patients undergoing ANT therapy, though it does not significantly impact mortality. Further research is needed to determine optimal dosing, timing, and long-term survival benefits.
{"title":"The efficacy of carvedilol in improving cardiac function and survival in patients with anthracycline-induced cardiotoxicity: a comprehensive systematic review and meta-analysis","authors":"Sabahat Ul Ain Munir Abbasi , Riya Bhagwan , Aamna Rehman , Neha Malik , Sanya Ashraf Khaskheli , Najaf Ahmed Rajpar , Rayyan Nabi , Ayesha Amir Basra , Shehdev Meghwar , Raheel Ahmed , Kalpana Singh","doi":"10.1016/j.ijcha.2025.101862","DOIUrl":"10.1016/j.ijcha.2025.101862","url":null,"abstract":"<div><h3>Background</h3><div>Anthracyclines (ANT) are widely used in chemotherapy, but their dose-dependent Cardiotoxicity limits long-term use. Carvedilol, a non-selective beta-blocker, has shown potential as a Cardioprotective agent for patients receiving ANT, though its overall effectiveness remains unclear. This systematic review and <em>meta</em>-analysis aimed to assess the impact of carvedilol on cardiac function and survival in patients with anthracycline-induced Cardiotoxicity.</div></div><div><h3>Methods</h3><div>We performed a comprehensive search of major electronic databases through March 2025 for studies comparing carvedilol with placebo or no treatment in human subjects with ANT-Induced Cardiotoxicity. Primary outcomes included left ventricular ejection fraction (LVEF), left ventricular systolic dysfunction (LVSD), left ventricular systolic and diastolic diameters (LVsD, LVdD), and mortality. Secondary outcomes included echocardiographic and Doppler parameters. Random-effects models were used to calculate standard mean differences (SMDs) and risk ratios (RR) using RevMan 5.4.</div></div><div><h3>Results</h3><div>A total of fourteen studies were included, thirteen in the <em>meta</em>-analysis and one in the systematic review only, comprising 1,245 participants (carvedilol: 679; control: 566). Carvedilol significantly preserved LVEF (SMD: 0.33, 95% CI: 0.09, 0.58) and reduced the risk of LVSD (RR: 0.26, 95% CI: 0.11, 0.62). It also decreased systolic (SMD: −0.39, 95% CI: −0.53, −0.26) as well as diastolic ventricular diameter (SMD: −0.19, 95% CI: −0.38, −0.00). However, no significant difference in short-term mortality was observed.</div></div><div><h3>Conclusion</h3><div>Carvedilol appears to protect cardiac function in patients undergoing ANT therapy, though it does not significantly impact mortality. Further research is needed to determine optimal dosing, timing, and long-term survival benefits.</div></div>","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101862"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924276","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}
Pub Date : 2026-02-01Epub Date: 2026-01-08DOI: 10.1016/j.ijcha.2026.101868
Man Huang , Yang Sun , Ke Li , Ting Yu , Hu Zhao , Min Tao , Xiuli Song , Linlin Wang , Xin Xu , Yanghui Chen , Guanglin Cui , Hu Ding , Jiangtao Yan , Jiangang Jiang , Hesong Zeng , Yan Wang , Xiaoqing Shen , Hong Wang , Dao Wen Wang
Background
Ticagrelor is recommended as the preferred antiplatelet agent for patients with acute coronary syndrome (ACS), which is controversial in East Asians, Chinese patients in particular. This study aimed to compare the efficacy and safety of ticagrelor vs. clopidogrel in Chinese ACS patients following coronary stenting.
Methods
Between August 2014 and October 2020, COSTIC recruited 9,040 patients prescribed with ticagrelor or clopidogrel. Applying propensity score matching, ticagrelor was compared with clopidogrel for 1-year risks of the primary efficacy endpoint (a composite of cardiovascular (CV) death, myocardial infarction and stroke) and bleeding endpoint.
Results
The risk of the primary efficacy endpoint was comparable between the two groups but numerically higher after clopidogrel at 6 months (HR, 1.33 [95 % CI, 0.98–1.80]; P = 0.07). Clopidogrel was associated with high incidences of CV death (HR, 1.49 [95 % CI, 1.04–2.15]; P = 0.03 at 6 months; HR, 1.42 [95 % CI, 1.04–1.93]; P = 0.02 at 12 months) and all-cause death (HR, 1.43 [95 % CI, 1.02–1.99]; P = 0.04 at 6 months). BARC type 3 or 5 bleeding (OR, 0.60 [95 % CI, 0.40–0.88]; P = 0.008 at 6 months; OR, 0.71 [95 % CI, 0.52–0.96]; P = 0.03 at 12 months) and BARC type 2 bleeding risks (OR, 0.47 [95 % CI, 0.34–0.66] at 1 month, OR, 0.41 [95 % CI, 0.32–0.52] at 6 months, OR, 0.43 [95 % CI, 0.35–0.53] at 12 months, P < 0.001 at 1, 6 and 12 months) were higher with ticagrelor, as compared to clopidogrel. In terms of the net clinical benefit events, clopidogrel was comparable to ticagrelor in the total cohort.
Conclusions
Among Chinese ACS patients with successful PCI, ticagrelor did not significantly reduce the risk of major ischemic events; instead, it was associated with a significant elevation bleeding risk.
{"title":"Comparison of efficacy and safety between TIcagrelor and clopidogrel in Chinese patients with acute coronary syndrome (COSTIC study)","authors":"Man Huang , Yang Sun , Ke Li , Ting Yu , Hu Zhao , Min Tao , Xiuli Song , Linlin Wang , Xin Xu , Yanghui Chen , Guanglin Cui , Hu Ding , Jiangtao Yan , Jiangang Jiang , Hesong Zeng , Yan Wang , Xiaoqing Shen , Hong Wang , Dao Wen Wang","doi":"10.1016/j.ijcha.2026.101868","DOIUrl":"10.1016/j.ijcha.2026.101868","url":null,"abstract":"<div><h3>Background</h3><div>Ticagrelor is recommended as the preferred antiplatelet agent for patients with acute coronary syndrome (ACS), which is controversial in East Asians, Chinese patients in particular. This study aimed to compare the efficacy and safety of ticagrelor vs. clopidogrel in Chinese ACS patients following coronary stenting.</div></div><div><h3>Methods</h3><div>Between August 2014 and October 2020, COSTIC recruited 9,040 patients prescribed with ticagrelor or clopidogrel. Applying propensity score matching, ticagrelor was compared with clopidogrel for 1-year risks of the primary efficacy endpoint (a composite of cardiovascular (CV) death, myocardial infarction and stroke) and bleeding endpoint.</div></div><div><h3>Results</h3><div>The risk of the primary efficacy endpoint was comparable between the two groups but numerically higher after clopidogrel at 6 months (HR, 1.33 [95 % CI, 0.98–1.80]; <em>P</em> = 0.07). Clopidogrel was associated with high incidences of CV death (HR, 1.49 [95 % CI, 1.04–2.15]; <em>P</em> = 0.03 at 6 months; HR, 1.42 [95 % CI, 1.04–1.93]; <em>P</em> = 0.02 at 12 months) and all-cause death (HR, 1.43 [95 % CI, 1.02–1.99]; <em>P</em> = 0.04 at 6 months). BARC type 3 or 5 bleeding (OR, 0.60 [95 % CI, 0.40–0.88]; <em>P</em> = 0.008 at 6 months; OR, 0.71 [95 % CI, 0.52–0.96]; <em>P</em> = 0.03 at 12 months) and BARC type 2 bleeding risks (OR, 0.47 [95 % CI, 0.34–0.66] at 1 month, OR, 0.41 [95 % CI, 0.32–0.52] at 6 months, OR, 0.43 [95 % CI, 0.35–0.53] at 12 months, <em>P</em> < 0.001 at 1, 6 and 12 months) were higher with ticagrelor, as compared to clopidogrel. In terms of the net clinical benefit events, clopidogrel was comparable to ticagrelor in the total cohort.</div></div><div><h3>Conclusions</h3><div>Among Chinese ACS patients with successful PCI, ticagrelor did not significantly reduce the risk of major ischemic events; instead, it was associated with a significant elevation bleeding risk.</div></div>","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101868"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924278","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}
Pub Date : 2026-02-01Epub Date: 2026-01-06DOI: 10.1016/j.ijcha.2025.101857
Andreas Goldschmied , Manuel Sigle , Ioannis Toskas , Mirac Senel , Livia Dingemann , Malte Kranert , Tobias Harm , Meinrad Gawaz , Michal Droppa , Andreas Brendlin , Karin Anne Lydia Mueller
Introduction
Transcutaneous cardiac pacing (TCP) is an important emergency treatment option in patients with symptomatic bradycardia. With the help of a portable pulse generator an electrical current is delivered through the patient́s thorax in order to induce ventricular contractions. Data on patients in sinus rhythm suggests favorable pacing thresholds when using an anteroposterior (AP) compared to an anterolateral (AL) pacer pad positioning. However, evidence in bradycardic patients is lacking.
Methods
We conducted a prospective crossover clinical study which included 16 patients with symptomatic bradycardia. Patients received consecutive TCP in an AP and AL position under sedoanalgesia. TCP was carried out in an AP and an AL pacer pad position if patients were hemodynamically stable (systolic blood pressure > 90 mmHg). Minimal required current and other variables were noted for both pacer pad positions and Wilcoxon Signed Rank tests were used to compare differences.
Results
We did not overserve a significant difference in minimal required pacing current between the AP and AL pacer pad position (median threshold AP = 125 mA [±48], median threshold AL = 140 mA [±78], p = 0.53). However, a linear mixed-effects model revealed higher pacing thresholds in patients on beta blockers (B = 72.1, p < 0.001, 95 % CI = 36.6–107.7) and with lower myocardial mass (B = -0.41, p < 0.001, 95 % CI = −0.59- −0.23).
Conclusion
We observed no significant difference in pacing thresholds between an AP and AL pacer pad position in patients with symptomatic bradycardia. These results do not align with prior work investigating a monitor with pulsed current delivery.
经皮心脏起搏(TCP)是症状性心动过缓患者的重要急诊治疗选择。在便携式脉冲发生器的帮助下,电流通过患者的胸腔传递,以诱导心室收缩。窦性心律患者的数据表明,与前外侧(AL)起搏器垫定位相比,采用正位(AP)起搏器定位有利于起搏阈值。然而,在心动过缓患者中缺乏证据。方法对16例症状性心动过缓患者进行前瞻性交叉临床研究。患者在sedo镇痛下连续接受AP位和AL位TCP。如果患者血流动力学稳定(收缩压>; 90 mmHg),则采用AP和AL起搏器垫位进行TCP。对起搏器垫位置的最小电流和其他变量进行了记录,并使用Wilcoxon Signed Rank检验来比较差异。结果AP和AL起搏器垫位置在最小起搏电流方面没有明显差异(AP阈值中位数为125 mA[±48],AL阈值中位数为140 mA[±78],p = 0.53)。然而,线性混合效应模型显示,服用受体阻滞剂的患者起搏阈值较高(B = 72.1, p < 0.001, 95% CI = 36.6-107.7),心肌质量较低(B = -0.41, p < 0.001, 95% CI = - 0.59- - 0.23)。结论:我们观察到AP和AL起搏器垫位在症状性心动过缓患者的起搏阈值无显著差异。这些结果与先前研究脉冲电流输送监测仪的工作不一致。
{"title":"Anteroposterior versus anterolateral pacer pad position in patients with symptomatic bradycardia","authors":"Andreas Goldschmied , Manuel Sigle , Ioannis Toskas , Mirac Senel , Livia Dingemann , Malte Kranert , Tobias Harm , Meinrad Gawaz , Michal Droppa , Andreas Brendlin , Karin Anne Lydia Mueller","doi":"10.1016/j.ijcha.2025.101857","DOIUrl":"10.1016/j.ijcha.2025.101857","url":null,"abstract":"<div><h3>Introduction</h3><div>Transcutaneous cardiac pacing (TCP) is an important emergency treatment option in patients with symptomatic bradycardia. With the help of a portable pulse generator an electrical current is delivered through the patient́s thorax in order to induce ventricular contractions. Data on patients in sinus rhythm suggests favorable pacing thresholds when using an anteroposterior (AP) compared to an anterolateral (AL) pacer pad positioning. However, evidence in bradycardic patients is lacking.</div></div><div><h3>Methods</h3><div>We conducted a prospective crossover clinical study which included 16 patients with symptomatic bradycardia. Patients received consecutive TCP in an AP and AL position under sedoanalgesia. TCP was carried out in an AP and an AL pacer pad position if patients were hemodynamically stable (systolic blood pressure > 90 mmHg). Minimal required current and other variables were noted for both pacer pad positions and Wilcoxon Signed Rank tests were used to compare differences.</div></div><div><h3>Results</h3><div>We did not overserve a significant difference in minimal required pacing current between the AP and AL pacer pad position (median threshold AP = 125 mA [±48], median threshold AL = 140 mA [±78], p = 0.53). However, a linear mixed-effects model revealed higher pacing thresholds in patients on beta blockers (B = 72.1, p < 0.001, 95 % CI = 36.6–107.7) and with lower myocardial mass (B = -0.41, p < 0.001, 95 % CI = −0.59- −0.23).</div></div><div><h3>Conclusion</h3><div>We observed no significant difference in pacing thresholds between an AP and AL pacer pad position in patients with symptomatic bradycardia. These results do not align with prior work investigating a monitor with pulsed current delivery.</div></div>","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101857"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924394","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}
Heart failure is one of the major public health concerns and a leading cause of hospitalization and mortality worldwide, including in Thailand. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have demonstrated significant cardiovascular benefits in clinical trials. This study aimed to evaluate the real-world effectiveness of SGLT2i in reducing all-cause mortality and heart failure hospitalization among patients with heart failure at Naresuan University Hospital.
Materials & Methods
This retrospective cohort study included patients newly diagnosed with heart failure at Naresuan University Hospital between January 1, 2019, and December 31, 2023. Patients were divided into those who received SGLT2i and those who did not. The primary outcome was a composite of all-cause mortality and hospitalization for worsening heart failure. Rate ratios were calculated using multilevel mixed-effects Poisson regression, adjusting for baseline characteristics.
Results
A total of 1,378 patients were included (1,080 SGLT2i visits; 5,243 non-SGLT2i visits). The proportion of patients with reduced left ventricular ejection fraction (LVEF ≤ 40%) was higher in the SGLT2i group than the non-SGLT2i group (39.9% vs. 29.4%, p < 0.001). The SGLT2i group also had a higher prevalence of coronary artery disease, myopathy, and chronic kidney disease. Rate of composite outcome (death or heart failure hospitalization) was lower in the SGLT2i group (rate 10.93 per 100 vs. 17.58 per 100). The incidence of the composite outcome was significantly lower in the SGLT2i group compared to the non-SGLT2i group (rate ratio 0.60, 95% CI: 0.42–0.87; p = 0.006). The all-cause mortality rate in the SGLT2i group was markedly lower (rate ratio 0.02, 95% CI: 0.00–0.18; p = 0.001), while heart failure hospitalization showed a favorable trend without reaching statistical significance.
Conclusion
SGLT2i were associated with a significantly lower risk of death and heart failure hospitalization in this real-world cohort of Thai heart failure patients. These findings reinforce the clinical benefits of SGLT2i and support their broader implementation in heart failure management in Thailand.
前言和目的心力衰竭是主要的公共卫生问题之一,也是包括泰国在内的世界范围内住院和死亡的主要原因。钠-葡萄糖共转运蛋白2抑制剂(SGLT2i)在临床试验中显示出显著的心血管益处。本研究旨在评估SGLT2i在降低那累大学医院心力衰竭患者全因死亡率和心力衰竭住院率方面的实际有效性。材料和方法本回顾性队列研究纳入2019年1月1日至2023年12月31日在那累大学医院新诊断为心力衰竭的患者。患者被分为接受SGLT2i治疗和未接受SGLT2i治疗的两组。主要结局是全因死亡率和因心衰恶化而住院的综合结果。采用多水平混合效应泊松回归计算比率,调整基线特征。结果共纳入1378例患者(SGLT2i患者1080例,非SGLT2i患者5243例)。SGLT2i组左室射血分数降低(LVEF≤40%)的患者比例高于非SGLT2i组(39.9% vs 29.4%, p < 0.001)。SGLT2i组也有更高的冠状动脉疾病、肌病和慢性肾脏疾病的患病率。SGLT2i组的综合转归率(死亡或心力衰竭住院)较低(10.93 / 100 vs. 17.58 / 100)。与非SGLT2i组相比,SGLT2i组的综合结局发生率显著降低(比率比0.60,95% CI: 0.42-0.87; p = 0.006)。SGLT2i组全因死亡率明显降低(比率比0.02,95% CI: 0.00-0.18; p = 0.001),心力衰竭住院率呈有利趋势,但无统计学意义。结论:在这个真实世界的泰国心力衰竭患者队列中,sglt2i与较低的死亡和心力衰竭住院风险相关。这些发现加强了SGLT2i的临床益处,并支持其在泰国心力衰竭管理中的更广泛实施。
{"title":"Clinical outcomes of SGLT2 inhibitor use in Thai patients with heart failure: a five-year retrospective cohort study","authors":"Thananan Chanchanayothin , Chuttikan Klomwong , Tanawit Saisri , Suphasin Panudom , Sakchai Chaiyamahapurk , Nonthikorn Theerasuwipakorn , Noppachai Siranart , Patavee Pajareya , Nattakorn Songsirisuk , Chalinee Pravarnpat , Akenarong Pipatputthapong , Pongpun Jittham , Paisit Kosum","doi":"10.1016/j.ijcha.2026.101873","DOIUrl":"10.1016/j.ijcha.2026.101873","url":null,"abstract":"<div><h3>Introduction & Objectives</h3><div>Heart failure is one of the major public health concerns and a leading cause of hospitalization and mortality worldwide, including in Thailand. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have demonstrated significant cardiovascular benefits in clinical trials. This study aimed to evaluate the real-world effectiveness of SGLT2i in reducing all-cause mortality and heart failure hospitalization among patients with heart failure at Naresuan University Hospital.</div></div><div><h3>Materials & Methods</h3><div>This retrospective cohort study included patients newly diagnosed with heart failure at Naresuan University Hospital between January 1, 2019, and December 31, 2023. Patients were divided into those who received SGLT2i and those who did not. The primary outcome was a composite of all-cause mortality and hospitalization for worsening heart failure. Rate ratios were calculated using multilevel mixed-effects Poisson regression, adjusting for baseline characteristics.</div></div><div><h3>Results</h3><div>A total of 1,378 patients were included (1,080 SGLT2i visits; 5,243 non-SGLT2i visits). The proportion of patients with reduced left ventricular ejection fraction (LVEF ≤ 40%) was higher in the SGLT2i group than the non-SGLT2i group (39.9% vs. 29.4%, p < 0.001). The SGLT2i group also had a higher prevalence of coronary artery disease, myopathy, and chronic kidney disease. Rate of composite outcome (death or heart failure hospitalization) was lower in the SGLT2i group (rate 10.93 per 100 vs. 17.58 per 100). The incidence of the composite outcome was significantly lower in the SGLT2i group compared to the non-SGLT2i group (rate ratio 0.60, 95% CI: 0.42–0.87; p = 0.006). The all-cause mortality rate in the SGLT2i group was markedly lower (rate ratio 0.02, 95% CI: 0.00–0.18; p = 0.001), while heart failure hospitalization showed a favorable trend without reaching statistical significance.</div></div><div><h3>Conclusion</h3><div>SGLT2i were associated with a significantly lower risk of death and heart failure hospitalization in this real-world cohort of Thai heart failure patients. These findings reinforce the clinical benefits of SGLT2i and support their broader implementation in heart failure management in Thailand.</div></div>","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101873"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146022482","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}
Pub Date : 2026-02-01Epub Date: 2026-01-06DOI: 10.1016/j.ijcha.2025.101855
Ayman Jubran , Raumil V Patel , Denis Qeska , Ragavie Manoragavan , Issac Yang , Anastasia Oikonomou , Harindra C Wijeysundera
{"title":"The role of membranous septum length as a predictor for post-TAVR pacemaker implantation in patients with pre-existing RBBB","authors":"Ayman Jubran , Raumil V Patel , Denis Qeska , Ragavie Manoragavan , Issac Yang , Anastasia Oikonomou , Harindra C Wijeysundera","doi":"10.1016/j.ijcha.2025.101855","DOIUrl":"10.1016/j.ijcha.2025.101855","url":null,"abstract":"","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101855"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924279","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}
Patients with heart failure (HF) often present with a relative deficiency of cyclic guanosine monophosphate (cGMP) despite elevated B-type natriuretic peptide (BNP) levels. Sacubitril/valsartan and vericiguat target the cGMP pathway, but the relative contribution of cardiac versus systemic cGMP production remains uncertain. This study evaluated the association between cGMP changes and hemodynamic changes in patients with HF with reduced ejection fraction (HFrEF) receiving these agents.
Methods
Fourteen symptomatic HFrEF patients (median age 65.0 [IQR: 56.0–72.3]years, EF 25.5 [24.0–33.3]%) and 20 control patients without HF (66.0 years, EF 66.5 %) were enrolled. Of the HFrEF patients, five received sacubitril/valsartan alone and nine received vericiguat (newly initiated or added to sacubitril/valsartan). All HFrEF patients underwent right heart catheterization before the treatment and two months after treatment. Blood samples were collected from the coronary sinus, arteries, and veins.
Results
HFrEF patients showed higher coronary sinus cGMP levels compared with controls (15.8 ± 1.7 vs. 10.9 ± 1.2 nM, p < 0.05) but a markedly lower cGMP/BNP ratio (0.09 ± 0.02 vs. 1.71 ± 0.63, p < 0.05), suggesting a relative cGMP deficiency. After the therapy, the cGMP/BNP ratio significantly increased (0.278, p < 0.05). The change in coronary sinus cGMP correlated with improvement in cardiac index (r = 0.57, p = 0.039). cGMP levels rose consistently across all sampling sites, indicating a systemic augmentation of the cGMP pathway.
Conclusion
Elevation of cGMP levels were associated with hemodynamic improvement in HFrEF patients treated with sacubitril/valsartan and vericiguat. These findings highlight the therapeutic relevance of cGMP pathway augmentation and provide mechanistic insights aligned with the known clinical effects of these agents in HFrEF.
{"title":"Association of elevated cyclic GMP levels with hemodynamic changes in HFrEF patients treated with sacubitril/valsartan and vericiguat: a pilot study","authors":"Takumi Inoue , Hiroyuki Takahama , Hideaki Suzuki , Marina Arai , Nobuhiro Kikuchi , Taijyu Satoh , Nobuhiro Yaoita , Saori Yamamoto , Kotaro Nochioka , Makoto Nakano , Shunsuke Tatebe , Jun Takahashi , Naoto Minamino , Satoshi Yasuda","doi":"10.1016/j.ijcha.2025.101863","DOIUrl":"10.1016/j.ijcha.2025.101863","url":null,"abstract":"<div><h3>Background</h3><div>Patients with heart failure (HF) often present with a relative deficiency of cyclic guanosine monophosphate (cGMP) despite elevated B-type natriuretic peptide (BNP) levels. Sacubitril/valsartan and vericiguat target the cGMP pathway, but the relative contribution of cardiac versus systemic cGMP production remains uncertain. This study evaluated the association between cGMP changes and hemodynamic changes in patients with HF with reduced ejection fraction (HFrEF) receiving these agents.</div></div><div><h3>Methods</h3><div>Fourteen symptomatic HFrEF patients (median age 65.0 [IQR: 56.0–72.3]years, EF 25.5 [24.0–33.3]%) and 20 control patients without HF (66.0 years, EF 66.5 %) were enrolled. Of the HFrEF patients, five received sacubitril/valsartan alone and nine received vericiguat (newly initiated or added to sacubitril/valsartan). All HFrEF patients underwent right heart catheterization before the treatment and two months after treatment. Blood samples were collected from the coronary sinus, arteries, and veins.</div></div><div><h3>Results</h3><div>HFrEF patients showed higher coronary sinus cGMP levels compared with controls (15.8 ± 1.7 vs. 10.9 ± 1.2 nM, p < 0.05) but a markedly lower cGMP/BNP ratio (0.09 ± 0.02 vs. 1.71 ± 0.63, p < 0.05), suggesting a relative cGMP deficiency. After the therapy, the cGMP/BNP ratio significantly increased (0.278, p < 0.05). The change in coronary sinus cGMP correlated with improvement in cardiac index (r = 0.57, p = 0.039). cGMP levels rose consistently across all sampling sites, indicating a systemic augmentation of the cGMP pathway.</div></div><div><h3>Conclusion</h3><div>Elevation of cGMP levels were associated with hemodynamic improvement in HFrEF patients treated with sacubitril/valsartan and vericiguat. These findings highlight the therapeutic relevance of cGMP pathway augmentation and provide mechanistic insights aligned with the known clinical effects of these agents in HFrEF.</div></div>","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101863"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924323","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}
Pub Date : 2026-02-01Epub Date: 2026-01-08DOI: 10.1016/j.ijcha.2025.101866
Julia M. Kröpfl , Christoph Hauser , Luca Beugger , Henner Hanssen , Fabian Schwendinger , Arno Schmidt-Trucksäss
Background
Cellular endothelial dysfunction in patients recovering from Coronavirus disease 2019 (COVID-19) remains poorly understood. This study examined circulating angiogenic progenitor cells (CAC) and mature endothelial cells (CEC) in individuals with persistent symptoms following hospitalization for COVID-19 (PH-PCS) at ≥ 18-months post-infection.
Methods
We compared PH-PCS (n = 14) to matched controls without symptomatic COVID-19 (n = 7). Examinations included macro- and microvascular structure and function and the analysis of CAC and CEC using flow cytometry.
Results
Estimates indicated somewhat lower apoptotic CAC concentrations (mean difference[md] [95 %CI] = 0.050 cells/µl [0.003, 0.137], p = 0.084) and proportions (% total CAC, 7.7 percentage points (pp) [0.3, 12.9], p = 0.066) in patients compared to controls, though estimates were imprecise. Similar results were observed for apoptotic CEC concentrations (1.202 cells/µl [0.040, 7.518], p = 0.066) and proportions (% total CEC, 2.7 pp [0.2, 23.8], p = 0.048). Live CAC (−7.6 pp [-12.7, −1.1], p = 0.084) and live CEC proportions (−4.9 pp [–23.7, −0.3], p = 0.042) were somewhat enhanced in PH-PCS. Brachial-arterial flow-mediated dilation (baFMD) and retinal vessel imaging parameters showed little evidence for differences between groups, except for maximal arteriolar constriction, where estimates suggested on average higher values in PH-PCS (md [95 %CI] = 1.64 [0.050, 3.63], p = 0.084), but estimates were uncertain. Pooling PH-PCS and controls, correlations were observed between reduced baFMD and both elevated total CEC concentrations (ρ = -0.56, p = 0.038) and decreased apoptotic CAC proportions (ρ = 0.56, p = 0.042).
Conclusions
This study suggests the possibility of unbalanced CAC and CEC apoptosis in PH-PCS, but with uncertain magnitude. The findings might inform hypothesis generation for future studies on (cellular) endothelial function in PH-PCS.
背景2019冠状病毒病(COVID-19)恢复期患者的细胞内皮功能障碍仍知之甚少。本研究检测了感染后≥18个月因COVID-19 (PH-PCS)住院后持续症状的个体的循环血管生成祖细胞(CAC)和成熟内皮细胞(CEC)。方法将PH-PCS (n = 14)与无症状的匹配对照组(n = 7)进行比较。检查包括大微血管结构和功能,流式细胞术分析CAC和CEC。结果估计显示,与对照组相比,患者的凋亡CAC浓度(平均差值[md] [95% CI] = 0.050细胞/µl [0.003, 0.137], p = 0.084)和比例(总CAC %, 7.7个百分点(pp) [0.3, 12.9], p = 0.066)有所降低,但估计不精确。凋亡的CEC浓度(1.202个细胞/µl [0.040, 7.518], p = 0.066)和比例(%总CEC, 2.7 pp [0.2, 23.8], p = 0.048)也有类似的结果。活性CAC (- 7.6 pp [-12.7, - 1.1], p = 0.084)和活性CEC比例(- 4.9 pp [-23.7, - 0.3], p = 0.042)在PH-PCS中有所提高。肱动脉血流介导的扩张(baFMD)和视网膜血管成像参数在两组之间几乎没有差异,除了最大动脉收缩,其中估计PH-PCS的平均值较高(md [95% CI] = 1.64 [0.050, 3.63], p = 0.084),但估计不确定。将PH-PCS和对照组合并,观察到baFMD降低与总CEC浓度升高(ρ = -0.56, p = 0.038)和凋亡CAC比例降低(ρ = 0.56, p = 0.042)之间的相关性。结论PH-PCS可能存在CAC和CEC不平衡凋亡,但凋亡程度不确定。这些发现可能为未来研究PH-PCS的(细胞)内皮功能提供假设。
{"title":"Circulating angiogenic progenitor cell apoptosis in Post-COVID-19 syndrome","authors":"Julia M. Kröpfl , Christoph Hauser , Luca Beugger , Henner Hanssen , Fabian Schwendinger , Arno Schmidt-Trucksäss","doi":"10.1016/j.ijcha.2025.101866","DOIUrl":"10.1016/j.ijcha.2025.101866","url":null,"abstract":"<div><h3>Background</h3><div>Cellular endothelial dysfunction in patients recovering from Coronavirus disease 2019 (COVID-19) remains poorly understood. This study examined circulating angiogenic progenitor cells (CAC) and mature endothelial cells (CEC) in individuals with persistent symptoms following hospitalization for COVID-19 (PH-PCS) at ≥ 18-months post-infection.</div></div><div><h3>Methods</h3><div>We compared PH-PCS (n = 14) to matched controls without symptomatic COVID-19 (n = 7). Examinations included macro- and microvascular structure and function and the analysis of CAC and CEC using flow cytometry.</div></div><div><h3>Results</h3><div>Estimates indicated somewhat lower apoptotic CAC concentrations (mean difference[md] [95 %CI] = 0.050 cells/µl [0.003, 0.137], p = 0.084) and proportions (% total CAC, 7.7 percentage points (pp) [0.3, 12.9], p = 0.066) in patients compared to controls, though estimates were imprecise. Similar results were observed for apoptotic CEC concentrations (1.202 cells/µl [0.040, 7.518], p = 0.066) and proportions (% total CEC, 2.7 pp [0.2, 23.8], p = 0.048). Live CAC (−7.6 pp [-12.7, −1.1], p = 0.084) and live CEC proportions (−4.9 pp [–23.7, −0.3], p = 0.042) were somewhat enhanced in PH-PCS. Brachial-arterial flow-mediated dilation (baFMD) and retinal vessel imaging parameters showed little evidence for differences between groups, except for maximal arteriolar constriction, where estimates suggested on average higher values in PH-PCS (md [95 %CI] = 1.64 [0.050, 3.63], p = 0.084), but estimates were uncertain. Pooling PH-PCS and controls, correlations were observed between reduced baFMD and both elevated total CEC concentrations (ρ = -0.56, p = 0.038) and decreased apoptotic CAC proportions (ρ = 0.56, p = 0.042).</div></div><div><h3>Conclusions</h3><div>This study suggests the possibility of unbalanced CAC and CEC apoptosis in PH-PCS, but with uncertain magnitude. The findings might inform hypothesis generation for future studies on (cellular) endothelial function in PH-PCS.</div></div>","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101866"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924277","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}
Pub Date : 2026-02-01Epub Date: 2026-01-06DOI: 10.1016/j.ijcha.2025.101865
Naomi E. Wattchow , Thalia Salagaras , Mau T. Nguyen , Lauren Y.J. Sandeman , Gemma A. Figtree , Giuseppe Di Giovanni , Dennis T.L. Wong , Stephen J. Nicholls , Christina A. Bursill , Peter J. Psaltis
Background
Syndecan-1 and endocan are biomarkers of endothelial damage, which associate with worse outcomes after myocardial infarction (MI). As it is unclear how this is mediated, we investigated how they associate with the composition of residual, non-culprit coronary atherosclerotic plaques following acute MI.
Methods
This post hoc analysis of the COCOMO-ACS trial used serum samples from forty-five patients with non-ST elevation MI who underwent blood collection and optical coherence tomography (OCT) imaging of non-culprit, lipid-rich coronary plaques at baseline and after a median of 17.8 months. Serum syndecan-1 and endocan concentrations at both time-points were measured by ELISA. Relationships between these biomarkers and OCT parameters of rupture-prone plaque were examined.
Results
Serum levels of syndecan-1 (median 161.0 ng/mL at baseline vs 93.5 ng/mL at follow-up, P < 0.0001) and endocan (225.7 pg/mL vs 191.2 pg/mL, P = 0.003) both decreased from time of MI to follow-up, with strong correlation between their changes (R2 = 0.64, P < 0.0001). Only syndecan-1 showed a weak negative correlation with minimum fibrous cap thickness at baseline (R2 = 0.10, P = 0.03) and a weak positive correlation with maximum lipid arc at follow-up (R2 = 0.14, P = 0.01). While syndecan-1 and endocan showed no relationship with plasma lipid concentrations, there were weak associations between follow-up syndecan-1 and interleukin-1-beta (R2 = 0.21, P = 0.001), and follow-up endocan and interleukin-6 (R2 = 0.15, P = 0.008).
Conclusions
Although serum syndecan-1 and endocan levels decreased in peripheral blood over time post-MI on guideline-directed therapy, this study identified only modest relationships between syndecan-1 (and not endocan) and OCT compositional characteristics of lipid-rich, rupture-prone plaque.
syndecan -1和endocan是内皮损伤的生物标志物,与心肌梗死(MI)后较差的预后相关。由于尚不清楚这是如何介导的,我们研究了它们与急性心肌梗死后残留的非罪魁祸首冠状动脉粥样硬化斑块的组成之间的关系。方法对COCOMO-ACS试验进行的事后分析使用了45例非st段抬高心肌梗死患者的血清样本,这些患者在基线和中位时间17.8个月后接受了采血和光学相干断层扫描(OCT)对非罪魁祸首、富含脂质的冠状动脉斑块进行了成像。ELISA法测定两个时间点血清syndecan-1和endocan浓度。研究了这些生物标志物与易破裂斑块OCT参数之间的关系。结果血清syndecan-1水平(基线时中位数为161.0 ng/mL,随访时中位数为93.5 ng/mL, P < 0.0001)和endocan水平(225.7 pg/mL,随访时中位数为191.2 pg/mL, P = 0.003)从心肌梗死到随访期间均下降,两者变化具有很强的相关性(R2 = 0.64, P < 0.0001)。只有syndecan-1与基线时最小纤维帽厚度呈弱负相关(R2 = 0.10, P = 0.03),与随访时最大脂质弧呈弱正相关(R2 = 0.14, P = 0.01)。虽然syndecan-1和endocan与血浆脂质浓度无相关性,但随访时syndecan-1与白细胞介素-1- β (R2 = 0.21, P = 0.001)、endocan与白细胞介素-6 (R2 = 0.15, P = 0.008)存在弱相关性。结论:尽管经指导治疗的心肌梗死后,外周血中血清syndecan-1和endocan水平随着时间的推移而下降,但本研究仅发现syndecan-1(而非endocan)与富含脂质、易破裂斑块的OCT组成特征之间存在适度关系。
{"title":"Syndecan-1, endocan and non-culprit coronary plaque composition following non-ST elevation myocardial infarction","authors":"Naomi E. Wattchow , Thalia Salagaras , Mau T. Nguyen , Lauren Y.J. Sandeman , Gemma A. Figtree , Giuseppe Di Giovanni , Dennis T.L. Wong , Stephen J. Nicholls , Christina A. Bursill , Peter J. Psaltis","doi":"10.1016/j.ijcha.2025.101865","DOIUrl":"10.1016/j.ijcha.2025.101865","url":null,"abstract":"<div><h3>Background</h3><div>Syndecan-1 and endocan are biomarkers of endothelial damage, which associate with worse outcomes after myocardial infarction (MI). As it is unclear how this is mediated, we investigated how they associate with the composition of residual, non-culprit coronary atherosclerotic plaques following acute MI.</div></div><div><h3>Methods</h3><div>This <em>post hoc</em> analysis of the COCOMO-ACS trial used serum samples from forty-five patients with non-ST elevation MI who underwent blood collection and optical coherence tomography (OCT) imaging of non-culprit, lipid-rich coronary plaques at baseline and after a median of 17.8 months. Serum syndecan-1 and endocan concentrations at both time-points were measured by ELISA. Relationships between these biomarkers and OCT parameters of rupture-prone plaque were examined.</div></div><div><h3>Results</h3><div>Serum levels of syndecan-1 (median 161.0 ng/mL at baseline vs 93.5 ng/mL at follow-up, P < 0.0001) and endocan (225.7 pg/mL vs 191.2 pg/mL, P = 0.003) both decreased from time of MI to follow-up, with strong correlation between their changes (R<sup>2</sup> = 0.64, P < 0.0001). Only syndecan-1 showed a weak negative correlation with minimum fibrous cap thickness at baseline (R<sup>2</sup> = 0.10, P = 0.03) and a weak positive correlation with maximum lipid arc at follow-up (R<sup>2</sup> = 0.14, P = 0.01). While syndecan-1 and endocan showed no relationship with plasma lipid concentrations, there were weak associations between follow-up syndecan-1 and interleukin-1-beta (R<sup>2</sup> = 0.21, P = 0.001), and follow-up endocan and interleukin-6 (R<sup>2</sup> = 0.15, P = 0.008).</div></div><div><h3>Conclusions</h3><div>Although serum syndecan-1 and endocan levels decreased in peripheral blood over time post-MI on guideline-directed therapy, this study identified only modest relationships between syndecan-1 (and not endocan) and OCT compositional characteristics of lipid-rich, rupture-prone plaque.</div></div>","PeriodicalId":38026,"journal":{"name":"IJC Heart and Vasculature","volume":"62 ","pages":"Article 101865"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924324","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}
Pub Date : 2026-02-01Epub Date: 2026-01-12DOI: 10.1016/j.ijcha.2025.101860
Mohammad Abumayyaleh, Tobias Schupp, Michael Behnes, Ibrahim Akin
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