首页 > 最新文献

Cardiology Research最新文献

英文 中文
Coronary Artery Disease as an Independent Predictor of Cardiovascular Mortality in COVID-19 Patients. 冠状动脉疾病是COVID-19患者心血管死亡率的独立预测因子
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.14740/cr1471
Hywel Soney, Nathan DeRon, Lucas Wang, Lawrence Hoang, Mujahed Abualfoul, Yi Zhao, Kristopher Aten, Victor Canela, Sri Prathivada, Michael Vu, Manavjot Sidhu

Background: Coronavirus disease 2019 (COVID-19) is associated with increased risk of cardiovascular mortality. However, little is known about the combined effect of coronary artery disease (CAD) and COVID-19 on mortality. We aimed to investigate the incidence of cardiovascular and all-cause mortality in COVID-19 patients with CAD.

Methods: This multicenter retrospective study identified 3,336 COVID-19 patients admitted between March and December 2020. Data points were manually reviewed in the patients' electronic health records. Multivariate logistic regression was used to assess whether CAD and its subtypes were associated with mortality.

Results: This study shows that CAD was not an independent predictor of all-cause mortality (odds ratio (OR): 1.512, 95% confidence interval (CI): 0.1529 - 14.95, P = 0.723). However, there was a significant increase in cardiovascular mortality in patients with CAD compared to those without (OR: 6.89, 95% CI: 2.706 - 17.53, P < 0.001). There was no significant difference in all-cause mortality in patients with left main artery and left anterior descending artery disease (OR: 1.29, 95% CI: 0.80 - 2.08, P = 0.29). However, CAD patients with a history of interventions (e.g., coronary stenting or coronary artery bypass graft) showed increased mortality compared to those solely treated by medical management (OR: 1.93, 95% CI: 1.12 - 3.33, P = 0.017).

Conclusions: CAD is associated with a higher incidence of cardiovascular mortality but not all-cause mortality in COVID-19 patients. Overall, this study will help clinicians identify characteristics of COVID-19 patients with increased risk of mortality in the setting of CAD.

背景:2019冠状病毒病(COVID-19)与心血管死亡风险增加相关。然而,冠状动脉疾病(CAD)和COVID-19对死亡率的联合影响知之甚少。我们的目的是调查COVID-19合并CAD患者的心血管和全因死亡率。方法:本多中心回顾性研究确定了2020年3月至12月期间入院的3336例COVID-19患者。在患者的电子健康记录中手动审查数据点。采用多变量logistic回归来评估CAD及其亚型是否与死亡率相关。结果:本研究显示CAD不是全因死亡率的独立预测因子(优势比(OR): 1.512, 95%可信区间(CI): 0.1529 - 14.95, P = 0.723)。然而,冠心病患者的心血管死亡率明显高于无冠心病患者(OR: 6.89, 95% CI: 2.706 - 17.53, P < 0.001)。左主干与左前降支病变患者的全因死亡率差异无统计学意义(OR: 1.29, 95% CI: 0.80 ~ 2.08, P = 0.29)。然而,有干预史的冠心病患者(如冠状动脉支架置入术或冠状动脉旁路移植术)的死亡率高于单纯接受药物治疗的患者(or: 1.93, 95% CI: 1.12 - 3.33, P = 0.017)。结论:在COVID-19患者中,CAD与较高的心血管死亡率相关,但与全因死亡率无关。总的来说,这项研究将帮助临床医生确定冠心病背景下死亡风险增加的COVID-19患者的特征。
{"title":"Coronary Artery Disease as an Independent Predictor of Cardiovascular Mortality in COVID-19 Patients.","authors":"Hywel Soney,&nbsp;Nathan DeRon,&nbsp;Lucas Wang,&nbsp;Lawrence Hoang,&nbsp;Mujahed Abualfoul,&nbsp;Yi Zhao,&nbsp;Kristopher Aten,&nbsp;Victor Canela,&nbsp;Sri Prathivada,&nbsp;Michael Vu,&nbsp;Manavjot Sidhu","doi":"10.14740/cr1471","DOIUrl":"https://doi.org/10.14740/cr1471","url":null,"abstract":"<p><strong>Background: </strong>Coronavirus disease 2019 (COVID-19) is associated with increased risk of cardiovascular mortality. However, little is known about the combined effect of coronary artery disease (CAD) and COVID-19 on mortality. We aimed to investigate the incidence of cardiovascular and all-cause mortality in COVID-19 patients with CAD.</p><p><strong>Methods: </strong>This multicenter retrospective study identified 3,336 COVID-19 patients admitted between March and December 2020. Data points were manually reviewed in the patients' electronic health records. Multivariate logistic regression was used to assess whether CAD and its subtypes were associated with mortality.</p><p><strong>Results: </strong>This study shows that CAD was not an independent predictor of all-cause mortality (odds ratio (OR): 1.512, 95% confidence interval (CI): 0.1529 - 14.95, P = 0.723). However, there was a significant increase in cardiovascular mortality in patients with CAD compared to those without (OR: 6.89, 95% CI: 2.706 - 17.53, P < 0.001). There was no significant difference in all-cause mortality in patients with left main artery and left anterior descending artery disease (OR: 1.29, 95% CI: 0.80 - 2.08, P = 0.29). However, CAD patients with a history of interventions (e.g., coronary stenting or coronary artery bypass graft) showed increased mortality compared to those solely treated by medical management (OR: 1.93, 95% CI: 1.12 - 3.33, P = 0.017).</p><p><strong>Conclusions: </strong>CAD is associated with a higher incidence of cardiovascular mortality but not all-cause mortality in COVID-19 patients. Overall, this study will help clinicians identify characteristics of COVID-19 patients with increased risk of mortality in the setting of CAD.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 3","pages":"221-227"},"PeriodicalIF":1.9,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/66/79/cr-14-221.PMC10257497.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9674211","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preliminary Study on the Association of Serum Branched-Chain Amino Acids With Lipid and Hepatic Markers. 血清支链氨基酸与脂质和肝脏标志物相关性的初步研究。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.14740/cr1454
Hari Krishnan Krishnamurthy, Swarnkumar Reddy, Vasanth Jayaraman, Karthik Krishna, Qi Song, Tianhao Wang, Kang Bei, John J Rajasekaran

Background: Serum levels of branched-chain amino acids (BCAAs) are associated with various vital physiological functions and thus elevation in circulating levels results in several metabolic disturbances. Serum levels of BCAAs are strong predictors of various metabolic disorders. Their association with cardiovascular health is uncertain. The study aimed to investigate the association of BCAAs with circulating levels of vital cardiovascular and hepatic markers.

Methods: The study population of 714 individuals was included from the population tested for the vital cardio and hepatic biomarkers at the Vibrant America Clinical Laboratories. The subjects were stratified into four quartiles based on the serum levels of BCAAs, and their association with vital markers was studied using the Kruskal-Wallis test. Pearson's correlation analyzed the univariant relationship of BCAAs with selected cardio and hepatic markers.

Results: BCAAs exhibited a strong negative correlation with serum HDL. Serum triglycerides were found to have a positive correlation with serum levels of leucine and valine. Univariant analysis exhibited a strong negative correlation between serum levels of BCAAs and HDL, and a positive correlation was observed between triglycerides and amino acids isoleucine and leucine. Among analyzed hepatic markers, alanine transaminase exhibited a considerable association with BCAAs.

Conclusions: The elevated levels of serum BCAAs are strongly associated with serum HDL and triglycerides. Consumption of these supplements must be in coordination with healthcare providers to avoid metabolic and cardiovascular risk.

背景:支链氨基酸(BCAAs)的血清水平与多种重要生理功能有关,因此循环水平升高会导致多种代谢紊乱。血清支链氨基酸水平是各种代谢紊乱的有力预测指标。它们与心血管健康的关系尚不确定。该研究旨在探讨支链氨基酸与重要心血管和肝脏标志物循环水平的关系。方法:研究人群为714人,这些人来自于在美国临床实验室进行重要心脏和肝脏生物标志物检测的人群。根据血清BCAAs水平将受试者分为四个四分之一,并使用Kruskal-Wallis测试研究其与生命标志物的相关性。Pearson相关性分析了BCAAs与选定的心脏和肝脏标志物的单变量关系。结果:支链氨基酸与血清HDL呈显著负相关。血清甘油三酯与血清亮氨酸和缬氨酸水平呈正相关。单变量分析显示血清BCAAs水平与HDL呈显著负相关,甘油三酯水平与氨基酸异亮氨酸和亮氨酸呈正相关。在分析的肝脏标志物中,丙氨酸转氨酶显示出与支链氨基酸相当大的关联。结论:血清BCAAs水平升高与血清HDL和甘油三酯密切相关。这些补充剂的使用必须与医疗保健提供者协调,以避免代谢和心血管风险。
{"title":"Preliminary Study on the Association of Serum Branched-Chain Amino Acids With Lipid and Hepatic Markers.","authors":"Hari Krishnan Krishnamurthy,&nbsp;Swarnkumar Reddy,&nbsp;Vasanth Jayaraman,&nbsp;Karthik Krishna,&nbsp;Qi Song,&nbsp;Tianhao Wang,&nbsp;Kang Bei,&nbsp;John J Rajasekaran","doi":"10.14740/cr1454","DOIUrl":"https://doi.org/10.14740/cr1454","url":null,"abstract":"<p><strong>Background: </strong>Serum levels of branched-chain amino acids (BCAAs) are associated with various vital physiological functions and thus elevation in circulating levels results in several metabolic disturbances. Serum levels of BCAAs are strong predictors of various metabolic disorders. Their association with cardiovascular health is uncertain. The study aimed to investigate the association of BCAAs with circulating levels of vital cardiovascular and hepatic markers.</p><p><strong>Methods: </strong>The study population of 714 individuals was included from the population tested for the vital cardio and hepatic biomarkers at the Vibrant America Clinical Laboratories. The subjects were stratified into four quartiles based on the serum levels of BCAAs, and their association with vital markers was studied using the Kruskal-Wallis test. Pearson's correlation analyzed the univariant relationship of BCAAs with selected cardio and hepatic markers.</p><p><strong>Results: </strong>BCAAs exhibited a strong negative correlation with serum HDL. Serum triglycerides were found to have a positive correlation with serum levels of leucine and valine. Univariant analysis exhibited a strong negative correlation between serum levels of BCAAs and HDL, and a positive correlation was observed between triglycerides and amino acids isoleucine and leucine. Among analyzed hepatic markers, alanine transaminase exhibited a considerable association with BCAAs.</p><p><strong>Conclusions: </strong>The elevated levels of serum BCAAs are strongly associated with serum HDL and triglycerides. Consumption of these supplements must be in coordination with healthcare providers to avoid metabolic and cardiovascular risk.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 3","pages":"167-175"},"PeriodicalIF":1.9,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cd/b8/cr-14-167.PMC10257501.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9674214","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Ultrasound-Accelerated Catheter-Directed Thrombolysis. 超声加速导管导向溶栓。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.14740/cr1490
Mrhaf Alsamman, Ali Mohsin Choudhry, Abdulaziz Mheir AlSaadi, Rakesh Prashad

Venous thromboembolism is a very common presentation in the hospital setting. In patients with high-risk pulmonary embolism (PE) or PE and hemodynamic instability, systemic thrombolytic treatment is generally indicated. In those with contraindications to systemic thrombolysis, catheter-directed local thrombolytic therapy and surgical embolectomy are currently considered. In particular, catheter-directed thrombolysis (CDT) is a drug delivery system coupling the endovascular drug administration nearby in the thrombus and the local facilitating effect of ultrasounds. The applications of CDT are currently debated. Here we provide a systematic review of the clinical utilization of CDT.

静脉血栓栓塞是一种非常常见的表现在医院设置。对于高危肺栓塞(PE)或PE伴血流动力学不稳定的患者,通常需要进行全身溶栓治疗。对于那些有全身性溶栓禁忌症的患者,目前考虑采用导管定向的局部溶栓治疗和手术栓塞切除术。特别是导管溶栓(CDT)是一种结合血栓附近血管内给药和超声局部促进作用的给药系统。CDT的应用目前存在争议。在此,我们对CDT的临床应用进行了系统的综述。
{"title":"Ultrasound-Accelerated Catheter-Directed Thrombolysis.","authors":"Mrhaf Alsamman,&nbsp;Ali Mohsin Choudhry,&nbsp;Abdulaziz Mheir AlSaadi,&nbsp;Rakesh Prashad","doi":"10.14740/cr1490","DOIUrl":"https://doi.org/10.14740/cr1490","url":null,"abstract":"<p><p>Venous thromboembolism is a very common presentation in the hospital setting. In patients with high-risk pulmonary embolism (PE) or PE and hemodynamic instability, systemic thrombolytic treatment is generally indicated. In those with contraindications to systemic thrombolysis, catheter-directed local thrombolytic therapy and surgical embolectomy are currently considered. In particular, catheter-directed thrombolysis (CDT) is a drug delivery system coupling the endovascular drug administration nearby in the thrombus and the local facilitating effect of ultrasounds. The applications of CDT are currently debated. Here we provide a systematic review of the clinical utilization of CDT.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 3","pages":"161-166"},"PeriodicalIF":1.9,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f4/7c/cr-14-161.PMC10257504.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9621243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chest Pain in Acute Myocardial Infarction and Its Association With the Culprit Artery and Fibrotic Segment Identified by Cardiac Magnetic Resonance. 急性心肌梗死胸痛及其与心脏磁共振鉴定的罪魁动脉和纤维化段的关系。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-04-01 DOI: 10.14740/cr1468
Weverton Ferreira Leite, Rui Manuel Dos Santos Povoa, Adriano Mendes Caixeta, Celso Amodeo, Gilberto Szarf, Maria Teresa Nogueira Bombig, Maria Cristina Oliveira Izar, Luciana Netto Gioia, Wilma Noia Ribeiro, Francisco Antonio Helfenstein Fonseca

Background: It is still very controversial whether the characteristics of pain in the acute myocardial infarction could be related to the culprit coronary artery. There are no data about associations of pain with the ST-segment elevation myocardial infarction (STEMI) and left ventricular (LV) fibrotic segments.

Methods: Data from 328 participants who had STEMI and were included in the B and T Types of Lymphocytes Evaluation in Acute Myocardial Infarction (BATTLE-AMI) study were analyzed. The culprit artery was identified by coronary angiography and the injured myocardial segments by cardiac magnetic resonance. The statistical significance was established by P value < 0.05.

Results: A total of 223 patients (68%) were selected. Association was not observed between chest pain and the culprit artery (P = 0.237), as well as between pain irradiation and the culprit artery (P = 0.473). No significant difference was observed in the pain localization in relation to the segments in the short axis basal, mid, apical, and long axis, except for the mid inferior segment. The data were not considered clinically relevant because this association was observed in only one of 17 segments after multiple comparisons.

Conclusions: In patients with STEMI, no associations were observed between the location or irradiation of acute chest pain and/or adjacent areas and the culprit artery, or between pain and segmental myocardial fibrosis in the LV.

背景:急性心肌梗死的疼痛特征是否与罪魁祸首冠状动脉有关,目前还存在很大争议。没有关于疼痛与st段抬高型心肌梗死(STEMI)和左心室(LV)纤维化段相关的数据。方法:对328名STEMI患者的数据进行分析,这些患者被纳入急性心肌梗死B型和T型淋巴细胞评估(BATTLE-AMI)研究。通过冠状动脉造影和心脏磁共振检查确定了损伤的心肌节段。P值< 0.05为差异有统计学意义。结果:共入选223例(68%)。胸痛与罪魁动脉无相关性(P = 0.237),疼痛照射与罪魁动脉无相关性(P = 0.473)。除中下节段外,短轴、基轴、中轴、尖轴和长轴节段的疼痛定位无显著差异。这些数据不被认为具有临床相关性,因为在多次比较后,在17个节段中仅观察到这种关联。结论:在STEMI患者中,急性胸痛和/或邻近区域的位置或照射与罪魁动脉之间,或左室疼痛与节段性心肌纤维化之间没有关联。
{"title":"Chest Pain in Acute Myocardial Infarction and Its Association With the Culprit Artery and Fibrotic Segment Identified by Cardiac Magnetic Resonance.","authors":"Weverton Ferreira Leite,&nbsp;Rui Manuel Dos Santos Povoa,&nbsp;Adriano Mendes Caixeta,&nbsp;Celso Amodeo,&nbsp;Gilberto Szarf,&nbsp;Maria Teresa Nogueira Bombig,&nbsp;Maria Cristina Oliveira Izar,&nbsp;Luciana Netto Gioia,&nbsp;Wilma Noia Ribeiro,&nbsp;Francisco Antonio Helfenstein Fonseca","doi":"10.14740/cr1468","DOIUrl":"https://doi.org/10.14740/cr1468","url":null,"abstract":"<p><strong>Background: </strong>It is still very controversial whether the characteristics of pain in the acute myocardial infarction could be related to the culprit coronary artery. There are no data about associations of pain with the ST-segment elevation myocardial infarction (STEMI) and left ventricular (LV) fibrotic segments.</p><p><strong>Methods: </strong>Data from 328 participants who had STEMI and were included in the B and T Types of Lymphocytes Evaluation in Acute Myocardial Infarction (BATTLE-AMI) study were analyzed. The culprit artery was identified by coronary angiography and the injured myocardial segments by cardiac magnetic resonance. The statistical significance was established by P value < 0.05.</p><p><strong>Results: </strong>A total of 223 patients (68%) were selected. Association was not observed between chest pain and the culprit artery (P = 0.237), as well as between pain irradiation and the culprit artery (P = 0.473). No significant difference was observed in the pain localization in relation to the segments in the short axis basal, mid, apical, and long axis, except for the mid inferior segment. The data were not considered clinically relevant because this association was observed in only one of 17 segments after multiple comparisons.</p><p><strong>Conclusions: </strong>In patients with STEMI, no associations were observed between the location or irradiation of acute chest pain and/or adjacent areas and the culprit artery, or between pain and segmental myocardial fibrosis in the LV.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 2","pages":"97-105"},"PeriodicalIF":1.9,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/27/e0/cr-14-097.PMC10116939.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9742655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Possible Exquisite Crosstalk of Urate Transporter 1 With Other Urate Transporters for Chronic Kidney Disease and Cardiovascular Disease Induced by Dotinurad. 尿酸转运蛋白1与其他尿酸转运蛋白的微妙串扰在多替努拉德诱导的慢性肾病和心血管疾病中可能存在。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-04-01 DOI: 10.14740/cr1496
Hidekatsu Yanai, Hiroki Adachi, Mariko Hakoshima, Hisayuki Katsuyama
We previously reported that the switching from fenofibrate to the selective peroxisome proliferator-activated receptor (PPAR) α modulator, pemafibrate, increased serum uric acid (UA) levels and reduced estimated glomerular filtration rate (eGFR) in patients with dyslipidemia [1]. Fenofibrate has a property to decrease serum UA by inhibition of urate transporter 1 (URAT1) by its major metabolite [2]. Although fenofibrate was reported to decrease the eGFR [3], the mechanism of fenofibrate-induced renal impairment has been remained unclear. Further, our previous discussion on such issue was premature [1]. Recently, the role of UA transporters has been clarified [4] (Fig. 1a). Renal excretion of UA is the major regulator of serum UA, and renal UA reabsorption is mainly mediated by URAT1 and glucose transporter 9 (GLUT9). Organic anion transporters (OATs) 1, 3 transport UA from the renal interstitial into renal proximal tubule epithelial cells. ATP-binding cassette, subfamily G, 2 (ABCG2) has been identified as a high-capacity UA exporter that mediates renal and/or extrarenal UA excretion. Indoxyl sulfate (IS) is a well-known uremic toxin that accumulates under renal impairment and is involved in the progression of chronic kidney disease (CKD) and cardiovascular disease (CVD), by inducing inflammation and free radical production [5, 6]. IS excretion is also mediated by OAT1/3 and ABCG2 as well as UA excretion [4]. ABCG2 inhibitors, such as febuxostat (xanthin oxidase (XO) inhibitor), caused renal IS accumulation by suppressing its excretion via ABCG2 in rats [7]. Fenofibrate completely inhibits ABCG2 which may lead to increase in renal IS [8], resulting in elevation of eGFR. Another XO inhibitor, topiroxostat, also inhibits ABCG2, however, allopurinol does not inhibit ABCG2. OAT inhibitors such as probenecid (uricosuric drug, URAT1, and GLUT9 inhibitor), suppressed IS uptake into the kidney, leading to increased plasma IS [7]. Increased plasma IS may be harmful to cardiovascular system by inducing inflammation and free radical production. Benzbromarone (uricosuric drug) inhibits OAT1 and OAT3, however, its inhibitory potency for OAT1/3 is lower than those of probenecid [9], which may not lead to an increase in plasma IS. Probenecid and benzbromarone inhibit ABCG2, which may be unfavorably associated with renal function. In short, the inhibition of OAT1/3 and ABCG2 increase IS in plasma and kidney, which may be unfavorably associated with the development of CVD and CKD, respectively. Very recently, we reported that the addition of the selective URAT1 inhibitor dotinurad to highly-evidence-proved drugs to improve CKD such as sodium-glucose cotransporter 2 (SGLT2) inhibitor and a glucagon-like peptide 1 (GLP-1) receptor agonist, improved eGFR in a diabetic patient with CKD stage G4 [10]. Dotinurad inhibits URAT1 specifically, however, does not inhibit ABCG2 [9], and reduces renal UA accumulation, which may increase the transport of renal accumulated IS b
{"title":"A Possible Exquisite Crosstalk of Urate Transporter 1 With Other Urate Transporters for Chronic Kidney Disease and Cardiovascular Disease Induced by Dotinurad.","authors":"Hidekatsu Yanai,&nbsp;Hiroki Adachi,&nbsp;Mariko Hakoshima,&nbsp;Hisayuki Katsuyama","doi":"10.14740/cr1496","DOIUrl":"https://doi.org/10.14740/cr1496","url":null,"abstract":"We previously reported that the switching from fenofibrate to the selective peroxisome proliferator-activated receptor (PPAR) α modulator, pemafibrate, increased serum uric acid (UA) levels and reduced estimated glomerular filtration rate (eGFR) in patients with dyslipidemia [1]. Fenofibrate has a property to decrease serum UA by inhibition of urate transporter 1 (URAT1) by its major metabolite [2]. Although fenofibrate was reported to decrease the eGFR [3], the mechanism of fenofibrate-induced renal impairment has been remained unclear. Further, our previous discussion on such issue was premature [1]. Recently, the role of UA transporters has been clarified [4] (Fig. 1a). Renal excretion of UA is the major regulator of serum UA, and renal UA reabsorption is mainly mediated by URAT1 and glucose transporter 9 (GLUT9). Organic anion transporters (OATs) 1, 3 transport UA from the renal interstitial into renal proximal tubule epithelial cells. ATP-binding cassette, subfamily G, 2 (ABCG2) has been identified as a high-capacity UA exporter that mediates renal and/or extrarenal UA excretion. Indoxyl sulfate (IS) is a well-known uremic toxin that accumulates under renal impairment and is involved in the progression of chronic kidney disease (CKD) and cardiovascular disease (CVD), by inducing inflammation and free radical production [5, 6]. IS excretion is also mediated by OAT1/3 and ABCG2 as well as UA excretion [4]. ABCG2 inhibitors, such as febuxostat (xanthin oxidase (XO) inhibitor), caused renal IS accumulation by suppressing its excretion via ABCG2 in rats [7]. Fenofibrate completely inhibits ABCG2 which may lead to increase in renal IS [8], resulting in elevation of eGFR. Another XO inhibitor, topiroxostat, also inhibits ABCG2, however, allopurinol does not inhibit ABCG2. OAT inhibitors such as probenecid (uricosuric drug, URAT1, and GLUT9 inhibitor), suppressed IS uptake into the kidney, leading to increased plasma IS [7]. Increased plasma IS may be harmful to cardiovascular system by inducing inflammation and free radical production. Benzbromarone (uricosuric drug) inhibits OAT1 and OAT3, however, its inhibitory potency for OAT1/3 is lower than those of probenecid [9], which may not lead to an increase in plasma IS. Probenecid and benzbromarone inhibit ABCG2, which may be unfavorably associated with renal function. In short, the inhibition of OAT1/3 and ABCG2 increase IS in plasma and kidney, which may be unfavorably associated with the development of CVD and CKD, respectively. Very recently, we reported that the addition of the selective URAT1 inhibitor dotinurad to highly-evidence-proved drugs to improve CKD such as sodium-glucose cotransporter 2 (SGLT2) inhibitor and a glucagon-like peptide 1 (GLP-1) receptor agonist, improved eGFR in a diabetic patient with CKD stage G4 [10]. Dotinurad inhibits URAT1 specifically, however, does not inhibit ABCG2 [9], and reduces renal UA accumulation, which may increase the transport of renal accumulated IS b","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 2","pages":"158-160"},"PeriodicalIF":1.9,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e1/15/cr-14-158.PMC10116931.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9742656","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sodium Chloride Physiological Saline Solution Versus Water Preparations Injectable in the Use of Shockwave Intravascular Lithotripsy: A Single-Center Experience. 在冲击波血管内碎石术中使用氯化钠生理盐水溶液与注射水制剂:单中心经验。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-04-01 DOI: 10.14740/cr1489
Quentin Landolff, Matthieu Godin, Alexandre Canville, Benjamin Honton, Jacques Monsegu, Marine Quillot, Jacques Berland, Rene Koning, Nicolas Amabile

Background: Shockwave intravascular lithotripsy (IVL) coronary system is a very useful new technology for de novo severely calcified coronary artery plaques before percutaneous coronary intervention (PCI). The device uses a semi-compliant low-pressure balloon, integrated into a sterile catheter, to deliver by vaporizing fluid an expanding bubble that generates high-pressure ultrasonic energy by waves that create multiplane longitudinal micro-macro fractures in calcified plaques, which facilitate optimal stent placement and expansion, and luminal gain.

Methods: The use of Shockwave IVL coronary system in our cardiac catheterization laboratory (Cath lab) at the "Clinique Saint-Hilaire" in Rouen, France, started in March 2019, with 42 procedures performed since this date: two patients in 2019, two patients in 2020, seven patients in 2021, 23 patients in 2022, and eight patients since the beginning of 2023.

Results: We had experienced problems at the beginning of our activity for the first 11 patients (two patients in 2019, two patients in 2020, and seven patients in 2021): after less than five pulses, the shock therapy stopped. We used initially for Shockwave IVL semi-compliant low-pressure integrated balloons a mixture of 50% contrast and 50% water preparations injectable (PPI). After changing water PPI by sodium chloride physiological saline solution, we never encountered this problem again for the following 31 patients (23 patients in 2022, and eight patients since the beginning of 2023). In fact, the proper functioning of Shockwave IVL system requires ions in balloon mixture in addition to the contrast. It is thanks to the ions contained in sodium chloride physiological saline solution that the spark necessary for shocks delivery after balloon inflation is produced.

Conclusions: Water PPI or sodium chloride physiological saline solution is used in angioplasty balloons in a lot of Cath labs worldwide. It is therefore essential to disseminate in the worldwide Cath lab the obligation to put in Shockwave IVL semi-compliant low-pressure integrated balloons sodium chloride physiological saline solution, rather than water PPI for optimal performance, and the importance of Shockwave Medical reporting this to interventional cardiologists.

背景:冲击波血管内碎石(IVL)冠状动脉系统是一种非常有用的新技术,用于经皮冠状动脉介入治疗(PCI)前新发严重钙化的冠状动脉斑块。该设备使用半兼容的低压球囊,整合到无菌导管中,通过汽化液体产生一个膨胀的气泡,通过波浪产生高压超声能量,在钙化斑块中产生多平面纵向微宏观断裂,从而促进最佳支架放置和扩张,并获得管腔增益。方法:我们在法国鲁昂“圣伊莱尔诊所”的心导管实验室(Cath lab)于2019年3月开始使用冲击波IVL冠状动脉系统,自该日起共进行了42例手术:2019年2例,2020年2例,2021年7例,2022年23例,2023年初至今8例。结果:前11例患者(2019年2例,2020年2例,2021年7例)在活动开始时就遇到了问题:在不到5次脉冲后,休克治疗停止。我们最初使用的冲击波IVL半顺从低压一体化气球是50%造影剂和50%可注射水制剂(PPI)的混合物。在用氯化钠生理盐水溶液改变水PPI后,以下31例患者(2022年23例,2023年初至今8例)没有再出现此问题。事实上,冲击波IVL系统的正常工作除了需要造影剂外,还需要球囊混合物中的离子。正是由于氯化钠生理盐水中所含的离子,才产生了气球充气后冲击传递所需的火花。结论:国内外许多导管实验室均采用水PPI或氯化钠生理盐水溶液作为血管成形术球囊。因此,有必要在世界范围内的导管室宣传在冲击波IVL半合规低压集成气囊中放入氯化钠生理盐水溶液,而不是水PPI以获得最佳性能的义务,以及冲击波医学向介入心脏病专家报告这一情况的重要性。
{"title":"Sodium Chloride Physiological Saline Solution Versus Water Preparations Injectable in the Use of Shockwave Intravascular Lithotripsy: A Single-Center Experience.","authors":"Quentin Landolff,&nbsp;Matthieu Godin,&nbsp;Alexandre Canville,&nbsp;Benjamin Honton,&nbsp;Jacques Monsegu,&nbsp;Marine Quillot,&nbsp;Jacques Berland,&nbsp;Rene Koning,&nbsp;Nicolas Amabile","doi":"10.14740/cr1489","DOIUrl":"https://doi.org/10.14740/cr1489","url":null,"abstract":"<p><strong>Background: </strong>Shockwave intravascular lithotripsy (IVL) coronary system is a very useful new technology for <i>de novo</i> severely calcified coronary artery plaques before percutaneous coronary intervention (PCI). The device uses a semi-compliant low-pressure balloon, integrated into a sterile catheter, to deliver by vaporizing fluid an expanding bubble that generates high-pressure ultrasonic energy by waves that create multiplane longitudinal micro-macro fractures in calcified plaques, which facilitate optimal stent placement and expansion, and luminal gain.</p><p><strong>Methods: </strong>The use of Shockwave IVL coronary system in our cardiac catheterization laboratory (Cath lab) at the \"Clinique Saint-Hilaire\" in Rouen, France, started in March 2019, with 42 procedures performed since this date: two patients in 2019, two patients in 2020, seven patients in 2021, 23 patients in 2022, and eight patients since the beginning of 2023.</p><p><strong>Results: </strong>We had experienced problems at the beginning of our activity for the first 11 patients (two patients in 2019, two patients in 2020, and seven patients in 2021): after less than five pulses, the shock therapy stopped. We used initially for Shockwave IVL semi-compliant low-pressure integrated balloons a mixture of 50% contrast and 50% water preparations injectable (PPI). After changing water PPI by sodium chloride physiological saline solution, we never encountered this problem again for the following 31 patients (23 patients in 2022, and eight patients since the beginning of 2023). In fact, the proper functioning of Shockwave IVL system requires ions in balloon mixture in addition to the contrast. It is thanks to the ions contained in sodium chloride physiological saline solution that the spark necessary for shocks delivery after balloon inflation is produced.</p><p><strong>Conclusions: </strong>Water PPI or sodium chloride physiological saline solution is used in angioplasty balloons in a lot of Cath labs worldwide. It is therefore essential to disseminate in the worldwide Cath lab the obligation to put in Shockwave IVL semi-compliant low-pressure integrated balloons sodium chloride physiological saline solution, rather than water PPI for optimal performance, and the importance of Shockwave Medical reporting this to interventional cardiologists.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 2","pages":"149-152"},"PeriodicalIF":1.9,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/4e/e3/cr-14-149.PMC10116940.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9445393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Left Atrial Remodeling in Patients With Severe Rheumatic Mitral Stenosis and Sinus Rhythm Using Two-Dimensional and Three-Dimensional Speckle Tracking Echocardiography. 二维和三维斑点跟踪超声心动图在严重风湿性二尖瓣狭窄和窦性心律患者左房重构中的应用。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-04-01 DOI: 10.14740/cr1465
Taher Said Abd Elkareem, Taghreed Abdelrahman Ahmed, Layla Ahmed Mohamed

Background: In mitral stenosis (MS), the combination of an increase in left atrium (LA) pressure and atrial inflammatory response is accompanied by increase in interstitial fibrosis of the atrial wall with disorganization of atrial muscle bundles, LA dysfunction and subsequently LA dilatation. We aimed to assess the effect of severe rheumatic MS on LA volumes and mechanics.

Methods: We enrolled 40 patients with pure severe rheumatic MS and sinus rhythm as a patient group and 30 healthy subjects as a control group. All patient and control groups underwent two-dimensional (2D) transthoracic echo to measure left ventricle (LV) dimensions, function, LA deformations, estimated systolic pulmonary artery pressure (EPAP), and left ventricle global longitudinal strain (LV GLS). Also LA volumes and mechanics (LA strain during LV systole (reservoir function) and LV diastole (early = conduit, and late = booster pump = atrial contraction)) were measured by three-dimensional (3D) transthoracic echo; mitral valve (MV) area was measured by 3D transesophageal echo (as routine pre-percutaneous MV commissurotomy using multiplanar reconstruction in mid-esophageal apical long-axis view from LA prospective).

Results: By 2D transthoracic echo, patient group revealed significantly lower all LA function vs. control group including LA strain during reservoir (24 ± 6 vs. 43 ± 3, P < 0.001), LA strain during conduit (-11 ± 3 vs. -25 ± 2, P < 0.001), and during booster pump (-13 ± 4 vs. -18 ± 1, P < 0.001). EPAP was significantly higher in patient group (48 ± 7 vs. 27 ± 4 in control group). LV GLS was significantly lower in patient group (-16±2% vs. -23±2% in control group). All 3D LA volumes were significantly higher in patient group than control group including maximum LA volume (LAVmax) (76 ± 18 vs. 50 ± 5, P < 0.001), indexed LA volume (LAVi) (44.6 ± 10.1 vs. 28.7 ± 3.7, P < 0.001), LV minimum volume (LAVmin) (51 ± 15 vs. 30 ± 4, P < 0.001), and LA volume pre atrial contraction (LAVpre A) (63 ± 15 vs. 41 ± 6, P < 0.001). Also, there was significantly decreased LA strain using 3D speckle tracking echo in patient group including systolic deformation of LA (reservoir function) (23 ± 6 vs. 41 ± 3, P < 0.001) and diastolic deformation, early diastole (conduit function) (-10 ± 2 vs. -24 ± 2, P < 0.001), and late diastole (booster pump function) (-13 ± 4 vs. -18 ± 1, P < 0.001).

Conclusions: All LA function markedly reduced in pure severe rheumatic MS. The reduction of LA mechanics is directly related to the degree of reduction of the stenotic MV area. LV GLS significantly reduced in severe MS and its reduction is directly related to the degree of reduction of the stenotic MV area and the LAVi by 3D echo.

背景:在二尖瓣狭窄(MS)中,左心房(LA)压力升高和心房炎症反应的结合伴随着心房壁间质纤维化的增加,并伴有心房肌束的紊乱、LA功能障碍和随后的LA扩张。我们的目的是评估严重风湿性MS对LA体积和力学的影响。方法:选取单纯重度风湿性MS合并窦性心律的患者40例作为患者组,健康者30例作为对照组。所有患者和对照组均行二维(2D)经胸超声测量左心室(LV)尺寸、功能、左室变形、估计收缩期肺动脉压(EPAP)和左心室整体纵向应变(LV GLS)。通过三维(3D)经胸回声测量左室容积和力学(左室收缩期(储层功能)和左室舒张期(早期=导管,晚期=增压泵=心房收缩)时的左室应变);通过三维经食管回声测量二尖瓣(MV)面积(作为常规经皮前二尖瓣融合切开术,在食管中端长轴视野下采用多平面重建)。结果:经胸二维超声显示,与对照组相比,患者组的所有LA功能均明显降低,包括储层期间LA应变(24±6比43±3,P < 0.001),导管期间LA应变(-11±3比-25±2,P < 0.001),增压泵期间LA应变(-13±4比-18±1,P < 0.001)。患者组EPAP(48±7)明显高于对照组(27±4)。患者组LV GLS明显低于对照组(-16±2%,对照组-23±2%)。患者组所有三维左室容积均显著高于对照组,包括最大左室容积(LAVmax)(76±18比50±5,P < 0.001)、指标左室容积(LAVi)(44.6±10.1比28.7±3.7,P < 0.001)、左室最小容积(LAVmin)(51±15比30±4,P < 0.001)、左室收缩前容积(LAVpre A)(63±15比41±6,P < 0.001)。3D斑点追踪回声显示,患者组LA应变明显降低,包括LA收缩变形(储层功能)(23±6比41±3,P < 0.001)和舒张变形、舒张早期(导管功能)(-10±2比-24±2,P < 0.001)和舒张晚期(增压泵功能)(-13±4比-18±1,P < 0.001)。结论:单纯重度风湿性ms的LA功能均明显降低,LA力学的降低与狭窄的MV区缩小程度直接相关。重度MS时左室GLS明显降低,其降低程度与狭窄MV区和三维回波对LAVi的降低程度直接相关。
{"title":"Left Atrial Remodeling in Patients With Severe Rheumatic Mitral Stenosis and Sinus Rhythm Using Two-Dimensional and Three-Dimensional Speckle Tracking Echocardiography.","authors":"Taher Said Abd Elkareem,&nbsp;Taghreed Abdelrahman Ahmed,&nbsp;Layla Ahmed Mohamed","doi":"10.14740/cr1465","DOIUrl":"https://doi.org/10.14740/cr1465","url":null,"abstract":"<p><strong>Background: </strong>In mitral stenosis (MS), the combination of an increase in left atrium (LA) pressure and atrial inflammatory response is accompanied by increase in interstitial fibrosis of the atrial wall with disorganization of atrial muscle bundles, LA dysfunction and subsequently LA dilatation. We aimed to assess the effect of severe rheumatic MS on LA volumes and mechanics.</p><p><strong>Methods: </strong>We enrolled 40 patients with pure severe rheumatic MS and sinus rhythm as a patient group and 30 healthy subjects as a control group. All patient and control groups underwent two-dimensional (2D) transthoracic echo to measure left ventricle (LV) dimensions, function, LA deformations, estimated systolic pulmonary artery pressure (EPAP), and left ventricle global longitudinal strain (LV GLS). Also LA volumes and mechanics (LA strain during LV systole (reservoir function) and LV diastole (early = conduit, and late = booster pump = atrial contraction)) were measured by three-dimensional (3D) transthoracic echo; mitral valve (MV) area was measured by 3D transesophageal echo (as routine pre-percutaneous MV commissurotomy using multiplanar reconstruction in mid-esophageal apical long-axis view from LA prospective).</p><p><strong>Results: </strong>By 2D transthoracic echo, patient group revealed significantly lower all LA function vs. control group including LA strain during reservoir (24 ± 6 vs. 43 ± 3, P < 0.001), LA strain during conduit (-11 ± 3 vs. -25 ± 2, P < 0.001), and during booster pump (-13 ± 4 vs. -18 ± 1, P < 0.001). EPAP was significantly higher in patient group (48 ± 7 vs. 27 ± 4 in control group). LV GLS was significantly lower in patient group (-16±2% vs. -23±2% in control group). All 3D LA volumes were significantly higher in patient group than control group including maximum LA volume (LAVmax) (76 ± 18 vs. 50 ± 5, P < 0.001), indexed LA volume (LAVi) (44.6 ± 10.1 vs. 28.7 ± 3.7, P < 0.001), LV minimum volume (LAVmin) (51 ± 15 vs. 30 ± 4, P < 0.001), and LA volume pre atrial contraction (LAVpre A) (63 ± 15 vs. 41 ± 6, P < 0.001). Also, there was significantly decreased LA strain using 3D speckle tracking echo in patient group including systolic deformation of LA (reservoir function) (23 ± 6 vs. 41 ± 3, P < 0.001) and diastolic deformation, early diastole (conduit function) (-10 ± 2 vs. -24 ± 2, P < 0.001), and late diastole (booster pump function) (-13 ± 4 vs. -18 ± 1, P < 0.001).</p><p><strong>Conclusions: </strong>All LA function markedly reduced in pure severe rheumatic MS. The reduction of LA mechanics is directly related to the degree of reduction of the stenotic MV area. LV GLS significantly reduced in severe MS and its reduction is directly related to the degree of reduction of the stenotic MV area and the LAVi by 3D echo.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 2","pages":"142-148"},"PeriodicalIF":1.9,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a5/0e/cr-14-142.PMC10116933.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9390008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Immobilizing Interstitial Cardiac Fibrosis. 固定化间质性心脏纤维化。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-04-01 DOI: 10.14740/cr1467
Yuriy L Shevchenko, Alexey V Plotnitsky, Daniil S Ulbashev

Background: The alterations in the endomysium and perimysium might cause compaction and gradual mechanical compression of cardiomyocytes resulting in their immobilization. This process finally leads to severe stiffening, so that the newly formed frame around individual cardiomyocytes and their clusters hinders normal diastole, and later systole. This phenomenon is referred to as immobilizing interstitial cardiac fibrosis (IICF). Deciphering the molecular and structural elements of myocardial changes is the key to understanding the pathogenetic foundations of heart failure development.

Methods: The study included 69 patients. Group I (n = 32) included patients with IICF; group II (n = 37) was comparison group. We evaluated the clinical picture, anamnesis of the disease, the results of physical examination, laboratory and instrumental examination of patients and autopsy data.

Results: In the anamnesis, patients with IICF were more likely to have diseases than patients in the control group: arrhythmia and impaired conductivity (88% vs. 19%, odds ratio (OR): 30.0; 95% confidence interval (CI): 7.918 - 113.7, P < 0.001), systemic connective tissue diseases (78% vs. 5%, OR: 62.5; 95% CI: 11.9 - 326.5, P < 0.001), viral infections (including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)) (53% vs. 19%, OR: 4.86; 95% CI: 1.66 - 14.25, P = 0.003), type 2 diabetes mellitus (47% vs. 8%, OR: 10.0; 95% CI: 2.54 - 39.34, P < 0.001), radiation therapy for mediastinal lymphoma and other oncological diseases (19% vs. 0%, P = 0.008), focal infections (sinusitis, osteomyelitis, periodontitis, nephritis, cystitis, pyelonephritis, pleurisy, etc.) within 12 months (31% vs. 11%, P = 0.069), chronic kidney disease (25% vs. 8%, P = 0.097), and tuberculosis (9% vs. 0%, P = 0.095). We have identified a statistically significant difference between the groups: the volume of the fibrosis zone (17.5±9.2% vs. 4.9±2.3%, P = 0.001), the expression of type I collagen (5,182 ± 1,301 vs. 2,189 ± 754 in 1 mm2, P = 0.0001), type III collagen (7,562 ± 1,405 vs. 2,320 ± 541 in 1 mm2, P = 0.0001), matrix metalloproteinase (MMP)-2 (12,850 ± 6,200 vs. 9,501 ± 7,145 in 1 mm2, P = 0.005), MMP-9 (15,745 ± 5,695 vs. 6,920 ± 3,125 in 1 mm2, P = 0.0001), connexin-43 (25,689 ± 14,871 vs. 37,523 ± 12,561 in 1 mm2, P = 0.001), fibronectin (3,448 ± 720 vs. 1,544 ± 610 in 1 mm2, P = 0.0001), and transforming growth factor β (TGF-β) (5,121 ± 1,243 vs. 2,531 ± 1,489 in 1 mm2, P = 0.001).

Conclusion: IICF is a separate pathological condition and one of the main causes of chronic heart failure. It is induced by changes in the myocardial connective tissue that prevent normal functioning of the myocardium.

背景:肌内膜和肌周膜的改变可能引起心肌细胞的压实和逐渐的机械压迫,导致它们的固定。这一过程最终导致严重的硬化,因此单个心肌细胞及其簇周围新形成的框架阻碍了正常的舒张和随后的收缩。这种现象被称为固定化间质性心脏纤维化(IICF)。破译心肌变化的分子和结构因素是了解心力衰竭发展的病理基础的关键。方法:纳入69例患者。第一组(n = 32)包括IICF患者;第二组(n = 37)为对照组。我们评估了临床表现,疾病的记忆,体检结果,实验室和仪器检查的病人和尸检数据。结果:在记忆中,IICF患者比对照组患者更容易出现疾病:心律失常和电导率受损(88%对19%,优势比(OR): 30.0;95%可信区间(CI): 7.918 ~ 113.7, P < 0.001),系统性结缔组织疾病(78% vs. 5%, OR: 62.5;95% CI: 11.9 - 326.5, P < 0.001),病毒感染(包括严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)) (53% vs. 19%, OR: 4.86;95% CI: 1.66 - 14.25, P = 0.003), 2型糖尿病(47%对8%,OR: 10.0;95% CI: 2.54 ~ 39.34, P < 0.001),纵隔淋巴瘤等肿瘤疾病(19% vs. 0%, P = 0.008), 12个月内局灶性感染(鼻窦炎、骨髓炎、牙周炎、肾炎、膀胱炎、肾盂肾炎、胸膜炎等)(31% vs. 11%, P = 0.069),慢性肾脏疾病(25% vs. 8%, P = 0.097),结核病(9% vs. 0%, P = 0.095)。我们发现两组之间存在统计学上的显著差异:纤维化区域的体积(17.5±9.2%和4.9±2.3%,P = 0.001), I型胶原蛋白的表达(5182±1301和2189±754年1平方毫米,P = 0.0001), III型胶原蛋白(7562±1405和2320±541年1平方毫米,P = 0.0001),基质金属蛋白酶(MMP) 2(12850±6200和9501±7145年1平方毫米,P = 0.005), MMP-9(15745±5695和6920±3125年1平方毫米,P = 0.0001), connexin-43(25689±14871和37523±12561年1平方毫米,P = 0.001),纤维连接蛋白(3,448±720比1,544±610,1 mm2, P = 0.0001)和转化生长因子β (TGF-β)(5,121±1,243比2,531±1,489,P = 0.001)。结论:IICF是一种独立的病理状态,是慢性心力衰竭的主要原因之一。它是由心肌结缔组织的变化引起的,这种变化阻止了心肌的正常功能。
{"title":"Immobilizing Interstitial Cardiac Fibrosis.","authors":"Yuriy L Shevchenko,&nbsp;Alexey V Plotnitsky,&nbsp;Daniil S Ulbashev","doi":"10.14740/cr1467","DOIUrl":"https://doi.org/10.14740/cr1467","url":null,"abstract":"<p><strong>Background: </strong>The alterations in the endomysium and perimysium might cause compaction and gradual mechanical compression of cardiomyocytes resulting in their immobilization. This process finally leads to severe stiffening, so that the newly formed frame around individual cardiomyocytes and their clusters hinders normal diastole, and later systole. This phenomenon is referred to as immobilizing interstitial cardiac fibrosis (IICF). Deciphering the molecular and structural elements of myocardial changes is the key to understanding the pathogenetic foundations of heart failure development.</p><p><strong>Methods: </strong>The study included 69 patients. Group I (n = 32) included patients with IICF; group II (n = 37) was comparison group. We evaluated the clinical picture, anamnesis of the disease, the results of physical examination, laboratory and instrumental examination of patients and autopsy data.</p><p><strong>Results: </strong>In the anamnesis, patients with IICF were more likely to have diseases than patients in the control group: arrhythmia and impaired conductivity (88% vs. 19%, odds ratio (OR): 30.0; 95% confidence interval (CI): 7.918 - 113.7, P < 0.001), systemic connective tissue diseases (78% vs. 5%, OR: 62.5; 95% CI: 11.9 - 326.5, P < 0.001), viral infections (including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)) (53% vs. 19%, OR: 4.86; 95% CI: 1.66 - 14.25, P = 0.003), type 2 diabetes mellitus (47% vs. 8%, OR: 10.0; 95% CI: 2.54 - 39.34, P < 0.001), radiation therapy for mediastinal lymphoma and other oncological diseases (19% vs. 0%, P = 0.008), focal infections (sinusitis, osteomyelitis, periodontitis, nephritis, cystitis, pyelonephritis, pleurisy, etc.) within 12 months (31% vs. 11%, P = 0.069), chronic kidney disease (25% vs. 8%, P = 0.097), and tuberculosis (9% vs. 0%, P = 0.095). We have identified a statistically significant difference between the groups: the volume of the fibrosis zone (17.5±9.2% vs. 4.9±2.3%, P = 0.001), the expression of type I collagen (5,182 ± 1,301 vs. 2,189 ± 754 in 1 mm<sup>2</sup>, P = 0.0001), type III collagen (7,562 ± 1,405 vs. 2,320 ± 541 in 1 mm<sup>2</sup>, P = 0.0001), matrix metalloproteinase (MMP)-2 (12,850 ± 6,200 vs. 9,501 ± 7,145 in 1 mm<sup>2</sup>, P = 0.005), MMP-9 (15,745 ± 5,695 vs. 6,920 ± 3,125 in 1 mm<sup>2</sup>, P = 0.0001), connexin-43 (25,689 ± 14,871 vs. 37,523 ± 12,561 in 1 mm<sup>2</sup>, P = 0.001), fibronectin (3,448 ± 720 vs. 1,544 ± 610 in 1 mm<sup>2</sup>, P = 0.0001), and transforming growth factor β (TGF-β) (5,121 ± 1,243 vs. 2,531 ± 1,489 in 1 mm<sup>2</sup>, P = 0.001).</p><p><strong>Conclusion: </strong>IICF is a separate pathological condition and one of the main causes of chronic heart failure. It is induced by changes in the myocardial connective tissue that prevent normal functioning of the myocardium.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 2","pages":"123-132"},"PeriodicalIF":1.9,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/0c/12/cr-14-123.PMC10116936.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9445391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mechanism of Increased Spinal Cord Blood Flow due to Noradrenaline Administration Using Vascular Resistance: An Experimental Study Using a Canine Model. 血管阻力对去甲肾上腺素给药后脊髓血流量增加的影响机制:犬模型实验研究。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-04-01 DOI: 10.14740/cr1478
Yuya Kise, Yukio Kuniyoshi, Keita Miyaishi, Mizuki Ando, Shotaro Higa, Tatuya Maeda, Moriyasu Nakaema, Hitoshi Inafuku, Kojiro Furukawa

Background: During thoracoabdominal aortic surgery, the spinal cord is placed under ischemic conditions. Elevation of systemic blood pressure is thus recommended as a method of increasing the blood supply from collateral networks. This study examined the mechanisms by which noradrenaline administration increases spinal cord blood flow (SCBF) by elevating systemic blood pressure.

Methods: In beagles (n = 7), the thoracoabdominal aorta and L2-L7 spinal cord segmental arteries (SAs) were exposed and a distal perfusion bypass was created to simulate clinical practice. SCBF was measured by laser flowmetry at the L5 dura mater and spinal cord perfusion pressure (SCPP) was measured inside the clamped aorta. The six pairs of SAs from L2 to L7 were clamped, and mean systemic blood pressure (mSBP), SCBF, and SCPP were measured before and after clamping and after starting continuous infusion of noradrenaline at 0.5 µg/kg/min. Rates of change in systemic vascular resistance (SVR) and spinal cord vascular resistance (SCVR) were calculated from the measured values.

Results: With no SA clamping (control), the rate of increase in SCVR was 0.74 times the rate of increase in SVR (y = 0.2 + 0.74x, r = 0.889, r2 = 0.789; P < 0.01). When all six pairs of SAs were clamped, a weak correlation was evident between rate of change in SCVR and rate of change in SVR, and the rate of increase in SCVR was lower than the rate of increase in SVR (y = 0.39 + 0.07x, r = 0.209, r2 = 0.039; P < 0.01). When all six pairs of SAs were clamped in the absence of distal perfusion, a weak correlation was also evident between rate of change in SCVR and rate of change in SVR, and the rate of increase in SCVR was lower than the rate of increase in SVR (y = 0.19 + 0.08x, r = 0.379, r2 = 0.144; P < 0.01).

Conclusions: The rate of increase in SCVR induced by noradrenaline administration was lower than the rate of increase in SVR in the control group with no spinal cord SA clamping and in both experimental groups with clamped SAs (with and without distal perfusion), creating an environment conducive to spinal cord flow distribution.

背景:在胸腹主动脉手术中,脊髓处于缺血状态。因此,建议将体表血压升高作为增加侧枝网络供血的一种方法。本研究探讨了去甲肾上腺素通过升高全身血压来增加脊髓血流量(SCBF)的机制。方法:取比格犬(n = 7),暴露胸腹主动脉和L2-L7脊髓节段动脉(SAs),建立远端灌注旁路模拟临床。采用激光血流仪测量L5硬脑膜SCBF,测定夹紧主动脉内脊髓灌注压(SCPP)。夹持L2 ~ L7的6对SAs,分别在夹持前后和开始以0.5µg/kg/min持续输注去甲肾上腺素后测量平均体血压(mSBP)、SCBF、SCPP。根据测量值计算全身血管阻力(SVR)和脊髓血管阻力(SCVR)的变化率。结果:未夹持SA组(对照组)SCVR的增加率是SVR增加率的0.74倍(y = 0.2 + 0.74x, r = 0.889, r2 = 0.789;P < 0.01)。当所有6对sa均夹持时,SCVR变化率与SVR变化率之间呈明显的弱相关,SCVR的增加速率低于SVR的增加速率(y = 0.39 + 0.07x, r = 0.209, r2 = 0.039;P < 0.01)。在没有远端灌注的情况下夹持所有6对sa时,SCVR变化率与SVR变化率之间也存在明显的弱相关,SCVR的增加速率低于SVR的增加速率(y = 0.19 + 0.08x, r = 0.379, r2 = 0.144;P < 0.01)。结论:未夹持脊髓SA的对照组和夹持脊髓SA(有远端灌注和无远端灌注)的实验组,去甲肾上腺素诱导SCVR的增加率低于SVR的增加率,创造了有利于脊髓血流分布的环境。
{"title":"Mechanism of Increased Spinal Cord Blood Flow due to Noradrenaline Administration Using Vascular Resistance: An Experimental Study Using a Canine Model.","authors":"Yuya Kise,&nbsp;Yukio Kuniyoshi,&nbsp;Keita Miyaishi,&nbsp;Mizuki Ando,&nbsp;Shotaro Higa,&nbsp;Tatuya Maeda,&nbsp;Moriyasu Nakaema,&nbsp;Hitoshi Inafuku,&nbsp;Kojiro Furukawa","doi":"10.14740/cr1478","DOIUrl":"https://doi.org/10.14740/cr1478","url":null,"abstract":"<p><strong>Background: </strong>During thoracoabdominal aortic surgery, the spinal cord is placed under ischemic conditions. Elevation of systemic blood pressure is thus recommended as a method of increasing the blood supply from collateral networks. This study examined the mechanisms by which noradrenaline administration increases spinal cord blood flow (SCBF) by elevating systemic blood pressure.</p><p><strong>Methods: </strong>In beagles (<i>n</i> = 7), the thoracoabdominal aorta and L2-L7 spinal cord segmental arteries (SAs) were exposed and a distal perfusion bypass was created to simulate clinical practice. SCBF was measured by laser flowmetry at the L5 dura mater and spinal cord perfusion pressure (SCPP) was measured inside the clamped aorta. The six pairs of SAs from L2 to L7 were clamped, and mean systemic blood pressure (mSBP), SCBF, and SCPP were measured before and after clamping and after starting continuous infusion of noradrenaline at 0.5 µg/kg/min. Rates of change in systemic vascular resistance (SVR) and spinal cord vascular resistance (SCVR) were calculated from the measured values.</p><p><strong>Results: </strong>With no SA clamping (control), the rate of increase in SCVR was 0.74 times the rate of increase in SVR (y = 0.2 + 0.74x, r = 0.889, r<sup>2</sup> = 0.789; P < 0.01). When all six pairs of SAs were clamped, a weak correlation was evident between rate of change in SCVR and rate of change in SVR, and the rate of increase in SCVR was lower than the rate of increase in SVR (y = 0.39 + 0.07x, r = 0.209, r<sup>2</sup> = 0.039; P < 0.01). When all six pairs of SAs were clamped in the absence of distal perfusion, a weak correlation was also evident between rate of change in SCVR and rate of change in SVR, and the rate of increase in SCVR was lower than the rate of increase in SVR (y = 0.19 + 0.08x, r = 0.379, r<sup>2</sup> = 0.144; P < 0.01).</p><p><strong>Conclusions: </strong>The rate of increase in SCVR induced by noradrenaline administration was lower than the rate of increase in SVR in the control group with no spinal cord SA clamping and in both experimental groups with clamped SAs (with and without distal perfusion), creating an environment conducive to spinal cord flow distribution.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 2","pages":"115-122"},"PeriodicalIF":1.9,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/fd/1a/cr-14-115.PMC10116934.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9445396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association Between Major Adverse Cardiovascular Events and the Gensini Score or Coronary Artery Calcification Score in Hypertensive Patients Who Have Undergone Coronary Computed Tomography Angiography. 接受冠状动脉ct血管造影的高血压患者的主要不良心血管事件与Gensini评分或冠状动脉钙化评分之间的关系
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-04-01 DOI: 10.14740/cr1453
Yuhei Shiga, Kohei Tashiro, Erica Miura, Sara Higashi, Yuto Kawahira, Takashi Kuwano, Makoto Sugihara, Shin-Ichiro Miura

Background: From the Fukuoka University Coronary Computed Tomography Angiography (FU-CCTA) registry, we present major adverse cardiovascular events (MACEs) in hypertensive patients who have undergone CCTA, and the association between MACEs and the Gensini score of coronary arteries or the coronary artery calcification (CAC) score.

Methods: Of the patients who underwent CCTA for coronary artery disease (CAD) screening at Fukuoka University Hospital, 318 hypertensive patients who had at least one cardiovascular risk factor or suspected CAD were enrolled. The patients were divided into two groups: MACEs and non-MACEs groups. The severity of atherosclerosis of coronary arteries was assessed by the Gensini score. The CAC score was also defined by computed tomography (CT) images at the time of CCTA. A primary endpoint was MACEs (all-cause death, ischemic stroke, acute myocardial infarction, coronary revascularization). The patients were followed for up to 5 years.

Results: The patients were 68 ± 10 years, and 50% were males. The percentages of smoking, dyslipidemia, diabetes, and chronic kidney disease were 39%, 70%, 26% and 37%, respectively. The %males, %smoking, CAC score and Gensini score in the MACEs group were significantly higher than those in the non-MACEs group. On the other hand, the differences in age, dyslipidemia, diabetes, or chronic kidney disease between the groups were not seen. A multivariate analysis was performed regarding the presence or absence of MACE by logistic regression analysis of the CAC score or Gensini score in addition to conventional risk factors as independent variables. A Cox regression analysis revealed significant relationships for both the CAC score (P = 0.043) and the Gensini score (P = 0.008).

Conclusions: The CAC score and the Gensini score could predict MACEs in hypertensive patients who have undergone CCTA.

背景:来自福冈大学冠状动脉计算机断层血管造影(FU-CCTA)登记,我们报告了接受CCTA的高血压患者的主要不良心血管事件(mace),以及mace与冠状动脉Gensini评分或冠状动脉钙化(CAC)评分之间的关系。方法:在福冈大学医院接受冠心病(CAD)筛查的患者中,纳入318例至少有一种心血管危险因素或疑似冠心病的高血压患者。患者分为两组:恶性肿瘤组和非恶性肿瘤组。冠状动脉粥样硬化的严重程度采用Gensini评分。CCTA时的计算机断层扫描(CT)图像也定义了CAC评分。主要终点是mace(全因死亡、缺血性卒中、急性心肌梗死、冠状动脉血运重建术)。对这些患者进行了长达5年的随访。结果:患者年龄68±10岁,男性占50%。吸烟、血脂异常、糖尿病和慢性肾病的比例分别为39%、70%、26%和37%。mace组男性百分比、吸烟百分比、CAC评分、Gensini评分均显著高于非mace组。另一方面,两组之间在年龄、血脂异常、糖尿病或慢性肾脏疾病方面没有差异。采用logistic回归分析CAC评分或Gensini评分,并将常规危险因素作为自变量,对MACE的存在与否进行多变量分析。Cox回归分析显示CAC评分(P = 0.043)与Gensini评分(P = 0.008)之间存在显著相关。结论:CAC评分和Gensini评分可以预测行CCTA的高血压患者的mace。
{"title":"Association Between Major Adverse Cardiovascular Events and the Gensini Score or Coronary Artery Calcification Score in Hypertensive Patients Who Have Undergone Coronary Computed Tomography Angiography.","authors":"Yuhei Shiga,&nbsp;Kohei Tashiro,&nbsp;Erica Miura,&nbsp;Sara Higashi,&nbsp;Yuto Kawahira,&nbsp;Takashi Kuwano,&nbsp;Makoto Sugihara,&nbsp;Shin-Ichiro Miura","doi":"10.14740/cr1453","DOIUrl":"https://doi.org/10.14740/cr1453","url":null,"abstract":"<p><strong>Background: </strong>From the Fukuoka University Coronary Computed Tomography Angiography (FU-CCTA) registry, we present major adverse cardiovascular events (MACEs) in hypertensive patients who have undergone CCTA, and the association between MACEs and the Gensini score of coronary arteries or the coronary artery calcification (CAC) score.</p><p><strong>Methods: </strong>Of the patients who underwent CCTA for coronary artery disease (CAD) screening at Fukuoka University Hospital, 318 hypertensive patients who had at least one cardiovascular risk factor or suspected CAD were enrolled. The patients were divided into two groups: MACEs and non-MACEs groups. The severity of atherosclerosis of coronary arteries was assessed by the Gensini score. The CAC score was also defined by computed tomography (CT) images at the time of CCTA. A primary endpoint was MACEs (all-cause death, ischemic stroke, acute myocardial infarction, coronary revascularization). The patients were followed for up to 5 years.</p><p><strong>Results: </strong>The patients were 68 ± 10 years, and 50% were males. The percentages of smoking, dyslipidemia, diabetes, and chronic kidney disease were 39%, 70%, 26% and 37%, respectively. The %males, %smoking, CAC score and Gensini score in the MACEs group were significantly higher than those in the non-MACEs group. On the other hand, the differences in age, dyslipidemia, diabetes, or chronic kidney disease between the groups were not seen. A multivariate analysis was performed regarding the presence or absence of MACE by logistic regression analysis of the CAC score or Gensini score in addition to conventional risk factors as independent variables. A Cox regression analysis revealed significant relationships for both the CAC score (P = 0.043) and the Gensini score (P = 0.008).</p><p><strong>Conclusions: </strong>The CAC score and the Gensini score could predict MACEs in hypertensive patients who have undergone CCTA.</p>","PeriodicalId":9424,"journal":{"name":"Cardiology Research","volume":"14 2","pages":"91-96"},"PeriodicalIF":1.9,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/29/23/cr-14-091.PMC10116937.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9445394","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Cardiology Research
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1