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Adolescent with Unexplained Cardiac Hypertrophy, Ventricular Pre-Excitation, Conduction System Disease: PRKAG2 Cardiac Syndrome as a Rare Mimicker of Hypertrophic Cardiomyopathy. 青少年不明原因心脏肥厚,心室预兴奋,传导系统疾病:PRKAG2心脏综合征是肥厚性心肌病的罕见模仿者。
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-02-04 DOI: 10.14744/AnatolJCardiol.2025.5695
Yafeng Guo, Dong Yi, Daoquan Liu, Qingkun Fan, Zhaokun Ma, Li Wang, Hongxu Chen, Bingyin Wang, Hua Yan
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引用次数: 0
Phenotypic, Epidemiologic, and Imaging Features of Hypertrophic Cardiomyopathy: A Single-Center Experience. 肥厚性心肌病的表型、流行病学和影像学特征:单中心经验。
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-02-04 DOI: 10.14744/AnatolJCardiol.2025.5686
Gamze Babur Güler, Arda Güler, İbrahim Halil Tanboğa, Mehmet Karacan, İrem Türkmen, Sezgin Atmaca, Aysel Türkvatan Cansever, Hasan Şahin, Gizemnur Coşkun, Sinem Aydın, Dilara Pay, Utku Yartası, Nail Güven Serbest, Muayad Almasri, Mustafa Can Gündoğdu, Duygu İnan, Özgür Sürgit, Mehmet Ertürk

Background: Hypertrophic cardiomyopathy (HCM) is a complex myocardial disorder with heterogeneous clinical presentations and structural manifestations. This study aimed to assess the distribution, clinical characteristics, and diagnostic approaches in a regional cohort of patients with HCM.

Methods: Patients diagnosed with HCM at a tertiary cardiomyopathy clinic between October 2021 and November 2024 were retrospectively analyzed. Patients were classified into obstructive, latent obstructive, non-obstructive, or apical phenotypes based on clinical and imaging findings. Comprehensive demographic, clinical, and imaging data were collected for detailed analysis, providing valuable insights into the phenotypic diversity of HCM.

Results: The cohort included 701 patients with a median age of 53 years of whom 68% were male. The phenotypic distribution comprised 9.3% apical, 38.1% non-obstructive, 32.5% resting obstructive, and 20.1% latent obstructive HCM. Implantable cardioverter-defibrillator implantation was more common in obstructive phenotypes, particularly in the latent obstructive group. Although late gadolinium enhancement (LGE) was more frequently observed in apical HCM, post-hoc analysis showed no significant difference in prevalence across subgroups. In contrast, LGE extent was significantly greater in the apical group. Genetic testing, performed in 32% of patients, revealed a 44% positivity rate, with MYBPC3 and MYH7 being the most commonly detected mutations. The overall mortality rate was 2.8%, with heart failure identified as the leading cause of death.

Conclusion: In this large regional cohort of HCM patients, obstructive and non-obstructive phenotypes were predominant, with a notable burden of genetic mutations and a low overall mortality rate primarily driven by heart failure. These findings emphasize the clinical heterogeneity of HCM and highlight the importance of comprehensive diagnostic evaluation.

背景:肥厚性心肌病(HCM)是一种复杂的心肌疾病,具有不同的临床表现和结构表现。本研究旨在评估HCM患者区域队列的分布、临床特征和诊断方法。方法:回顾性分析2021年10月至2024年11月在三级心肌病诊所诊断为HCM的患者。根据临床和影像学表现将患者分为阻塞性、潜伏性阻塞性、非阻塞性或根尖型。收集了全面的人口学、临床和影像学数据进行详细分析,为HCM的表型多样性提供了有价值的见解。结果:该队列包括701例患者,中位年龄53岁,其中68%为男性。表型分布为9.3%的根尖型HCM, 38.1%的非阻塞性HCM, 32.5%的静息性阻塞性HCM和20.1%的潜伏性阻塞性HCM。植入式心律转复除颤器植入在梗阻性表型中更为常见,特别是在潜伏性梗阻性组。虽然晚期钆增强(LGE)在根尖HCM中更常见,但事后分析显示,亚组间的患病率无显著差异。相比之下,根尖组的LGE程度明显更大。在32%的患者中进行的基因检测显示,44%的阳性率,其中MYBPC3和MYH7是最常检测到的突变。总体死亡率为2.8%,心力衰竭被确定为主要死亡原因。结论:在这个大型区域性HCM患者队列中,梗阻性和非梗阻性表型占主导地位,基因突变负担显著,主要由心力衰竭引起的总死亡率较低。这些发现强调了HCM的临床异质性,并强调了综合诊断评估的重要性。
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引用次数: 0
TRAFFIC study, Sarcopenia and Obesity…. TRAFFIC研究,肌肉减少症和肥胖症....
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-02-01 DOI: 10.14744/AnatolJCardiol.2026.2
Çetin Erol
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引用次数: 0
Reply to the Letter to the Editor: "Comment on 'Delayed-Onset Type 1 Kounis Syndrome Caused Ventricular Fibrillation: A Case Report'". 复函编者:《关于“迟发性1型Kounis综合征致心室颤动1例报告”的评论》
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-28 DOI: 10.14744/AnatolJCardiol.2025.6078
Honggen Cui, Yaqin Li, Yi Liu
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引用次数: 0
Commentary on the Prognostic Interpretation of the Triglyceride-Glucose Index in Patients with HCM and HFpEF. HCM和HFpEF患者的甘油三酯-葡萄糖指数的预后解释评论。
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-15 DOI: 10.14744/AnatolJCardiol.2025.6029
Ahmet Yılmaz
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引用次数: 0
Ventricular Fibrillation and Kounis Syndrome Can Result from a More Severe Delayed-Onset Allergic Reaction. 心室颤动和库尼斯综合征可由更严重的延迟性过敏反应引起。
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-15 DOI: 10.14744/AnatolJCardiol.2025.6022
Nicholas G Kounis
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引用次数: 0
When Myxoma Jumps Chambers: Direct Seeding from Left Atrium to Right Ventricular Outflow Tract via Patent Foramen Ovale. 当黏液瘤跳跃腔室时:从左心房经卵圆孔未闭直接播种至右心室流出道。
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-15 DOI: 10.14744/AnatolJCardiol.2025.6062
Wan Li, Ping Hu, Jie Wang, Xiao-Jing Ma, Yi Gao
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引用次数: 0
Transcatheter Versus Surgical Closure of Atrial Septal Defect in Children and Adults: A Systematic Review and Meta-Analysis of Observational Studies. 经导管与手术治疗儿童和成人房间隔缺损:观察性研究的系统回顾和荟萃分析。
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-15 DOI: 10.14744/AnatolJCardiol.2025.5766
Johnson Kannady, Putri Amelia, Ahmad Dwi Rifa'i, Grace Hany Hot Asi Sianturi

Background: Atrial septal defect closure can be performed surgically or via transcatheter intervention, yet comparative outcomes remain inconsistent between children and adults. This review synthesizes observational evidence to evaluate procedural success, complications, and periprocedural characteristics across both populations.

Methods: A systematic review and meta-analysis following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines was conducted, including 36 observational studies published through 2024. Study quality was assessed using the Newcastle-Ottawa Scale. Random effects models were applied, with subgroup analyses by age and procedure type. Publication bias was examined using funnel plots and Egger's test.

Results: The pooled procedural success rate was 95% (95% CI: 92%-97%; I² = 90.2%). Among children, raw procedural success was 87% (1445/1656) for transcatheter closure and 99% (505/510) with surgery. In adults, transcatheter closure achieved 97% (95% CI: 90%-99%), whereas surgery reached 98% (95% CI: 70%-100%). Transcatheter closure resulted in shorter hospitalization (mean difference: -3.86 days, 95% CI: -6.03 to -1.69; P = .0004) and fewer major complications (risk ratio: 0.58, 95% CI: 0.39-0.86; P = .006). Sensitivity analysis restricted to high-quality studies (n = 12) remained consistent. Egger's regression did not indicate significant publication bias (P = .069).

Conclusion: Both approaches provide high closure success, yet transcatheter intervention offers lower complication rates and faster recovery, particularly in anatomically suitable patients. These findings support individualized treatment selection based on age, anatomy, and institutional experience.

背景:房间隔缺损闭合可通过手术或经导管介入治疗,但儿童和成人的比较结果仍不一致。本综述综合了观察证据来评估两种人群的手术成功率、并发症和围手术期特征。方法:根据系统评价和荟萃分析首选报告项目(PRISMA) 2020指南进行系统评价和荟萃分析,包括36项到2024年发表的观察性研究。使用纽卡斯尔-渥太华量表评估研究质量。采用随机效应模型,按年龄和手术类型进行亚组分析。采用漏斗图和Egger检验检验发表偏倚。结果:合并手术成功率为95% (95% CI: 92% ~ 97%; I²= 90.2%)。在儿童中,经导管闭合的原始手术成功率为87%(1445/1656),手术成功率为99%(505/510)。在成人中,经导管闭合达到97% (95% CI: 90%-99%),而手术达到98% (95% CI: 70%-100%)。经导管关闭缩短了住院时间(平均差值:-3.86天,95% CI: -6.03 ~ -1.69; P = 0.0004),减少了主要并发症(风险比:0.58,95% CI: 0.39 ~ 0.86; P = 0.006)。局限于高质量研究(n = 12)的敏感性分析保持一致。Egger回归未显示显著的发表偏倚(P = 0.069)。结论:两种方法均能获得较高的闭合成功率,但经导管介入治疗的并发症发生率更低,恢复速度更快,尤其是在解剖结构合适的患者中。这些发现支持基于年龄、解剖结构和机构经验的个性化治疗选择。
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引用次数: 0
A Fishbone-Like Bone Cement Fragment Crossing the Tricuspid Valve and Penetrating the Septum: Rare Sequela of Percutaneous Vertebroplasty. 鱼骨样骨水泥碎片穿过三尖瓣并穿透中隔:经皮椎体成形术的罕见后遗症。
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-15 DOI: 10.14744/AnatolJCardiol.2025.6015
Xin Xie, Yibing Fang
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引用次数: 0
Revisiting Triglyceride-Glucose Index in HCM and HFpEF: Clarifying Confounders and Interpretative Limitations. 重新审视HCM和HFpEF的甘油三酯-葡萄糖指数:澄清混杂因素和解释局限性。
IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-15 DOI: 10.14744/AnatolJCardiol.2025.5969
Hüseyin Bektaş, Fatih Akkaya, Yusuf Hoşoğlu
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引用次数: 0
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Anatolian Journal of Cardiology
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