Division of Cardiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Division of General Internal Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland.
JACC Heart Fail. 2020 Sep;8(9):712-724. doi: 10.1016/j.jchf.2020.04.007. Epub 2020 Jul 8.
This study prospectively evaluated endomyocardial biopsies in patients with heart failure with preserved ejection fraction (HFpEF) to identify histopathologic phenotypes and their association with clinical characteristics.
Myocardial tissue analysis from a prospectively defined HFpEF cohort reflecting contemporary comorbidities is lacking.
Patients with HFpEF (EF ≥50%) referred to the Johns Hopkins HFpEF Clinic between August 2014 and September 2018 were enrolled for right heart catheterization and endomyocardial biopsy. Clinical features, echocardiography, hemodynamics, and tissue histology were determined and compared with controls (unused donor hearts) and HF with reduced EF (HFrEF).
Of the 108 patients enrolled, median age was 66 years (25th to 75th percentile: 57 to 74 years), 61% were women, 57% were African American, 62% had a previous HF hospitalization, median systolic blood pressure was 141 mm Hg (25th to 75th percentile: 125 to 162 mm Hg), body mass index (BMI) was 37 kg/m (25th to 75th percentile: 32 to 45 kg/m), and 97% were on a loop diuretic. Myocardial fibrosis and myocyte hypertrophy were often present (93% and 88%, respectively); however, mild in 71% with fibrosis and in 52% with hypertrophy. Monocyte infiltration (CD68+ cells/mm) was greater in patients with HFpEF versus controls (60.4 cells/mm [25th to 75th percentile: 36.8 to 97.8] vs. 32.1 cells/mm [25th to 75th percentile: 22.3 to 59.2]; p = 0.02) and correlated with age and renal disease. Cardiac amyloidosis (CA) was diagnosed in 15 (14%) patients (HFpEF-CA: 7 patients with wild-type transthyretin amyloidosis [ATTR], 4 patients with hereditary ATTR, 3 patients with light-chain amyloidosis, and 1 patient with AA (secondary) amyloidosis), of which 7 cases were unsuspected. Patients with HFpEF-CA were older, with lower BMI, higher left ventricular mass index, and higher N-terminal pro-B-type natriuretic peptide and troponin I levels.
In this large, prospective myocardial tissue analysis of HFpEF, myocardial fibrosis and hypertrophy were common, CD68+ inflammation was increased, and CA prevalence was 14%. Tissue analysis in HFpEF might improve precision therapies by identifying relevant myocardial mechanisms.
本研究前瞻性评估射血分数保留型心力衰竭(HFpEF)患者的心内膜心肌活检,以确定组织病理学表型及其与临床特征的关系。
缺乏反映当代合并症的前瞻性定义的 HFpEF 队列的心肌组织分析。
2014 年 8 月至 2018 年 9 月期间,因 HFpEF 被转诊至约翰霍普金斯 HFpEF 诊所的患者接受右心导管检查和心内膜心肌活检。确定临床特征、超声心动图、血液动力学和组织病理学,并与对照组(未使用的供体心脏)和射血分数降低的心力衰竭(HFrEF)进行比较。
在纳入的 108 例患者中,中位年龄为 66 岁(25%至 75%分位:57 至 74 岁),61%为女性,57%为非裔美国人,62%有 HF 住院史,中位收缩压为 141mmHg(25%至 75%分位:125 至 162mmHg),体重指数(BMI)为 37kg/m(25%至 75%分位:32 至 45kg/m),97%服用袢利尿剂。心肌纤维化和心肌细胞肥大常存在(分别为 93%和 88%);然而,纤维化中有 71%和肥大中有 52%为轻度。与对照组相比,HFpEF 患者的单核细胞浸润(CD68+细胞/mm)更高(60.4 个细胞/mm[25%至 75%分位:36.8 至 97.8]比 32.1 个细胞/mm[25%至 75%分位:22.3 至 59.2];p=0.02),并与年龄和肾脏疾病相关。15 例(14%)患者诊断为心脏淀粉样变性(CA)(HFpEF-CA:7 例野生型转甲状腺素蛋白淀粉样变性[ATTR],4 例遗传性ATTR,3 例轻链淀粉样变性,1 例 AA(继发性)淀粉样变性),其中 7 例为意外发现。HFpEF-CA 患者年龄较大,BMI 较低,左心室质量指数较高,N 末端脑钠肽前体和肌钙蛋白 I 水平较高。
在这项针对 HFpEF 的大规模前瞻性心肌组织分析中,心肌纤维化和肥大很常见,CD68+炎症增加,CA 患病率为 14%。HFpEF 中的组织分析可能通过识别相关的心肌机制来改善精准治疗。