Orihuela Rodríguez Oscar, Valle Nava Leobardo, Ferreira-Hermosillo Aldo, Carmona-Ruiz Héctor A, Acevedo Meléndez Ariana, Jacobo Ruvalcaba Andrés, Sosa-Eroza Ernesto
Clinical Department of Cardiology, Hospital de Especialidades "Dr. Benardo Sepúlveda", Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City 06720, Mexico.
Unidad de Investigación Médica en Enfermedades Endocrinas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City 06720, Mexico.
Biomedicines. 2025 Mar 1;13(3):605. doi: 10.3390/biomedicines13030605.
: Cardiomyopathy is the leading cause of morbidity and mortality in patients with acromegaly. Pharmacological and surgical treatment of the disease has been associated with morphological and functional benefits for the heart, but other studies have shown that the condition and its effects may be irreversible. This study aims to uncover the most frequent echocardiographic changes in patients with cardiomyopathy due to acromegaly. : An observational, descriptive, cross-sectional study was performed. Patients were referred from the Endocrinology department to the Cardiology department. This study was conducted from November 2020 to November 2022. Patients with the following criteria were included: over 18 years of age, of both genders, and with a complete clinical record and complete laboratory studies. : A total of 89 men (38%) and 148 women (62%) were included, with a mean age of 48 ± 12 years in the men and 49 ± 13 years in the women ( = 0.223). The most frequent cardiac findings were concentric hypertrophy (CHT) in 116 patients (49%), concentric remodeling (CR) in 52 patients (22%), and eccentric hypertrophy (EH) in 18 patients (8%). The left ventricular ejection fraction (LVEF) was preserved in the entire population. Left atrial enlargement (LAE) was observed in 88 patients (37%), diastolic dysfunction in 61 patients (26%), right ventricular dilatation in 47 patients (20%), right atrial enlargement in 120 patients (51), and pulmonary hypertension in 28 patients (12%). Valvular insufficiencies (VIs) were observed: tricuspid VIs in 73%, mitral VIs in 49%, and aortic VIs in 24% of the population. : The frequency of changes in the four chambers is elevated in cardiomyopathy due to acromegaly.
心肌病是肢端肥大症患者发病和死亡的主要原因。该疾病的药物和手术治疗已显示对心脏有形态和功能方面的益处,但其他研究表明,这种病症及其影响可能是不可逆的。本研究旨在揭示肢端肥大症所致心肌病患者最常见的超声心动图变化。
进行了一项观察性、描述性横断面研究。患者从内分泌科转诊至心内科。本研究于2020年11月至2022年11月进行。纳入符合以下标准的患者:年龄超过18岁,男女不限,有完整的临床记录和完整的实验室检查结果。
共纳入89名男性(38%)和148名女性(62%),男性平均年龄为48±12岁,女性平均年龄为49±13岁(P = 0.223)。最常见的心脏检查结果为116例患者(49%)出现向心性肥厚(CHT),52例患者(22%)出现向心性重塑(CR),18例患者(8%)出现离心性肥厚(EH)。整个人群的左心室射血分数(LVEF)均保留。88例患者(37%)观察到左心房扩大(LAE),61例患者(26%)出现舒张功能障碍,47例患者(20%)出现右心室扩张,120例患者(51%)出现右心房扩大,28例患者(12%)出现肺动脉高压。观察到瓣膜关闭不全(VIs):三尖瓣VIs占73%,二尖瓣VIs占49%,主动脉VIs占24%。
肢端肥大症所致心肌病患者四个心腔变化的发生率升高。