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骨髓增殖性疾病的心脏功能和形态学改变(临床研究)

Functional and morphological cardiac changes in myeloproliferative disorders (clinical study).

作者信息

Kadikoylu Gurhan, Onbasili Alper, Tekten Tarkan, Barutca Sabri, Bolaman Zahit

机构信息

Department of Hematology, Medical Faculty, Adnan Menderes University, Aydin, Turkey.

出版信息

Int J Cardiol. 2004 Nov;97(2):213-20. doi: 10.1016/j.ijcard.2003.08.013.

Abstract

PURPOSE

Cardiac involvement is not well defined in myeloproliferative disorders (MPD). The purpose of this study was to evaluate the cardiac involvement by transthoracic echocardiography in MPD.

MATERIALS AND METHODS

The study groups were 36 patients (mean age: 58+/-15 years, 20 female and 16 male) with MPD and 30 age-matched healthy controls. MPD group included 15 essential thrombocythemia (ET), eight chronic phase chronic myelogenous leukemia (CML), seven idiopathic myelofibrosis (MF) and six polcythemia vera patients.

RESULTS

Valvular regurgitations were present in 14 patients (39%) and eight controls (27%), (P>0.05). Mitral regurgitation (MR) was more prominent in CML compared to controls (P=0.044). The rates of annular calcifications, valvular thickening, and vegetation like lesions were not different between MPD and control groups. Pulmonary hypertension (PHT) was present in six (17%) patients, but none of the controls (P=0.021). The rates of PHT in CML and MF were significantly higher than controls (P<0.05). The rate of PHT was not different in-between MPD patients with and without thromboembolic events, however, in MPD cases with thromboembolic events PHT was more common compared to controls (P=0.037).

CONCLUSION

This study showed that valvular lesions were not more prevalent in MPD. PHT was the most prominent cardiac pathology in MPD (especially in CML, MF and thromboembolic events subgroups) compared to controls. Further evaluation of the cardiac changes in MPD subgroups with extended studies including trans-oesophageal echocardiography and longer follow-up periods would be appropriate.

摘要

目的

骨髓增殖性疾病(MPD)中心脏受累情况尚未明确界定。本研究旨在通过经胸超声心动图评估MPD患者的心脏受累情况。

材料与方法

研究组为36例MPD患者(平均年龄:58±15岁,女性20例,男性16例)和30例年龄匹配的健康对照者。MPD组包括15例原发性血小板增多症(ET)、8例慢性期慢性粒细胞白血病(CML)、7例特发性骨髓纤维化(MF)和6例真性红细胞增多症患者。

结果

14例患者(39%)和8例对照者(27%)存在瓣膜反流(P>0.05)。与对照组相比,CML患者的二尖瓣反流(MR)更为显著(P=0.044)。MPD组和对照组之间,瓣环钙化、瓣膜增厚及赘生物样病变的发生率无差异。6例(17%)患者存在肺动脉高压(PHT),而对照组无一例出现(P=0.021)。CML和MF患者的PHT发生率显著高于对照组(P<0.05)。有无血栓栓塞事件的MPD患者之间PHT发生率无差异,然而,有血栓栓塞事件的MPD患者中PHT比对照组更常见(P=0.037)。

结论

本研究表明MPD患者中瓣膜病变并不更普遍。与对照组相比,PHT是MPD中最突出的心脏病理改变(尤其是在CML、MF和血栓栓塞事件亚组中)。对MPD亚组的心脏变化进行进一步评估,采用包括经食管超声心动图和更长随访期的扩展研究是合适的。

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