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DOI 10.1111/eci.12492

Медицинская библиотека · European journal of clinical investigation · 2015

Echocardiographic evaluation in subjects with α1-Antitrypsin deficiency.

Vizzardi Enrico, Corda Luciano, Sciatti Edoardo, Roca Elisa, Redolfi Stefania, Arici Marianna, Pini Laura, Bonadei Ivano, Metra Marco, Tantucci Claudio

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Аннотация

BACKGROUND

α1-Antitrypsin (AAT) deficiency (AATD) is a genetic condition associated with early-onset panacinar emphysema and, less often, vascular disease. Recently, abnormal elastic properties of ascending aortic wall were described in ZZ genotype AATD subjects who incidentally showed an increased left ventricular mass.

MATERIALS AND

METHODS

To evaluate biventricular dimensions, valvular apparatus, systolic and diastolic function, 33 AATD subjects with ZZ genotype and 33 healthy subjects matched for age and sex underwent a complete echocardiographic assessment.

RESULTS

Compared to controls, AATD subjects showed increased left ventricular mass (160 ± 59 g vs. 121 ± 70 g, P < 0.001), a higher incidence of left and right ventricular diastolic dysfunction (30% vs. 16%, P < 0.001 and 45% vs. 20%, P < 0.001, respectively) and mitral valve prolapse (35% vs. 6%, P < 0.001). In contrast, there was no difference between the two groups in diameters and systolic function of both ventricles and in the ejection fraction of left ventricle. The functions of aortic and tricuspidal valves were also similar.

CONCLUSIONS

In the presence of greater left ventricular mass, a significantly higher incidence of left and right ventricular diastolic dysfunction and mitral valve prolapse occurs in AATD subjects (ZZ genotype). These findings strongly suggest an abnormal remodelling process in cardiac tissue in AATD.

Для цитирования: Vizzardi Enrico, Corda Luciano, Sciatti Edoardo, Roca Elisa, Redolfi Stefania, Arici Marianna, Pini Laura, Bonadei Ivano, Metra Marco, Tantucci Claudio. Echocardiographic evaluation in subjects with α1-Antitrypsin deficiency.. European journal of clinical investigation. 2015. DOI: 10.1111/eci.12492.

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