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DOI 10.1016/j.jacc.2011.12.052

Медицинская библиотека · Journal of the American College of Cardiology · 2012

Aggressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variants.

van der Linde Denise, van de Laar Ingrid M B H, Bertoli-Avella Aida M, Oldenburg Rogier A, Bekkers Jos A, Mattace-Raso Francesco U S, van den Meiracker Anton H, Moelker Adriaan, van Kooten Fop, Frohn-Mulder Ingrid M E, Timmermans Janneke, Moltzer Els, Cobben Jan M, van Laer Lut, Loeys Bart, De Backer Julie, Coucke Paul J, De Paepe Anne, Hilhorst-Hofstee Yvonne, Wessels Marja W, Roos-Hesselink Jolien W

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVES

The purpose of this study was describe the cardiovascular phenotype of the aneurysms-osteoarthritis syndrome (AOS) and to provide clinical recommendations.

BACKGROUND

AOS, caused by pathogenic SMAD3 variants, is a recently described autosomal dominant syndrome characterized by aneurysms and arterial tortuosity in combination with osteoarthritis.

METHODS

AOS patients in participating centers underwent extensive cardiovascular evaluation, including imaging, arterial stiffness measurements, and biochemical studies.

RESULTS

We included 44 AOS patients from 7 families with pathogenic SMAD3 variants (mean age: 42 ± 17 years). In 71%, an aortic root aneurysm was found. In 33%, aneurysms in other arteries in the thorax and abdomen were diagnosed, and in 48%, arterial tortuosity was diagnosed. In 16 patients, cerebrovascular imaging was performed, and cerebrovascular abnormalities were detected in 56% of them. Fifteen deaths occurred at a mean age of 54 ± 15 years. The main cause of death was aortic dissection (9 of 15; 60%), which occurred at mildly increased aortic diameters (range: 40 to 63 mm). Furthermore, cardiac abnormalities were diagnosed, such as congenital heart defects (6%), mitral valve abnormalities (51%), left ventricular hypertrophy (19%), and atrial fibrillation (22%). N-terminal brain natriuretic peptide (NT-proBNP) was significantly higher in AOS patients compared with matched controls (p < 0.001). Aortic pulse wave velocity was high-normal (9.2 ± 2.2 m/s), indicating increased aortic stiffness, which strongly correlated with NT-proBNP (r = 0.731, p = 0.005).

CONCLUSIONS

AOS predisposes patients to aggressive and widespread cardiovascular disease and is associated with high mortality. Dissections can occur at relatively mildly increased aortic diameters; therefore, early elective repair of the ascending aorta should be considered. Moreover, cerebrovascular abnormalities were encountered in most patients.

Для цитирования: van der Linde Denise, van de Laar Ingrid M B H, Bertoli-Avella Aida M, Oldenburg Rogier A, Bekkers Jos A, Mattace-Raso Francesco U S, van den Meiracker Anton H, Moelker Adriaan, van Kooten Fop, Frohn-Mulder Ingrid M E, Timmermans Janneke, Moltzer Els, Cobben Jan M, van Laer Lut, Loeys Bart, De Backer Julie, Coucke Paul J, De Paepe Anne, Hilhorst-Hofstee Yvonne, Wessels Marja W, Roos-Hesselink Jolien W. Aggressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variants.. Journal of the American College of Cardiology. 2012. DOI: 10.1016/j.jacc.2011.12.052.

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