Prophylactic effect of angiotensin receptor blockers in children with genetic aortopathies: the early bird catches the worm

被引:2
作者
Olfe, J. [1 ,3 ]
Kanitz, J. J. [1 ]
Stark, V. C. [1 ]
Stute, F. [1 ]
von Kodolitsch, Y. [2 ,3 ]
Biermann, D. [1 ,3 ]
Huebler, M. [1 ]
Kozlik-Feldmann, R. [1 ,3 ]
Mir, T. S. [1 ,3 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Childrens Heart Clin, Martinistr 52, D-20246 Hamburg, Germany
[2] Univ Med Ctr Hamburg Eppendorf, German Aort Ctr, Hamburg, Germany
[3] German Ctr Cardiovasc Res DZHK, Partner Site Kiel Lubeck, Hamburg, Germany
关键词
Marfan; Children; Sartan; Betablocker; Genetic aortopathies; AORTIC-ROOT DILATION; MARFAN-SYNDROME; PEDIATRIC-PATIENTS; YOUNG-ADULTS; BETA-BLOCKER; LOSARTAN; ADOLESCENTS; PREVENTION; ATENOLOL; COHORT;
D O I
10.1007/s00392-023-02221-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimsIn genetic aortopathies (GA) particular attention is paid to aortic root dilatation which has an impact on morbidity and mortality. This study focuses on the effects of therapy with angiotensin-II-receptor-blockers (ARB) or beta-blockers (BB) on aortic root growth and the question which therapy should be initiated at which dosage and at what age.MethodsSince 1998 we diagnosed 208 patients with GA (170 FBN-1). 81 patients between 5 months and 18 years receiving either ARB or BB therapy were included. We retrospectively analyzed the progression of the dilatation of Sinus Valsalva aortae (SV) using calculated z-scores before and after therapy initiation and compared BB and ARB treatment.ResultsBoth ARB and BB (p < 0.05) therapy showed significant improvement in aortic root growth, while the effect is significantly more pronounced in ARB (p < 0.01) independent of age and genetic cause. A detailed comparison of the two drug groups showed a more sustained effect in limiting the progression of the dilatation of the aortic root in patients treated with ARB. Progression of dilatation of the SV was significantly lower in children treated with ARBs compared to BB (delta z-score, p < 0.05). In addition, ARBs were better tolerated and had a significantly lower discontinuation rate (3%) compared to BB (50%) (p < 0.01). Independently of age at initiation all children and adolescents were able to reach the target dose under ARB.ConclusionWe demonstrated a significant change in both treatment options, with the effect of ARB being more pronounced while being better tolerated throughout the treatment period.
引用
收藏
页码:1610 / 1619
页数:10
相关论文
共 34 条
[11]  
HALPERN BL, 1971, JOHNS HOPKINS MED J, V129, P123
[12]   The translational science of Marfan syndrome [J].
Jondeau, Guillaume ;
Michel, Jean Baptiste ;
Boileau, Catherine .
HEART, 2011, 97 (15) :1206-1214
[13]  
Judge D.P., 2005, LANCET, P1965, DOI DOI 10.1016/S0140-6736(05)67789-6
[14]   Medical management of Marfan syndrome [J].
Keane, Martin G. ;
Pyeritz, Reed E. .
CIRCULATION, 2008, 117 (21) :2802-2813
[15]   Atenolol versus Losartan in Children and Young Adults with Marfan's Syndrome [J].
Lacro, R. V. ;
Dietz, H. C. ;
Sleeper, L. A. ;
Yetman, A. T. ;
Bradley, T. J. ;
Colan, S. D. ;
Pearson, G. D. ;
Tierney, E. S. Selamet ;
Levine, J. C. ;
Atz, A. M. ;
Benson, D. W. ;
Braverman, A. C. ;
Chen, S. ;
De Backer, J. ;
Gelb, B. D. ;
Grossfeld, P. D. ;
Klein, G. L. ;
Lai, W. W. ;
Liou, A. ;
Loeys, B. L. ;
Markham, L. W. ;
Olson, A. K. ;
Paridon, S. M. ;
Pemberton, V. L. ;
Pierpont, M. E. ;
Pyeritz, R. E. ;
Radojewski, E. ;
Roman, M. J. ;
Sharkey, A. M. ;
Stylianou, M. P. ;
Wechsler, S. Burns ;
Young, L. T. ;
Mahony, L. .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (22) :2061-2071
[16]   The revised Ghent nosology for the Marfan syndrome [J].
Loeys, Bart L. ;
Dietz, Harry C. ;
Braverman, Alan C. ;
Callewaert, Bert L. ;
De Backer, Julie ;
Devereux, Richard B. ;
Hilhorst-Hofstee, Yvonne ;
Jondeau, Guillaume ;
Faivre, Laurence ;
Milewicz, Dianna M. ;
Pyeritz, Reed E. ;
Sponseller, Paul D. ;
Wordsworth, Paul ;
De Paepe, Anne M. .
JOURNAL OF MEDICAL GENETICS, 2010, 47 (07) :476-485
[17]   Retrospective analysis of the effect of angiotensin II receptor blocker versus β-blocker on aortic root growth in paediatric patients with Marfan syndrome [J].
Mueller, Goetz C. ;
Stierle, Lydia ;
Stark, Veronika ;
Steiner, Kristoffer ;
von Kodolitsch, Yskert ;
Weil, Jochen ;
Mir, Thomas S. .
HEART, 2014, 100 (03) :214-218
[18]   Impact of Age and Gender on Cardiac Pathology in Children and Adolescents With Marfan Syndrome [J].
Mueller, Goetz C. ;
Stark, Veronika ;
Steiner, Kristoffer ;
von Kodolitsch, Yskert ;
Rybczynski, Meike ;
Weil, Jochen ;
Mir, Thomas S. .
PEDIATRIC CARDIOLOGY, 2013, 34 (04) :991-998
[19]   Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial [J].
Mullen, Michael ;
Jin, Xu Yu ;
Child, Anne ;
Stuart, A. Graham ;
Dodd, Matthew ;
Aragon-Martin, Jose Antonio ;
Gaze, David ;
Kiotsekoglou, Anatoli ;
Yuan, Li ;
Hu, Jiangting ;
Foley, Claire ;
Van Dyck, Laura ;
Knight, Rosemary ;
Clayton, Tim ;
Swan, Lorna ;
Thomson, John D. R. ;
Erdem, Guliz ;
Crossman, David ;
Flather, Marcus .
LANCET, 2019, 394 (10216) :2263-2270
[20]   LIFE EXPECTANCY AND CAUSES OF DEATH IN MARFAN SYNDROME [J].
MURDOCH, JL ;
KUZMA, JW ;
HALPERN, BL ;
WALKER, BA ;
MCKUSICK, VA .
NEW ENGLAND JOURNAL OF MEDICINE, 1972, 286 (15) :804-+