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
[1]   Update on Clinical Trials of Losartan With and Without β-Blockers to Block Aneurysm Growth in Patients With Marfan Syndrome A Review [J].
Bowman, Marion A. Hofmann ;
Eagle, Kim A. ;
Milewicz, Dianna M. .
JAMA CARDIOLOGY, 2019, 4 (07) :702-707
[2]   Angiotensin II blockade and aortic-root dilation in Marfan's syndrome [J].
Brooke, Benjamin S. ;
Habashi, Jennifer P. ;
Judge, Daniel P. ;
Patel, Nishant ;
Loeys, Bart ;
Dietz, Harry C., III .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (26) :2787-2795
[3]   Angiotensin II type 1 receptor blockers [J].
Burnier, M .
CIRCULATION, 2001, 103 (06) :904-912
[4]  
DePaepe A, 1996, AM J MED GENET, V62, P417, DOI 10.1002/(SICI)1096-8628(19960424)62:4<417::AID-AJMG15>3.0.CO
[5]  
2-R
[6]   MUTATIONS IN THE HUMAN GENE FOR FIBRILLIN-1 (FBN1) IN THE MARFAN-SYNDROME AND RELATED DISORDERS [J].
DIETZ, HC ;
PYERITZ, RE .
HUMAN MOLECULAR GENETICS, 1995, 4 :1799-1809
[7]   MARFAN-SYNDROME CAUSED BY A RECURRENT DENOVO MISSENSE MUTATION IN THE FIBRILLIN GENE [J].
DIETZ, HC ;
CUTTING, GR ;
PYERITZ, RE ;
MASLEN, CL ;
SAKAI, LY ;
CORSON, GM ;
PUFFENBERGER, EG ;
HAMOSH, A ;
NANTHAKUMAR, EJ ;
CURRISTIN, SM ;
STETTEN, G ;
MEYERS, DA ;
FRANCOMANO, CA .
NATURE, 1991, 352 (6333) :337-339
[8]  
Dominiak P., 1999, J KARDIOLOGIE AUST J, V6, P488
[9]   Replacement of the aortic root in patients with Marfan's syndrome [J].
Gott, VL ;
Greene, PS ;
Alejo, DE ;
Cameron, DE ;
Naftel, DC ;
Miller, DC ;
Gillinov, AM ;
Laschinger, JC ;
Pyeritz, RE .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (17) :1307-1313
[10]   Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome [J].
Habashi, JP ;
Judge, DP ;
Holm, TM ;
Cohn, RD ;
Loeys, BL ;
Cooper, TK ;
Myers, L ;
Klein, EC ;
Liu, GS ;
Calvi, C ;
Podowski, M ;
Neptune, ER ;
Halushka, MK ;
Bedja, D ;
Gabrielson, K ;
Rifkin, DB ;
Carta, L ;
Ramirez, F ;
Huso, DL ;
Dietz, HC .
SCIENCE, 2006, 312 (5770) :117-121