The effectiveness of enzyme replacement therapy on cardiac findings in patients with mucopolysaccharidosis

被引:9
作者
Gurbuz, Berrak Bilginer [1 ]
Aypar, Ebru [2 ]
Coskun, Turgay [1 ]
Alehan, Dursun [2 ]
Dursun, Ali [1 ]
Tokatli, Aysegul [1 ]
Sivri, Hatice Serap [1 ]
机构
[1] Hacettepe Univ, Med Fac, Div Pediat Metab, Ankara, Turkey
[2] Hacettepe Univ, Med Fac, Div Pediat Cardiol, Ankara, Turkey
关键词
cardiac findings; enzyme replacement therapy; left ventricular hypertrophy; mucopolysaccharidosis; CARDIOVASCULAR CHANGES; DISEASE; VI; EXPERIENCE; DIAGNOSIS; FEATURES;
D O I
10.1515/jpem-2019-0293
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: This study aimed to determine cardiac findings in patients with mucopolysaccharidosis (MPS) and to assess the changes in these findings after enzyme replacement therapy (ERT). Methods: A retrospective clinical cohort study was conducted on patients who were diagnosed with MPS between 1995 and 2018 in Hacettepe University, Division of Pediatric Metabolism. A total of 96 patients were diagnosed with MPS during the study period. Of these patients, 81(84.3%) received ER'L Echocardiographic findings of the patients together with the 6-min walking test (6MWT) results before and after ERT were compared. Results: Thirty-one participants (38.2%) were female, while 50 (61.8%) were male. The mean age of the participants was 11.97 +/- 6.33 years (range: 1.8-30). Five patients (6.2%) had MPS type I, 14 (17.3%) had type II, 28 (34.6%) had type IVa, 33 (40.7%) had type VI and one (1.2%) had type VII. Before ERT, 69.4% of patients had mitral insufficiency (MI; mild: 40.5%, moderate: 16.5%, severe: 12.7%), 35.4% had aortic insufficiency (AI; mild: 22.8%, moderate: 12.7%) and 45.1% had tricuspid insufficiency (TI; mild: 39.2%, moderate: 2.5%). The median duration of the ERT was 3.5 years. The ERT significantly improved left ventricular hypertrophy (LVH), but all other study variables returned non-significant before and after treatment. ERT may improve LVH in MPS. Bearing in mind that MPS is a progressive disease, ERT seems to prevent significant deterioration of this ailment but is not able to reverse the already settled pathologies except for LVH. ERT is not able to reverse the damage, but provides stabilization; so it is best to initiate treatment before cardiac damage.
引用
收藏
页码:1049 / 1053
页数:5
相关论文
共 24 条
[1]   Enzyme replacement therapy in Hurler syndrome after failure of hematopoietic transplant [J].
Arranz, Leonor ;
Aldamiz-Echevarria, Luis .
MOLECULAR GENETICS AND METABOLISM REPORTS, 2015, 3 :88-91
[2]   Early diagnosis and management of cardiac manifestations in mucopolysaccharidoses: a practical guide for paediatric and adult cardiologists [J].
Boffi, Lucia ;
Russo, Pierluigi ;
Limongelli, Giuseppe .
ITALIAN JOURNAL OF PEDIATRICS, 2018, 44
[3]   Up to five years experience with 11 mucopolysaccharidosis type VI patients [J].
Brands, Marion M. M. G. ;
Oussoren, Esmee ;
Ruijter, George J. G. ;
Vollebregt, Audrey A. M. ;
van den Hout, Hannerieke M. P. ;
Joosten, Koen F. M. ;
Hop, Wim C. J. ;
Plug, Iris ;
van der Ploeg, Ans T. .
MOLECULAR GENETICS AND METABOLISM, 2013, 109 (01) :70-76
[4]   Cardiac functional and histopathologic findings in humans and mice with mucopolysaccharidosis type I: Implications for assessment of therapeutic interventions in Hurler syndrome [J].
Braunlin, E ;
Mackey-Bojack, S ;
Panoskaltsis-Mortari, A ;
Berry, JM ;
McElmurry, RT ;
Riddle, M ;
Sun, LY ;
Clarke, LA ;
Tolar, J ;
Blazar, BR .
PEDIATRIC RESEARCH, 2006, 59 (01) :27-32
[5]   Cardiac findings after enzyme replacement therapy for mucopolysaccharidosis type I [J].
Braunlin, Elizabeth A. ;
Berry, James M. ;
Whitley, Chester B. .
AMERICAN JOURNAL OF CARDIOLOGY, 2006, 98 (03) :416-418
[6]   Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management [J].
Braunlin, Elizabeth A. ;
Harmatz, Paul R. ;
Scarpa, Maurizio ;
Furlanetto, Beatriz ;
Kampmann, Christoph ;
Loehr, James P. ;
Ponder, Katherine P. ;
Roberts, William C. ;
Rosenfeld, Howard M. ;
Giugliani, Roberto .
JOURNAL OF INHERITED METABOLIC DISEASE, 2011, 34 (06) :1183-1197
[7]   Cardiovascular changes in mucopolysaccharidoses in Taiwan [J].
Chen, MR ;
Lin, SP ;
Hwang, HK ;
Yu, CH .
ACTA CARDIOLOGICA, 2005, 60 (01) :51-53
[8]   Enzyme replacement therapy: efficacy and limitations [J].
Concolino, Daniela ;
Deodato, Federica ;
Parini, Rossella .
ITALIAN JOURNAL OF PEDIATRICS, 2018, 44
[9]   The natural course and the impact of therapies of cardiac involvement in the mucopolysaccharidoses [J].
Fesslova, Vlasta ;
Corti, Paola ;
Sersale, Giovanna ;
Rovelli, Attilio ;
Russo, Pierluigi ;
Mannarino, Savina ;
Butera, Gianfranco ;
Parini, Rossella .
CARDIOLOGY IN THE YOUNG, 2009, 19 (02) :170-178
[10]   ECHOCARDIOGRAPHIC ABNORMALITIES IN THE MUCOPOLYSACCHARIDE STORAGE DISEASES [J].
GROSS, DM ;
WILLIAMS, JC ;
CAPRIOLI, C ;
DOMINGUEZ, B ;
HOWELL, RR .
AMERICAN JOURNAL OF CARDIOLOGY, 1988, 61 (01) :170-176