The analysis of echocardiographic results in patients suffering from epidermolysis bullosa

被引:2
|
作者
Kurnicka, Katarzyna [1 ]
Osipowicz, Katarzyna [2 ]
Dzikowska-Diduch, Olga [1 ]
Wertheim-Tysarowska, Katarzyna [3 ]
Kowalewski, Cezary [2 ]
Pruszczyk, Piotr [1 ]
机构
[1] Med Univ Warsaw, Dept Internal Med & Cardiol, Warsaw, Poland
[2] Med Univ Warsaw, Dept Dermatol & Immunodermatol, Warsaw, Poland
[3] Inst Mother & Child Hlth, Dept Med Genet, Warsaw, Poland
来源
POSTEPY DERMATOLOGII I ALERGOLOGII | 2020年 / 37卷 / 06期
关键词
epidermolysis bullosa; echocardiography; cardiomyopathy; DILATED CARDIOMYOPATHY; AMERICAN SOCIETY; VENTRICULAR DYSFUNCTION; EUROPEAN ASSOCIATION; RECOMMENDATIONS; QUANTIFICATION; PERFORMANCE; DIAGNOSIS; UPDATE; ADULTS;
D O I
10.5114/ada.2020.102101
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Introduction: Cardiac abnormalities revealed in patients suffering from epidermolysis bullosa (EB) include dilated cardiomyopathy (DC) and aortopathy. DC is a rare but serious complication associated with an increased mortality, predominantly observed in recessive dystrophic EB. Echocardiography is the most available diagnostic tool used to detect heart disease in EB patients. Aim: To analyse echocardiographic results obtained in Polish EB patients and compare them between the EB group and healthy persons. Material and methods: We analysed retrospectively echocardiograms of 23 patients with EB (14 F, mean age 17.3 years) performed from 2017 to 2019. The incidence of left ventricular (LV) systolic and diastolic dysfunction, right heart disease and congenital heart disease was evaluated. A comparison of echo-parameters between EB patients and 20 matched healthy subjects was performed. Results: We did not find any cases of DC and aortopathy in the EB group. One bicuspid aortic valve case was revealed. Analysis of LV diastolic parameters showed that the mean value of mitral A velocity was significantly higher and the pulmonary venous flow D velocity was lower in the EB group than in controls. Tissue Doppler analysis revealed lower values of E' velocities of mitral annulus in the EB group, what may suggest discreetly slower LV relaxation, however, this will definitely require further research. Conclusions: Although most EB patients do not present cardiac symptoms, there is still a risk of developing cardiomyopathy associated with poor prognosis. It seems reasonable to perform a scheduled echocardiographic screening including LV systolic and diastolic function assessment to detect preclinical cardiac abnormalities.
引用
收藏
页码:871 / 878
页数:8
相关论文
共 50 条
  • [31] Analysis of chemokines in blister fluids of epidermolysis bullosa patients: Implications for therapy
    Alexeev, V.
    Mukhtarzada, L.
    Alanis, J. Salas
    Palisson, F.
    Uitto, J.
    South, A.
    Igoucheva, O.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2017, 137 (10) : B13 - B13
  • [32] Plectin deficiency results in muscular dystrophy with epidermolysis bullosa
    Smith, FJD
    Eady, RAJ
    Leigh, IM
    McMillan, JR
    Rugg, EL
    Kelsell, DP
    Bryant, SP
    Spurr, NK
    Geddes, JF
    Kirtschig, G
    Milana, G
    deBono, AG
    Owaribe, K
    Wiche, G
    Pulkkinen, L
    Uitto, J
    McLean, WHI
    Lane, EB
    NATURE GENETICS, 1996, 13 (04) : 450 - 457
  • [33] Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosa
    Danescu, S.
    Has, C.
    Senila, S.
    Ungureanu, L.
    Cosgarea, R.
    JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2015, 29 (05) : 899 - 903
  • [34] Are existing validated severity scores for epidermolysis bullosa reflective of the burden of disease in patients with epidermolysis bullosa simplex?
    Hunjan, Manrup K.
    Bardhan, Ajoy
    Zuzarte, Louise
    Balacco, Dario Leonardo
    Harper, Natasha
    Heagerty, Adrian
    CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2023, 48 (06) : 706 - 707
  • [35] The new cell cultures from dystrophic epidermolysis bullosa patients in Russia
    Beilin, A.
    Evtushenko, N.
    Murashkin, N.
    Savostyanov, K.
    Fisenko, A.
    Ambarchyan, E.
    Vorotelyak, E.
    Gurskaya, N.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2019, 139 (09) : S267 - S267
  • [36] A review of the obstetric management of patients with epidermolysis bullosa
    Bolt, L. A.
    O'Sullivan, G.
    Rajasingham, D.
    Shennan, A.
    OBSTETRIC MEDICINE, 2010, 3 (03) : 101 - 105
  • [37] Eruptive naevi in epidermolysis bullosa hereditaria patients
    Miquel, J.
    Chevrant-Breton, J.
    Dupuy, A.
    Le Gall, F.
    Bourdon-Lannoy, E.
    Adamski, H.
    Bodemer, C.
    ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE, 2012, 139 (6-7): : 435 - 443
  • [38] THE ITALIAN REGISTRY FOR PATIENTS AFFECTED BY EPIDERMOLYSIS BULLOSA
    Brena, Michela
    Tadini, Gianluca
    Marchisio, Paola
    Pilo, Cinzia
    Guez, Sophie
    ACTA DERMATO-VENEREOLOGICA, 2020, 100 : 43 - 43
  • [39] Mucosal morbidity in patients with epidermolysis bullosa acquisita
    Luke, MC
    Darling, TN
    Hsu, R
    Summers, RM
    Smith, JA
    Solomon, BI
    Thomas, GR
    Yancey, KB
    ARCHIVES OF DERMATOLOGY, 1999, 135 (08) : 954 - 959
  • [40] Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China
    Chen, Fuying
    Wei, Ruoqu
    Deng, Dan
    Zhang, Xue
    Cao, Yu
    Pan, Chaolan
    Wang, Yumeng
    Cao, Qiaoyu
    Wang, Jianbo
    Zeng, Ming
    Huang, Linting
    Gu, Yan
    Yao, Zhirong
    Li, Ming
    JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2023, 37 (02) : 411 - 419