Cardioprotective Effects of Spirulina Therapy in Children With Beta-Thalassemia Major

被引:1
|
作者
El-Shanshory, Mohammed [1 ]
Tolba, Osama [1 ]
El-Shafiey, Rasha [1 ]
Mawlana, Wegdan [1 ]
Ibrahim, Magda [1 ]
El-Gamasy, Mohamed [1 ]
机构
[1] Tanta Univ Hosp, Dept Pediat, Tanta, Egypt
关键词
thalassemia major; cardiomyopathy; spirulina; speckle tracking imaging; IRON OVERLOAD CARDIOMYOPATHY; SPECKLE TRACKING; ANTIINFLAMMATORY ACTIVITIES; MYOCARDIAL DEFORMATION; ECHOCARDIOGRAPHY; ANTIOXIDANT;
D O I
10.1097/MPH.0000000000001380
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Cardiac failure in children with Thalassemia major (TM) is the major cause of death due to iron overload. Spirulina is a micro alga with proven anti-inflammatory, antioxidant and may have a cardioprotective effect. Aim of the Work: The aim of this study was to evaluate the possible beneficial effect of spirulina supplement in TM children. Subject and Methods: It is an interventional study carried out in 60 children with TM and 30 healthy children matched for age and sex as control. Both groups received spirulina supplement at a dose of 250 mg/kg/d for 3 months. 2D Echo, Tissue Doppler, and speckle tracking imaging (STI) were done for all the studied cohort before and after the 3-month duration of spirulina supplement. Results: There was significant improvement in hemoglobin level at the end of 3-month period (8.27 +/- 1.3 vs. 9.023 +/- 1.7; P <0.033) with decrease the frequency of blood transfusion in TM patients (66.6% vs. 40% required transfusion at interval less than 2 wk). Left ventricle global longitudinal strain (LVGLS) significantly improved after 3-month period (-21.7 +/- 4.64 vs. -24.67 +/- 4.478; P <0.002). Conclusions: Spirulina supplement has possible beneficial effect in minimizing the frequency of blood transfusion as well as cardioprotective effect against cardiac damage in TM patients.
引用
收藏
页码:202 / 206
页数:5
相关论文
共 50 条
  • [31] Hematuria in Patients With Beta-Thalassemia Major
    Fallahzadeh, Mohammad Hossein
    Fallahzadeh, Mohammad Kazem
    Shahriari, Mehdi
    Rastegar, Shervin
    Derakhshan, Ali
    Fallahzadeh, Mohammad Amin
    IRANIAN JOURNAL OF KIDNEY DISEASES, 2010, 4 (02) : 133 - 136
  • [32] SUSCEPTIBILITY TO INFECTIONS IN BETA-THALASSEMIA MAJOR
    SCHILIRO, G
    ROMEO, MA
    RUSSO, A
    DIGREGORIO, F
    MUSUMECI, S
    RUSSO, G
    AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1982, 136 (12): : 1099 - 1099
  • [33] IMMUNOLOGICAL DYSFUNCTION AND BETA-THALASSEMIA MAJOR
    MANDALENAKILAMBROU, C
    VRACHNOU, E
    KALOGEROPOULOU, K
    LADIS, V
    KATTAMIS, C
    EUROPEAN JOURNAL OF PEDIATRICS, 1985, 144 (01) : 112 - 112
  • [34] LYMPHOCYTE CHANGE IN BETA-THALASSEMIA MAJOR
    MUSUMECI, S
    SCHILIRO, G
    ROMEO, MA
    SCIOTTO, A
    ROSALBA, A
    PIZZARELLI, G
    ARCHIVES OF DISEASE IN CHILDHOOD, 1979, 54 (12) : 954 - 957
  • [35] Beta-Thalassemia major with Gaucher disease
    Ibrahimi, Mohammad Akbar
    Hakimi, Turyalai
    Halimi, Sultan Ahmad
    INTERNATIONAL JOURNAL OF SURGERY OPEN, 2022, 42
  • [36] NEUROLOGICAL COMPLICATIONS OF BETA-THALASSEMIA MAJOR
    SINNIAH, D
    VIGNAENDRA, V
    AHMAD, K
    ARCHIVES OF DISEASE IN CHILDHOOD, 1977, 52 (12) : 977 - 979
  • [37] CARDIOPULMONARY ASSESSMENT IN BETA-THALASSEMIA MAJOR
    GRISARU, D
    RACHMILEWITZ, EA
    MOSSERI, M
    GOTSMAN, M
    LAFAIR, JS
    OKON, E
    GOLDFARB, A
    HASIN, Y
    CHEST, 1990, 98 (05) : 1138 - 1142
  • [38] LYMPHOCYTE CHANGES IN BETA-THALASSEMIA MAJOR
    MUSUMECI, S
    SCHILIRO, G
    ROMEO, MA
    SCIOTTO, A
    ROSALBA, A
    PIZZARELLI, G
    CLINICAL RESEARCH, 1979, 27 (02): : A302 - A302
  • [39] HEMORRHAGIC TENDENCY IN BETA-THALASSEMIA MAJOR
    ELDOR, A
    ISRAEL JOURNAL OF MEDICAL SCIENCES, 1978, 14 (11): : 1132 - 1134
  • [40] Aortic Distensibility in beta-Thalassemia Major
    Kojuri, J.
    Aslani, A.
    Jannati, M.
    INTERNATIONAL CARDIOVASCULAR RESEARCH JOURNAL, 2008, 2 (01) : 21 - 23