Evidence for a Proatherogenic Biochemical Phenotype in Beta Thalassemia Minor and Intermedia

被引:6
|
作者
Lai, Maria Eliana [1 ]
Vacquer, Stefania [1 ]
Carta, Maria Paola [1 ]
Spiga, Alessandra [1 ]
Cocco, Pierluigi [1 ]
Abete, Claudia [1 ]
Dessi, Sandra [1 ]
Mandas, Antonella [1 ]
机构
[1] Univ Cagliari, Dept Internal Med Sci, IT-09042 Cagliari, Italy
关键词
Thalassemia; Cholesterol; Iron; IRON-METABOLISM; MYOCARDIAL-INFARCTION; HEART-DISEASE; CHOLESTEROL; HEPCIDIN; TRAIT; MORTALITY; ADHESION; PLASMA;
D O I
10.1159/000327252
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The purpose of this study was to focus on pathophysiological mechanisms linking beta-thalassemia intermedia (beta-TI) and minor (beta-TMI) with cardiovascular risk. Iron status, prooxidant-antioxidant balance and lipid profiles in serum, and lipid content in peripheral blood mononuclear cells (PBMCs) were evaluated in 20 beta-TMI subjects, 22 beta-TI patients and in 30 nonthalassemic blood donors. The mRNA levels of some genes involved in the regulation of iron and cholesterol metabolism were also determined. In beta-TI and in beta-TMI, serum iron, prooxidant-antioxidant ratio, transferrin saturation and erythropoietin levels were higher, while transferrin and hepcidin were lower compared to controls. Hepcidin and interleukin-1 alpha mRNA levels were found to be reduced in beta-TI- and beta-TMI-PBMCs, while those of tumor necrosis factor alpha were increased. A reduction in high-density lipoprotein cholesterol in serum and an accumulation of neutral lipids coupled with increased mRNA levels of acetyl-coenzyme A: cholesterol acyltransferase and decreased neutral cholesterol ester hydrolase in PBMCs were also observed in beta-TI and beta-TMI compared to controls. Taken together, these findings provide experimental support for the idea that not only beta-TI patients but also beta-TMI have a proatherogenic biochemical phenotype which may contribute to increase their cardiovascular disease risk. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:87 / 94
页数:8
相关论文
共 50 条
  • [1] Thalassemia intermedia is associated with a proatherogenic biochemical phenotype
    Lai, Maria Eliana
    Vacquer, Stefania
    Carta, Maria Paola
    Spiga, Alessandra
    Cocco, Pierluigi
    Angius, Fabrizio
    Mandas, Antonella
    Dessi, Sandra
    BLOOD CELLS MOLECULES AND DISEASES, 2011, 46 (04) : 294 - 299
  • [3] AHSP expression in beta-thalassemia carriers with thalassemia intermedia phenotype
    Perseu, L
    Giagu, N
    Sole, G
    Perra, C
    BLOOD, 2003, 102 (11) : 516A - 516A
  • [4] Heterozygous β-thalassemia with thalassemia intermedia phenotype
    Gasperini, D
    Perseu, L
    Melis, MA
    Maccioni, L
    Sollaino, MC
    Paglietti, E
    Cao, A
    Galanello, R
    AMERICAN JOURNAL OF HEMATOLOGY, 1998, 57 (01) : 43 - 47
  • [5] The First report of sextuplicated alpha genes in a heterozygote beta thalassemia revealed by a severe beta thalassemia intermedia phenotype
    Achour, Ahlem
    Koopmann, Tamara
    Knijnenburg, Jeroen
    Amir, Raz
    Harteveld, Cornelis
    Baas, Frank
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 162 - 162
  • [6] SILENT BETA-THALASSEMIA AND THALASSEMIA INTERMEDIA
    HUISMAN, THJ
    HAEMATOLOGICA, 1990, 75 : 1 - 8
  • [7] BIOCHEMICAL AND GENETIC FEATURES OF THALASSEMIA INTERMEDIA
    COSTA, FF
    COVAS, DT
    ZAGO, MA
    BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1985, 18 (5-6) : A773 - A773
  • [9] HOMOZYGOUS BETA-THALASSEMIA PRESENTING AS THALASSEMIA INTERMEDIA
    HELLER, P
    YAKULIS, VJ
    ROSENZWEIG, AI
    RUCKNAGEL, DL
    JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1964, 64 (05): : 868 - &
  • [10] Relationship between genotype and phenotype - Thalassemia intermedia
    Galanello, R
    Cao, A
    COOLEYS ANEMIA: SEVENTH SYMPOSIUM, 1998, 850 : 325 - 333