2006
DOI: 10.1157/13085509
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Correlación de los perfiles lipoproteicos y variables antropométricas con concentraciones séricas de lipoproteína(a) en la infancia

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Cited by 3 publications
(5 citation statements)
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References 17 publications
(17 reference statements)
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“…Regarding the laboratory parameters, this study showed that patients belonging to the lower tertiles (T1) and to the upper tertiles Lp(a) (T3) did not show significant differences in all conventional lipid profile with respect to the reference category (middle tertile Lp(a)T2)) with (all P > 0.05), the median concentrations of LDL-c were similar between the higher Lp(a) tertile (T3) and the middle Lp(a) tertile (T2) with (2.5 mmol.L -1 (IQR 1.9-3.3) vs. 2.5 mmol.L -1 (IQR 1.9-3.1), P > 0.05), the some finding was reported by several sudies [35][36][37][38], Qayum, et al [36] did not find a significant association between Lp(a) and LDL-c in a cohort of 257 children with high risk cardiovascular. In contrast, Meabe YS, et al [37] found a positive correlation between Lp(a), LDL-c and apo B in a cohort of Spanish children, the same findings were reported by Gannagé-Yared MH, et al [38]. In our data, only AIP was significantly lower in patient with normal Lp(a) (T2) compared to a group with very-low Lp(a) (T1) and elevated Lp(a) (T3).…”
Section: Statements and Declarationsmentioning
confidence: 71%
“…Regarding the laboratory parameters, this study showed that patients belonging to the lower tertiles (T1) and to the upper tertiles Lp(a) (T3) did not show significant differences in all conventional lipid profile with respect to the reference category (middle tertile Lp(a)T2)) with (all P > 0.05), the median concentrations of LDL-c were similar between the higher Lp(a) tertile (T3) and the middle Lp(a) tertile (T2) with (2.5 mmol.L -1 (IQR 1.9-3.3) vs. 2.5 mmol.L -1 (IQR 1.9-3.1), P > 0.05), the some finding was reported by several sudies [35][36][37][38], Qayum, et al [36] did not find a significant association between Lp(a) and LDL-c in a cohort of 257 children with high risk cardiovascular. In contrast, Meabe YS, et al [37] found a positive correlation between Lp(a), LDL-c and apo B in a cohort of Spanish children, the same findings were reported by Gannagé-Yared MH, et al [38]. In our data, only AIP was significantly lower in patient with normal Lp(a) (T2) compared to a group with very-low Lp(a) (T1) and elevated Lp(a) (T3).…”
Section: Statements and Declarationsmentioning
confidence: 71%
“…A positive correlation was observed between Lp(a) and LDL cholesterol (LDL-c) (3,8,9), Lp(a) and total cholesterol (TC) ( 9 , 10 ) and Lp(a) and apolipoprotein B (Apo B) ( 3 , 9 ) , which suggests an association between Lp(a) levels and lipid profile. According to Meabe et al ( 3 ) , the fact that high Lp(a) levels are associated with high LDL-c levels proposes that the LDL metabolism may be involved in the Lp(a) synthesis. In patients with high LDL-c levels, Lp(a) is an important factor to determine atherosclerotic disease, as well as its severity and progression rate ( 15 ) .…”
Section: Discussionmentioning
confidence: 99%
“…Observou-se correlação positiva entre Lp(a) e colesterol LDL (LDL-c) ( 3 , 8 , 9 ) , Lp(a) e colesterol total (CT) ( 9 , 10 ) e Lp(a) e apolipoproteína B (Apo B) ( 3 , 9 ) , o que sugere uma associação entre concentrações de Lp(a) e perfil lipídico. Segundo Meabe et al ( 3 ) , o fato de níveis elevados de Lp(a) se associarem a níveis elevados de LDL-c sugere que o metabolismo da LDL pode estar envolvido na síntese de Lp(a). Em pacientes com altos níveis de LDL-c, a Lp(a) é um fator importante na determinação da doença aterosclerótica, bem como da sua gravidade e velocidade de progressão ( 15 ) .…”
Section: Discussionunclassified
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