Brachial artery flow-mediated dilatation and carotid intima medial thickness in pediatric nephrotic syndrome: a cross-sectional case-control study

被引:16
作者
Rahul, Illaparambath [1 ]
Krishnamurthy, Sriram [1 ]
Satheesh, Santhosh [2 ]
Biswal, Niranjan [1 ]
Bobby, Zachariah [3 ]
Lakshminarayanan, Subitha [4 ]
机构
[1] JIPMER, Dept Pediat, Pondicherry 605006, India
[2] JIPMER, Dept Cardiol, Pondicherry, India
[3] JIPMER, Dept Biochem, Pondicherry, India
[4] JIPMER, Dept Community Med, Pondicherry, India
关键词
Nephrotic syndrome; FMD; CIMT; Endothelial dysfunction; Oxidative stress; MDA; Structural atherosclerosis; ENDOTHELIAL FUNCTION; DENSITY-LIPOPROTEIN; RISK-FACTORS; OXIDATIVE STRESS; CHILDREN; ATHEROSCLEROSIS; SERUM; VASODILATION; CHOLESTEROL; DYSFUNCTION;
D O I
10.1007/s10157-014-0958-1
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Children with nephrotic syndrome (NS) have hyperlipidemia, which may lead to endothelial dysfunction. This study evaluated endothelial function and structural atherosclerosis in NS children with disease duration more than 2 years, by assessment of brachial artery flow-mediated dilatation (FMD) and carotid intima medial thickness (CIMT). This is a cross-sectional case-control study recruiting 32 subjects aged 1-13 years with NS and 32 matched controls. Clinical details, FMD and CIMT were recorded. Lipid profile and oxidative stress were also analyzed in the subjects. The proportionate change in FMD was significantly lower in cases (5.65 +/- A 6.08 %) compared to controls (15.21 +/- A 9.41 %) (p < 0.01). No significant differences in CIMT were observed (p = 0.383). Blood malondialdehyde was significantly higher (p = 0.006) in the cases. Overall, 25 NS children (78 %) were in remission for more than 6 months, and in them, 9 (36 %) had deranged lipid profile. On stepwise linear regression, age of the patient was found to be a determinant of FMD (model R (2) = 18.9 %, p value = 0.048). The significantly low proportionate change in FMD in NS children suggests an ongoing process of endothelial dysfunction. Further studies are needed to confirm these findings. A long-term follow-up of children with NS may be required for identification of CIMT derangements.
引用
收藏
页码:125 / 132
页数:8
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