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 ORIGINAL ARTICLE
Year : 2019  |  Volume : 29  |  Issue : 3  |  Page : 186-190

Plasma free homocysteine levels in children with idiopathic nephrotic syndrome


1 Division of Pediatric Nephrology, Department of Pediatrics, Postgraduate Institute of Medical Education and Research and Associated, Dr. Ram Manohar Lohia Hospital, Baba Kharak Singh Marg, New Delhi, India
2 Division of Pediatric Nephrology, Department of Pediatrics, Lady Hardinge Medical College and associated Kalawati Saran Children Hospital, New Delhi, India
3 Genomics and Molecular Medicine CSIR-Institute of Genomics and Integrative Biology; Academy of Scientific and Innovative Research, New Delhi, India
4 Genomics and Molecular Medicine CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
5 Department of Pathology, GB Pant Institute of Postgraduate Medical Education and Research, New Delhi, India
6 Department of Biostatistics, All India Institute of Medical Sciences, New Delhi, India

Correspondence Address:
Abhijeet Saha
Division of Pediatric Nephrology, Room No 102, Lady Hardinge Medical College and Kalawati Saran Children Hospital, New Delhi - 110 001
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijn.IJN_293_17

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Altered metabolism of homocysteine in children with idiopathic nephrotic syndrome leads to raised plasma-free homocysteine levels. Elevated free homocysteine causes endothelial cell dysfunction and promotes early atherosclerosis and glomerulosclerosis. In this analytical study with a longitudinal follow-up, 29 children with first episode of nephrotic syndrome (FENS) aged 1–16 years along with 30 age andgender-matched healthy controls were enrolled. Plasma-free homocysteine was measured using high-performance liquid chromatography (HPLC). Other variables were measured using standard biochemical methods. The primary outcome measure was plasma-free homocysteine level in children with FENS and in controls. The secondary outcome measure was to observe the levels of plasma-free homocysteine in children with FENS at 12 weeks in remission and in steroid resistant states. Plasma-free homocysteine levels were significantly elevated in children with FENS at disease onset [Median (IQR) 2.170 (1.54–2.71); N = 29; P < 0.001], at 12 weeks of steroid-induced remission [Median (IQR) 1.946 (1.53–2.71); N = 22; P < 0.001], and in steroid-resistant states [Median (IQR) 2.262 (1.53–2.74); N = 7; P < 0.001] compared to controls. The levels did not decrease significantly at 12 weeks of steroid-induced remission compared to onset of nephrotic syndrome. Plasma-free homocysteine levels correlated positively with serum total cholesterol (P = 0.005; r = 0.362) and negatively with serum albumin (P = 0.032; r = 0.281). Plasma-free homocysteine levels are raised in children with FENS posing a risk of endothelial dysfunction which persists at least in short term. Long-term effects of raised plasma-free homocysteine needs to be studied.






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Indian Journal of Nephrology
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Online since 20th Sept '07