Literature DB >> 24633472

Apolipoprotein AII levels are associated with the UP/UCr levels in idiopathic steroid-sensitive nephrotic syndrome.

Takahiro Kanai1, Takanori Yamagata, Takane Ito, Jun Odaka, Takashi Saito, Jun Aoyagi, Mariko Y Momoi.   

Abstract

BACKGROUND: Various humoral factors have been proposed as causal agents of idiopathic steroid-sensitive nephrotic syndrome (ISSNS), resulting in varying data. We used mass spectrometry (MS) to analyze serum proteins in a search for proteins that might be involved in ISSNS pathophysiology.
METHODS: Serial serum samples were obtained from 33 children with ISSNS. Samples were collected during Phase A1 [the acute phase prior to steroid treatment (STx)], Phase A2 (remission with STx), and Phase A3 (remission without any medication). We also included age- and sex-matched two control groups comprising children with normal urinalysis (Group B) and children with a nephrotic syndrome other than ISSNS (Group C). The urinary protein/urinary creatinine (UP/UCr) ratios were not statistically different between Phase A1 and Group C. Samples were analyzed using surface-enhanced laser desorption/ionization time of flight MS.
RESULTS: A total of 207 peptide ion peaks were detected in the range of m/z 2000-10000. Four peptide ions (m/z 6444, 6626, 8695, and 8915) were detected at significant elevation during Phase A1 compared with Phase A2, Phase A3, and Group C. The intensities of m/z 6444 and 8695 were higher in Phase A3 than in Group B. There were significant correlations between the intensities of m/z 6626, 8695, and 8915 and UP/UCr levels. The m/z 8695 was identified as apolipoprotein AII.
CONCLUSIONS: Apolipoprotein AII was detected as a protein associated with the UP/UCr levels in pediatric ISSNS. Our findings present an interesting starting point for further investigation into the pathophysiology of ISSNS.

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Year:  2014        PMID: 24633472     DOI: 10.1007/s10157-014-0957-2

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


  29 in total

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5.  Minimal-change glomerular nephritis. Normal kidneys in an abnormal environment?

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7.  Steroid-responsive and nephrotic syndrome and allergy: clinical studies.

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8.  Isolation and characterization of an apoA-II-containing lipoprotein (LP-A-II:B complex) from plasma very low density lipoproteins of patients with Tangier disease and type V hyperlipoproteinemia.

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9.  The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children.

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Review 10.  Vascular permeability factors in steroid-sensitive nephrotic syndrome and focal segmental glomerulosclerosis.

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  2 in total

1.  Apolipoprotein C-I Levels Are Associated with the Urinary Protein/Urinary Creatinine Ratio in Pediatric Idiopathic Steroid-Sensitive Nephrotic Syndrome: A Case Control Study.

Authors:  Jun Odaka; Takahiro Kanai; Takane Ito; Takashi Saito; Jun Aoyagi; Hiroyuki Betsui; Takanori Yamagata
Journal:  Int J Nephrol       Date:  2017-01-30

Review 2.  Long-term Outcomes of Childhood Onset Nephrotic Syndrome.

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Journal:  Front Pediatr       Date:  2016-05-25       Impact factor: 3.418

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