Evidence map›Paper›PMID 19636666›Full record

ArticleClinical and experimental nephrology2009

Histopathological spectrum of childhood nephrotic syndrome in Pakistan.

Muhammed Mubarak, Ali Lanewala, Javed Iqbal Kazi, Fazal Akhter, Atika Sher, Amir Fayyaz, Sajid Bhatti

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Article in Clinical and experimental nephrology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
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  3. Screening of theFrontiers in genetics · 2018
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  6. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.Clinical journal of the American Society of Nephrology : CJASN · 2015
    Article
  7. Article
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  10. IgM nephropathy; can we still ignore it.Journal of nephropathology · 2013
    Review
  11. Article
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  13. Article
  14. Journal of Nephropathology: A need of the hour.Journal of nephropathology · 2012
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Muhammed MubarakDepartment of Histopathology, Sindh Institute of Urology and Transplantation, Civil Hospital, Karachi, Pakistan. drmubaraksiut@yahoo.com
Ali Lanewala
Javed Iqbal Kazi
Fazal Akhter
Atika Sher
Amir Fayyaz
Sajid Bhatti
Sindh Institute of Urology and Transplantation · PKCivil Hospital Karachi · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is no information in international literature on the pattern of glomerulopathies in children with idiopathic nephrotic syndrome (INS) in Pakistan. We undertook this study to determine the pattern of glomerulopathies based on renal biopsies studied by light (LM), immunofluorescence (IF), and electron microscopy (EM).

methodsThe study was conducted at Sindh Institute of Urology and Transplantation (SIUT), Karachi over 12 years (1996-2008). All children (<or=18 years) with INS in whom renal biopsy was performed were included. Renal biopsies were studied by LM, IF, and EM.

resultsOf 538 children, 347 (64.4%) were male and 191 (35.5%) were female. Mean age was 9.79 +/- 4.59 years. The histopathological lesions comprised: minimal change disease (MCD) and its variants, 43.8%; focal segmental glomerulosclerosis (FSGS), 38.14%; membranous glomerulonephritis (GN) (MGN), 7.96%; mesangioproliferative GN (MesPGN), 4.81%; mesangiocapillary GN (MPGN), 3.14%; IgA nephropathy (IgAN), 1.11%; and other rare lesions.

conclusionMCD and its variants are the leading cause of overall INS in children, followed by FSGS, which is the predominant pathology in steroid-resistant and adolescent nephrotic syndrome (NS). Our data are in accordance with recent series from around the world with similar biopsy indications. The study defines the true pattern of glomerulopathies in childhood INS for the first time in Pakistan.

Indexed as

AdolescentBiopsyChildChild, PreschoolFemaleFluorescent Antibody TechniqueGlomerulonephritis, IGAGlomerulonephritis, MembranousGlomerulosclerosis, Focal SegmentalHumansInfantKidneyMaleMicroscopy, ElectronNephrotic SyndromePakistanSteroids

Identifiers

PMID19636666
OpenAlexW1967456983

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.