ArticleIndian journal of pediatrics2012
IgM nephropathy in India: a single centre experience.
Article in Indian journal of pediatrics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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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.
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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.
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Who cites it
9 citing papers in PubMed, 13 citations in OpenAlex.
- Article
- IgM mesangial deposition as a risk factor for relapses of adult-onset minimal change disease.BMC nephrology · 2021Article
- IgM nephropathy: is it closer to minimal change disease or to focal segmental glomerulosclerosis?Journal of nephrology · 2016Review
- Article
- Pediatric Renal Biopsies in India: A Single-Centre Experience of Six Years.Nephro-urology monthly · 2015Article
- IgM nephropathy: timely response to a call for action.Journal of renal injury prevention · 2014Article
- IgM nephropathy; time to act.Journal of nephropathology · 2014Article
- Comment on: IgM nephropathy: Can we still ignore it.Journal of nephropathology · 2013Article
- IgM nephropathy; can we still ignore it.Journal of nephropathology · 2013Review
Corrections and comments
- Commented on byIgM nephropathy.2013
- Commented on byAuthors' reply.2013
Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveTo find out the incidence and natural history of IgMN in India.
methodsRenal biopsies of children ≤12 y age of last 6 y were retrospectively evaluated. Their clinical and biochemical presentation were correlated. Patients with systemic diseases/disorders were excluded from the study.
resultsImmunoglobulin M nephropathy (IgMN) constituted 11.9% (n = 28) of 236 renal biopsies. Mean age was 10 y, predominant in boys (n = 24), most of the patients presented with proteinuria and edema. The most common associated histopathological finding was mesangial proliferative glomerulonephritis (MePGN) in 60.7% (n = 17) followed by minimal change disease (MCD) in 28.6% (n = 8) and focal segmental glomerulosclerosis (FSGS) in 10.7% (n = 3). In 85.7%, IgM appeared as the sole immunoglobulin deposit mainly in mesangial regions, followed by accompanied C3 in 3.6% (n = 1) and C1q + C3 in 10.7% (n = 3) biopsies.
conclusionsIgMN was observed in 11.9% biopsies with commonest morphology of MePGN followed by MCD and FSGS; proteinuria was bad prognosticator in addition to FSGS and co-deposition of other immunoglobulins had no significance.
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Registered trials
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