Evidence map›Paper›PMID 36348611›Full record

ArticleSaudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association

Identification of celiac disease associated IgA nephropathy by IgA anti-tissue transglutaminase2 antibody deposits in archived formalin-fixed tissues.

Rimlee Dutta, Ramakant Rawat, Prasenjit Das, Geetika Singh, Alka Kumari, Muzafer Ahmad, Ashish Chauhan, Vineet Ahuja, Sanjay K Agrawal, Govind K Makharia

Open access · diamondAbstract read
In one paragraph

Article in Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
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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

10 authors at 1 institution in 1 country.

Rimlee DuttaDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Ramakant RawatDepartment of Gastroenterology & Human Nutrition, All India Institute of Medical Sciences, New Delhi, India.
Prasenjit DasDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Geetika SinghDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Alka KumariDepartment of Gastroenterology & Human Nutrition, All India Institute of Medical Sciences, New Delhi, India.
Muzafer AhmadDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Ashish ChauhanDepartment of Gastroenterology & Human Nutrition, All India Institute of Medical Sciences, New Delhi, India.
Vineet AhujaDepartment of Gastroenterology & Human Nutrition, All India Institute of Medical Sciences, New Delhi, India.
Sanjay K AgrawalDepartment of Nephrology, All India Institute of Medical Sciences, New Delhi, India.
Govind K MakhariaDepartment of Gastroenterology & Human Nutrition, All India Institute of Medical Sciences, New Delhi, India.
All India Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The causal association between IgA nephropathy (IgAN) and celiac disease (CeD) is based on their clinical coexistence. In this prospective study, we screened patients with IgAN for CeD and explored the utility of analysis of IgA anti-TG2 antibody deposits, for establishing a causal association. Methods: Biopsy-proven patients of IgAN were screened for serum IgA anti-tissue transglutaminase antibody (IgA anti-tTG Ab) titer and thereafter were invited to undergo endoscopic duodenal biopsy. Corresponding duodenal and kidney biopsies were subjected to IgA anti-TG2 antibody colocalization study using dual-color immunohistochemistry and immunofluorescence techniques. Additionally, kidney biopsies from 105 patients with IgAN who did not give consent for serology analysis, 30 non-IgA nephropathies, and 10 normal controls were also included. Dual-color-stained slides were interpreted based on stain distribution and intensity scores, and Pearson's index >0.3-1 on confocal imaging was considered significant. Results: Of a cohort of 151 patients with IgAN, 32 consented to undergo sero-screening and 5 of them had high serum anti-tTG Ab titer. Two out of the latter consented to endoscopic duodenal biopsies, in whom modified Marsh grade 3b changes were identified. Strong IgA anti-TG2 antibody deposits were noted in the kidney and duodenal biopsies of these patients. One patient out of non-consenting 105 patients with IgAN and 3 out of 30 patients with other non-IgA nephropathies also showed IgA anti-TG2 deposits. None of the healthy kidney tissues showed IgA anti-TG2 Ab deposits. Conclusions: Co-localized IgA anti-TG2 deposits in the kidney biopsies in patients with IgAN help to establish a pathogenic link with CeD. A small proportion of patients with IgAN have associated CeD.

Indexed as

Celiac DiseaseGlomerulonephritis, IGAAutoantibodiesBiopsyGTP-Binding ProteinsHumansImmunoglobulin AProspective StudiesProtein Glutamine gamma Glutamyltransferase 2TransglutaminasesAutoantibodiesGTP-Binding ProteinsImmunoglobulin AProtein Glutamine gamma Glutamyltransferase 2TransglutaminasesAnti-tissue transglutaminase 2celiac diseaseduodenal biopsyIgAIgA nephropathynephropathypathogenesis

Identifiers

PMID36348611
PMCPMC10117010
OpenAlexW4308634368

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.