Evidence map›Paper›PMID 35645421›Full record

ArticleReumatologia2022

Routine IgG4 staining in minor salivary gland biopsy in a cohort of Italian Caucasian patients suffering from xerostomia.

Edoardo Conticini, Roberto D'Alessandro, Marco Bardelli, Paolo Falsetti, Stefano Gentileschi, Virginia Mancini, Luca Cantarini, Bruno Frediani

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Article in Reumatologia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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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

8 authors at 2 institutions in 2 countries.

Edoardo ConticiniDepartment of Medicine, Surgery, and Neurosciences, Rheumatology Unit, University of Siena, Italy.ORCID https://orcid.org/0000-0002-3974-6606
Roberto D'AlessandroDepartment of Medicine, Surgery, and Neurosciences, Rheumatology Unit, University of Siena, Italy.ORCID https://orcid.org/0000-0002-0165-5901
Marco BardelliDepartment of Medicine, Surgery, and Neurosciences, Rheumatology Unit, University of Siena, Italy.ORCID https://orcid.org/0000-0003-1893-0401
Paolo FalsettiDepartment of Medicine, Surgery, and Neurosciences, Rheumatology Unit, University of Siena, Italy.ORCID https://orcid.org/0000-0003-2667-4866
Stefano GentileschiDepartment of Medicine, Surgery, and Neurosciences, Rheumatology Unit, University of Siena, Italy.ORCID https://orcid.org/0000-0001-9682-4706
Virginia ManciniDepartment of Medical Biotechnology, Section of Pathology, University of Siena, Italy.
Luca CantariniDepartment of Medicine, Surgery, and Neurosciences, Rheumatology Unit, University of Siena, Italy.
Bruno FredianiDepartment of Medicine, Surgery, and Neurosciences, Rheumatology Unit, University of Siena, Italy.ORCID https://orcid.org/0000-0002-9375-5984
Center for Rheumatology · USUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: IgG4-related disease is a potentially systemic disease mimicking and overlapping with different autoimmune diseases, such as primary Sjögren's syndrome (pSS). The involvement of salivary glands, previously called Mikulicz's disease, has been reclassified as IgG4-related sialadenitis (SA). The aim of this study was to assess the prevalence of IgG4-SA in a cohort of Italian Caucasian patients presenting with xerostomia and to evaluate the eventual overlap between IgG4-SA and pSS. Material and methods: We included 154 patients - 15 males and 139 females, mean age 54.18 ±14.24 years, who underwent minor salivary gland biopsy between March and December 2019 for xerostomia. Histopathology was evaluated using Chisholm-Mason (CM) and focus score (FS) for pSS and immunohistochemical study with IgG4 staining for IgG4-SA were performed. Serum autoantibodies (anti-SSa/RoAb, anti-SSB/LaAb, antinuclear antibodies, rheumatoid factor) were also assessed. Results: In 69 patients (44.8%) FS 0 was found, while FS ≥ 1 was presented in 85 (55.2%). Chisholm-Mason score < 3 and CM ≥ 3 was found in 73 (47.4%) and 81 (52.6%) cases, respectively. IgG4/high-power field level was 20 in 3 pSS patients (1.9%), but none of them had an IgG4/IgG ratio ≥ 40, as well as tissue fibrosis with storiform pattern, obliterative vasculitis, and tissue eosinophilia. The diagnosis of pSS, was confirmed in 92 patients (59.74%). No patient was definitively diagnosed with an IgG4-related disease. Conclusions: In the case of xerostomia, the evaluation of the histopathological specimen for IgG4 should not be routinely performed, at least in an Italian-based Caucasian population. Moreover, immunohistochemistry should not be requested in the case of a negative result of biopsy for pSS.

Indexed as

IgG4-related diseaseminor salivary glands biopsySjögren’s syndromexerostomia

Identifiers

PMID35645421
PMCPMC9132120
OpenAlexW4225659988

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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.