Evidence map›Paper›PMID 40257948›Full record

Observational studyBiomedica : revista del Instituto Nacional de Salud2025

Clinical, histopathological, and immunohistochemical characteristics of patients with sicca syndrome with a focus score ≥ 1 in the minor salivary gland biopsy

Andrés Felipe Lamos-Duarte, Rafael Parra-Medina, Carlos Santiago Rivadeneira-Chamorro, Juan Pablo Castañeda-González, Alejandro Escobar, Adriana Rojas-Villarraga, Gabriel Santiago Rodríguez-Vargas, Ana María Arredondo, Héctor Cubides, José Fernando Polo and 3 more

Abstract readObservational StudyEnglish Abstract
In one paragraph

Observational study in Biomedica : revista del Instituto Nacional de Salud, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Andrés Felipe Lamos-DuarteDepartamento de Reumatología, Fundación Universitaria de Ciencias de la Salud - FUCS, Hospital de San José, Bogotá, D. C., Colombia.ORCID 0000-0002-1783-6598
Rafael Parra-MedinaLaboratorio de Patología, Instituto Nacional de Cancerología y Fundación Universitaria de Ciencias de la Salud - FUCS, Bogotá, D. C., Colombia.ORCID 0000-0002-8428-5837
Carlos Santiago Rivadeneira-ChamorroDepartamento de Reumatología, Fundación Universitaria de Ciencias de la Salud - FUCS, Hospital de San José, Bogotá, D. C., Colombia.ORCID 0000-0002-2674-285X
Juan Pablo Castañeda-GonzálezInstituto de Investigaciones, Fundación Universitaria de Ciencias de la Salud - FUCS, Bogotá, D. C., Colombia.ORCID 0000-0001-5400-9068
Alejandro EscobarDepartamento de Reumatología, Fundación Universitaria de Ciencias de la Salud - FUCS, Hospital de San José, Bogotá, D. C., Colombia.ORCID 0000-0001-7125-1462
Adriana Rojas-VillarragaInstituto de Investigaciones, Fundación Universitaria de Ciencias de la Salud - FUCS, Bogotá, D. C., Colombia.ORCID 0000-0003-3145-2440
Gabriel Santiago Rodríguez-VargasDirección Científica, Biomab I.P.S., Bogotá, D. C., Colombia.ORCID 0000-0003-1613-7100
Ana María ArredondoDepartamento de Reumatología, Fundación Universitaria de Ciencias de la Salud - FUCS, Hospital de San José, Bogotá, D. C., Colombia.ORCID 0009-0005-4738-7323
Héctor CubidesDepartamento de Reumatología, Fundación Universitaria de Ciencias de la Salud - FUCS, Hospital de San José, Bogotá, D. C., Colombia.ORCID 0009-0008-5304-8135
José Fernando PoloDepartamento de Patología, Hospital Infantil Universitario de San José, Fundación Universitaria de Ciencias de la Salud - FUCS, Bogotá, D. C., Colombia.ORCID 0000-0001-5043-4577
Juan José CapassoDepartamento de Patología, Hospital de San José, Fundación Universitaria de Ciencias de la Salud - FUCS, Bogotá D. C., Colombia.ORCID 0009-0003-5347-1930
Claudia IbañezInstituto de Investigaciones, Fundación Universitaria de Ciencias de la Salud - FUCS, Bogotá, D. C., Colombia.ORCID 0000-0001-6063-277X
Jairo Hernán Cajamarca-BarónDepartamento de Reumatología, Fundación Universitaria de Ciencias de la Salud - FUCS, Hospital de San José, Bogotá, D. C., Colombia.ORCID 0000-0003-0468-4908

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Sjögren’s syndrome is a systemic autoimmune disease. The usefulness of immunohistochemistry in minor salivary gland biopsies has been described to be helpful in indirectly characterizing the lymphocyte phenotype in difficult diagnosis cases. Objective: To describe sociodemographic, clinical, serological, histopathological, and immunohistochemical variables in patients with sicca syndrome and a minor salivary gland biopsy focus score greater than or equal to one. Materials and methods: We conducted an observational, retrospective study that included patients under study for potential sicca syndrome whose minor salivary gland biopsy was available and had obtained a focus score greater than or equal to one. Immunohistochemistry was performed on the minor salivary gland biopsy with chromogen red staining for CD8 T lymphocytes and brown staining for CD4 T lymphocytes. Expression ratio of CD20:CD3 and CD4:CD8 markers was determined with the MoticEasyScan Pro 6™ (MOTIC) device and the QuPath™ software. Qualitative variables were analyzed using the chi-square or Fisher’s exact test, and quantitative variables were analyzed according to their assumption of normality. Results: Twenty-eight patients were analyzed: 16 patients had Sjögren’s syndrome, and 8 of them had polyautoimmunity. An association was found between atrophy in the minor salivary gland biopsy and development of polyautoimmunity (OR = 11.1; 95% CI: 1.12-112; p value = 0.033). The CD20:CD3 and CD4:CD8 ratios were normal, with no statistically significant differences between patients with and without Sjögren’s syndrome. In the subgroup of patients with Sjögren’s syndrome, CD4 T lymphocytes were predominant, with 15 cases out of 16 with CD4:CD8 ratios equal to or greater than 2:1. Conclusions: Glandular atrophy was associated with the development of polyautoimmunity and a predominance of CD4 T lymphocytes in patients with Sjögren’s syndrome. This finding highlights the potential value of immunohistochemistry of minor salivary gland biopsies in this group.

Indexed as

Salivary GlandsSalivary Glands, MinorSjogren's SyndromeAdultAgedBiopsyCD8-Positive T-LymphocytesFemaleHumansImmunohistochemistryMaleMiddle AgedRetrospective Studiesautoimmune diseasesbiopsyimmunohistochemistrylymphocytesSjogren’s syndrome

Identifiers

PMID40257948
PMCPMC12178605

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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.