Evidence map›Paper›PMID 41891412›Full record

ArticleSarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG2026

Late-Onset Sjögren disease: A different clinical entity?

Celil Barlas Cengiz, Tuğba Kahraman Denizhan, Hüseyin Kaplan, Emel Oğuz Kökoğlu, Melih Kızıltepe, Burcu Eren Cengiz, Hanife Oğuz, Abdurrahman Soner Şenel

Abstract read
In one paragraph

Article in Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG, 2026. 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
–field-weighted citation impact
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

8 authors.

Celil Barlas CengizDepartment of Rheumatology, Erciyes University, Kayseri, Türkiye.
Tuğba Kahraman DenizhanDepartment of Rheumatology, Erciyes University, Kayseri, Türkiye.
Hüseyin KaplanDepartment of Rheumatology, Aksaray University Training and Research Hospital, Aksaray, Türkiye.
Emel Oğuz KökoğluDepartment of Rheumatology, Kayseri City Education and Research Hospital, Kayseri, Türkiye.
Melih KızıltepeDepartment of Rheumatology, Kayseri City Education and Research Hospital, Kayseri, Türkiye.
Burcu Eren CengizDepartment of Geriatrics, Kayseri City Education and Research Hospital, Kayseri, Türkiye.
Hanife OğuzDepartment of İnternal Medicine, Erciyes University, Kayseri, Türkiye.
Abdurrahman Soner ŞenelDepartment of Rheumatology, Erciyes University, Kayseri, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimSjögren's disease(SjD) exhibits heterogeneous clinical phenotypes influenced by age at onset. This study aimed to evaluate the impact of onset age on the clinical and serological characteristics of SjD in a Turkish cohort.

methodsWe retrospectively analyzed 411 patients diagnosed with SjD between 2013 and 2024, fulfilling the 2002 AECG or 2016 ACR/EULAR criteria. Patients were classified as young-onset (<40 years; YoSjD), adult-onset (40-60 years; AoSjD), or elderly-onset (>60 years; EoSjD). Demographic, clinical, laboratory, and treatment characteristics were compared among groups.

resultsThe cohort comprised predominantly females (93.4%) with a median age of 55 years. RF positivity was significantly higher in EoSjS (35.5%) compared to YoSjD (27.9%) and AoSjD (19.2%, p=0.007). Inflammatory markers (ESR, CRP) were more frequently elevated in EoSjD. Interstitial lung disease (ILD) prevalence was highest in EoSjD (25.8%, p<0.05), particularly in males. Artropathy was more frequent in EoSjD (80.6%) and YoSjD (76%) than in AoSjD (64.5%, p=0.007). Anemia was more common in EoSjD (20.4%, p=0.040). Hydroxychloroquine was widely used (86.6%), with glucocorticoid and azathioprine use significantly higher in EoSjD.

conclusionsElderly-onset SjD demonstrates a distinct phenotype characterized by higher ILD prevalence, increased RF positivity, greater inflammatory activity, and more frequent artropathy and anemia compared to younger-onset groups. These findings highlight the need for age-tailored diagnostic vigilance, proactive ILD screening, and cautious use of immunosuppressants in older patients. Prospective multicenter studies are warranted to refine management strategies in this subgroup.

Identifiers

PMID41891412
PMCPMC13101011

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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 Socratic graph.