Evidence map›Paper›PMID 42772944›Full record

Observational studyBMJ open gastroenterology2026

Clinical characteristics and treatment patterns of elderly versus non-elderly adults with inflammatory bowel disease in Brazil: a cross-sectional study.

Vanessa Teixeira Martins Campos, Genalva de Almeida Couto, Valdiana Cristina Surlo, Raisa Araújo Lisboa, Jaciane Araujo Mota, Andrea Maia Pimentel, Neogélia Pereira de Almeida Morais, Flora Maria Lorenzo Fortes, Adriana Ribas Andrade, Bruno Cesar da Silva and 7 more

Abstract readComparative StudyObservational StudyComparative Study
In one paragraph

Observational study in BMJ open gastroenterology, 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

17 authors.

Vanessa Teixeira Martins CamposCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.ORCID http://orcid.org/0000-0003-4519-5481
Genalva de Almeida CoutoCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.
Valdiana Cristina SurloCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.
Raisa Araújo LisboaCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.
Jaciane Araujo MotaDepartment of Gastroenterology, Hospital Geral Roberto Santos, Salvador, Bahia, Brazil.
Andrea Maia PimentelDepartment of Gastroenterology, Hospital Geral Roberto Santos, Salvador, Bahia, Brazil.
Neogélia Pereira de Almeida MoraisDepartment of Gastroenterology, Hospital Geral Roberto Santos, Salvador, Bahia, Brazil.
Flora Maria Lorenzo FortesDepartment of Gastroenterology, Hospital Geral Roberto Santos, Salvador, Bahia, Brazil.
Adriana Ribas AndradeDepartment of Gastroenterology, Hospital Geral Roberto Santos, Salvador, Bahia, Brazil.
Bruno Cesar da SilvaZane Cohen Centre for Digestive Diseases, Lunenfeld-Tanenbaum Research Institute, Toronto, Ontario, Canada.
Gustavo Gabriel Silva CardosoCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.
João Vitor Xavier SantosCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.
Maria Luisa Rocha TerencioCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.
Erick Santos NeryCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.
Lidiane Matos Almeida MouraCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil.
Adam CheifetzMedicine/Gastroenterology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Genoile Oliveira SantanaCiências da Vida, Universidade do Estado da Bahia, Salvador, Bahia, Brazil genoile@uol.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveInflammatory bowel disease (IBD) is increasingly diagnosed in older adults, but data from Latin America remain limited. This study aimed to compare the clinical, phenotypic and therapeutic characteristics of elderly and non-elderly adults with IBD in Brazil.

methodsThis cross-sectional study included adults with confirmed Crohn's disease (CD) or ulcerative colitis (UC) attending an IBD clinic in Brazil. Patients were stratified as elderly (≥60 years) or non-elderly (<60 years); elderly individuals were further categorised according to age at diagnosis (<60 years vs ≥60 years). Clinical, therapeutic and frailty-related data were collected from medical records and structured interviews. The primary outcome was biologic therapy use.

results450 patients were included in the study (115 elderly, 335 non-elderly). UC was more common among the elderly patients (77.4% vs 56.7%, p<0.001). Elderly patients had higher comorbidity scores (2.6 vs 0.3 for CD; 2.6 vs 0.4 for UC; p<0.001) and greater polypharmacy (21.7% vs 3.3%, p<0.001) but similar disease activity (CD: Harvey-Bradshaw Index <5, 92.2% vs 79.3%; UC: Mayo Score <2, 88.6% vs 78.3%). They received fewer biologics (26.1% vs 43.6%, p=0.001) and immunosuppressants (22.6% vs 47.5%, p<0.001). Among elderly patients, immunosuppressant use was lower in those diagnosed at ≥60 years (2.9% vs 30.9%, p=0·001). Most elderly patients (82.3%) were robust according to the Clinical Frailty Scale.

conclusionElderly patients were less likely to receive biologic and immunosuppressive therapy despite similar disease activity and had substantially greater comorbidity burden and polypharmacy. These findings suggest that therapeutic decisions in older adults should incorporate frailty and comorbidity assessment to support individualised age-adapted management.

Indexed as

Age FactorsBiological ProductsColitis, UlcerativeCrohn DiseaseImmunosuppressive AgentsAdultAgedBrazilComorbidityCross-Sectional StudiesFemaleFrailtyHumansMaleMiddle AgedPhenotypeBiological ProductsImmunosuppressive AgentsCROHN'S DISEASEELDERLYINFLAMMATORY BOWEL DISEASEULCERATIVE COLITIS

Identifiers

PMID42772944
PMCPMC13599941

What Socratic holds

Textmetadata
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.