Evidence map›Paper›PMID 32573825›Full record

ArticleAlimentary pharmacology & therapeutics2020

No benefit of continuing vs stopping 5-aminosalicylates in patients with ulcerative colitis escalated to anti-metabolite therapy.

Siddharth Singh, Jihoon Kim, Wenhong Zhu, Parambir S Dulai, William J Sandborn, Vipul Jairath

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Alimentary pharmacology & therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06878495 (Optimizing IBD Management), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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.

NCT06878495 nanot yet recruitingnot on this mapstarted 2025, after this paper: background citation

Optimizing IBD Management: A Comparative Study on the Efficacy and Safety of 5-ASA De-escalation in Patients With Ulcerative Colitis and Crohn's Disease on Stable Biologic or Immunomodulator Therapy

TypeinterventionalSponsorPusan National University HospitalRan2025 to 2025Enrolled100ConditionsUlcerative Colitis (UC), Crohn&#39, s Disease, Inflammatory Bowel Disease (IBD)ArmsDiscontinuation of 5-ASA
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
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

6 authors at 3 institutions in 2 countries.

Siddharth SinghDivision of Gastroenterology, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-2640-7269
Jihoon KimDivision of Biomedical Informatics, University of California San Diego, La Jolla, CA, USA.
Wenhong ZhuVisting Fellow, OptumLabs, Cambridge, MA, USA.
Parambir S DulaiDivision of Gastroenterology, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-9514-2321
William J SandbornDivision of Gastroenterology, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-3314-7960
Vipul JairathRobarts Clinical Trials, Inc., London, ON, Canada.ORCID 0000-0002-1092-0033
Tellabs (Canada) · CAUniversity of California San Diego · USWestern University · CA

Funding

UC San Diego Clinical and Translational Research InstituteUL1TR001442 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S, HOGARTH, MICHAEL · 2015 to 2024
$88.3M
San Diego Digestive Diseases Research CenterP30DK120515 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ROHIT LOOMBA · 2019 to 2026
$10.8M
Comparative Risks and Benefits of Pharmacological Therapies for Older Patients with Inflammatory Bowel DiseasesK23DK117058 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SINGH, SIDDHARTH · 2018 to 2022
$971k
NCATS NIH HHS UL1 TR001442NCATS NIH HHS UL1TR001442NIDDK NIH HHS K23 DK117058NIDDK NIH HHS K23DK117058NIDDK NIH HHS P30 DK120515
6 · The paper itself

Abstract

backgroundWhilst continuation of 5-aminosalicylates (5-ASA) after escalation to biologic therapy is considered ineffective in patients with ulcerative colitis (UC), their role in patients escalated to anti-metabolites is unclear.

aimTo compared patterns and outcomes of continuing vs stopping 5-ASA in patients with UC who escalated to anti-metabolite monotherapy, using a de-identified administrative claims database.

methodsWe identified patients with UC who were new users of anti-metabolite monotherapy who were receiving 5-ASA, and were followed for at least 12 months after starting anti-metabolite therapy. We evaluated patterns of 5-ASA use (stopped 5-ASA, short-term 5-ASA use for <6 months after starting anti-metabolites, persistent 5-ASA use for >6 months after starting anti-metabolites). We compared outcomes (risk of UC-related hospitalisation and/or surgery, need for corticosteroids, treatment escalation to biologic therapy) by pattern of 5-ASA use, using Cox proportional hazard analysis adjusting for age, sex, race, comorbidity burden, and hospitalisation or emergency department visit, abdominal surgery and corticosteroid use in the previous 12 months (as measures of disease severity), with a 12-month immortal time period.

resultsOf 4068 patients with UC who were new-users of anti-metabolite monotherapy, 578 (14.2%), 782 (19.2%) and 2708 (66.6%) stopped 5-ASA, used 5-ASA transiently or persistently, respectively. Compared to patients who stopped 5-ASA after starting anti-metabolites, persistent 5-ASA use was associated with a higher risk of UC-related hospitalisation (HR, 1.40 [1.07-1.83]) and corticosteroid use (HR, 1.48 [1.28-1.70]), without an increase in risk of UC-related surgery (HR, 1.32 [0.86-2.00]) or treatment escalation (HR, 0.80 [0.53-1.20]). Sensitivity analyses using a 3 months window after initiation of anti-metabolites to classify patients as continuing vs stopping 5-ASA showed similar results. Residual confounding by disease severity could not be excluded.

conclusion5-ASA are usually continued long-term even after escalating to anti-metabolite therapy in patients with UC without clinical benefit.

Indexed as

Adrenal Cortex HormonesAdultAnti-Inflammatory Agents, Non-SteroidalAntimetabolitesBiological TherapyColitis, UlcerativeEmergency Service, HospitalFemaleHospitalizationHumansMaleMesalamineMiddle AgedWithholding TreatmentYoung AdultAdrenal Cortex HormonesAnti-Inflammatory Agents, Non-SteroidalAntimetabolitesMesalamine

Identifiers

PMID32573825
PMCPMC8015755
OpenAlexW3038123023

What OpenQuestion holds

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Registered trials

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.