Introduction
What “Remission” Means in IBD (Treat-to-Target)
Last Updated Dec 3, 2025

Remission in inflammatory bowel disease (IBD) means much more than “having a good day.” Modern care uses a treat‑to‑target approach that sets clear short- and long-term goals, tracks progress with tests, and adjusts therapy until the gut is as quiet and healed as safely possible. Understanding these layers of remission helps explain why symptoms, lab results, and scope findings all matter over time.
Key Takeaways
In IBD, remission has several layers: symptom control, quiet inflammation on tests, and healing of the bowel lining.
Treat‑to‑target is a strategy where the care team aims for specific measurable goals, not just “feeling better.” (pubmed.ncbi.nlm.nih.gov)
Short‑term targets focus on symptom relief and calming inflammation on blood and stool tests. (pubmed.ncbi.nlm.nih.gov)
Long‑term targets include clinical remission, mucosal healing on endoscopy, and steroid‑free control of disease. (journals.lww.com)
Deeper goals, like histologic or transmural healing, show how “deep” remission is but are not yet standard targets for everyone. (pubmed.ncbi.nlm.nih.gov)
Quality of life, ability to work or study, and growth in children are now recognized as important long‑term targets too. (cris.tau.ac.il)
Why “remission” is more than feeling better
Everyday language often uses remission to mean “no symptoms.” In IBD, that is only one piece of the picture. People can feel fairly well even while hidden inflammation continues in the gut, which raises the risk of flares, strictures, surgery, or colon cancer over time. Others can feel unwell from scarring, IBS, or fatigue even when inflammation is quiet.
To manage this mismatch, expert groups created more precise definitions of remission that combine:
How a person feels and functions
What blood and stool tests show
What scopes or imaging reveal about the bowel
Whether strong medicines like steroids are still needed
This multi‑layered view is the foundation of treat‑to‑target care. (pubmed.ncbi.nlm.nih.gov)
Treat‑to‑target: a roadmap for IBD care
Treat‑to‑target (T2T) means setting clear, shared goals and adjusting treatment until those goals are met, rather than waiting for big flares or only reacting to symptoms. The STRIDE and STRIDE‑II initiatives from the International Organization for the Study of IBD (IOIBD) defined the main targets for Crohn’s disease and ulcerative colitis. (pubmed.ncbi.nlm.nih.gov)
T2T in IBD uses three time frames:
Short term (weeks to a few months): reduce symptoms and start calming inflammation on tests.
Medium term (about 3–6 months): achieve clinical remission and normal or near‑normal blood and stool markers. (pubmed.ncbi.nlm.nih.gov)
Long term (6–12 months and beyond): show mucosal healing on scopes, stay in steroid‑free remission, and protect quality of life. (journals.lww.com)
Treatment and monitoring plans are adapted to each person’s disease type, risks, and life circumstances, but the basic targets are similar across Crohn’s and ulcerative colitis.
Short‑term goals: calming the fire
Short‑term goals focus on bringing active inflammation under control and improving daily life. STRIDE‑II highlights: (pubmed.ncbi.nlm.nih.gov)
Symptomatic response: fewer stools, less rectal bleeding, less abdominal pain, and reduced urgency.
Biochemical response: improving or normalizing markers of inflammation such as C‑reactive protein (CRP), erythrocyte sedimentation rate (ESR), and fecal calprotectin.
Short‑term response shows that a treatment is starting to work. If these early goals are not met, the care team may adjust doses or consider different therapies rather than waiting for a full flare.
Long‑term goals: protecting the gut
Long‑term treat‑to‑target goals aim to change the disease course, not only the current flare. STRIDE‑II and major guidelines emphasize: (pubmed.ncbi.nlm.nih.gov)
Clinical remission: minimal or no symptoms such as abdominal pain, rectal bleeding, or urgency, with normal stool frequency.
Endoscopic remission (mucosal healing): the lining of the bowel looks healed and free of ulcers on colonoscopy or sigmoidoscopy. In ulcerative colitis, this often means a Mayo endoscopic subscore of 0 or 1. (journals.lww.com)
Biomarker normalization: CRP, ESR, and fecal calprotectin are within the normal range or at a stable, low level for that individual. (pubmed.ncbi.nlm.nih.gov)
Steroid‑free remission: disease control without ongoing corticosteroids for a sustained period, often defined as at least 12 weeks. (journals.lww.com)
Quality of life and functioning: absence of IBD‑related disability and restoration of normal daily activities, with normal growth in children. (cris.tau.ac.il)
Research shows that achieving mucosal healing and steroid‑free remission is linked with fewer hospitalizations, fewer surgeries, and more durable control of disease. (journals.lww.com)
Types of remission and healing targets
The term remission can apply to different layers of disease control.
Target type | What it means | How it is checked | Why it matters |
|---|---|---|---|
Symptomatic or clinical remission | Near‑normal stool frequency and consistency, no rectal bleeding, minimal abdominal pain or urgency | Symptom history or patient‑reported questionnaires | Directly reflects how a person feels and functions day to day (journals.lww.com) |
Biochemical remission | Normal CRP/ESR and low fecal calprotectin | Blood tests and stool tests | Shows whether inflammation is controlled without always needing a scope (pubmed.ncbi.nlm.nih.gov) |
Endoscopic remission (mucosal healing) | Healed lining with no ulcers or only minimal changes | Colonoscopy or flexible sigmoidoscopy | Linked with sustained remission and lower risk of surgery and complications (journals.lww.com) |
Histologic remission | Biopsies show no active microscopic inflammation | Pathology review of tissue samples | Associated with lower relapse risk, but not yet a universal treatment target (journals.lww.com) |
Transmural remission (mainly Crohn’s) | Healing through the full bowel wall, no active inflammation on imaging | MRI, CT enterography, or intestinal ultrasound | Signals very deep control of Crohn’s disease, but still considered an aspirational goal (pubmed.ncbi.nlm.nih.gov) |
Deep remission | Combination of clinical remission and mucosal healing, often steroid‑free | Symptoms plus endoscopy, medication review | Preferred goal in many guidelines, associated with better long‑term outcomes (journals.lww.com) |
The special role of biomarkers
Biomarkers such as CRP and fecal calprotectin are key tools in treat‑to‑target care. They are less invasive and can be checked more often than scopes. STRIDE‑II treats normalization of these markers as a short‑term and intermediate target that guides decisions about continued therapy or escalation. (pubmed.ncbi.nlm.nih.gov)
Biomarkers are not perfect. Some people flare with only mild changes in blood work, and others have chronically raised CRP for unrelated reasons. For that reason, guidelines recommend combining biomarkers with symptom tracking and imaging or endoscopy, rather than relying on any single measure alone. (journals.lww.com)
Mucosal, histologic, and transmural healing
Endoscopic mucosal healing is now a central long‑term target in both Crohn’s disease and ulcerative colitis guidelines. (journals.lww.com)
In ulcerative colitis, an endoscopic score of 0 or 1 with no friability is often used to define healing. (journals.lww.com)
In Crohn’s disease, healing is defined as disappearance of ulcers on colonoscopy or resolution of inflammation on cross‑sectional imaging when scopes are not feasible. (pubmed.ncbi.nlm.nih.gov)
Histologic healing (normal biopsies) and transmural healing (full‑thickness healing on imaging) appear to predict even better outcomes, but STRIDE‑II currently treats them as measures of remission depth rather than formal targets for all patients. (pubmed.ncbi.nlm.nih.gov)
What remission can look like in real life
When treat‑to‑target goals are met, remission often includes:
Little to no abdominal pain, rectal bleeding, or urgency, with stable, predictable bowel habits
Normal or stable‑low inflammatory markers on repeated tests
Scopes showing a healed or nearly healed bowel lining at recommended intervals
No need for continuous steroids, relying instead on maintenance therapies that keep inflammation quiet
Ability to attend school or work, participate in social life, and maintain energy, with normal growth and puberty in children (cris.tau.ac.il)
Remission is not a cure. IBD remains a chronic condition, and targets may need to be revisited if symptoms or tests change over time. But using a clear treat‑to‑target framework helps align the goals of the person with IBD and the care team, with the shared aim of quiet inflammation, healed bowel tissue, and a fuller life outside the bathroom and hospital.
FAQs
Does remission mean stopping IBD medicines?
Not usually. Most people stay on maintenance therapy to keep inflammation under control and prevent flares. Stopping effective medicines can raise the chance of relapse, so any change in therapy is usually planned carefully and monitored closely. (journals.lww.com)
Why are steroids not counted as “real” remission?
Steroids can quickly reduce symptoms but do not reliably heal the bowel lining, and long‑term use causes serious side effects. Guidelines therefore emphasize steroid‑free remission, where symptoms and inflammation are controlled without ongoing steroid treatment. (journals.lww.com)
Can a person feel fine but still have active IBD?
Yes. Some people have few symptoms yet still show ulcers on endoscopy or elevated biomarkers. This “silent” inflammation can lead to complications over time, which is why regular objective monitoring is recommended even in those who feel well. (pubmed.ncbi.nlm.nih.gov)
Is deep remission realistic for everyone?
Deep remission is an ideal goal but not always achievable or appropriate for every individual, especially when other health issues or treatment risks are present. STRIDE‑II suggests individualizing targets, balancing the benefits of deeper control with safety, side effects, and personal preferences. (pubmed.ncbi.nlm.nih.gov)