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Persistent disease burden despite advanced therapies in inflammatory bowel disease: a real-world patient-reported survey from Greece.
Frontiers in immunology

Cure8 research brief

Persistent disease burden despite advanced therapies in inflammatory bowel disease: a real-world patient-reported survey from Greece.

2 min read
Mental health and quality of life Observational Study Adult patients Patients On Biologics Clinicians Researchers Newly Diagnosed Inflammatory bowel disease

Why This Matters

Many people with IBD still experience active disease, poor quality of life, work impairment, and depression even while on advanced therapies — highlighting gaps in how we measure and manage treatment success. Who this affects: patients on biologics/advanced treatments and their care teams.

Who Should Pay Attention

Adult patients with IBD on advanced therapies, clinicians treating IBD, patient advocates, and researchers focused on real-world patient-reported outcomes.

Study Snapshot

Story typeResearch paper
Evidence typeResearch paper
Source depthJournal abstract

What To Know

This survey of 287 adult Greek patients with Crohn’s disease (CD) or ulcerative colitis (UC) who were receiving advanced therapies found a high residual disease burden despite treatment.

Over half (57.1%) reported active disease; about three-quarters had impaired quality of life; nearly 1 in 3 reported work productivity loss; almost half had moderate-to-severe depressive symptoms; and about 39% were dissatisfied with their advanced therapy.

The data come from a structured, self-reported questionnaire administered to members of a national patient organization (HELLESCC) between October 2023 and January 2024.

Analyses included associations between disease activity and patient-reported outcomes (SIBDQ, WPAI, PHQ-9), showing higher disease activity linked to worse QoL, greater work impairment, more depressive symptoms, and lower treatment satisfaction.

These findings highlight persistent unmet needs among patients on advanced treatments and the importance of assessing mental health, work impact, treatment satisfaction, and adherence alongside disease activity in routine care.

Keep In Mind

Survey participants were members of a national patient group and responded to a self-reported questionnaire between Oct 2023–Jan 2024. Results are associative and may not generalize beyond this population. Structured content depth: abstract.

Source Details

Review the original publication for the complete reporting, methods, and context.

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Research paper Evidence type derived from source or registry metadata.
PublicationFrontiers in immunology
AuthorsTzanetakos C, Vakouftsi VR, Mavridoglou G +2 more
Study typeJournal article
Indexed viaEurope PMC
Source typeResearch paper
PublishedJul 10, 2026, 12:00 AM
Content availableJournal abstract

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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