# Challenges and Treatment Strategies in Elderly Patients with Inflammatory Bowel Disease: A Systematic Review and Narrative Synthesis

**Authors:** John K. Triantafillidis, Konstantinos Malgarinos, Georgia Kontrarou, Emmanouil Kritsotakis, Victoria Polydorou, Konstantinos Pantos, Konstantinos Sfakianoudis, Agni Pantou, Anastasios Karandreas, Manousos M. Konstandoulakis, Apostolos E. Papalois

PMC · DOI: 10.3390/jpm16020059 · 2026-01-23

## TL;DR

This paper reviews how to best treat inflammatory bowel disease in elderly patients, considering their unique health challenges and the effectiveness of biological therapies.

## Contribution

The paper provides a systematic review and synthesis of recent data on the treatment of IBD in elderly patients, emphasizing practical guidelines for biological therapies.

## Key findings

- Elderly IBD patients often have a milder clinical course and a higher ratio of UC to CD.
- Biologic therapies like anti-TNF agents, vedolizumab, and ustekinumab are effective and safer in elderly patients compared to traditional therapies.
- JAK inhibitors are a practical option but require careful patient selection due to increased thromboembolic risk.

## Abstract

Introduction: The proportion of elderly patients with IBD is steadily increasing due to the aging population and improved survival. Patients in this age group present specificities in diagnosis and treatment, particularly regarding the use of biological agents, where immunosenescence, multimorbidity, and polypharmacy affect the precise assessment of benefit and risk. Aim: This systematic review, which was conducted in accordance with the PRISMA 2020 statement, aims to synthesize available data on the epidemiology, clinical characteristics, and therapeutic management of IBD in the elderly, with emphasis on the most recent data and practical guidelines for the use of biological therapies. Methods: A systematic search of PubMed, Scopus, and Embase was conducted. A total of 40 studies were included, comprising 5 randomized controlled trials, 15 prospective cohort studies, and 20 retrospective observational studies. Eligible studies included randomized controlled trials, observational cohort studies, and population-based analyses. Given substantial clinical and methodological heterogeneity, findings were synthesized narratively. Data on demographics, disease phenotype, comorbidities, and treatment outcomes were extracted and analyzed. In addition, a narrative synthesis of major randomized trials of biologic therapies, recent guidelines, and data from prospective studies and patient registries was performed with a focus on safety and real-world outcomes in the elderly. Risk of bias was assessed using the Newcastle–Ottawa Scale (NOS) and the Cochrane Risk of Bias tool. Results: The majority of included studies (85%) were found to have a low to moderate risk of bias, providing a reliable basis for the synthesis. Data show an increasing incidence of IBD in the elderly, often with a milder clinical course and a higher ratio of UC to CD. Multimorbidity and polypharmacy are significant challenges that increase the risk of adverse events. Although classic therapies remain effective, in many cases, a lower threshold is required to initiate advanced therapies, such as biologic agents. Anti-tumor necrosis factor (anti-TNF) agents, as well as biologics with alternative mechanisms of action such as vedolizumab (α4β7 integrin antagonist) and ustekinumab (interleukin-12/23 inhibitor), represent key therapeutic options in elderly patients with IBD. These biologic factors have efficacy comparable to that in younger patients and are considered attractive options due to reduced systemic immunosuppression and favorable safety profiles. JAK inhibitors are a practical option but are associated with an increased thromboembolic risk and require careful patient selection. Older age is associated with higher absolute rates of serious infections, hospitalizations, and, in some series, mortality. Individualized decision-making, including frailty assessment, vaccination coverage, infection control, and dose adjustments based on renal and hepatic function, is essential for optimal care. Conclusions: IBD in the elderly is a distinct clinical entity with unique challenges in diagnosis and management. A multidisciplinary approach and individualized treatment strategies are essential to ensure the balance between disease control and minimizing the risks associated with comorbidity and polypharmacy. Further research, including specifically designed clinical trials, is needed to optimize treatment and outcomes in this unique patient group.

## Linked entities

- **Diseases:** inflammatory bowel disease (MONDO:0005265), CD (MONDO:0016063)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, KRT88P (keratin 88, pseudogene) [NCBI Gene 85348] {aka HBC, KRT122P, KRTHBP3}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** Cancer (MESH:D009369), opportunistic infections (MESH:D009894), ischemic (MESH:D002545), diverticulitis (MESH:D004238), diabetes (MESH:D003920), anxiety (MESH:D001007), chronic kidney disease (MESH:D051436), anorexia (MESH:D000855), hepatitis B (MESH:D006509), abdominal pain (MESH:D015746), rectal bleeding (MESH:D012002), hyperglycemia (MESH:D006943), cardiometabolic diseases (MESH:D024821), abscess (MESH:D000038), gastrointestinal symptoms (MESH:D012817), chronic intestinal inflammation (MESH:D007249), sarcopenia (MESH:D055948), complications (MESH:D008107), injury to (MESH:D014947), Disease (MESH:D004194), dysplasia (MESH:D015792), acute coronary syndrome (MESH:D054058), dyslipidemia (MESH:D050171), influenza (MESH:D007251), fractures (MESH:D050723), fever (MESH:D005334), intestinal strictures (MESH:D003251), enteropathies (MESH:C538273), systemic disease (MESH:D034721), Frail (MESH:D000073496), nutritional deficits (MESH:D009748), latent infections (MESH:D000085343), nonmelanoma skin cancer (MESH:D012878), Fall (MESH:C537863), musculoskeletal pain (MESH:D059352), bleeding (MESH:D006470), mood disturbances (MESH:D019964), interstitial nephritis (MESH:D009395), vitamin D deficiency (MESH:D014808), bloody diarrhea (MESH:D003967), metabolic toxicity (MESH:D065606), Fatigue (MESH:D005221), postoperative complications (MESH:D011183), colitides (MESH:D003092), ischemic lesions (MESH:D017202), COVID-19 (MESH:D000086382), gastrointestinal diseases (MESH:D005767), cardiovascular disease (MESH:D002318), Infection (MESH:D007239), -bowel CD (MESH:D003424), osteoporosis (MESH:D010024), latent tuberculosis (MESH:D055985), weight loss (MESH:D015431), toxicity (MESH:D064420), bone loss (MESH:D001847), thrombotic (MESH:D013927), bowel motility (MESH:D015835), anemia (MESH:D000740), colorectal cancer (MESH:D015179), malnutrition (MESH:D044342)
- **Chemicals:** tofacitinib (MESH:C479163), azathioprine (MESH:D001379), Etrasimod (MESH:C000656249), Mesalamine (MESH:D019804), vitamin D (MESH:D014807), Risankizumab (MESH:C000601773), Thiopurines (MESH:C520399), upadacitinib (MESH:C000613732), Ustekinumab (MESH:D000069549), Obefazimod (MESH:C000623073), infliximab (MESH:D000069285), adalimumab (MESH:D000068879), methylprednisolone (MESH:D008775), 6-mercaptopurine (MESH:D015122), golimumab (MESH:C529000), Vedolizumab (MESH:C543529), prednisolone (MESH:D011239), Mirikizumab (MESH:C000708407), PCV15 (-), Guselkumab (MESH:C000588857), filgotinib (MESH:C584571), calcium (MESH:D002118), SCFA (MESH:D005232), Budesonide (MESH:D019819), creatinine (MESH:D003404), steroid (MESH:D013256), prednisone (MESH:D011241), certolizumab pegol (MESH:D000068582), lipid (MESH:D008055)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Hepatitis B virus (no rank) [taxon 10407], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941479/full.md

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Source: https://tomesphere.com/paper/PMC12941479