# Metabolic Disorders and Inflammatory Bowel Diseases: Unraveling Shared Pathways and Clinical Interactions

**Authors:** Fotios Fousekis, Afroditi Lamprou, Maria Saridi, Ioanna Nefeli Mastorogianni, Konstantinos Mpakogiannis, Georgios D. Lianos, Konstantinos H. Katsanos

PMC · DOI: 10.3390/metabo16030181 · Metabolites · 2026-03-09

## TL;DR

Inflammatory bowel diseases and metabolic disorders are linked through shared mechanisms, affecting each other's progression and treatment outcomes.

## Contribution

The paper highlights bidirectional interactions and shared pathways between IBD and metabolic disorders, emphasizing integrated management strategies.

## Key findings

- IBD patients often have metabolic comorbidities like obesity and diabetes, which worsen disease outcomes.
- Metabolic disorders can be exacerbated by IBD inflammation and corticosteroid treatments.
- Integrated care involving lifestyle and nutritional strategies is crucial for managing both conditions.

## Abstract

Inflammatory bowel diseases (IBDs) and metabolic disorders are increasingly recognized as interconnected conditions that frequently coexist and influence each other’s clinical course. Accumulating evidence indicates that patients with IBD face a substantial burden of obesity, metabolic syndrome, metabolic dysfunction-associated steatotic liver disease, osteoporosis, and type 2 diabetes. These associations appear to be driven by shared and interacting mechanisms, including intestinal barrier disruption, gut microbiota dysbiosis, chronic systemic inflammation, and adipose tissue-mediated immunometabolic pathways. Metabolic comorbidities may worsen IBD activity, reduce response to therapy, increase complications, and contribute to higher health care utilization. Conversely, intestinal inflammation and commonly used treatments, particularly corticosteroids, can adversely affect glucose metabolism, lipid metabolism, body composition and bone homeostasis. Advanced therapies have demonstrated variable metabolic effects, some of which may be beneficial through suppression of systemic inflammation. Recognition of these bidirectional interactions highlights the importance of routine metabolic screening and integrated, multidisciplinary management. Lifestyle interventions, nutritional optimization and individualized therapeutic strategies represent central parts of comprehensive management.

## Linked entities

- **Diseases:** obesity (MONDO:0011122), metabolic syndrome (MONDO:0000816), metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), osteoporosis (MONDO:0005298), type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, MUC2 (mucin 2, oligomeric mucus/gel-forming) [NCBI Gene 4583] {aka MLP, MUC-2, SMUC}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, APOC3 (apolipoprotein C3) [NCBI Gene 345] {aka APOCIII, Apo-C3, ApoC-3}, TNFRSF11B (TNF receptor superfamily member 11b) [NCBI Gene 4982] {aka OCIF, OPG, PDB5, TR1}, 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}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}, SOST (sclerostin) [NCBI Gene 50964] {aka CDD, DAND6, SOST1, VBCH}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, ANGPTL3 (angiopoietin like 3) [NCBI Gene 27329] {aka ANG-5, ANGPT5, ANL3, FHBL2}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, TNFSF11 (TNF superfamily member 11) [NCBI Gene 8600] {aka CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B}, NPC1L1 (NPC1 like intracellular cholesterol transporter 1) [NCBI Gene 29881] {aka LDLCQ7, NPC11L1, SLC65A2}, NOD2 (nucleotide binding oligomerization domain containing 2) [NCBI Gene 64127] {aka ACUG, BLAU, BLAUS, CARD15, CD, CLR16.3}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, LDLR (low density lipoprotein receptor) [NCBI Gene 3949] {aka LDLCQ2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, CETP (cholesteryl ester transfer protein) [NCBI Gene 1071] {aka BPIFF, HDLCQ10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** depression (MESH:D003866), NAFLD (MESH:D065626), Diabetes Type 2 (MESH:D003924), bone resorption (MESH:D001862), Obese (MESH:D009765), nutritional deficiencies (MESH:D044342), Bone loss (MESH:D001847), Intestinal Barrier Dysfunction (MESH:D007410), sarcopenia (MESH:D055948), Vitamin D deficiency (MESH:D014808), Insulin Resistance (MESH:D007333), abdominal pain (MESH:D015746), infections (MESH:D007239), injury to (MESH:D014947), IBD (MESH:D015212), metabolic dysregulation (MESH:D021081), Malabsorption (MESH:D008286), end-organ damage (MESH:C564816), dyslipidemia (MESH:D050171), fragility fracture (MESH:D005600), micronutrient deficiencies (MESH:D007153), psoriasis (MESH:D011565), atherosclerosis (MESH:D050197), Diabetic (MESH:D003920), venous thromboembolism (MESH:D054556), osteopenia (MESH:D001851), visceral obesity (MESH:D056128), psoriatic arthritis (MESH:D015535), impaired bone formation (MESH:D058426), Dysbiosis (MESH:D064806), Systemic (MESH:D015619), pain (MESH:D010146), cardiovascular disease (MESH:D002318), weight loss (MESH:D015431), CD (MESH:D003424), fibrosis (MESH:D005355), UC (MESH:D003093), endotoxemia (MESH:D019446), overweight (MESH:D050177), chronic (MESH:D002908), weight gain (MESH:D015430), Metabolic (MESH:D008659), gastrointestinal symptoms (MESH:D012817), viral hepatitis (MESH:D014777), fracture (MESH:D050723), Intestinal inflammation (MESH:D007249), Fatty Liver (MESH:D005234), Adipose Tissue Dysfunction (MESH:D018205), bone erosion (MESH:D014077), biliary disease (MESH:D001660), visceral adiposity (MESH:D007418), Gut (MESH:C536735), anxiety (MESH:D001007), immune-mediated disorders (MESH:C567355), tract (MESH:D014570), liver condition (MESH:D017093), Metabolic Syndrome (MESH:D024821), colitis (MESH:D003092), fatigue (MESH:D005221), hypertension (MESH:D006973)
- **Chemicals:** carnitine (MESH:D002331), branched-chain amino acids (MESH:D000597), risankizumab (MESH:C000601773), certolizumab pegol (MESH:D000068582), cholesterol (MESH:D002784), luminal (MESH:D010634), Antilipidemic Agents (-), B12 (MESH:C034730), H2S (MESH:D006862), infliximab (MESH:D000069285), Vedolizumab (MESH:C543529), calcium (MESH:D002118), tryptophan (MESH:D014364), natalizumab (MESH:D000069442), bempedoic acid (MESH:C581236), Lipid (MESH:D008055), golimumab (MESH:C529000), zinc (MESH:D015032), mirikizumab (MESH:C000708407), Ezetimibe (MESH:D000069438), iron (MESH:D007501), guselkumab (MESH:C000588857), amino acid (MESH:D000596), bile acid (MESH:D001647), p-cresyl sulfate (MESH:C408690), sphingolipid (MESH:D013107), salt (MESH:D012492), upadacitinib (MESH:C000613732), ustekinumab (MESH:D000069549), omega-3 fatty acids (MESH:D015525), folate (MESH:D005492), sodium (MESH:D012964), Thiazolidinediones (MESH:D045162), adalimumab (MESH:D000068879), nitrogen (MESH:D009584), filgotinib (MESH:C584571), glucose (MESH:D005947), butyrate (MESH:D002087), TMA (MESH:C023336), sugars (MESH:D000073893), SCFA (MESH:D005232), carbohydrate (MESH:D002241), metformin (MESH:D008687), steroid (MESH:D013256), LPS (MESH:D008070), Vitamin D (MESH:D014807), tofacitinib (MESH:C479163), vitamin B12 (MESH:D014805)
- **Species:** gut metagenome (species) [taxon 749906], Akkermansia muciniphila (species) [taxon 239935], Roseburia (genus) [taxon 841], Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606], Faecalibacterium prausnitzii (species) [taxon 853], Actinomycetota (actinobacteria, phylum) [taxon 201174], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

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## References

178 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028057/full.md

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Source: https://tomesphere.com/paper/PMC13028057