# From Adipose Dysfunction to Multi-Organ Steatosis: Defining the Metabolic Steatotic Axis

**Authors:** Almir Fajkić, Yun Wah Lam, Rijad Jahić, Ivan Ćavar, Antonio Markotić, Andrej Belančić

PMC · DOI: 10.3390/cimb48020178 · 2026-02-04

## TL;DR

This paper introduces a new framework called the Metabolic Steatotic Axis to better understand how fat accumulation in multiple organs contributes to metabolic diseases.

## Contribution

The paper introduces the Metabolic Steatotic Axis as a novel conceptual framework for understanding multi-organ steatosis and systemic metabolic dysfunction.

## Key findings

- Steatosis in multiple organs is interconnected through lipotoxicity and inflammatory signaling.
- The MSA framework can improve disease staging and risk stratification using composite biomarkers.
- Interventions should be viewed as systemic modulators rather than organ-specific treatments.

## Abstract

Steatosis extends beyond the liver to the pancreas, heart, and skeletal muscle, yet prevailing definitions remain narrowly organ-focused. This narrative review introduces the Metabolic Steatotic Axis (MSA) as a framework that captures the dynamic, bidirectional interactions among these organs, driving systemic metabolic dysfunction. We synthesize evidence linking lipotoxicity, inflammatory signaling, and endocrine cross-talk into a self-amplifying network accelerating insulin resistance, β-cell failure, and cardiometabolic risk. The MSA concept provides a rationale for axis-based staging systems and composite biomarker panels to quantify cumulative disease burden better and refine risk stratification. We highlight phenotypic heterogeneity within MSA stages, the possible hierarchy of organ vulnerability, and the implications for prognosis and therapy. Viewing pharmacological and lifestyle interventions through the MSA lens reframes them as systemic modulators rather than organ-specific treatments, underscoring the need for multi-organ endpoints in clinical trials. Finally, we outline priorities for longitudinal imaging, multi-omics integration, and global harmonization to translate the MSA from a conceptual construct to a clinically actionable paradigm. By unifying fragmented observations into a systemic model, the MSA has the potential to reshape disease classification, therapeutic strategies, and precision medicine in metabolic disorders.

## Full-text entities

- **Genes:** MIR1225 (microRNA 1225) [NCBI Gene 100188847] {aka MIRN1225}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, AHR (aryl hydrocarbon receptor) [NCBI Gene 196] {aka FVH3, RP85, bHLHe76}, CLOCK (clock circadian regulator) [NCBI Gene 9575] {aka KAT13D, bHLHe8}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, KRT18 (keratin 18) [NCBI Gene 3875] {aka CK-18, CYK18, K18}, PRKCE (protein kinase C epsilon) [NCBI Gene 5581] {aka PKCE, nPKC-epsilon}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IAPP (islet amyloid polypeptide) [NCBI Gene 3375] {aka DAP, IAP}, CD36 (CD36 molecule (CD36 blood group)) [NCBI Gene 948] {aka BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV}, AGRP (agouti related neuropeptide) [NCBI Gene 181] {aka AGRT, ART, ASIP2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, AHSG (alpha 2-HS glycoprotein) [NCBI Gene 197] {aka A2HS, AHS, APMR1, FETUA, HSGA}, EIF2AK3 (eukaryotic translation initiation factor 2 alpha kinase 3) [NCBI Gene 9451] {aka PEK, PERK, WRS}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, XBP1 (X-box binding protein 1) [NCBI Gene 7494] {aka TREB-5, TREB5, XBP-1, XBP2}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, FFAR3 (free fatty acid receptor 3) [NCBI Gene 2865] {aka FFA3R, GPR41}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], IRS1 (insulin receptor substrate 1) [NCBI Gene 3667] {aka HIRS-1}, FABP3 (fatty acid binding protein 3) [NCBI Gene 2170] {aka FABP11, H-FABP, M-FABP, MDGI, O-FABP}, PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891] {aka LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, SREBF1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 6720] {aka HMD, IFAP2, SREBP1, bHLHd1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, TRB (T cell receptor beta locus) [NCBI Gene 6957] {aka TCRB, TRB@}, SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476] {aka BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA}, FETUB (fetuin B) [NCBI Gene 26998] {aka 16G2, Gugu, IRL685}, FGF21 (fibroblast growth factor 21) [NCBI Gene 26291], NPY (neuropeptide Y) [NCBI Gene 4852] {aka PYY4}, FFAR2 (free fatty acid receptor 2) [NCBI Gene 2867] {aka FFA2R, GPR43}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465] {aka NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR}, ERN1 (endoplasmic reticulum to nucleus signaling 1) [NCBI Gene 2081] {aka IRE1, IRE1P, IRE1a, hIRE1p}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, PYY (peptide YY) [NCBI Gene 5697] {aka PYY-I, PYY1}, BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406] {aka ARNTL, ARNTL1, BMAL1c, JAP3, MOP3, PASD3}, TRA (T cell receptor alpha locus) [NCBI Gene 6955] {aka IMD7, TCRA, TRA@}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, SELENOP (selenoprotein P) [NCBI Gene 6414] {aka SELP, SEPP, SEPP1, SeP}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, GPR119 (G protein-coupled receptor 119) [NCBI Gene 139760] {aka GPCR2}, FNDC5 (fibronectin type III domain containing 5) [NCBI Gene 252995] {aka FRCP2, irisin}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, EIF2A (eukaryotic translation initiation factor 2A) [NCBI Gene 83939] {aka CDA02, EIF-2A, MST089, MSTP004, MSTP089}
- **Diseases:** overnutrition (MESH:D044343), Pancreatic steatosis (MESH:D010195), neuroinflammation (MESH:D000090862), diabetes (MESH:D003920), NAFLD (MESH:D065626), beta-cell failure (MESH:D051437), Pancreas (MESH:D010190), atherogenic dyslipidemia (MESH:D050171), sleep disorders (MESH:D012893), metabolic syndrome (MESH:D024821), fibrosis (MESH:D005355), mitochondrial overload (MESH:D019190), Inflammation (MESH:D007249), MASLD (MESH:D008107), steatotic disease (MESH:D004194), injury to (MESH:D014947), visceral adiposity (MESH:D007418), Cushing's syndrome (MESH:D003480), lipodystrophy (MESH:D008060), MASPD (MESH:D008659), choline deficiency (MESH:D002796), Deficiencies in vitamin B12 (MESH:D014806), lipotoxic cardiomyopathy (MESH:D009202), Dysautonomia (MESH:D054969), Obesity (MESH:D009765), metabolic organ failure (MESH:D009102), diastolic dysfunction (MESH:D018487), Multi-Organ Steatosis (MESH:D005234), hepatic insulin resistance (MESH:D007333), diastolic impairment (MESH:D006337), weight loss (MESH:D015431), toxic (MESH:D064420), hypertrophy (MESH:D006984), cardiovascular disease (MESH:D002318), hypothyroidism (MESH:D007037), metabolic endotoxemia (MESH:D019446), gliosis (MESH:D005911), MSA (MESH:C566610), ectopic (MESH:C566852), tissue injury (MESH:D017695), lipid (MESH:D011017), impaired glucose tolerance (MESH:D018149), cardiac ectopic fat (MESH:D006331), hepatic disease (MESH:D056486), Adipose Dysfunction (MESH:D018205), type 2 diabetes (MESH:D003924)
- **Chemicals:** carbon (MESH:D002244), Triglyceride (MESH:D014280), choline (MESH:D002794), cortisol (MESH:D006854), sugar (MESH:D000073893), Ceramides (MESH:D002518), testosterone (MESH:D013739), FFAs (MESH:D005230), indoles (MESH:D007211), luminal (MESH:D010634), fatty acid (MESH:D005227), carbohydrate (MESH:D002241), natriuretic peptides (MESH:D045265), Catecholamines (MESH:D002395), bile acids (MESH:D001647), melatonin (MESH:D008550), T4 (MESH:D013974), hepatic lipid (-), ROS (MESH:D017382), folate (MESH:D005492), calcium (MESH:D002118), SCFAs (MESH:D005232), glucose (MESH:D005947), T3 (MESH:D014284), DAG (MESH:D004075), tryptophan (MESH:D014364), alcohol (MESH:D000438), vitamin B12 (MESH:D014805), resmetirom (MESH:C588408), Lipid (MESH:D008055), LPS (MESH:D008070), thiazolidinediones (MESH:D045162), ATP (MESH:D000255)
- **Species:** Homo sapiens (human, species) [taxon 9606], gut metagenome (species) [taxon 749906]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12939849/full.md

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Source: https://tomesphere.com/paper/PMC12939849