Small-Nerve Fibre Pathology in Metabolic Dysfunction-Associated Steatotic Liver Disease Is Associated with Liver Fat/Inflammation and Improves with Weight Loss

@article{henney2026smallnerve,
  title = {{Small-Nerve Fibre Pathology in Metabolic Dysfunction-Associated Steatotic Liver Disease Is Associated with Liver Fat/Inflammation and Improves with Weight Loss}},
  author = {Alex E. Henney and Azlinda Hamid and Jamie Burgess and David R. Riley and Barbara Fielding and Anne Marshall and Khansa Makawi and Abdel-Naser Elzouki and Einas Elgassim and Graham J. Kemp and Rayaz A. Malik and Uazman Alam and Daniel J. Cuthbertson},
  journal = {Nutrients},
  year = {2026},
  month = oct,
  doi = {10.3390/nu18193242},
  url = {https://europepmc.org/article/PMC/PMC13666698},
  note = {CC BY},
}

TY  - JOUR
TI  - Small-Nerve Fibre Pathology in Metabolic Dysfunction-Associated Steatotic Liver Disease Is Associated with Liver Fat/Inflammation and Improves with Weight Loss
AU  - Alex E. Henney
AU  - Azlinda Hamid
AU  - Jamie Burgess
AU  - David R. Riley
AU  - Barbara Fielding
AU  - Anne Marshall
AU  - Khansa Makawi
AU  - Abdel-Naser Elzouki
AU  - Einas Elgassim
AU  - Graham J. Kemp
AU  - Rayaz A. Malik
AU  - Uazman Alam
AU  - Daniel J. Cuthbertson
PY  - 2026
DA  - 2026/10/01
JO  - Nutrients
DO  - 10.3390/nu18193242
UR  - https://europepmc.org/article/PMC/PMC13666698
AB  - Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) is associated with multiple extrahepatic complications, but its relationship with peripheral neuropathy, even without co-existing type 2 diabetes (T2D), remains poorly understood. Furthermore, to what extent addressing liver and metabolic health would be associated with improvements in small nerve fibre morphology (that mediate neuropathy) is unknown. We investigated the relationship between liver health and small nerve fibre morphology in adults with MASLD before and after diet-induced weight loss and improvements in liver health. Methods: Adults with MASLD (n = 12) and controls without MASLD or T2D (n = 16) underwent anthropometry, biochemistry, transient elastography (TE) and corneal confocal microscopy (CCM). Participants with MASLD then completed a 12-week low-calorie diet (LCD; Counterweight-Plus, ~850 kcal/day) with repeat assessments including multi-organ magnetic resonance imaging (MRI). TE quantified hepatic steatosis (controlled attenuation parameter, CAP), while MRI measured hepatic and pancreatic fat (proton density fat fraction, PDFF) and fibroinflammation (iron-corrected T1, cT1). Neuropathy was assessed using validated questionnaires and CCM-derived corneal nerve fibre density (CNFD), branch density (CNBD) and fibre length (CNFL). The primary outcome measure was change in liver PDFF. Associations between hepatic and neuropathy measures were assessed using correlation and multivariable linear regression. Results: Compared with controls, MASLD participants had higher liver fat and metabolic dysfunction, with reduced CNFD (25.7 vs. 28.4 fibres/mm2, p = 0.03) and CNFL (14.1 vs. 17.1 mm/mm2, p = 0.02). In multivariable regression, TE-derived CAP was independently associated with CNFD (β −0.03 (95% CI −0.06, −0.01), p < 0.05), while total cholesterol was associated with CNFL (β −1.54 (95% CI −2.81, −0.27), p < 0.02). After LCD, participants lost 12.5 kg with reductions in metabolic syndrome components (p = 0.04) and liver fat (ΔPDFF −5.0%, p = 0.03). Neuropathic symptoms improved and CNFD increased (+1.87 fibres/mm2, p = 0.05). Reduction in liver fat correlated with increased CNFL (r = −0.63, p = 0.03), while change in hepatic fibroinflammation (ΔcT1) correlated with neuropathy disability (r = 0.62, p = 0.04) and small-fibre symptom scores (r = 0.47, p = 0.05). Conclusions: These exploratory findings suggest that MASLD, even without T2D, may be associated with small nerve fibre abnormalities and neuropathic symptoms. Diet-induced weight loss improved liver, metabolic and neural health in parallel. Larger prospective confirmatory studies are required to more precisely establish this relationship both at baseline and with interventions.
SN  - 2072-6643
ER  -