1 Research Professor, Department of Health Care, Universidad Autónoma Metropolitana, Xochimilco Campus.
2 MD, Universidad Autónoma Metropolitana, Xochimilco Campus.
3 Medical Social Service Intern, Universidad Autónoma Metropolitana, Xochimilco Campus.
4 Medical Student, Universidad Autónoma Metropolitana, Xochimilco Campus.
World Journal of Biology Pharmacy and Health Sciences, 2026, 25(01), 118-123
Article DOI: 10.30574/wjbphs.2026.25.1.0026
Received on 06 December 2025; revised on 10 January 2026; accepted on 13 January 2026
This systematic review details the pathophysiology of metabolic dysfunction–associated steatotic liver disease (MASLD), identifying it as the intrinsic hepatic manifestation of metabolic syndrome. The process is primarily triggered by insulin resistance, which disrupts lipid metabolism and promotes a massive influx of fatty acids into the liver, leading to lipotoxicity and oxidative stress. Under the “multiple-hit” model, factors such as chronic inflammation derived from dysfunctional adipose tissue, dysbiosis of the gut–liver axis, and genetic polymorphisms (such as those in the PNPLA3 gene) act synergistically to promote progression from simple steatosis to severe conditions such as metabolic dysfunction–associated steatohepatitis (MASH), fibrosis, cirrhosis, and hepatocellular carcinoma. Therefore, it is concluded that therapeutic management must be comprehensive, focusing on visceral obesity and systemic inflammation beyond the hepatic organ itself.
Metabolic syndrome; MASLD / NAFLD; Insulin resistance; MASH / NASH; Multiple-hit model; Lipotoxicity; Adipokines
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Alejandro Alonso Altamirano, Araceli Chalte Valencia, Jazmin Mendoza Olivares and Roman Rodriguez Milan. Systematic Review: Pathophysiology of Hepatic Alterations Associated with Metabolic Syndrome. World Journal of Biology Pharmacy and Health Sciences, 2026, 25(01), 118-123. Article DOI: https://doi.org/10.30574/wjbphs.2026.25.1.0026