# Malondialdehyde as a Predictor of Disease Severity and Cardiovascular Risk in Population with Metabolic Dysfunction-Associated Steatotic Liver Disease

**Authors:** Roberto Lugo, Ana Ligia Gutiérrez-Solis, Ricardo Emmanuel Jimeno-Figueroa, Paul Góngora-Chan, Mayra Vera-Aviles, Dayana Williams-Jacquez, Marlene Chaurand-Lara, Jorge Arturo Valdivieso-Jimenez, Isabel Medina-Vera, Martha Guevara-Cruz, Brenda Pacheco-Hernández, Noriyouky Ix-Ruiz, Rodolfo Chim-Aké, Azalia Avila-Nava

PMC · DOI: 10.3390/metabo16030203 · Metabolites · 2026-03-19

## TL;DR

This study shows that higher levels of malondialdehyde (MDA) are linked to more severe liver disease and higher cardiovascular risk in people with metabolic dysfunction-associated steatotic liver disease.

## Contribution

The study identifies MDA as a potential predictor of steatosis severity and cardiovascular risk in MASLD patients.

## Key findings

- An MDA cut-off of ≥ 0.13 nmol/mL was associated with higher steatosis severity (grade II–III vs. grade I).
- Higher body fat percentage and elevated MDA levels correlated with increased cardiovascular risk markers.
- WHR and TyG index were higher in patients with more severe steatosis, indicating greater cardiovascular risk.

## Abstract

Background/Objectives: Metabolic dysfunction-associated steatotic liver disease (MASLD) is characterized by excessive triglyceride accumulation in the liver, the presence of one or more cardiometabolic risk factors, and an absence of harmful alcohol intake. Oxidative stress plays a crucial role in the development and severity of this disease, contributing to an increased cardiovascular risk (CVR). Malondialdehyde (MDA), an oxidative biomarker resulting from lipid peroxidation, is closely associated with metabolic dysfunction. This study aimed to evaluate the role of MDA as a predictor of steatosis severity and CVR. Methodology: An observational cross-sectional study was conducted in a population with MASLD with hepatic steatosis confirmed by ultrasonography and computed tomography. Subjects were classified according to severity of the hepatic steatosis as grade I or grade II-III. Nutritional, anthropometric, and serum biochemical parameters were measured. MDA levels were determined using a spectrophotometric method. The CVR was assessed using waist-to-hip ratio (WHR), triglycerides-glucose (TyG) index, lipid accumulation product (LAP), and atherogenic index of plasma (AIP). Receiver operating characteristic (ROC) curve analysis was performed to identify MDA cut-off value, followed by multivariable logistic regression to assess its association with severity of steatosis adjusted for body fat percentage. Results: A total of 50 patients were included (21 men and 29 women). An MDA cut-off value ≥ 0.13 nmol/mL was associated with higher severity (grade II–III vs. grade I) (OR = 5.0; 95% CI: 1.20–20.0; p = 0.022). Higher WHR values were found in subjects with grade I (p = 0.049), and elevated TyG index values were observed in patients with grade I-III (p = 0.042) both indicating increased CVR. Conclusions: Elevated MDA levels and higher body fat percentage were associated with higher degree of hepatic steatosis and increased CVR in the population from southeastern Mexico.

## Linked entities

- **Chemicals:** Malondialdehyde (PubChem CID 10964), triglyceride (PubChem CID 5460048)
- **Diseases:** Metabolic dysfunction-associated steatotic liver disease (MONDO:0013209)

## Full-text entities

- **Genes:** LAP (Laryngeal adductor paralysis) [NCBI Gene 7939], GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, AIP (AHR interacting HSP90 co-chaperone) [NCBI Gene 9049] {aka ARA9, FKBP16, FKBP37, PITA1, SMTPHN, XAP-2}
- **Diseases:** cirrhosis (MESH:D005355), hepatic OS (MESH:D056486), Metabolic Dysfunction (MESH:D008659), Hepatic Steatosis (MESH:D005234), inflammation (MESH:D007249), allergy (MESH:D004342), endothelial dysfunction (MESH:D014652), adiposity (MESH:D018205), ischemic heart disease (MESH:D017202), metabolic disturbances (MESH:D024821), liver injury (MESH:D017093), hypertension (MESH:D006973), MASLD (MESH:D008107), obesity (MESH:D009765), type 2 diabetes (MESH:D003924), hypertriglyceridemia (MESH:D015228), NAFLD (MESH:D065626), II-III (MESH:C536044), deaths (MESH:D003643), chronic liver failure (MESH:D058625), hepatitis B or hepatitis C virus infection (MESH:D006509), insulin resistance (MESH:D007333), injury to (MESH:D014947), human immunodeficiency virus infection (MESH:D015658), dyslipidemia (MESH:D050171), OS (MESH:D000079225), mitochondrial dysfunction (MESH:D028361), atherogenesis (MESH:D050197), hepatocellular carcinoma (MESH:D006528), central obesity (MESH:D056128), alcoholism (MESH:D000437), CVR (MESH:D002318)
- **Chemicals:** polyunsaturated fatty acids (MESH:D005231), ROS (MESH:D017382), tetramethoxypropane (MESH:C041295), glucose (MESH:D005947), sodium fluorescein (MESH:D019793), free fatty acids (MESH:D005230), carbohydrates (MESH:D002241), Trolox (MESH:C010643), hydrochloric acid (MESH:D006851), 2,2-Azobis (2-methylpropionamidine) dihydrochloride (MESH:C046728), 1-methyl-2-phenylindole (MESH:C520322), oxygen (MESH:D010100), MDA (MESH:D008315), LDL-C (-), cholesterol (MESH:D002784), peroxyl radicals (MESH:C049375), Lipid (MESH:D008055), TG (MESH:D014280), alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028847/full.md

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Source: https://tomesphere.com/paper/PMC13028847