# Beyond Taste: The Impact of Chocolate on Cardiovascular and Steatotic Liver Disease Risk Factors

**Authors:** Júlia Mayumi Tomaru, Iara Ribeiro Nunes, Caroline Fernandes de Souza Santiago, Alda Maria Machado Bueno Otoboni, Claudemir Gregorio Mendes, Adriana Maria Ragassi Fiorini, Elen Landgraf Guiguer, Claudia Cristina Teixeira Nicolau, Antonelly Cassio Alves Carvalho, Caio Sérgio Galina Spilla, José Luiz Yanaguizawa Junior, Vitor Engrácia Valenti, Ricardo de Alvares Goulart, Luiz Carlos de Abreu, Lucas Fornari Laurindo, Sandra Maria Barbalho

PMC · DOI: 10.3390/nu18040636 · 2026-02-14

## TL;DR

Dark chocolate may help reduce risks of heart disease and fatty liver by improving factors like inflammation and cholesterol, though more research is needed.

## Contribution

This review uniquely integrates evidence on chocolate's effects on both cardiovascular and liver health, highlighting shared mechanisms.

## Key findings

- Chocolate improves flow-mediated dilation and lipid profiles, including increased HDL-c and reduced LDL-c.
- It reduces intestinal permeability and endotoxemia while increasing plasma polyphenols.
- Chocolate consumption may attenuate hepatocyte apoptosis and improve platelet function.

## Abstract

Cardiovascular diseases and metabolic dysfunction-associated steatotic liver disease (MASLD) are increasing sharply worldwide and share overlapping pathophysiological pathways, including oxidative stress, inflammation, hyperglycemia, obesity, dyslipidemia, and hypertension. Dark chocolate, rich in cocoa flavanols such as epicatechin and catechin, exhibits antioxidant and anti-inflammatory effects. Based on these properties, this narrative review uniquely integrates evidence on chocolate’s effects on both cardiovascular and hepatic health, exploring shared mechanisms and clinical implications. Evidence from clinical studies suggests that chocolate modulates nitric oxide bioavailability and NADPH oxidase activity. Clinical findings demonstrate improvements in flow-mediated dilation, decreased NT-proBNP, reduced intestinal permeability and endotoxemia, improved lipid profile (increased HDL-c and reduced total cholesterol, LDL-c, and triglycerides), increased plasma polyphenols, improved platelet function, and attenuated hepatocyte apoptosis. These findings suggest a potential role for cocoa flavanol-rich dark chocolate in cardiometabolic health; however, the evidence remains preliminary and is limited by heterogeneous study designs, small sample sizes, and short intervention durations. Despite these limitations, current evidence supports the inclusion of moderate dark chocolate consumption as a possible adjunct strategy to mitigate cardiometabolic and hepatic metabolic risks. Further large-scale, long-term trials are needed to confirm these beneficial effects and to standardize the dosage and formulation of cocoa flavanols.

## Linked entities

- **Chemicals:** epicatechin (PubChem CID 1203), catechin (PubChem CID 1203)
- **Diseases:** metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), obesity (MONDO:0011122), dyslipidemia (MONDO:0002525)

## Full-text entities

- **Genes:** AP-1 [NCBI Gene 18593467], Glutathione S-transferase [NCBI Gene 18613516]
- **Diseases:** preeclampsia (MESH:D011225), DM2 (MESH:D009223), insulin resistance (MESH:D007333), FMD (MESH:D002311), CVD (MESH:D002318), non-alcoholic fatty liver disease (MESH:D065626), gastrointestinal and hepatic (MESH:D005767), diabetes (MESH:D003920), Endothelial Dysfunction (MESH:D014652), ischemic heart disease (MESH:D017202), cancer (MESH:D009369), Hypertension (MESH:D006973), death (MESH:D003643), dyslipidemia (MESH:D050171), mitochondrial dysfunction (MESH:D028361), coronary heart disease (MESH:D003327), atherogenic (MESH:D050197), injury to (MESH:D014947), Cardiovascular and Steatotic Liver Disease (MESH:D008107), conditions (MESH:D020763), Inflammation (MESH:D007249), platelet aggregation (MESH:D001791), fibrosis (MESH:D005355), endotoxemia (MESH:D019446), MetS (MESH:D024821), hyperglycemia (MESH:D006943), chronic diseases (MESH:D002908), Metabolic disorders (MESH:D008659), glucose intolerance (MESH:D018149), lipid disorders (MESH:D011017), hepatic (MESH:D056486), prehypertension (MESH:D058246), coronary artery disease (MESH:D003324), systemic (MESH:D015619), overweight (MESH:D050177), stroke (MESH:D020521), liver and gastrointestinal disorders (MESH:D017093), Peripheral Artery Disease (MESH:D058729), MASH (MESH:D005234), Diabetes Mellitus type II (MESH:D003924), weight gain (MESH:D015430), organ dysfunction (MESH:D009102), heart failure (MESH:D006333), NASH (MESH:D005235), Obesity (MESH:D009765), depression (MESH:D003866), inflammatory bowel disease (MESH:D015212)
- **Chemicals:** triglyceride (MESH:D014280), ADP (MESH:D000244), amines (MESH:D000588), tricarboxylic acid (MESH:D014233), flavonols (MESH:D044948), theobromine (MESH:D013805), MC (MESH:C061001), Saturated Fatty Acids (MESH:D005227), carbohydrates (MESH:D002241), aspartic acid (MESH:D001224), methylxanthines (MESH:C008514), procyanidins (MESH:D044945), flavanones (MESH:D044950), PUFA (MESH:D005231), acids (MESH:D000143), sugar (MESH:D000073893), caffeine (MESH:D002110), Dark Chocolate (-), superoxide (MESH:D013481), flavan-3-ol (MESH:C404987), fat (MESH:D005223), clopidogrel (MESH:D000077144), hydrogen peroxide (MESH:D006861), histamine (MESH:D006632), glucose (MESH:D005947), serotonin (MESH:D012701), NR (MESH:C018613), flavonoid (MESH:D005419), NO (MESH:D009569), cholesterol (MESH:D002784), hydroxyl (MESH:D017665), ROS (MESH:D017382), phenylethylamine (MESH:D010627), lysine (MESH:D008239), isoprostanes (MESH:D028421), GA (MESH:D005708), flavones (MESH:D047309), oxysterols (MESH:D000072376), tryptophan (MESH:D014364), CD (MESH:D002104), anthocyanins (MESH:D000872), glutamic acid (MESH:D018698), DC (MESH:D003841), LPS (MESH:D008070), acetyl-CoA (MESH:D000105), Lipids (MESH:D008055), phenolic acids (MESH:C017616), resmetirom (MESH:C588408), GAL (MESH:C101993), (-)-epicatechin (MESH:D002392), aspirin (MESH:D001241), Lycopene (MESH:D000077276), leucine (MESH:D007930), Polyphenols (MESH:D059808), ATP (MESH:D000255), AGEs (MESH:D017127)
- **Species:** Theobroma cacao (cacao, species) [taxon 3641], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], gut metagenome (species) [taxon 749906]
- **Cell lines:** CaCo-2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025)

## Figures

17 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943539/full.md

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Source: https://tomesphere.com/paper/PMC12943539