# Tirzepatide and Cardiovascular Outcomes: A Narrative Review of Mechanisms, Efficacy and Implications for Heart Failure Management

**Authors:** Hamza A. Abdul‐Hafez, Ameer Awashra, Sosana Bdir, Sarah Saife, Qasem Salah, Mohammed Barbarawi, Thabet Swaileh, Ahmed Emara, Mohamed S. Elgendy, Abdalhakim Shubietah

PMC · DOI: 10.1002/edm2.70152 · 2026-01-22

## TL;DR

Tirzepatide, a new drug targeting heart failure, helps reduce weight and improve heart function in obesity-related cases.

## Contribution

This paper reviews tirzepatide's mechanisms and clinical outcomes, emphasizing its potential for obesity-related heart failure.

## Key findings

- Tirzepatide improves heart function and reduces heart failure events in obesity-related HFpEF.
- It shows renal stabilisation and minimal hypoglycemia risk.
- Data on HFrEF is limited and requires further study.

## Abstract

Tirzepatide, a dual GIP/GLP‐1 receptor agonist, offers a novel cardiometabolic strategy beyond glycemic control with important implications for heart failure care. By producing potent, sustained weight reduction and favourable changes in lipids, blood pressure, systemic inflammation and endothelial biology, tirzepatide targets central pathophysiologic drivers of obesity‐related HFpEF.

We conducted this review to synthesise current evidence on the mechanisms, clinical efficacy and therapeutic implications of tirzepatide for heart failure management, with emphasis on obesity‐related HFpEF, cardiorenal effects and safety considerations. Randomised clinical programmes and the SUMMIT outcomes trial have demonstrated symptomatic and functional improvements, reverse cardiac remodelling on imaging, reduced circulating markers of myocardial stress and fewer worsening heart‐failure events versus placebo, alongside signals of renal stabilisation.

The tolerability profile aligns with the GLP‐1 class, with gastrointestinal events predominating and a low risk of clinically important hypoglycemia; biliary events may be more likely at higher doses, while pancreatitis risk has not been clearly elevated. Data in HFrEF remain limited and caution is advised given prior mixed results with incretin therapies and theoretical concerns about rapid weight loss in advanced systolic failure.

This review integrates mechanistic insights and contemporary trial evidence to clarify how dual incretin agonism may modify the trajectory of obesity‐driven heart failure, to inform multidisciplinary clinical decision making, and to highlight key unanswered questions and research priorities needed to define tirzepatide's full role in heart failure management.

Integrated framework for tirzepatide in HFpEF management. Through metabolic, haemodynamic, structural and anti‐inflammatory pathways, tirzepatide modifies the disease trajectory of HFpEF, leading to improvements in symptoms, functional capacity and reduction in HF events.

## Linked entities

- **Chemicals:** tirzepatide (PubChem CID 163285897)
- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, GIPR (gastric inhibitory polypeptide receptor) [NCBI Gene 2696] {aka PGQTL2}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, CHI3L1 (chitinase 3 like 1) [NCBI Gene 1116] {aka ASRT7, CGP-39, GP-39, GP39, HC-gp39, HCGP-3P}, NPPA (natriuretic peptide A) [NCBI Gene 4878] {aka ANF, ANP, ATFB6, ATRST2, CDD, CDD-ANF}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, SLC9A3 (solute carrier family 9 member A3) [NCBI Gene 6550] {aka DIAR8, NHE-3, NHE3}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, SST (somatostatin) [NCBI Gene 6750] {aka SMST, SST1}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, APOC3 (apolipoprotein C3) [NCBI Gene 345] {aka APOCIII, Apo-C3, ApoC-3}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** MEN-2 (MESH:D018813), congestion (MESH:D002311), developmental abnormalities (MESH:D006130), abortion (MESH:D000026), T2D (MESH:D003924), cardiac abnormality (MESH:D018376), cachexia (MESH:D002100), muscle loss (MESH:D009135), ectopic pregnancy (MESH:D011271), vascular stiffness (MESH:C566112), hypoglycemia (MESH:D007003), GI adverse effects (MESH:D064420), BP (MESH:D007022), HFpEF (MESH:D054144), growth restriction (MESH:D005317), visceral adiposity (MESH:D007418), thyroid C-cell tumours (MESH:D013964), biliary problems (MESH:D001658), stroke (MESH:D020521), dyspepsia (MESH:D004415), Obesity (MESH:D009765), volume overload (MESH:D019190), frailty (MESH:D000073496), ischemic (MESH:D002545), gallbladder disease (MESH:D005705), psychiatric (MESH:D001523), hypertension (MESH:D006973), decreased appetite (MESH:D001068), systemic (MESH:D015619), cardiac loading (MESH:C536761), cardiac remodelling (MESH:D020257), thyroid nodules (MESH:D016606), hyperglycemia (MESH:D006943), vomiting (MESH:D014839), kidney failure (MESH:D051437), Endothelial dysfunction (MESH:D014652), albuminuria (MESH:D000419), chronic kidney disease (MESH:D051436), hypertrophy (MESH:D006984), adiposity (MESH:D018205), myocardial infarction (MESH:D009203), ischemic heart disease (MESH:D017202), cardiorenal syndrome (MESH:D059347), Cardiomyopathy (MESH:D009202), LA (MESH:C535395), arrhythmia (MESH:D001145), diarrhoea (MESH:D003967), metabolic dysfunction (MESH:D008659), pulmonary or systemic congestion (MESH:D001261), Inflammation (MESH:D007249), renal impairment (MESH:D007674), dyslipidemia (MESH:D050171), venous congestion (MESH:D006940), cholecystitis (MESH:D002764), CKD (MESH:D012080), medullary thyroid carcinoma (MESH:C536914), depression (MESH:D003866), pancreatitis (MESH:D010195), atherogenic (MESH:D050197), orthostatic symptoms (MESH:D006261)
- **Chemicals:** GLP-1RA (-), nitric oxide (MESH:D009569), sodium (MESH:D012964), creatinine (MESH:D003404), 8-iso-PGF2alpha (MESH:C075750), Lipids (MESH:D008055), NO (MESH:D009614), sulfonylureas (MESH:D013453), RA (MESH:D011883), glucose (MESH:D005947), cholesterol (MESH:D002784), glycemia (MESH:D001786), triglyceride (MESH:D014280), BP (MESH:C038809), TC (MESH:D013667), MRA (MESH:C502936), exenatide (MESH:D000077270), reactive oxygen species (MESH:D017382)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12824524/full.md

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Source: https://tomesphere.com/paper/PMC12824524