# Electrocardiogram abnormalities in patients with acne undergoing isotretinoin therapy: a focused review

**Authors:** Afra Wasama Islam, Prarthana Motdhare, Shreya Mohan, Swapna Bejoy, Harsahaj Singh Wilkhoo

PMC · DOI: 10.1016/j.abd.2026.501304 · 2026-03-19

## TL;DR

This review examines the rare but potentially serious heart-related side effects of isotretinoin, a common acne treatment, and highlights the need for better monitoring and research.

## Contribution

The paper uniquely integrates dermatological and cardiac perspectives to address gaps in ECG monitoring and research on isotretinoin.

## Key findings

- ECG abnormalities with isotretinoin are rare, affecting fewer than 1%–2% of users.
- Most reported cardiac effects are reversible upon discontinuation of isotretinoin.
- Large studies have not found a significant increase in major cardiovascular events.

## Abstract

Isotretinoin is an extremely successful treatment for acne, widely prescribed for moderate to severe cases unresponsive to conventional therapy that is commonly used in dermatology. While its systemic side effects, particularly those related to hepatic and lipid metabolism, are extensively documented, its impact on cardiac electrophysiology is little understood. Metabolic abnormalities are frequent, with hypertriglyceridemia occurring in up to 44% of patients, elevated total cholesterol in 30%, and transient liver enzyme elevation in approximately 10%–11%. This focused review summarizes the existing research on electrocardiographic (ECG) alterations associated with isotretinoin medication. Reported cardiac abnormalities are rare, with isolated case reports and small studies describing transient arrhythmias in fewer than 1%–2% of users, including premature ventricular contractions (PVCs), atrial tachycardia, and, in exceptionally rare instances, cardiomyopathy < 0.01%. Mechanistic ideas suggest changes in human ether-a-go-go-related gene (hERG) potassium channels, dyslipidemia-induced atherosclerosis, electrolyte imbalances, and sympathetic overactivity. However, large population-based studies have not found a significant increase in major cardiovascular events. Most ECG abnormalities, when noted, appear to be reversible with discontinuing isotretinoin. This review is unique in that it focuses on isotretinoin from both dermatological and cardiac viewpoints. It identifies important shortcomings in standardized ECG monitoring procedures and underscores the scarcity of large, prospective, controlled trials. Future research should focus on longitudinal, multicenter trials using serial ECG evaluations to better define risk profiles and guide clinical monitoring. Understanding infrequent but potentially serious cardiac effects is critical for improving isotretinoin's safety profile and guiding evidence-based therapy.

## Linked entities

- **Genes:** KCNH2 (potassium voltage-gated channel subfamily H member 2) [NCBI Gene 3757]
- **Chemicals:** isotretinoin (PubChem CID 5282379)
- **Diseases:** acne (MONDO:0011438), hypertriglyceridemia (MONDO:0005347), cardiomyopathy (MONDO:0004994), atherosclerosis (MONDO:0005311)

## Full-text entities

- **Genes:** CYP2C8 (cytochrome P450 family 2 subfamily C member 8) [NCBI Gene 1558] {aka CPC8, CYP2C8DM, CYPIIC8, MP-12/MP-20}, CYP2C9 (cytochrome P450 family 2 subfamily C member 9) [NCBI Gene 1559] {aka CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9}, CYP2B6 (cytochrome P450 family 2 subfamily B member 6) [NCBI Gene 1555] {aka CPB6, CYP2B, CYP2B7, CYPIIB6, EFVM, IIB1}, TNFSF10 (TNF superfamily member 10) [NCBI Gene 8743] {aka APO2L, Apo-2L, CD253, TANCR, TL2, TNLG6A}, CYP4F3 (cytochrome P450 family 4 subfamily F member 3) [NCBI Gene 4051] {aka CPF3, CYP4F, CYPIVF3, LTB4H}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, LDLR (low density lipoprotein receptor) [NCBI Gene 3949] {aka LDLCQ2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, ERG (ETS transcription factor ERG) [NCBI Gene 2078] {aka LMPHM14, erg-3, p55}, PPIG (peptidylprolyl isomerase G) [NCBI Gene 9360] {aka CARS-Cyp, CYP, SCAF10, SRCyp}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, KCNH2 (potassium voltage-gated channel subfamily H member 2) [NCBI Gene 3757] {aka ERG-1, ERG1, H-ERG, HERG, HERG1, Kv11.1}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}
- **Diseases:** acne inflammation (MESH:D007249), Ventricular Tachycardia (MESH:D017180), arrhythmia (MESH:D001145), hypersensitivity (MESH:D004342), cheilitis (MESH:D002613), Chronic kidney disease (MESH:D051436), heart abnormalities (MESH:D006330), cardiac abnormalities (MESH:D018376), ORCID ID (MESH:C537985), DRESS (MESH:D063926), bradyarrhythmias (MESH:D001919), chest discomfort (MESH:D013898), cardiovascular, cerebrovascular, or thromboembolic (MESH:D013923), heart failure (MESH:D006333), eosinophilia (MESH:D004802), PVCs (MESH:D018879), ECG abnormalities (MESH:C566733), Acne vulgaris (MESH:D000152), Metabolic abnormalities (MESH:D008659), arrhythmic (OMIM:212500), sinus tachycardia (MESH:D013616), migraine with aura (MESH:D020325), Myocardial infarction (MESH:D009203), CKD (MESH:D012080), pericardial effusion (MESH:D010490), Lab abnormalities (MESH:D000014), shortening (MESH:C535850), cardiomyopathy (MESH:D009202), atherosclerosis (MESH:D050197), Venous thromboembolism (MESH:D054556), atrial tachycardia (MESH:D013617), laboratory abnormalities (MESH:D007757), dilated cardiomyopathy (MESH:D002311), Long QT syndrome (MESH:D008133), Hypokalemia (MESH:D007008), Right bundle branch block (MESH:D002037), QT interval elongation (OMIM:610141), T-wave abnormalities (MESH:D001260), cardiovascular adverse effects (MESH:D002318), Myocarditis (MESH:D009205), renal infarction (MESH:D007238), hypertriglyceridemia (MESH:D015228), cardiac dysfunction (MESH:D006331), conduction abnormalities (MESH:D054537), dizziness (MESH:D004244), syncope (MESH:D013575), Dyslipidemia (MESH:D050171), torsades de pointes (MESH:D016171), conduction anomalies (OMIM:617300), stroke (MESH:D020521)
- **Chemicals:** retinoic acid (MESH:D014212), P (MESH:D010758), spironolactone (MESH:D013148), tetracycline (MESH:D013752), retinoid (MESH:D012176), tazarotene (MESH:C086827), minocycline (MESH:D008911), phospholipids (MESH:D010743), 4-oxo-isotretinoin (MESH:C002202), doxycycline (MESH:D004318), Magnesium (MESH:D008274), lipid (MESH:D008055), K (MESH:D011188), Zinc (MESH:D015032), Triglycerides (MESH:D014280), vitamin A (MESH:D014801), Tetracyclines (MESH:D013754), fatty acid (MESH:D005227), adapalene (MESH:D000068816), 13-cis-retinoic acid (MESH:D015474), cholesterol (MESH:D002784), QT-prolonging medicines (-), TG (MESH:D013866), Ca (MESH:D002118)
- **Species:** Cutibacterium acnes (species) [taxon 1747], Gallus gallus (bantam, species) [taxon 9031], Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13015224/full.md

---
Source: https://tomesphere.com/paper/PMC13015224