# From Exposure to Atherosclerosis: Mechanistic Insights into Phthalate-Driven Ischemic Heart Disease and Prevention Strategies

**Authors:** Francesca Gorini, Alessandro Tonacci, Mariangela Palazzo, Andrea Borghini

PMC · DOI: 10.3390/life16020327 · 2026-02-13

## TL;DR

This paper reviews how phthalates, common plasticizers, may contribute to ischemic heart disease through mechanisms like oxidative stress and atherosclerosis.

## Contribution

The paper provides a comprehensive synthesis of phthalate-induced IHD mechanisms and novel prevention strategies using AI.

## Key findings

- Phthalates are linked to atherosclerosis through oxidative stress and mitochondrial dysfunction.
- Epidemiological and experimental evidence supports phthalate-induced endothelial damage and atherogenesis.
- AI-based frameworks could improve risk prediction and prevention of phthalate-related heart disease.

## Abstract

Despite decades of interventions targeting modifiable risk factors to reduce the burden of cardiovascular disease, ischemic heart disease (IHD) remains the leading cause of mortality and the second leading cause of disability-adjusted life-years worldwide. Growing evidence suggests that phthalates–plasticizers widely used in consumer products, cosmetics, and medical devices, and therefore ubiquitous across environmental media, may contribute to IHD development. Epidemiological studies have reported associations between phthalate exposure and multiple markers of atherosclerosis, the pathological hallmark of IHD, with or without mediation by traditional cardiovascular risk factors. Experimental models support these findings, showing that phthalates can induce oxidative stress, mitochondrial dysfunction, apoptosis, lipid accumulation, and epigenetic alterations, all of which promote endothelial damage and atherogenesis. In this review, we synthesize current epidemiological findings linking phthalate exposure to IHD, describe the main cellular and molecular mechanisms involved, and outline research gaps and regulatory perspectives. We also discuss how novel analytical frameworks—including artificial intelligence—may enhance the integration of environmental, clinical, and molecular data to advance risk prediction and prevention strategies.

## Linked entities

- **Diseases:** ischemic heart disease (MONDO:0024644), atherosclerosis (MONDO:0005311)

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Crp (C-reactive protein, pentraxin-related) [NCBI Gene 12944], NMRK2 (nicotinamide riboside kinase 2) [NCBI Gene 27231] {aka ITGB1BP3, MIBP, NRK2}, PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, SPHK1 (sphingosine kinase 1) [NCBI Gene 8877] {aka SPHK}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, GP9 (glycoprotein IX platelet) [NCBI Gene 2815] {aka CD42a, GPIX}, CEBPA (CCAAT enhancer binding protein alpha) [NCBI Gene 1050] {aka C/EBP-alpha, CEBP}, FABP4 (fatty acid binding protein 4) [NCBI Gene 2167] {aka A-FABP, AFABP, ALBP, HEL-S-104, aP2}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, POLK (DNA polymerase kappa) [NCBI Gene 51426] {aka DINB1, DINP, POLQ}, NR1I2 (nuclear receptor subfamily 1 group I member 2) [NCBI Gene 8856] {aka BXR, ONR1, PAR, PAR1, PAR2, PARq}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, FASLG (Fas ligand) [NCBI Gene 356] {aka ALPS1B, APT1LG1, APTL, CD178, CD95-L, CD95L}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, GSDMD (gasdermin D) [NCBI Gene 79792] {aka DF5L, DFNA5L, FKSG10, GSDMDC1}, Sphk1 (sphingosine kinase 1) [NCBI Gene 20698] {aka 1110006G24Rik, Sk1, Spk1}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, SMN1 (survival of motor neuron 1, telomeric) [NCBI Gene 6606] {aka BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3}, MAP1LC3A (microtubule associated protein 1 light chain 3 alpha) [NCBI Gene 84557] {aka ATG8E, LC3, LC3A, MAP1ALC3, MAP1BLC3}, GAS5 (growth arrest specific 5) [NCBI Gene 60674] {aka NCRNA00030, SNHG2}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}, MYOCD (myocardin) [NCBI Gene 93649] {aka MGBL, MYCD}, MIR155 (microRNA 155) [NCBI Gene 406947] {aka MIRN155, miRNA155, mir-155}, CYCS (cytochrome c, somatic) [NCBI Gene 54205] {aka CYC, HCS, THC4}, MBP (myelin basic protein) [NCBI Gene 4155], ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, ANXA5 (annexin A5) [NCBI Gene 308] {aka ANX5, CPB-I, ENX2, HEL-S-7, PP4, RPRGL3}, gc (GC vitamin D binding protein) [NCBI Gene 436841] {aka zgc:110389, zgc:92753}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, SELP (selectin P) [NCBI Gene 6403] {aka CD62, CD62P, GMP140, GRMP, LECAM3, PADGEM}, ACSL4 (acyl-CoA synthetase long chain family member 4) [NCBI Gene 2182] {aka ACS4, FACL4, LACS4, MRX63, MRX68, XLID63}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}, PYCARD (PYD and CARD domain containing) [NCBI Gene 29108] {aka ASC, CARD5, TMS, TMS-1, TMS1}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, CTSL (cathepsin L) [NCBI Gene 1514] {aka CATL, CTSL1, MEP}, SCNN1G (sodium channel epithelial 1 subunit gamma) [NCBI Gene 6340] {aka BESC3, ENaCg, ENaCgamma, LDLS2, PHA1, PHA1B3}, FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, CASP1 (caspase 1) [NCBI Gene 834] {aka ICE, IL1BC, P45}, CD14 (CD14 molecule) [NCBI Gene 929], ECE1 (endothelin converting enzyme 1) [NCBI Gene 1889] {aka ECE}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, TAGLN (transgelin) [NCBI Gene 6876] {aka SM22, SM22-alpha, SMCC, TAGLN1, TGLN, WS3-10}, SCNN1A (sodium channel epithelial 1 subunit alpha) [NCBI Gene 6337] {aka BESC2, ENaCa, ENaCalpha, LIDLS3, PHA1B1, SCNEA}, SP1 (Sp1 transcription factor) [NCBI Gene 6667], NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, CTSB (cathepsin B) [NCBI Gene 1508] {aka APPS, CPSB, KWE, RECEUP}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, S1pr2 (sphingosine-1-phosphate receptor 2) [NCBI Gene 14739] {aka 1100001A16Rik, Edg5, Gpcr13, H218, LPb2, S1P2}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, SERPINE1 (serpin family E member 1) [NCBI Gene 5054] {aka PAI, PAI-1, PAI1, PLANH1}
- **Diseases:** angina pectoris (MESH:D000787), ischemic (MESH:D002545), endothelial damage (MESH:D014652), diabetes (MESH:D003920), cancer (MESH:D009369), dyslipidemia (MESH:D050171), chronic coronary syndrome (MESH:D054058), CHD (MESH:D003327), Mitochondrial DNA Alterations and Dysfunction (MESH:D028361), Disease (MESH:D004194), injury to (MESH:D014947), Inflammation (MESH:D007249), cardiac fibrosis (MESH:D005355), cardiometabolic disease (MESH:D024821), hyperglycemia (MESH:D006943), carotid plaques (MESH:D016893), stenosis (MESH:D003251), cardiotoxic (MESH:D066126), ischemia (MESH:D007511), metabolic disorders (MESH:D008659), myocardial damage (MESH:D009202), mtDNA injury (MESH:C536350), stroke (MESH:D020521), apolipoprotein E-deficient (MESH:C566260), overweight (MESH:D050177), AI (MESH:C538142), obesity (MESH:D009765), bone and joint problems (MESH:D001847), endothelial injury (MESH:D057772), toxicity (MESH:D064420), insulin resistance (MESH:D007333), AMI (MESH:D009203), CVD (MESH:D002318), COVID-19 (MESH:D000086382), IHD (MESH:D017202), embryonal carcinoma (MESH:D018236), endocrine disruptors (MESH:D004700), ischemic stroke (MESH:D002544), EBP (MESH:D006973), DIDP (MESH:D003643), atherogenesis (MESH:D050197), carotid atherosclerosis (MESH:D002340), Stress (MESH:D000079225), thrombosis (MESH:D013927), birth (MESH:D000014), tissue injury (MESH:D017695), Atherosclerotic plaques (MESH:D058226), Coronary (MESH:D003323), pathology (MESH:D005598), liver toxicity (MESH:D056486), CAC (MESH:D003324), Cardiac (MESH:D006331), T2D (MESH:D003924), membrane damage (MESH:D015433), mitochondrial fragmentation (MESH:D012892), peripheral arterial disease (MESH:D058729), transient ischemic attacks (MESH:D002546), hypercholesterolemia (MESH:D006937), heart failure (MESH:D006333), Calcium (MESH:D002128)
- **Chemicals:** DnBP (MESH:C018527), substances (MESH:C012600), triglyceride (MESH:D014280), esters (MESH:D004952), 2',7'-dichlorodihydrofluorescein diacetate (MESH:C110400), polymer (MESH:D011108), DnOP (MESH:C010715), acid (MESH:D000143), mono-methyl phthalate (MESH:C517284), PI (MESH:D010716), DIBP (MESH:C025605), MCPP (MESH:C015068), MECPP (MESH:C078327), DEP (MESH:C007379), mono-n-butyl phthalate (MESH:C028577), cholesterol (MESH:D002784), nitric oxide (MESH:D009569), iodide (MESH:D007454), 8-OHdG (MESH:D000080242), MEHP (MESH:C016599), ceramide (MESH:D002518), DEHP (MESH:D004051), MBzP (MESH:C103325), testosterone (MESH:D013739), DCFH-DA (MESH:C029569), thiobarbituric acid (MESH:C029684), bisphenol A (MESH:C006780), CCK-8 (MESH:D012844), MEOHP (MESH:C080276), 5-methylcytosine (MESH:D044503), water (MESH:D014867), DIDP (MESH:C042080), BBP (MESH:C027561), di-n-butyl phthalate (MESH:D003993), 5-methyl-2'-deoxycytidine (MESH:C016569), MDA (MESH:D008315), fatty acid (MESH:D005227), polyvinyl chloride (MESH:D011143), dG (MESH:D003849), MTT (MESH:C070243), JC-1 (MESH:C068624), Phthalate (MESH:C032279), mono-isobutyl phthalate (MESH:C575690), sodium (MESH:D012964), polychlorinated biphenyls (MESH:D011078), propidium iodide (MESH:D011419), 2-ethylhexyl phthalate (-), DMP (MESH:C024629), dioxins (MESH:D004147), NO (MESH:D009614), DCHP (MESH:C036042), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), creatinine (MESH:D003404), phthalic anhydride (MESH:C043103), glucose (MESH:D005947), diisononyl phthalate (MESH:C012125), ROS (MESH:D017382), calcium (MESH:D002118), sphingolipid (MESH:D013107), PMP (MESH:C091421)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Danio rerio (leopard danio, species) [taxon 7955]
- **Cell lines:** 3T3-L1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0123), CCK-8 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_2873), THP-1 — Homo sapiens (Human), Childhood acute monocytic leukemia, Cancer cell line (CVCL_0006), VSMC — Homo sapiens (Human), Finite cell line (CVCL_4009), smooth muscle — Homo sapiens (Human), Finite cell line (CVCL_F640), EA.hy926 — Homo sapiens (Human), Hybrid cell line (CVCL_3901)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942049/full.md

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Source: https://tomesphere.com/paper/PMC12942049