Abstract
Drug-eluting stents are frequently employed in cardiovascular coronary revascularization procedures, primarily because of their capacity to limit intimal hyperplasia. Stent stenosis has the potential to manifest within the artery that has been treated, which can ultimately result in procedural failure. One potential factor that may contribute to this failure is the genetic composition of the patients. The aim of this study is to investigate the correlation between genetic diversity, as reported in existing literature, and the incidence of coronary revascularization subsequent to angioplasty and the use of drug-eluting stents. Consequently, the involvement of various genetic systems, including antioxidant genes, the inflammatory system, the renin angiotensin system, the anticoagulant system, and the homeostasis system, is assessed in the context of stent restenosis. In conclusion, the utilization of genetic diagnosis for the NOS3, AGT, ACE, and CYP2C19 genes holds promise in improving treatment outcomes through the implementation of personalized interventions to tackle coronary stent restenosis.
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References
Buccheri, D., Piraino, D., Andolina, G., Cortese, B.: Understanding and managing in-stent restenosis: a review of clinical data, from pathogenesis to treatment. J. Thoracic Disease 8(10), E1150–E1162 (2016). https://doi.org/10.21037/jtd.2016.10.93
Virmani, R., Kolodgie, F.D., Finn, A.V., Gold, H.K.: Pathological Anatomy of Restenosis. In: Duckers, H.J., Nabel, E.G., Serruys, P.W. (eds.) Essentials of Restenosis, pp. 47–58. Humana Press, Totowa, NJ (2007). https://doi.org/10.1007/978-1-59745-001-0_4
Farooq, V., Gogas, B.D., Serruys, P.W.: Restenosis. Circ. Cardiovasc. Interv. 4(2), 195–205 (2011).https://doi.org/10.1161/CIRCINTERVENTIONS.110.959882
Omeh, D.J., Restenosis, E.S.: StatPearls Publishing (2020). Consulté le: 13 août 2021. [En ligne]. Disponible sur: https://www.ncbi.nlm.nih.gov/books/NBK545139/
Geary, R.L., Koudy Williams, J., Golden, D., Brown, D.G., Benjamin, M.E., Adams, M.R.: Time course of cellular proliferation, intimal hyperplasia, and remodeling following angioplasty in monkeys with established atherosclerosis: a nonhuman primate model of restenosis. Arteriosclerosis, Thrombosis, Vascular Biol. 16(1), 34–43 (1996). https://doi.org/10.1161/01.ATV.16.1.34
Mintz, G.S., et al.: Arterial remodeling after coronary angioplasty: a serial intravascular ultrasound study. Circulation 94(1), 35–43 (1996). https://doi.org/10.1161/01.cir.94.1.35
Sheppard Mondy, J., Koudy Williams, J., Adams, M.R., Dean, R.H., Geary, R.L.: Structural determinants of lumen narrowing after angioplasty in atherosclerotic nonhuman primates. J. Vascular Surg. 26(5), 875–883 (1997). https://doi.org/10.1016/S0741-5214(97)70103-4
Dai, Z., et al.: Mean platelet volume as a predictor for restenosis after carotid angioplasty and stenting. Stroke 49(4), 872–876 (2018). https://doi.org/10.1161/STROKEAHA.117.019748
Fox, J.: Platelet biology and restenosis. Restenosis Summit VIII Clevel. Clin. Heart Cent., p. 234 (1996)
Bornfeldt, K.E., Raines, E.W., Nakano, T., Graves, L.M., Krebs, E.G., Ross, R.: Insulin-like growth factor-I and platelet-derived growth factor-BB induce directed migration of human arterial smooth muscle cells via signaling pathways that are distinct from those of proliferation. J. Clin. Invest.Clin. Invest. 93(3), 1266–1274 (1994)
Huang, C., Mei, H., Zhou, M., Zheng, X.: A novel PDGF receptor inhibitor-eluting stent attenuates in-stent neointima formation in a rabbit carotid model. Molecular Med. Reports 15(1), 21–28 (2017). https://doi.org/10.3892/mmr.2016.5986
Jingzhou Chen, Y., et al.: PDGF-D contributes to neointimal hyperplasia in rat model of vessel injury. Biochem. Biophys. Res. Commun.. Biophys. Res. Commun. 329(3), 976–983 (2005). https://doi.org/10.1016/j.bbrc.2005.02.062
Kirchner, G.I., Meier-Wiedenbach, I., Manns, M.P.: Clinical pharmacokinetics of everolimus. Clin. Pharmacokinet. 43(2), 83–95 (2004). https://doi.org/10.2165/00003088-200443020-00002
Bae, I.-H., et al.: Novel polymer-free everolimus-eluting stent fabricated using femtosecond laser improves re-endothelialization and anti-inflammation. Sci. Rep. 8(1), 7383 (2018). https://doi.org/10.1038/s41598-018-25629-9
Wang, W., Wang, B., Chen, Y., Wei, S.: Late stent thrombosis after drug-coated balloon coronary angioplasty for in-stent restenosis: a case report. Int. Heart J. 62(1), 171–174 (2021). https://doi.org/10.1536/ihj.20-309
Seawright, J.W., et al.: Vascular smooth muscle contractile function declines with age in skeletal muscle feed arteries. Front. Physiol. 9, 856 (2018). https://doi.org/10.3389/fphys.2018.00856
Huckle, W.R., et al.: Effects of subtype-selective and balanced angiotensin II receptor antagonists in a porcine coronary artery model of vascular restenosis. Circulation 93(5), 1009–1019 (1996). https://doi.org/10.1161/01.CIR.93.5.1009
Ichikawa, N., et al.: Angiotensin II type 1 receptor blockers suppress neointimal hyperplasia after stent implantation in carotid arteries of hypercholesterolemic rabbits. Neurol. Res. 37(2), 147–152 (2015). https://doi.org/10.1179/1743132814Y.0000000436
Yoshikawa, M., et al.: Effects of Combined Treatment with Angiotensin II Type 1 Receptor Blocker and Statin on Stent Restenosis. J. Cardiovasc. Pharmacol.Cardiovasc. Pharmacol. 53(2), 179–186 (2009). https://doi.org/10.1097/FJC.0b013e318199f30b
Tang, B., et al.: Overexpression of angiotensin II type 2 receptor suppresses neointimal hyperplasia in a rat carotid arterial balloon injury model. Mol. Med. Rep. 4(2), 249–254 (2011). https://doi.org/10.3892/mmr.2011.433
Ahanchi, S.S., Tsihlis, N.D., Kibbe, M.R.: The role of nitric oxide in the pathophysiology of intimal hyperplasia. J. Vasc. Surg.Vasc. Surg. 45(6), A64–A73 (2007). https://doi.org/10.1016/j.jvs.2007.02.027
Wolf, Y.G., Rasmussen, L.M., Ruoslahti, E.: Antibodies against transforming growth factor-beta 1 suppress intimal hyperplasia in a rat model. J. Clin. Invest.Clin. Invest. 93(3), 1172–1178 (1994). https://doi.org/10.1172/JCI117070
Ryan, S.T., Koteliansky, V.E., Gotwals, P.J., Lindner, V.: Transforming growth factor- beta-dependent events in vascular remodeling following arterial injury. J. Vasc. Res.Vasc. Res. 40(1), 37–46 (2003). https://doi.org/10.1159/000068937
Guerri-Guttenberg, R.A., Castilla, R., Francos, G.C., Müller, A., Ambrosio, G., Milei, J.: Transforming growth factor β1 and coronary intimal hyperplasia in pediatric patients with congenital heart disease. Can. J. Cardiol.Cardiol. 29(7), 849–857 (2013). https://doi.org/10.1016/j.cjca.2012.11.018
Casscells, W., et al.: Elimination of smooth muscle cells in experimental restenosis: targeting of fibroblast growth factor receptors. Proc. Natl. Acad. Sci. 89(15), 7159–7163 (1992). https://doi.org/10.1073/pnas.89.15.7159
Clowes, A.W., Reidy, M.A., Clowes, M.M.: Kinetics of cellular proliferation after arterial injury. I. Smooth muscle growth in the absence of endothelium. Lab. Investig. J. Tech. Methods Pathol. 49(3), 327–333 (1983)
Marx, S.O., Marks, A.R.: Bench to Bedside. Circulation 104(8), 852–855 (2001). https://doi.org/10.1161/01.CIR.104.8.852
Dong, S.H., Frane, N.D., Christensen, Q.H., Greenberg, E.P., Nagarajan, R., Nair, S.K.: Molecular basis for the substrate specificity of quorum signal synthases. Proc. Natl. Acad. Sci. U.S.A. 114(34), 9092–9097 (2017). https://doi.org/10.1073/pnas.1705400114
Yang, D., et al.: Proliferation of vascular smooth muscle cells under inflammation is regulated by NF-κB p65/microRNA-17/RB pathway activation. Int. J. Molecular Med. 41(1), 43–50 (2017). https://doi.org/10.3892/ijmm.2017.3212
Howson, J.M.M., et al.: Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms. Nat. Genet. 49(7), 1113–1119 (2017). https://doi.org/10.1038/ng.3874
Zago, A.C., et al.: Identification of Genes Involved in Smooth Muscle Cell Protein Synthesis with Increased Expression in Atheromatous Plaques Associated with Neointimal Hyperplasia after Bare-Metal Stenting: A GENESIS-R Study. Revista Brasileira de Cardiologia Invasiva (English Edition) 20(2), 140–145 (2012). https://doi.org/10.1016/S2214-1235(15)30043-0
Kallenbach, K., Salcher, R., Heim, A., Karck, M., Mignatti, P., Haverich, A.: Inhibition of smooth muscle cell migration and neointima formation in vein grafts by overexpression of matrix metalloproteinase-3. J. Vasc. Surg.Vasc. Surg. 49(3), 750–758 (2009). https://doi.org/10.1016/j.jvs.2008.11.001
Sun, Q., et al.: Oral intake of hydrogen-rich water inhibits intimal hyperplasia in arterialized vein grafts in rats. Cardiovasc. Res.. Res. 94(1), 144–153 (2012). https://doi.org/10.1093/cvr/cvs024
Song, M.-J., et al.: Purification and characterization of Prodigiosin produced by integrated bioreactor from Serratia sp. KH-95. J. Biosci. Bioeng.Biosci. Bioeng. 101(2), 157–161 (2006). https://doi.org/10.1263/jbb.101.157
Kanta, K., et al.: The Effects of Chymase on matrix metalloproteinase-2 activation in neointimal hyperplasia after balloon injury in dogs. Hypertens. Res.. Res. 30(1), 77–83 (2007). https://doi.org/10.1291/hypres.30.77
Frants, R.R., (John) Kastelein, J.J.P., (Wouter) Jukema, J.W.: Genetic determinants of restenosis (GENDER). (1998). Consulté le: 10 février 2022. [En ligne]. Disponible sur: https://www.narcis.nl/research/RecordID/OND1277043
Hubert, C., Houot, A.M., Corvol, P., Soubrier, F.: Structure of the angiotensin I-converting enzyme gene. Two alternate promoters correspond to evolutionary steps of a duplicated gene. J. Biol. Chem. 266(23), 15377–15383 (1991)
Riordan, J.F.: Angiotensin-I-converting enzyme and its relatives. Genome Biol. 4(8), 225 (2003). https://doi.org/10.1186/gb-2003-4-8-225
Miao, H.-W., Gong, H.: Association of ACE insertion or deletion polymorphisms with the risk of coronary restenosis after percutaneous coronary intervention: a meta-analysis. J. Renin-Angiotensin-Aldosterone Syst. 16(4), 844–850 (2015). https://doi.org/10.1177/1470320315588233
Wang, S., et al.: Genetic polymorphism of angiotensin converting enzyme and risk of coronary restenosis after percutaneous transluminal coronary angioplasties: evidence from 33 cohort studies. PLoS ONE 8(9), e75285 (2013). https://doi.org/10.1371/journal.pone.0075285
Azova, M., et al.: Gene polymorphisms of the renin-angiotensin-aldosterone system as risk factors for the development of in-stent restenosis in patients with stable coronary artery disease. Biomolecules 11(5), 763 (2021). https://doi.org/10.3390/biom11050763
Thomas Michel, O.F.: Cell and molecular biology of nitric oxide synthases. In: Nitric Oxide and the Cardiovascular System, Joseph Loscalzo and Joseph A., p. 12–14‑15 (2000)
NOS3 nitric oxide synthase 3 [Homo sapiens (human)] - Gene - NCBI. https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=DetailsSearch&Term=4846 (consulté le 6 septembre 2021)
Ben Ali, M., Messaoudi, S., Ezzine, H., Mahjoub, T.: Contribution of eNOS Variants to the genetic susceptibility of coronary artery disease in a tunisian population. Genet. Test. Mol. Biomark. 19(4), 203–208 (2015). https://doi.org/10.1089/gtmb.2014.0261
Gomma, A.H., et al.: The endothelial nitric oxide synthase (Glu298Asp and –786T>C) gene polymorphisms are associated with coronary in-stent restenosis. Eur Heart J. 23(24), 8 (2002)
Derynck, R., et al.: Human transforming growth factor-β complementary DNA sequence and expression in normal and transformed cells. Nature 316(6030), 701–705 (1985). https://doi.org/10.1038/316701a0
TGFB1 Functional Gene Polymorphisms (C‐509T and T869C) in the Maternal Susceptibility to Pre‐eclampsia in South Indian Women - Deepthi - 2015 - Scandinavian Journal of Immunology - Wiley Online Library. https://onlinelibrary.wiley.com/doi/10.1111/sji.12342 (consulté le 5 juin 2022)
Osadnik, T., Lekston, A., Bujak, K., Strzelczyk, J.K., Poloński, L., Gąsior, M.: The Relationship between VEGFA and TGFB1 Polymorphisms and Target lesion revascularization after elective percutaneous coronary intervention. Dis. Markers 2017, 8165219 (2017). https://doi.org/10.1155/2017/8165219
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Elmansouri, R., Tazzite, A., Dehbi, H., Habbal, R. (2024). Gene’s Association with Coronary Stent Stenosis After Drug Eluting Stent: Review. In: Ezziyyani, M., Kacprzyk, J., Balas, V.E. (eds) International Conference on Advanced Intelligent Systems for Sustainable Development (AI2SD’2023). AI2SD 2023. Lecture Notes in Networks and Systems, vol 905. Springer, Cham. https://doi.org/10.1007/978-3-031-52385-4_39
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