Pathological findings after third- and second-generation everolimus-eluting stent implantations in coronary arteries from autopsy cases and an atherosclerotic porcine model
Pathological changes after third-generation drug-eluting stent implantation remain unclear. We compared the tissue responses of coronary arteries after the implantation of third-generation abluminal biodegradable-polymer everolimus-eluting stent (3rd EES) and second-generation durable-polymer EES (2...
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Published in | Scientific reports Vol. 11; no. 1; p. 6281 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
18.03.2021
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Abstract | Pathological changes after third-generation drug-eluting stent implantation remain unclear. We compared the tissue responses of coronary arteries after the implantation of third-generation abluminal biodegradable-polymer everolimus-eluting stent (3rd EES) and second-generation durable-polymer EES (2nd EES) using autopsy specimens and an atherosclerotic porcine model. We compared the histology of stented coronary arteries obtained by autopsy performed 1–10 months after 3rd EES (n (number of cases) = 4, stent-implanted period of 3–7 months) and 2nd EES (n (number of cases) = 9, stent-implanted period of 1–10 months) implantations. The ratio of covered stent struts was higher with 3rd EESs than with 2nd EESs (3rd; 0.824 ± 0.032 vs. 2nd; 0.736 ± 0.022,
p
= 0.035). Low-density lipoprotein receptor knockout minipigs were stented with 3rd or 2nd EES in the coronary arteries and the stented regions were investigated. The fibrin deposition around the 2nd EES was more prominent. Additionally, higher density of smooth muscle cells was confirmed after the 3rd EES implantation. Pathological examination after the 3rd EES demonstrated a combination of less fibrin deposition and more rapid acquisition of well-developed neointima as compared to the 2nd EES at autopsy and the atherosclerotic porcine model. |
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AbstractList | Pathological changes after third-generation drug-eluting stent implantation remain unclear. We compared the tissue responses of coronary arteries after the implantation of third-generation abluminal biodegradable-polymer everolimus-eluting stent (3rd EES) and second-generation durable-polymer EES (2nd EES) using autopsy specimens and an atherosclerotic porcine model. We compared the histology of stented coronary arteries obtained by autopsy performed 1–10 months after 3rd EES (n (number of cases) = 4, stent-implanted period of 3–7 months) and 2nd EES (n (number of cases) = 9, stent-implanted period of 1–10 months) implantations. The ratio of covered stent struts was higher with 3rd EESs than with 2nd EESs (3rd; 0.824 ± 0.032 vs. 2nd; 0.736 ± 0.022, p = 0.035). Low-density lipoprotein receptor knockout minipigs were stented with 3rd or 2nd EES in the coronary arteries and the stented regions were investigated. The fibrin deposition around the 2nd EES was more prominent. Additionally, higher density of smooth muscle cells was confirmed after the 3rd EES implantation. Pathological examination after the 3rd EES demonstrated a combination of less fibrin deposition and more rapid acquisition of well-developed neointima as compared to the 2nd EES at autopsy and the atherosclerotic porcine model. Pathological changes after third-generation drug-eluting stent implantation remain unclear. We compared the tissue responses of coronary arteries after the implantation of third-generation abluminal biodegradable-polymer everolimus-eluting stent (3rd EES) and second-generation durable-polymer EES (2nd EES) using autopsy specimens and an atherosclerotic porcine model. We compared the histology of stented coronary arteries obtained by autopsy performed 1–10 months after 3rd EES (n (number of cases) = 4, stent-implanted period of 3–7 months) and 2nd EES (n (number of cases) = 9, stent-implanted period of 1–10 months) implantations. The ratio of covered stent struts was higher with 3rd EESs than with 2nd EESs (3rd; 0.824 ± 0.032 vs. 2nd; 0.736 ± 0.022, p = 0.035). Low-density lipoprotein receptor knockout minipigs were stented with 3rd or 2nd EES in the coronary arteries and the stented regions were investigated. The fibrin deposition around the 2nd EES was more prominent. Additionally, higher density of smooth muscle cells was confirmed after the 3rd EES implantation. Pathological examination after the 3rd EES demonstrated a combination of less fibrin deposition and more rapid acquisition of well-developed neointima as compared to the 2nd EES at autopsy and the atherosclerotic porcine model. Pathological changes after third-generation drug-eluting stent implantation remain unclear. We compared the tissue responses of coronary arteries after the implantation of third-generation abluminal biodegradable-polymer everolimus-eluting stent (3rd EES) and second-generation durable-polymer EES (2nd EES) using autopsy specimens and an atherosclerotic porcine model. We compared the histology of stented coronary arteries obtained by autopsy performed 1-10 months after 3rd EES (n (number of cases) = 4, stent-implanted period of 3-7 months) and 2nd EES (n (number of cases) = 9, stent-implanted period of 1-10 months) implantations. The ratio of covered stent struts was higher with 3rd EESs than with 2nd EESs (3rd; 0.824 ± 0.032 vs. 2nd; 0.736 ± 0.022, p = 0.035). Low-density lipoprotein receptor knockout minipigs were stented with 3rd or 2nd EES in the coronary arteries and the stented regions were investigated. The fibrin deposition around the 2nd EES was more prominent. Additionally, higher density of smooth muscle cells was confirmed after the 3rd EES implantation. Pathological examination after the 3rd EES demonstrated a combination of less fibrin deposition and more rapid acquisition of well-developed neointima as compared to the 2nd EES at autopsy and the atherosclerotic porcine model. Abstract Pathological changes after third-generation drug-eluting stent implantation remain unclear. We compared the tissue responses of coronary arteries after the implantation of third-generation abluminal biodegradable-polymer everolimus-eluting stent (3rd EES) and second-generation durable-polymer EES (2nd EES) using autopsy specimens and an atherosclerotic porcine model. We compared the histology of stented coronary arteries obtained by autopsy performed 1–10 months after 3rd EES (n (number of cases) = 4, stent-implanted period of 3–7 months) and 2nd EES (n (number of cases) = 9, stent-implanted period of 1–10 months) implantations. The ratio of covered stent struts was higher with 3rd EESs than with 2nd EESs (3rd; 0.824 ± 0.032 vs. 2nd; 0.736 ± 0.022, p = 0.035). Low-density lipoprotein receptor knockout minipigs were stented with 3rd or 2nd EES in the coronary arteries and the stented regions were investigated. The fibrin deposition around the 2nd EES was more prominent. Additionally, higher density of smooth muscle cells was confirmed after the 3rd EES implantation. Pathological examination after the 3rd EES demonstrated a combination of less fibrin deposition and more rapid acquisition of well-developed neointima as compared to the 2nd EES at autopsy and the atherosclerotic porcine model. |
ArticleNumber | 6281 |
Author | Okumura, Yasuo Hao, Hiroyuki Tsujimoto, Masahiko Li, Yuxin Matsuyama, Taka-aki Fuchimoto, Daiichiro Suzuki, Shunichi Koyama, Yutaka Hirota, Seiichi Nakamura, Yoshiyuki Shimodai-Yamada, Sayaka Sakuma, Masashi Kitano, Daisuke Hirayama, Atsushi Onishi, Akira Migita, Suguru |
Author_xml | – sequence: 1 givenname: Suguru surname: Migita fullname: Migita, Suguru organization: Division of Human Pathology, Department of Pathology and Microbiology, Nihon University School of Medicine, Division of Cardiology, Department of Medicine, Nihon University School of Medicine – sequence: 2 givenname: Daisuke surname: Kitano fullname: Kitano, Daisuke organization: Division of Cardiology, Department of Medicine, Nihon University School of Medicine – sequence: 3 givenname: Yuxin surname: Li fullname: Li, Yuxin email: li.yuxin@nihon-u.ac.jp organization: Division of Cell Regeneration and Transplantation, Department of Functional Morphology, Nihon University School of Medicine – sequence: 4 givenname: Yutaka surname: Koyama fullname: Koyama, Yutaka organization: Division of Human Pathology, Department of Pathology and Microbiology, Nihon University School of Medicine, Division of Cardiology, Department of Medicine, Nihon University School of Medicine – sequence: 5 givenname: Sayaka surname: Shimodai-Yamada fullname: Shimodai-Yamada, Sayaka organization: Division of Human Pathology, Department of Pathology and Microbiology, Nihon University School of Medicine – sequence: 6 givenname: Akira surname: Onishi fullname: Onishi, Akira organization: Department of Animal Science and Resources, College of Bioresource Sciences, Nihon University – sequence: 7 givenname: Daiichiro surname: Fuchimoto fullname: Fuchimoto, Daiichiro organization: Institute of Agrobiological Sciences, National Agriculture and Food Research Organization (NARO) – sequence: 8 givenname: Shunichi surname: Suzuki fullname: Suzuki, Shunichi organization: Institute of Agrobiological Sciences, National Agriculture and Food Research Organization (NARO) – sequence: 9 givenname: Yoshiyuki surname: Nakamura fullname: Nakamura, Yoshiyuki organization: Swine and Poultry Research, Saitama Prefectural Agricultural Technology Research Center – sequence: 10 givenname: Taka-aki surname: Matsuyama fullname: Matsuyama, Taka-aki organization: Department of Legal Medicine, Showa University School of Medicine – sequence: 11 givenname: Seiichi surname: Hirota fullname: Hirota, Seiichi organization: Department of Surgical Pathology, Hyogo College of Medicine – sequence: 12 givenname: Masashi surname: Sakuma fullname: Sakuma, Masashi organization: Department of Cardiovascular Medicine, Dokkyo Medical University School of Medicine – sequence: 13 givenname: Masahiko surname: Tsujimoto fullname: Tsujimoto, Masahiko organization: Department of Pathology, Osaka Police Hospital – sequence: 14 givenname: Atsushi surname: Hirayama fullname: Hirayama, Atsushi organization: Department of Cardiology, Osaka Police Hospital – sequence: 15 givenname: Yasuo surname: Okumura fullname: Okumura, Yasuo organization: Division of Cardiology, Department of Medicine, Nihon University School of Medicine – sequence: 16 givenname: Hiroyuki surname: Hao fullname: Hao, Hiroyuki email: hao.hiroyuki@nihon-u.ac.jp organization: Division of Human Pathology, Department of Pathology and Microbiology, Nihon University School of Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33737695$$D View this record in MEDLINE/PubMed |
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Snippet | Pathological changes after third-generation drug-eluting stent implantation remain unclear. We compared the tissue responses of coronary arteries after the... Abstract Pathological changes after third-generation drug-eluting stent implantation remain unclear. We compared the tissue responses of coronary arteries... |
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StartPage | 6281 |
SubjectTerms | 631/154 692/308 692/4019 Arteriosclerosis Atherosclerosis Autopsy Biodegradability Biodegradation Coronary artery Coronary vessels Drug delivery Fibrin Histology Humanities and Social Sciences Implants multidisciplinary Polymers Receptor density Science Science (multidisciplinary) Smooth muscle Stents |
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Title | Pathological findings after third- and second-generation everolimus-eluting stent implantations in coronary arteries from autopsy cases and an atherosclerotic porcine model |
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