Inflammation in Coronary Microvascular Dysfunction
Open accessAbstract
Chronic low-grade inflammation is involved in coronary atherosclerosis, presenting multiple clinical manifestations ranging from asymptomatic to stable angina, acute coronary syndrome, heart failure and sudden cardiac death. Coronary microvasculature consists of vessels with a diameter less than 500 μm, whose potential structural and functional abnormalities can lead to inappropriate dilatation and an inability to meet the required myocardium oxygen demands. This review focuses on the pathogenesis of coronary microvascular dysfunction and the capability of non-invasive screening methods to detect the phenomenon. Anti-inflammatory agents, such as statins and immunomodulators, including anakinra, tocilizumab, and tumor necrosis factor-alpha inhibitors, have been assessed recently and may constitute additional or alternative treatment approaches to reduce cardiovascular events in atherosclerotic heart disease characterized by coronary microvascular dysfunction.
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Excessive or dysregulated inflammation is a major driver of tissue damage and the pathogenesis of numerous diseases, including stroke, Parkinson's disease, atherosclerosis, and cancer.
“Excessive or dysregulated inflammation is a major driver of tissue damage and the pathogenesis of numerous diseases, including stroke, Parkinson’s disease, atherosclerosis, and cancer [9,30,31,32,33].”
From Picroside II as a Potential Anti-Inflammatory Agent (2026) · cites this paper as [31]
The Introduction and section 3.1 link inflammation to coronary atherosclerosis and coronary microvascular dysfunction. The copy does not establish the broader claim about tissue damage or the pathogenesis of stroke, Parkinson’s disease, and cancer; searches for those diseases found no supporting passage. No page numbers were available in the copy. (LLM, conf=0.86)
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Inflammation and Atherosclerosis
Libby, P., Ridker, P. M., & Maseri, A. (2002) · Circulation · doi:10.1161/hc0902.104353 · Cited by 7,724 · see citing works
Rosuvastatin to Prevent Vascular Events in Men and Women with Elevated C-Reactive Protein
Ridker, P. M., Danielson, E., Fonseca, F. A. H., Genest, J., Gotto, A. M., Kastelein, J. J. P., Koenig, W., Libby, P., Lorenzatti, A. J., MacFadyen, J. G., et al. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0807646 · Cited by 6,674 · see citing works
Type 2 diabetes as an inflammatory disease
Donath, M. Y., & Shoelson, S. E. (2011) · Nature Reviews Immunology · doi:10.1038/nri2925 · Cited by 3,737 · see citing works
Efficacy and safety of low-dose colchicine after myocardial infarction
Tardif, J.-C., Kouz, S., Waters, D. D., Bertrand, O. F., Diaz, R., Maggioni, A. P., Pinto, F. J., Ibrahim, R., Gamra, H., Kiwan, G. S., et al. (2019) · New England Journal of Medicine · doi:10.1056/nejmoa1912388 · Cited by 3,159 · cited 2× · see citing works
“Cholesterol crystals are present through all stages of atherosclerosis and can activate the NLRP3 inflammasome within these inflammatory cells to produce IL-1β and IL-18, key mediators in the inflammatory cascade that drive plaque progression and instability [6].”
BackgroundRegulation of coronary blood flow during exercise
Duncker, D. J., & Bache, R. J. (2008) · Physiological Reviews · doi:10.1152/physrev.00045.2006 · Cited by 936 · see citing works
Seldin, M. M., Meng, Y., Qi, H., Zhu, W., Wang, Z., Hazen, S. L., Lusis, A. J., & Shih, D. M. (2016) · Journal of the American Heart Association · doi:10.1161/jaha.115.002767 · Cited by 911 · see citing works
Adipocytokines in Obesity and Metabolic Disease
Cao, H. (2014) · Journal of Endocrinology · doi:10.1530/joe-13-0339 · Cited by 705 · see citing works
Packer, M. (2018) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2018.03.509 · Cited by 656 · cited 1× · see citing works
“Resistin hormone stimulates the proliferation of smooth muscle cells and the over-secretion of endotelin-1, leading to endothelial dysfunction [92].”
BackgroundMa, G., Pan, B., Chen, Y., Guo, C., Zhao, M., Zheng, L., & Chen, B. (2017) · Bioscience Reports · doi:10.1042/bsr20160244 · Cited by 267 · see citing works
Villeneuve, L. M., Kato, M., Reddy, M. A., Wang, M., Lanting, L., & Natarajan, R. (2010) · Diabetes · doi:10.2337/db10-0208 · Cited by 186 · see citing works
Brunt, V. E., Gioscia‐Ryan, R. A., Richey, J. J., Zigler, M. C., Cuevas, L. M., Gonzalez, A., Vázquez‐Baeza, Y., Battson, M. L., Smithson, A. T., Gilley, A. D., et al. (2019) · The Journal of Physiology · doi:10.1113/jp277336 · Cited by 182 · see citing works
Bays, H. E. (2012) · The American Journal of Cardiology · doi:10.1016/j.amjcard.2012.08.029 · Cited by 73 · see citing works
Flagged first, then by citations
Research works printed but not linked: 128
- [1]Johnson B.D. Shaw L.J. Buchthal S.D. Bairey Merz C.N. Kim H.W. Scott K.N. Doyle M. Olson M.B. Pepine C.J. den Hollander J. Prognosis in women with myocardial ischemia in the absence of obstructive coronary disease: Results from the National Institutes of Health-National Heart, Lung, and Blood Institute-Sponsored Women’s Ischemia Syndrome Evaluation (WISE) Circulation 2004 109 2993 2999 10.1161/01.CIR.0000130642.79868.B2 15197152 · DOI
- [2]Lin F.Y. Shaw L.J. Dunning A.M. Labounty T.M. Choi J.H. Weinsaft J.W. Koduru S. Gomez M.J. Delago A.J. Callister T.Q. Mortality risk in symptomatic patients with nonobstructive coronary artery disease: A prospective 2-center study of 2583 patients undergoing 64-detector row coronary computed tomographic angiography J. Am. Coll. Cardiol. 2011 58 510 519 10.1016/j.jacc.2010.11.078 21777749 · DOI
- [3]Lichtlen P.R. Bargheer K. Wenzlaff P. Long-term prognosis of patients with anginalike chest pain and normal coronary angiographic findings J. Am. Coll. Cardiol. 1995 25 1013 1018 10.1016/0735-1097(94)00519-V 7897110 · DOI
- [4]Elgendy I.Y. Pepine C.J. Heart Failure With Preserved Ejection Fraction: Is Ischemia Due to Coronary Microvascular Dysfunction a Mechanistic Factor? Am. J. Med. 2019 132 692 697 10.1016/j.amjmed.2018.12.038 30684452 PMC7722793 · DOI
- [5]Ridker P.M. Everett B.M. Thuren T. MacFadyen J.G. Chang W.H. Ballantyne C. Fonseca F. Nicolau J. Koenig W. Anker S.D. Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease N. Engl. J. Med. 2017 377 1119 1131 10.1056/NEJMoa1707914 28845751 · DOI · Paper page
- [7]Sagris M. Antonopoulos A.S. Theofilis P. Oikonomou E. Siasos G. Tsalamandris S. Antoniades C. Brilakis E.S. Kaski J.C. Tousoulis D. Risk factors profile of young and older patients with Myocardial Infarction Cardiovasc. Res. 2021 cvab264 10.1093/cvr/cvab264 34358302 · DOI
- [8]Zanatta E. Colombo C. D’Amico G. d’Humieres T. Dal Lin C. Tona F. Inflammation and Coronary Microvascular Dysfunction in Autoimmune Rheumatic Diseases Int. J. Mol. Sci. 2019 20 5563 10.3390/ijms20225563 PMC6888405 31703406 · DOI
- [9]Wei K. Jayaweera A.R. Firoozan S. Linka A. Skyba D.M. Kaul S. Quantification of myocardial blood flow with ultrasound-induced destruction of microbubbles administered as a constant venous infusion Circulation 1998 97 473 483 10.1161/01.CIR.97.5.473 9490243 · DOI
- [10]Caiati C. Montaldo C. Zedda N. Montisci R. Ruscazio M. Lai G. Cadeddu M. Meloni L. Iliceto S. Validation of a new noninvasive method (contrast-enhanced transthoracic second harmonic echo Doppler) for the evaluation of coronary flow reserve: Comparison with intracoronary Doppler flow wire J. Am. Coll. Cardiol. 1999 34 1193 1200 10.1016/S0735-1097(99)00342-3 10520812 · DOI
- [11]Lethen H. H P.T. Kersting S. Lambertz H. Validation of noninvasive assessment of coronary flow velocity reserve in the right coronary artery. A comparison of transthoracic echocardiographic results with intracoronary Doppler flow wire measurements Eur. Heart J. 2003 24 1567 1575 10.1016/S0195-668X(03)00284-7 12927192 · DOI
- [12]Cortigiani L. Rigo F. Gherardi S. Bovenzi F. Picano E. Sicari R. Implication of the continuous prognostic spectrum of Doppler echocardiographic derived coronary flow reserve on left anterior descending artery Am. J. Cardiol. 2010 105 158 162 10.1016/j.amjcard.2009.08.669 20102911 · DOI
- [13]Danad I. Szymonifka J. Schulman-Marcus J. Min J.K. Static and dynamic assessment of myocardial perfusion by computed tomography Eur. Heart J. Cardiovasc. Imaging 2016 17 836 844 10.1093/ehjci/jew044 27013250 PMC4955293 · DOI
- [14]George R.T. Jerosch-Herold M. Silva C. Kitagawa K. Bluemke D.A. Lima J.A. Lardo A.C. Quantification of myocardial perfusion using dynamic 64-detector computed tomography Investig. Radiol. 2007 42 815 822 10.1097/RLI.0b013e318124a884 18007153 · DOI
- [15]Camici P.G. d’Amati G. Rimoldi O. Coronary microvascular dysfunction: Mechanisms and functional assessment Nat. Rev. Cardiol. 2015 12 48 62 10.1038/nrcardio.2014.160 25311229 · DOI
- [16]Blankstein R. Shturman L.D. Rogers I.S. Rocha-Filho J.A. Okada D.R. Sarwar A. Soni A.V. Bezerra H. Ghoshhajra B.B. Petranovic M. Adenosine-induced stress myocardial perfusion imaging using dual-source cardiac computed tomography J. Am. Coll. Cardiol. 2009 54 1072 1084 10.1016/j.jacc.2009.06.014 19744616 · DOI
- [17]Antonopoulos A.S. Sanna F. Sabharwal N. Thomas S. Oikonomou E.K. Herdman L. Margaritis M. Shirodaria C. Kampoli A.M. Akoumianakis I. Detecting human coronary inflammation by imaging perivascular fat Sci. Transl. Med. 2017 9 10.1126/scitranslmed.aal2658 28701474 · DOI
- [18]Yu M. Dai X. Deng J. Lu Z. Shen C. Zhang J. Diagnostic performance of perivascular fat attenuation index to predict hemodynamic significance of coronary stenosis: A preliminary coronary computed tomography angiography study Eur. Radiol. 2020 30 673 681 10.1007/s00330-019-06400-8 31444596 · DOI
- [19]Hoshino M. Yang S. Sugiyama T. Zhang J. Kanaji Y. Yamaguchi M. Hada M. Sumino Y. Horie T. Nogami K. Peri-coronary inflammation is associated with findings on coronary computed tomography angiography and fractional flow reserve J. Cardiovasc. Comput. Tomogr. 2020 14 483 489 10.1016/j.jcct.2020.02.002 32057707 · DOI
- [20]Kwiecinski J. Dey D. Cadet S. Lee S.E. Otaki Y. Huynh P.T. Doris M.K. Eisenberg E. Yun M. Jansen M.A. Peri-Coronary Adipose Tissue Density Is Associated With (18)F-Sodium Fluoride Coronary Uptake in Stable Patients With High-Risk Plaques JACC Cardiovasc. Imaging 2019 12 2000 2010 10.1016/j.jcmg.2018.11.032 30772226 PMC6689460 · DOI
- [21]Goeller M. Achenbach S. Cadet S. Kwan A.C. Commandeur F. Slomka P.J. Gransar H. Albrecht M.H. Tamarappoo B.K. Berman D.S. Pericoronary Adipose Tissue Computed Tomography Attenuation and High-Risk Plaque Characteristics in Acute Coronary Syndrome Compared With Stable Coronary Artery Disease JAMA Cardiol. 2018 3 858 863 10.1001/jamacardio.2018.1997 30027285 PMC6233643 · DOI
- [22]Sugiyama T. Kanaji Y. Hoshino M. Yamaguchi M. Hada M. Ohya H. Sumino Y. Hirano H. Kanno Y. Horie T. Determinants of Pericoronary Adipose Tissue Attenuation on Computed Tomography Angiography in Coronary Artery Disease J. Am. Heart Assoc. 2020 9 e016202 10.1161/JAHA.120.016202 32750306 PMC7792233 · DOI
- [23]Oikonomou E.K. Williams M.C. Kotanidis C.P. Desai M.Y. Marwan M. Antonopoulos A.S. Thomas K.E. Thomas S. Akoumianakis I. Fan L.M. A novel machine learning-derived radiotranscriptomic signature of perivascular fat improves cardiac risk prediction using coronary CT angiography Eur. Heart J. 2019 40 3529 3543 10.1093/eurheartj/ehz592 31504423 PMC6855141 · DOI · Paper page
- [24]Oikonomou E.K. Marwan M. Desai M.Y. Mancio J. Alashi A. Hutt Centeno E. Thomas S. Herdman L. Kotanidis C.P. Thomas K.E. Non-invasive detection of coronary inflammation using computed tomography and prediction of residual cardiovascular risk (the CRISP CT study): A post-hoc analysis of prospective outcome data Lancet 2018 392 929 939 10.1016/S0140-6736(18)31114-0 30170852 PMC6137540 · DOI
- [25]Slomka P. Berman D.S. Alexanderson E. Germano G. The role of PET quantification in cardiovascular imaging Clin. Transl. Imaging 2014 2 343 358 10.1007/s40336-014-0070-2 26247005 PMC4523308 · DOI
- [26]Taqueti V.R. Solomon S.D. Shah A.M. Desai A.S. Groarke J.D. Osborne M.T. Hainer J. Bibbo C.F. Dorbala S. Blankstein R. Coronary microvascular dysfunction and future risk of heart failure with preserved ejection fraction Eur. Heart J. 2018 39 840 849 10.1093/eurheartj/ehx721 29293969 PMC5939665 · DOI
- [27]Gould K.L. Johnson N.P. Coronary Physiology beyond Coronary Flow Reserve in Microvascular Angina: JACC State-of-the-Art Review J. Am. Coll. Cardiol. 2018 72 2642 2662 10.1016/j.jacc.2018.07.106 30466522 · DOI
- [28]Biglands J.D. Magee D.R. Sourbron S.P. Plein S. Greenwood J.P. Radjenovic A. Comparison of the Diagnostic Performance of Four Quantitative Myocardial Perfusion Estimation Methods Used in Cardiac MR Imaging: CE-MARC Substudy Radiology 2015 275 393 402 10.1148/radiol.14140433 25521666 PMC4455679 · DOI
- [29]Carrick D. Haig C. Ahmed N. Carberry J. Yue May V.T. McEntegart M. Petrie M.C. Eteiba H. Lindsay M. Hood S. Comparative Prognostic Utility of Indexes of Microvascular Function Alone or in Combination in Patients With an Acute ST-Segment-Elevation Myocardial Infarction Circulation 2016 134 1833 1847 10.1161/CIRCULATIONAHA.116.022603 27803036 PMC5131697 · DOI
- [30]Thomson L.E. Wei J. Agarwal M. Haft-Baradaran A. Shufelt C. Mehta P.K. Gill E.B. Johnson B.D. Kenkre T. Handberg E.M. Cardiac magnetic resonance myocardial perfusion reserve index is reduced in women with coronary microvascular dysfunction. A National Heart, Lung, and Blood Institute-sponsored study from the Women’s Ischemia Syndrome Evaluation Circ. Cardiovasc. Imaging 2015 8 e002481 10.1161/CIRCIMAGING.114.002481 25801710 PMC4375783 · DOI
- [31]Indorkar R. Kwong R.Y. Romano S. White B.E. Chia R.C. Trybula M. Evans K. Shenoy C. Farzaneh-Far A. Global Coronary Flow Reserve Measured During Stress Cardiac Magnetic Resonance Imaging Is an Independent Predictor of Adverse Cardiovascular Events JACC Cardiovasc. Imaging 2019 12 1686 1695 10.1016/j.jcmg.2018.08.018 30409558 · DOI
- [32]Schroder J. Mygind N.D. Frestad D. Michelsen M. Suhrs H.E. Bove K.B. Gustafsson I. Kastrup J. Prescott E. Pro-inflammatory biomarkers in women with non-obstructive angina pectoris and coronary microvascular dysfunction Int. J. Cardiol. Heart Vasc. 2019 24 100370 10.1016/j.ijcha.2019.100370 31193994 PMC6545380 · DOI
- [33]Aslan G. Polat V. Bozcali E. Opan S. Cetin N. Ural D. Evaluation of serum sST2 and sCD40L values in patients with microvascular angina Microvasc. Res. 2019 122 85 93 10.1016/j.mvr.2018.11.009 30502363 · DOI
- [34]Dollard J. Kearney P. Clarke G. Moloney G. Cryan J.F. Dinan T.G. A prospective study of C-reactive protein as a state marker in Cardiac Syndrome X Brain Behav. Immun. 2015 43 27 32 10.1016/j.bbi.2014.07.011 25064176 · DOI
- [35]Theofilis P. Sagris M. Antonopoulos A.S. Oikonomou E. Tsioufis C. Tousoulis D. Inflammatory Mediators of Platelet Activation: Focus on Atherosclerosis and COVID-19 Int. J. Mol. Sci. 2021 22 11170 10.3390/ijms222011170 34681830 PMC8539848 · DOI
- [36]Safdar B. Guo X. Johnson C. D’Onofrio G. Dziura J. Sinusas A.J. Testani J. Rao V. Desir G. Elevated renalase levels in patients with acute coronary microvascular dysfunction - A possible biomarker for ischemia Int. J. Cardiol. 2019 279 155 161 10.1016/j.ijcard.2018.12.061 30630613 PMC6482834 · DOI
- [37]Suhrs H.E. Schroder J. Bove K.B. Mygind N.D. Frestad D. Michelsen M.M. Lange T. Gustafsson I. Kastrup J. Prescott E. Inflammation, non-endothelial dependent coronary microvascular function and diastolic function-Are they linked? PLoS ONE 2020 15 e0236035 10.1371/journal.pone.0236035 32673354 PMC7365405 · DOI
- [38]Siasos G. Bletsa E. Stampouloglou P.K. Oikonomou E. Tsigkou V. Paschou S.A. Vlasis K. Marinos G. Vavuranakis M. Stefanadis C. MicroRNAs in cardiovascular disease Hell. J. Cardiol. HJC = Hell. Kardiol. Ep. 2020 61 165 173 10.1016/j.hjc.2020.03.003 32305497 · DOI
- [39]Vogiatzi G. Oikonomou E. Deftereos S. Siasos G. Tousoulis D. Peripheral artery disease: A micro-RNA-related condition? Curr. Opin. Pharmacol. 2018 39 105 112 10.1016/j.coph.2018.04.001 29679926 · DOI
- [40]Theofilis P. Oikonomou E. Vogiatzi G. Antonopoulos A.S. Siasos G. Iliopoulos D.C. Perrea D. Tsioufis C. Tousoulis D. The impact of proangiogenic microRNA modulation on blood flow recovery following hind limb ischemia. A systematic review and meta-analysis of animal studies Vasc. Pharmacol. 2021 106906 10.1016/j.vph.2021.106906 34509635 · DOI
- [41]Theofilis P. Vogiatzi G. Oikonomou E. Gazouli M. Siasos G. Katifelis H. Perrea D. Vavuranakis M. Iliopoulos D.C. Tsioufis C. The Effect of MicroRNA-126 Mimic Administration on Vascular Perfusion Recovery in an Animal Model of Hind Limb Ischemia Front. Mol. Biosci. 2021 8 724465 10.3389/fmolb.2021.724465 34513927 PMC8423909 · DOI
- [43]Sun X. He S. Wara A.K.M. Icli B. Shvartz E. Tesmenitsky Y. Belkin N. Li D. Blackwell T.S. Sukhova G.K. Systemic delivery of microRNA-181b inhibits nuclear factor-kappaB activation, vascular inflammation, and atherosclerosis in apolipoprotein E-deficient mice Circ. Res. 2014 114 32 40 10.1161/CIRCRESAHA.113.302089 24084690 PMC4051320 · DOI
- [44]Reddy M.A. Jin W. Villeneuve L. Wang M. Lanting L. Todorov I. Kato M. Natarajan R. Pro-inflammatory role of microrna-200 in vascular smooth muscle cells from diabetic mice Arterioscler. Thromb. Vasc. Biol. 2012 32 721 729 10.1161/ATVBAHA.111.241109 22247255 PMC3288534 · DOI
- [45]Cowan C. Muraleedharan C.K. O’Donnell J.J. 3rd Singh P.K. Lum H. Kumar A. Xu S. MicroRNA-146 inhibits thrombin-induced NF-kappaB activation and subsequent inflammatory responses in human retinal endothelial cells Investig. Ophthalmol. Vis. Sci. 2014 55 4944 4951 10.1167/iovs.13-13631 24985472 · DOI
- [46]Liang K.W. Sheu W.H. Lee W.J. Lee W.L. Fu C.P. Wang J.S. Differential expression of circulating vascular cell adhesion molecule-1 in subjects with coronary artery disease and cardiac syndrome X without known diabetes mellitus Biomark. Biochem. Indic. Expo. Response Susceptibility Chem. 2017 22 798 804 10.1080/1354750X.2017.1351003 28675064 · DOI
- [47]Efe S.C. Demirci K. Ozturk S. Gurbuz A.S. Poci N. Kilicgedik A. Guler A. Yilmaz M.F. Izgi I.A. Kirma C. Serum endocan levels in patients with cardiac syndrome X Herz 2018 43 359 363 10.1007/s00059-017-4580-3 28589439 · DOI
- [48]Prasad M. Matteson E.L. Herrmann J. Gulati R. Rihal C.S. Lerman L.O. Lerman A. Uric Acid Is Associated With Inflammation, Coronary Microvascular Dysfunction, and Adverse Outcomes in Postmenopausal Women Hypertension 2017 69 236 242 10.1161/HYPERTENSIONAHA.116.08436 27993955 PMC5233565 · DOI
- [49]Altiparmak I.H. Erkus M.E. Sezen H. Demirbag R. Kaya Z. Sezen Y. Gunebakmaz O. Asoglu R. Besli F. Neselioglu S. Evaluation of thiol levels, thiol/disulfide homeostasis and their relation with inflammation in cardiac syndrome X Coron. Artery Dis. 2016 27 295 301 10.1097/MCA.0000000000000362 26928883 · DOI
- [50]Mekonnen G. Corban M.T. Hung O.Y. Eshtehardi P. Eapen D.J. Al-Kassem H. Rasoul-Arzrumly E. Gogas B.D. McDaniel M.C. Pielak T. Plasma soluble urokinase-type plasminogen activator receptor level is independently associated with coronary microvascular function in patients with non-obstructive coronary artery disease Atherosclerosis 2015 239 55 60 10.1016/j.atherosclerosis.2014.12.025 25574858 · DOI
- [51]Bozcali E. Polat V. Aciksari G. Opan S. Bayrak I.H. Paker N. Karakaya O. Serum concentrations of galectin-3 in patients with cardiac syndrome X Atherosclerosis 2014 237 259 263 10.1016/j.atherosclerosis.2014.09.014 25282685 · DOI
- [52]Tenekecioglu E. Yilmaz M. Demir S. Bekler A. Ozluk O.A. Aydin U. Goncu T. Yontar O.C. HDL-cholesterol is associated with systemic inflammation in cardiac syndrome X Minerva Med. 2015 106 133 141 25028863
- [53]Faccini A. Kaski J.C. Camici P.G. Coronary microvascular dysfunction in chronic inflammatory rheumatoid diseases Eur. Heart J. 2016 37 1799 1806 10.1093/eurheartj/ehw018 26912605 · DOI
- [54]Oikonomou E. Leopoulou M. Theofilis P. Antonopoulos A.S. Siasos G. Latsios G. Mystakidi V.C. Antoniades C. Tousoulis D. A link between inflammation and thrombosis in atherosclerotic cardiovascular diseases: Clinical and therapeutic implications Atherosclerosis 2020 309 16 26 10.1016/j.atherosclerosis.2020.07.027 32858395 · DOI
- [55]Puddu P. Puddu G.M. Cravero E. Muscari S. Muscari A. The involvement of circulating microparticles in inflammation, coagulation and cardiovascular diseases Can. J. Cardiol. 2010 26 140 145 10.1016/S0828-282X(10)70371-8 20386775 PMC2886541 · DOI
- [57]Clarke J.G. Davies G.J. Kerwin R. Hackett D. Larkin S. Dawbarn D. Lee Y. Bloom S.R. Yacoub M. Maseri A. Coronary artery infusion of neuropeptide Y in patients with angina pectoris Lancet 1987 1 1057 1059 10.1016/S0140-6736(87)90483-1 2883396 · DOI
- [58]Crea F. Camici P.G. Bairey Merz C.N. Coronary microvascular dysfunction: An update Eur. Heart J. 2014 35 1101 1111 10.1093/eurheartj/eht513 24366916 PMC4006091 · DOI
- [59]Choudhury L. Rosen S.D. Patel D. Nihoyannopoulos P. Camici P.G. Coronary vasodilator reserve in primary and secondary left ventricular hypertrophy. A study with positron emission tomography Eur. Heart J. 1997 18 108 116 10.1093/oxfordjournals.eurheartj.a015090 9049522 · DOI
- [60]Sagris M. Theofilis P. Antonopoulos A.S. Tsioufis C. Oikonomou E. Antoniades C. Crea F. Kaski J.C. Tousoulis D. Inflammatory Mechanisms in COVID-19 and Atherosclerosis: Current Pharmaceutical Perspectives Int. J. Mol. Sci. 2021 22 6607 10.3390/ijms22126607 34205487 PMC8234423 · DOI
- [61]Theofilis P. Sagris M. Oikonomou E. Antonopoulos A.S. Siasos G. Tsioufis C. Tousoulis D. Inflammatory Mechanisms Contributing to Endothelial Dysfunction Biomedicines 2021 9 781 10.3390/biomedicines9070781 34356845 PMC8301477 · DOI
- [62]Benjamin E.J. Blaha M.J. Chiuve S.E. Cushman M. Das S.R. Deo R. de Ferranti S.D. Floyd J. Fornage M. Gillespie C. Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association Circulation 2017 135 e146 e603 10.1161/CIR.0000000000000485 28122885 PMC5408160 · DOI · Paper page
- [63]Carrick D. Haig C. Ahmed N. McEntegart M. Petrie M.C. Eteiba H. Hood S. Watkins S. Lindsay M.M. Davie A. Myocardial Hemorrhage After Acute Reperfused ST-Segment-Elevation Myocardial Infarction: Relation to Microvascular Obstruction and Prognostic Significance Circ. Cardiovasc. Imaging 2016 9 e004148 10.1161/CIRCIMAGING.115.004148 26763281 PMC4718183 · DOI
- [64]Eitel I. Kubusch K. Strohm O. Desch S. Mikami Y. de Waha S. Gutberlet M. Schuler G. Friedrich M.G. Thiele H. Prognostic value and determinants of a hypointense infarct core in T2-weighted cardiac magnetic resonance in acute reperfused ST-elevation-myocardial infarction Circ. Cardiovasc. Imaging 2011 4 354 362 10.1161/CIRCIMAGING.110.960500 21518773 · DOI
- [65]Duprez D.A. Role of the renin-angiotensin-aldosterone system in vascular remodeling and inflammation: A clinical review J. Hypertens. 2006 24 983 991 10.1097/01.hjh.0000226182.60321.69 16685192 · DOI
- [66]Hao Y. Tsuruda T. Sekita-Hatakeyama Y. Kurogi S. Kubo K. Sakamoto S. Nakamura M. Udagawa N. Sekimoto T. Hatakeyama K. Cardiac hypertrophy is exacerbated in aged mice lacking the osteoprotegerin gene Cardiovasc. Res. 2016 110 62 72 10.1093/cvr/cvw025 26825553 · DOI
- [67]Siedlinski M. Nosalski R. Szczepaniak P. Ludwig-Galezowska A.H. Mikolajczyk T. Filip M. Osmenda G. Wilk G. Nowak M. Wolkow P. Vascular transcriptome profiling identifies Sphingosine kinase 1 as a modulator of angiotensin II-induced vascular dysfunction Sci. Rep. 2017 7 44131 10.1038/srep44131 28276483 PMC5343497 · DOI
- [68]Wang M. Kim S.H. Monticone R.E. Lakatta E.G. Matrix metalloproteinases promote arterial remodeling in aging, hypertension, and atherosclerosis Hypertension 2015 65 698 703 10.1161/HYPERTENSIONAHA.114.03618 25667214 PMC4359070 · DOI · Paper page
- [69]Camici P.G. Olivotto I. Rimoldi O.E. The coronary circulation and blood flow in left ventricular hypertrophy J. Mol. Cell Cardiol. 2012 52 857 864 10.1016/j.yjmcc.2011.08.028 21924273 · DOI
- [70]Cortigiani L. Rigo F. Gherardi S. Galderisi M. Bovenzi F. Sicari R. Prognostic meaning of coronary microvascular disease in type 2 diabetes mellitus: A transthoracic Doppler echocardiographic study J. Am. Soc. Echocardiogr. 2014 27 742 748 10.1016/j.echo.2014.02.010 24679741 · DOI
- [71]Murthy V.L. Naya M. Foster C.R. Gaber M. Hainer J. Klein J. Dorbala S. Blankstein R. Di Carli M.F. Association between coronary vascular dysfunction and cardiac mortality in patients with and without diabetes mellitus Circulation 2012 126 1858 1868 10.1161/CIRCULATIONAHA.112.120402 22919001 PMC3495105 · DOI
- [72]Sagris M. Giannopoulos S. Giannopoulos S. Tzoumas A. Texakalidis P. Charisis N. Kokkinidis D.G. Malgor R.D. Mouawad N.J. Bakoyiannis C. Transcervical carotid artery revascularization: A systematic review and meta-analysis of outcomes J. Vasc. Surg. 2021 74 657 665.e612 10.1016/j.jvs.2021.03.032 33864829 · DOI
- [73]Tabit C.E. Chung W.B. Hamburg N.M. Vita J.A. Endothelial dysfunction in diabetes mellitus: Molecular mechanisms and clinical implications Rev. Endocr. Metab. Disord. 2010 11 61 74 10.1007/s11154-010-9134-4 20186491 PMC2882637 · DOI
- [74]Suzuki L.A. Poot M. Gerrity R.G. Bornfeldt K.E. Diabetes accelerates smooth muscle accumulation in lesions of atherosclerosis: Lack of direct growth-promoting effects of high glucose levels Diabetes 2001 50 851 860 10.2337/diabetes.50.4.851 11289052 · DOI
- [75]Salmi M. Jalkanen S. Vascular Adhesion Protein-1: A Cell Surface Amine Oxidase in Translation Antioxid. Redox Signal. 2019 30 314 332 10.1089/ars.2017.7418 29065711 PMC6306676 · DOI
- [76]Stolen C.M. Madanat R. Marti L. Kari S. Yegutkin G.G. Sariola H. Zorzano A. Jalkanen S. Semicarbazide sensitive amine oxidase overexpression has dual consequences: Insulin mimicry and diabetes-like complications FASEB J. Off. Publ. Fed. Am. Soc. Exp. Biol. 2004 18 702 704 10.1096/fj.03-0562fje 14977883 · DOI
- [77]Diavati S. Sagris M. Terentes-Printzios D. Vlachopoulos C. Anticoagulation Treatment in Venous Thromboembolism: Options and Optimal Duration Curr. Pharm. Des. 2021 10.2174/1381612827666211111150705 34766887 · DOI
- [79]Sorop O. Heinonen I. van Kranenburg M. van de Wouw J. de Beer V.J. Nguyen I.T.N. Octavia Y. van Duin R.W.B. Stam K. van Geuns R.J. Multiple common comorbidities produce left ventricular diastolic dysfunction associated with coronary microvascular dysfunction, oxidative stress, and myocardial stiffening Cardiovasc. Res. 2018 114 954 964 10.1093/cvr/cvy038 29432575 PMC5967461 · DOI
- [80]Costantino S. Paneni F. Battista R. Castello L. Capretti G. Chiandotto S. Tanese L. Russo G. Pitocco D. Lanza G.A. Impact of Glycemic Variability on Chromatin Remodeling, Oxidative Stress, and Endothelial Dysfunction in Patients With Type 2 Diabetes and With Target HbA1c Levels Diabetes 2017 66 2472 2482 10.2337/db17-0294 28634176 · DOI
- [81]Siasos G. Skotsimara G. Oikonomou E. Sagris M. Vasiliki-Chara M. Bletsa E. Stampouloglou P. Theofilis P. Charalampous G. Tousoulis D. Antithrombotic Treatment in Diabetes Mellitus: A Review of the Literature about Antiplatelet and Anticoagulation Strategies Used for Diabetic Patients in Primary and Secondary Prevention Curr. Pharm. Des. 2020 26 2780 2788 10.2174/1381612826666200417145605 32303164 · DOI
- [82]Neeland I.J. Ross R. Despres J.P. Matsuzawa Y. Yamashita S. Shai I. Seidell J. Magni P. Santos R.D. Arsenault B. Visceral and ectopic fat, atherosclerosis, and cardiometabolic disease: A position statement Lancet Diabetes Endocrinol. 2019 7 715 725 10.1016/S2213-8587(19)30084-1 31301983 · DOI · Paper page
- [83]Shulman G.I. Ectopic Fat in Insulin Resistance, Dyslipidemia, and Cardiometabolic Disease N. Engl. J. Med. 2014 371 1131 1141 10.1056/NEJMra1011035 25229917 · DOI · Paper page
- [84]Goossens G.H. Blaak E.E. Adipose Tissue Dysfunction and Impaired Metabolic Health in Human Obesity: A Matter of Oxygen? Front. Endocrinol. 2015 6 55 10.3389/fendo.2015.00055 PMC4408910 25964776 · DOI
- [85]Frayn K.N. Karpe F. Regulation of human subcutaneous adipose tissue blood flow Int. J. Obes. 2014 38 1019 1026 10.1038/ijo.2013.200 24166067 · DOI
- [86]Lempesis I.G. van Meijel R.L.J. Manolopoulos K.N. Goossens G.H. Oxygenation of adipose tissue: A human perspective Acta Physiol. 2019 228 e13298 10.1111/apha.13298 PMC6916558 31077538 · DOI
- [87]Bays H.E. Adiposopathy is “sick fat” a cardiovascular disease? J. Am. Coll. Cardiol. 2011 57 2461 2473 10.1016/j.jacc.2011.02.038 21679848 · DOI · Paper page
- [90]Karam B.S. Chavez-Moreno A. Koh W. Akar J.G. Akar F.G. Oxidative stress and inflammation as central mediators of atrial fibrillation in obesity and diabetes Cardiovasc. Diabetol. 2017 16 120 10.1186/s12933-017-0604-9 28962617 PMC5622555 · DOI
- [91]Sagris M. Kokkinidis D.G. Lempesis I.G. Giannopoulos S. Rallidis L. Mena-Hurtado C. Bakoyiannis C. Nutrition, dietary habits, and weight management to prevent and treat patients with peripheral artery disease Rev. Cardiovasc. Med. 2020 21 565 575 10.31083/j.rcm.2020.04.202 33388001 · DOI
- [93]Naoumova R.P. Kindler H. Leccisotti L. Mongillo M. Khan M.T. Neuwirth C. Seed M. Holvoet P. Betteridge J. Camici P.G. Pioglitazone improves myocardial blood flow and glucose utilization in nondiabetic patients with combined hyperlipidemia: A randomized, double-blind, placebo-controlled study J. Am. Coll. Cardiol. 2007 50 2051 2058 10.1016/j.jacc.2007.07.070 18021872 · DOI
- [94]Lang D.H. Yeung C.K. Peter R.M. Ibarra C. Gasser R. Itagaki K. Philpot R.M. Rettie A.E. Isoform specificity of trimethylamine N-oxygenation by human flavin-containing monooxygenase (FMO) and P450 enzymes: Selective catalysis by FMO3 Biochem. Pharmacol. 1998 56 1005 1012 10.1016/S0006-2952(98)00218-4 9776311 · DOI · Paper page
- [97]Ross R. Atherosclerosis--an inflammatory disease N. Engl. J. Med. 1999 340 115 126 10.1056/NEJM199901143400207 9887164 · DOI · Paper page
- [100]Liu H. Tian R. Wang H. Feng S. Li H. Xiao Y. Luan X. Zhang Z. Shi N. Niu H. Gut microbiota from coronary artery disease patients contributes to vascular dysfunction in mice by regulating bile acid metabolism and immune activation J. Transl. Med. 2020 18 382 10.1186/s12967-020-02539-x 33036625 PMC7547479 · DOI
- [101]Tenore G.C. Caruso D. Buonomo G. D’Avino M. Ciampaglia R. Maisto M. Schisano C. Bocchino B. Novellino E. Lactofermented Annurca Apple Puree as a Functional Food Indicated for the Control of Plasma Lipid and Oxidative Amine Levels: Results from a Randomised Clinical Trial Nutrients 2019 11 122 10.3390/nu11010122 PMC6356833 30634393 · DOI
- [102]Ford T.J. Stanley B. Good R. Rocchiccioli P. McEntegart M. Watkins S. Eteiba H. Shaukat A. Lindsay M. Robertson K. Stratified Medical Therapy Using Invasive Coronary Function Testing in Angina: The CorMicA Trial J. Am. Coll. Cardiol. 2018 72 2841 2855 10.1016/j.jacc.2018.09.006 30266608 · DOI
- [103]Bouabdallaoui N. Tardif J.C. Waters D.D. Pinto F.J. Maggioni A.P. Diaz R. Berry C. Koenig W. Lopez-Sendon J. Gamra H. Time-to-treatment initiation of colchicine and cardiovascular outcomes after myocardial infarction in the Colchicine Cardiovascular Outcomes Trial (COLCOT) Eur. Heart J. 2020 41 4092 4099 10.1093/eurheartj/ehaa659 32860034 PMC7700755 · DOI
- [104]Ikonomidis I. Lekakis J.P. Nikolaou M. Paraskevaidis I. Andreadou I. Kaplanoglou T. Katsimbri P. Skarantavos G. Soucacos P.N. Kremastinos D.T. Inhibition of interleukin-1 by anakinra improves vascular and left ventricular function in patients with rheumatoid arthritis Circulation 2008 117 2662 2669 10.1161/CIRCULATIONAHA.107.731877 18474811 · DOI
- [105]Holte E. Kleveland O. Ueland T. Kunszt G. Bratlie M. Broch K. Michelsen A.E. Bendz B. Amundsen B.H. Aakhus S. Effect of interleukin-6 inhibition on coronary microvascular and endothelial function in myocardial infarction Heart 2017 103 1521 1527 10.1136/heartjnl-2016-310875 28432157 · DOI
- [106]Portman M.A. Olson A. Soriano B. Dahdah N. Williams R. Kirkpatrick E. Etanercept as adjunctive treatment for acute Kawasaki disease: Study design and rationale Am. Heart J. 2011 161 494 499 10.1016/j.ahj.2010.12.003 21392603 · DOI
- [107]Almeida S.O. Budoff M. Effect of statins on atherosclerotic plaque Trends Cardiovasc. Med. 2019 29 451 455 10.1016/j.tcm.2019.01.001 30642643 · DOI
- [108]Sakellarios A.I. Fotiadis D.I. Editorial commentary: The pleiotropic effect of statins on the atherosclerotic plaque and coronary heart disease Trends Cardiovasc. Med. 2019 29 456 457 10.1016/j.tcm.2019.02.001 30770174 · DOI
- [109]Stumpf C. Petzi S. Seybold K. Wasmeier G. Arnold M. Raaz D. Yilmaz A. Daniel W.G. Garlichs C.D. Atorvastatin enhances interleukin-10 levels and improves cardiac function in rats after acute myocardial infarction Clin. Sci. 2009 116 45 52 10.1042/CS20080042 18459941 · DOI
- [110]Shen Y. Wu H. Wang C. Shao H. Huang H. Jing H. Li D. Simvastatin attenuates cardiopulmonary bypass-induced myocardial inflammatory injury in rats by activating peroxisome proliferator-activated receptor gamma Eur. J. Pharmacol. 2010 649 255 262 10.1016/j.ejphar.2010.08.058 20858481 · DOI
- [112]Giles J.T. Sattar N. Gabriel S. Ridker P.M. Gay S. Warne C. Musselman D. Brockwell L. Shittu E. Klearman M. Cardiovascular Safety of Tocilizumab Versus Etanercept in Rheumatoid Arthritis: A Randomized Controlled Trial Arthritis Rheumatol. 2020 72 31 40 10.1002/art.41095 31469238 · DOI
- [113]Luo W.H. Guo Y. Huang J.W. Zhang P.D. Do Statins Have a Positive Impact on Patients with Coronary Microvascular Dysfunction on Long-Term Clinical Outcome? A Large Retrospective Cohort Study Biomed. Res. Int. 2019 2019 10.1155/2019/4069097 31008104 PMC6441523 · DOI
- [114]Hetzel S. DeMets D. Schneider R. Borzak S. Schneider W. Serebruany V. Schroder H. Hennekens C.H. Aspirin increases nitric oxide formation in chronic stable coronary disease J. Cardiovasc. Pharmacol. Ther. 2013 18 217 221 10.1177/1074248413482753 23524841 PMC4014131 · DOI
- [115]Yang Y. Hwang E. Lee S.A. Lee S. Kim D.H. Song J.M. Kang D.H. Effect of Rosuvastatin on Coronary Flow Reserve in Hypertensive Patients at Cardiovascular Risk J. Cardiovasc. Imaging 2021 29 255 262 10.4250/jcvi.2020.0244 34080332 PMC8318809 · DOI
- [116]Sun B.J. Hwang E. Jang J.Y. Kim D.H. Song J.M. Kang D.H. Effect of rosuvastatin on coronary flow reserve in patients with systemic hypertension Am. J. Cardiol. 2014 114 1234 1237 10.1016/j.amjcard.2014.07.046 25159238 · DOI
- [117]Ishida K. Geshi T. Nakano A. Uzui H. Mitsuke Y. Okazawa H. Ueda T. Lee J.D. Beneficial effects of statin treatment on coronary microvascular dysfunction and left ventricular remodeling in patients with acute myocardial infarction Int. J. Cardiol. 2012 155 442 447 10.1016/j.ijcard.2011.11.015 22146235 · DOI
- [118]Yong J. Tian J. Yang X. Xing H. He Y. Song X. Effects of Oral Drugs on Coronary Microvascular Function in Patients Without Significant Stenosis of Epicardial Coronary Arteries: A Systematic Review and Meta-Analysis of Coronary Flow Reserve Front. Cardiovasc. Med. 2020 7 580419 10.3389/fcvm.2020.580419 33195465 PMC7661556 · DOI
- [119]Kattoor A.J. Pothineni N.V.K. Palagiri D. Mehta J.L. Oxidative Stress in Atherosclerosis Curr. Atheroscler. Rep. 2017 19 42 10.1007/s11883-017-0678-6 28921056 · DOI
- [120]Naderi S. Microvascular Coronary Dysfunction-an Overview Curr. Atheroscler. Rep. 2018 20 7 10.1007/s11883-018-0710-5 29383530 · DOI
- [121]Nidorf M. Thompson P.L. Effect of colchicine (0.5 mg twice daily) on high-sensitivity C-reactive protein independent of aspirin and atorvastatin in patients with stable coronary artery disease Am. J. Cardiol. 2007 99 805 807 10.1016/j.amjcard.2006.10.039 17350370 · DOI
- [122]Nidorf S.M. Thompson P.L. Why Colchicine Should Be Considered for Secondary Prevention of Atherosclerosis: An Overview Clin. Ther. 2019 41 41 48 10.1016/j.clinthera.2018.11.016 30591286 · DOI
- [123]Castaneda S. Martinez-Quintanilla D. Martin-Varillas J.L. Garcia-Castaneda N. Atienza-Mateo B. Gonzalez-Gay M.A. Tocilizumab for the treatment of adult-onset Still’s disease Expert Opin. Biol. Ther. 2019 19 273 286 10.1080/14712598.2019.1590334 30827128 · DOI
- [124]Monteagudo L.A. Boothby A. Gertner E. Continuous Intravenous Anakinra Infusion to Calm the Cytokine Storm in Macrophage Activation Syndrome ACR Open Rheumatol. 2020 2 276 282 10.1002/acr2.11135 32267081 PMC7231518 · DOI
- [125]Ikonomidis I. Pavlidis G. Katsimbri P. Andreadou I. Triantafyllidi H. Tsoumani M. Varoudi M. Vlastos D. Makavos G. Kostelli G. Differential effects of inhibition of interleukin 1 and 6 on myocardial, coronary and vascular function Clin. Res. Cardiol. Off. J. Ger. Card. Soc. 2019 108 1093 1101 10.1007/s00392-019-01443-9 30859382 · DOI
- [126]Zhu Y. Xian X. Wang Z. Bi Y. Chen Q. Han X. Tang D. Chen R. Research Progress on the Relationship between Atherosclerosis and Inflammation Biomolecules 2018 8 80 10.3390/biom8030080 PMC6163673 30142970 · DOI
- [127]Cacciapaglia F. Anelli M.G. Rinaldi A. Fornaro M. Lopalco G. Scioscia C. Lapadula G. Iannone F. Lipids and Atherogenic Indices Fluctuation in Rheumatoid Arthritis Patients on Long-Term Tocilizumab Treatment Mediat. Inflamm. 2018 2018 10.1155/2018/2453265 30405318 PMC6204176 · DOI
- [128]Toniati P. Piva S. Cattalini M. Garrafa E. Regola F. Castelli F. Franceschini F. Airo P. Bazzani C. Beindorf E.A. Tocilizumab for the treatment of severe COVID-19 pneumonia with hyperinflammatory syndrome and acute respiratory failure: A single center study of 100 patients in Brescia, Italy Autoimmun. Rev. 2020 102568 10.1016/j.autrev.2020.102568 32376398 PMC7252115 · DOI
- [129]Van Kraaij T.D. Mostard R.L. Ramiro S. Magro Checa C. van Dongen C.M. van Haren E.H. Buijs J. Landewe R.B. Tocilizumab in Severe COVID-19 Pneumonia and Concomitant Cytokine Release Syndrome Eur. J. Case Rep. Intern. Med. 2020 7 001675 10.12890/2020_001675 32399455 PMC7213824 · DOI
- [130]Strang A.C. Bisoendial R.J. Kootte R.S. Schulte D.M. Dallinga-Thie G.M. Levels J.H. Kok M. Vos K. Tas S.W. Tietge U.J. Pro-atherogenic lipid changes and decreased hepatic LDL receptor expression by tocilizumab in rheumatoid arthritis Atherosclerosis 2013 229 174 181 10.1016/j.atherosclerosis.2013.04.031 23746537 · DOI
- [131]Broch K. Anstensrud A.K. Woxholt S. Sharma K. Tollefsen I.M. Bendz B. Aakhus S. Ueland T. Amundsen B.H. Damas J.K. Randomized Trial of Interleukin-6 Receptor Inhibition in Patients With Acute ST-Segment Elevation Myocardial Infarction J. Am. Coll. Cardiol. 2021 77 1845 1855 10.1016/j.jacc.2021.02.049 33858620 · DOI
- [132]Ahlehoff O. Skov L. Gislason G. Gniadecki R. Iversen L. Bryld L.E. Lasthein S. Lindhardsen J. Kristensen S.L. Torp-Pedersen C. Cardiovascular outcomes and systemic anti-inflammatory drugs in patients with severe psoriasis: 5-year follow-up of a Danish nationwide cohort J. Eur. Acad. Dermatol. Venereol. JEADV 2015 29 1128 1134 10.1111/jdv.12768 25303139 · DOI
- [133]Jacobsson L.T. Turesson C. Gulfe A. Kapetanovic M.C. Petersson I.F. Saxne T. Geborek P. Treatment with tumor necrosis factor blockers is associated with a lower incidence of first cardiovascular events in patients with rheumatoid arthritis J. Rheumatol. 2005 32 1213 1218 15996054
- [134]Bergstrom U. Jovinge S. Persson J. Jacobsson L.T.H. Turesson C. Effects of Treatment with Adalimumab on Blood Lipid Levels and Atherosclerosis in Patients with Rheumatoid Arthritis Curr. Ther. Res. Clin. Exp. 2018 89 1 6 10.1016/j.curtheres.2018.07.001 30128057 PMC6097545 · DOI
- [135]Chen X.Y. Yan B.X. Man X.Y. TNFalpha inhibitor may be effective for severe COVID-19: Learning from toxic epidermal necrolysis Ther. Adv. Respir. Dis. 2020 14 10.1177/1753466620926800 PMC7243041 32436460 · DOI
- [136]Guzik T.J. Hoch N.E. Brown K.A. McCann L.A. Rahman A. Dikalov S. Goronzy J. Weyand C. Harrison D.G. Role of the T cell in the genesis of angiotensin II induced hypertension and vascular dysfunction J. Exp. Med. 2007 204 2449 2460 10.1084/jem.20070657 17875676 PMC2118469 · DOI · Paper page
- [137]Kroetsch J.T. Levy A.S. Zhang H. Aschar-Sobbi R. Lidington D. Offermanns S. Nedospasov S.A. Backx P.H. Heximer S.P. Bolz S.S. Constitutive smooth muscle tumour necrosis factor regulates microvascular myogenic responsiveness and systemic blood pressure Nat. Commun. 2017 8 14805 10.1038/ncomms14805 28378814 PMC5382284 · DOI
- [138]Ikonomidis I. Papadavid E. Makavos G. Andreadou I. Varoudi M. Gravanis K. Theodoropoulos K. Pavlidis G. Triantafyllidi H. Moutsatsou P. Lowering Interleukin-12 Activity Improves Myocardial and Vascular Function Compared With Tumor Necrosis Factor-a Antagonism or Cyclosporine in Psoriasis Circulation. Cardiovasc. Imaging 2017 10 e006283 10.1161/CIRCIMAGING.117.006283 28899951 · DOI
- [139]Piaserico S. Osto E. Famoso G. Zanetti I. Gregori D. Poretto A. Iliceto S. Peserico A. Tona F. Treatment with tumor necrosis factor inhibitors restores coronary microvascular function in young patients with severe psoriasis Atherosclerosis 2016 251 25 30 10.1016/j.atherosclerosis.2016.05.036 27236353 · DOI
- [140]Dominguez H. Storgaard H. Rask-Madsen C. Steffen Hermann T. Ihlemann N. Baunbjerg Nielsen D. Spohr C. Kober L. Vaag A. Torp-Pedersen C. Metabolic and vascular effects of tumor necrosis factor-alpha blockade with etanercept in obese patients with type 2 diabetes J. Vasc. Res. 2005 42 517 525 10.1159/000088261 16155368 · DOI · Paper page
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Picroside II as a Potential Anti-Inflammatory Agent
Ren, Y., Liu, Z., Wei, L., Wang, Y., Wang, Y., Guo, Y., & Ma, Z. (2026) · Pharmaceutics · doi:10.3390/pharmaceutics18040499 · Cited by 2 · see citing works
- Authors
- Sagris, M., Theofilis, P., Antonopoulos, A. S., Oikonomou, E., Paschaliori, C., Galiatsatos, N., Tsioufis, K., & Tousoulis, D.
- Affiliations
- Cardiology Clinic, ‘Hippokration’ General Hospital, School of Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece
- National and Kapodistrian University of Athens (GR)
- ORCID
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2021-12-15
- Volume
- 22
- Issue
- 24
- Pages
- 13471
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC8703507
- OpenAlex
- W4200256560
- Cited by
- 115
- References
- 12
- Citations by year
- 2026: 15 · 2025: 39 · 2024: 19 · 2023: 19 · 2022: 23
- FWCI
- 1.56
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Cardiac Imaging and Diagnostics
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Keywords
- coronary microvascular dysfunction, low-grade inflammation, coronary artery disease, coronary microcirculation, myocardial ischemia, non-invasive screening, anti-inflammatory therapy, statins, anakinra, tocilizumab, TNF-alpha inhibitors, atherosclerotic heart disease
- MeSH terms
- Coronary Artery Disease, Coronary Circulation, Coronary Vessels, Heart Failure, Humans, Inflammation, Microcirculation, Myocardial Infarction, Risk Factors, Death, Sudden, Cardiac, Myocardial Ischemia, Acute Coronary Syndrome, Microvessels
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