Biomarkers of subclinical atherosclerosis in patients with psoriasis.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
02 11 2021
Historique:
received: 06 06 2021
accepted: 20 10 2021
entrez: 3 11 2021
pubmed: 4 11 2021
medline: 27 1 2022
Statut: epublish

Résumé

Psoriasis is linked with increased risk of cardiovascular disease (CVD) that is underestimated by traditional risk stratification. We conducted a large-scale plasma proteomic analysis by use of a proximity extension assay in 85 patients with a history of moderate-to-severe psoriasis with or without established atherosclerotic CVD. Differentially expressed proteins associated with CVD were correlated with subclinical atherosclerotic markers including vascular inflammation determined by

Identifiants

pubmed: 34728734
doi: 10.1038/s41598-021-00999-9
pii: 10.1038/s41598-021-00999-9
pmc: PMC8564536
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

21438

Subventions

Organisme : LEO Fondet
ID : LF16115

Informations de copyright

© 2021. The Author(s).

Références

Boehncke, W. H. Systemic inflammation and cardiovascular comorbidity in psoriasis patients: Causes and consequences. Front. Immunol. 9, 579 (2018).
pubmed: 29675020 pmcid: 5895645 doi: 10.3389/fimmu.2018.00579
Parisi, R. et al. National, regional, and worldwide epidemiology of psoriasis: Systematic analysis and modelling study. BMJ 369, m1590 (2020).
pubmed: 32467098 pmcid: 7254147 doi: 10.1136/bmj.m1590
Armstrong, E. J., Harskamp, C. T. & Armstrong, A. W. Psoriasis and major adverse cardiovascular events: A systematic review and meta-analysis of observational studies. J. Am. Heart. Assoc. 2, e000062 (2013).
pubmed: 23557749 pmcid: 3647278 doi: 10.1161/JAHA.113.000062
Salahadeen, E., Torp-Pedersen, C., Gislason, G., Hansen, P. R. & Ahlehoff, O. Nationwide population-based study of cause-specific death rates in patients with psoriasis. J. Eur. Acad. Dermatol. Venereol. 29, 1002–1005 (2015).
pubmed: 24909271 doi: 10.1111/jdv.12523
Elmets, C. A. et al. Joint AAD-NPF guidelines of care for the management and treatment of psoriasis with awareness and attention to comorbidities. J. Am. Acad. Dermatol. 80, 1073–1113 (2019).
pubmed: 30772097 doi: 10.1016/j.jaad.2018.11.058
Grundy, S. M. et al. 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA guideline on the management of blood cholesterol: A report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation 139, E1082–E1143 (2019).
pubmed: 30586774
Gyldenløve, M. et al. Psoriasis and the framingham risk score in a danish hospital cohort. Int. J. Dermatol. 53, 1086–1090 (2014).
pubmed: 23879194 doi: 10.1111/ijd.12196
Eder, L., Chandran, V. & Gladman, D. D. The Framingham risk score underestimates the extent of subclinical atherosclerosis in patients with psoriatic disease. Ann. Rheum. Dis. 73, 1990–1996 (2014).
pubmed: 23887287 doi: 10.1136/annrheumdis-2013-203433
Zhou, W. et al. The application of molecular imaging to advance translational research in chronic inflammation. J. Nucl. Cardiol. https://doi.org/10.1007/s12350-020-02439-z (2020).
doi: 10.1007/s12350-020-02439-z pubmed: 33244675
Joshi, A. A. et al. Association between aortic vascular inflammation and coronary artery plaque characteristics in psoriasis. JAMA Cardiol. 3, 949–956 (2018).
pubmed: 30208407 pmcid: 6233814 doi: 10.1001/jamacardio.2018.2769
Figueroa, A. L. et al. Measurement of arterial activity on routine FDG PET/CT images improves prediction of risk of future CV events. JACC. Cardiovasc. Imaging 6, 1250–1259 (2013).
pubmed: 24269261 doi: 10.1016/j.jcmg.2013.08.006
Hjuler, K. F. et al. Increased global arterial and subcutaneous adipose tissue inflammation in patients with moderate-to-severe psoriasis. Br. J. Dermatol. 176, 732–740 (2017).
pubmed: 27787888 doi: 10.1111/bjd.15149
Kaiser, H., Abdulla, J., Henningsen, K. M. A., Skov, L. & Hansen, P. R. Coronary artery disease assessed by computed tomography in patients with psoriasis: A systematic review and meta-analysis. Dermatology 235, 478–487 (2019).
pubmed: 31480039 doi: 10.1159/000502138
Balci, D. D. et al. Increased carotid artery intima-media thickness and impaired endothelial function in psoriasis. J. Eur. Acad. Dermatol. Venereol. 23, 1–6 (2009).
pubmed: 18702627 doi: 10.1111/j.1468-3083.2008.02936.x
Joshi, A. A. et al. GlycA is a novel biomarker of inflammation and subclinical cardiovascular disease in psoriasis. Circ. Res. 119, 1242–1253 (2016).
pubmed: 27654120 pmcid: 5215065 doi: 10.1161/CIRCRESAHA.116.309637
Balta, I. et al. Elevated serum levels of endocan in patients with psoriasis vulgaris: Correlations with cardiovascular risk and activity of disease. Br. J. Dermatol. 169, 1066–1070 (2013).
pubmed: 23889284 doi: 10.1111/bjd.12525
Erfan, G. et al. Serum YKL-40: A potential biomarker for psoriasis or endothelial dysfunction in psoriasis? Mol. Cell. Biochem. 400, 207–212 (2015).
pubmed: 25421412 doi: 10.1007/s11010-014-2277-y
Robati, R. M., Partovi-Kia, M., Haghighatkhah, H. R., Younespour, S. & Abdollahimajd, F. Increased serum leptin and resistin levels and increased carotid intima-media wall thickness in patients with psoriasis: Is psoriasis associated with atherosclerosis? J. Am. Acad. Dermatol. 71, 642–648 (2014).
pubmed: 25043845 doi: 10.1016/j.jaad.2014.06.006
Elnabawi, Y. A. et al. CCL20 in psoriasis: A potential biomarker of disease severity, inflammation, and impaired vascular health. J. Am. Acad. Dermatol. 84, 913–920 (2021).
pubmed: 33259876 doi: 10.1016/j.jaad.2020.10.094
Adamstein, N. H. et al. The neutrophil–lymphocyte ratio and incident atherosclerotic events: Analyses from five contemporary randomized trials. Eur. Heart J. 42, 896–903 (2021).
pubmed: 33417682 doi: 10.1093/eurheartj/ehaa1034 pmcid: 7936519
Paliogiannis, P. et al. Associations between the neutrophil-to-lymphocyte and the platelet-to-lymphocyte ratios and the presence and severity of psoriasis: A systematic review and meta-analysis. Clin. Exp. Med. 19, 37–45 (2019).
pubmed: 30478648 doi: 10.1007/s10238-018-0538-x
Dey, A. K. et al. Association of neutrophil-to-lymphocyte ratio with non-calcified coronary artery burden in psoriasis: Findings from an observational cohort study. J. Cardiovasc. Comput. Tomogr. 15, 372–379 (2021).
pubmed: 33390348 doi: 10.1016/j.jcct.2020.12.006
Kaiser, H. et al. Multiscale biology of cardiovascular risk in psoriasis: Protocol for a case-control study. JMIR Res. Protoc. 10, e28669 (2021).
pubmed: 34581684 doi: 10.2196/28669 pmcid: 8512189
Assarsson, E. et al. Homogenous 96-plex PEA immunoassay exhibiting high sensitivity, specificity, and excellent scalability. PLoS ONE 9, e95192 (2014).
pubmed: 24755770 pmcid: 3995906 doi: 10.1371/journal.pone.0095192
Brunner, P. M. et al. The atopic dermatitis blood signature is characterized by increases in inflammatory and cardiovascular risk proteins. Sci. Rep. 7, 8707 (2017).
pubmed: 28821884 pmcid: 5562859 doi: 10.1038/s41598-017-09207-z
Bucerius, J. et al. Position paper of the cardiovascular committee of the european association of nuclear medicine (EANM) on PET imaging of atherosclerosis. Eur. J. Nucl. Med. Mol. Imaging 43, 780–792 (2016).
pubmed: 26678270 doi: 10.1007/s00259-015-3259-3
Agatston, A. S. et al. Quantification of coronary artery calcium using ultrafast computed tomography. J. Am. Coll. Cardiol. 15, 827–832 (1990).
pubmed: 2407762 doi: 10.1016/0735-1097(90)90282-T
Touboul, P.-J. et al. Mannheim carotid intima-media thickness and plaque consensus (2004–2006–2011). Cerebrovasc. Dis. 34, 290–296 (2012).
pubmed: 23128470 doi: 10.1159/000343145
Ritchie, M. E. et al. Limma powers differential expression analyses for RNA-sequencing and microarray studies. Nucleic Acids Res. 43, e47 (2015).
pubmed: 25605792 pmcid: 4402510 doi: 10.1093/nar/gkv007
Benjamini, Y. & Hochberg, Y. Controlling the false discovery rate: A practical and powerful approach to multiple testing. J. R. Stat. Soc. Ser. B 57, 289–300 (1995).
Hou, Z. H. et al. Prognostic value of coronary CT angiography and calcium score for major adverse cardiac events in outpatients. JACC Cardiovasc. Imaging 5, 990–999 (2012).
pubmed: 23058065 doi: 10.1016/j.jcmg.2012.06.006
Goff, D. C. et al. 2013 ACC/AHA guideline on the assessment of cardiovascular risk: A report of the American college of cardiology/American heart association task force on practice guidelines. Circulation 129, 49–73 (2014).
doi: 10.1161/01.cir.0000437741.48606.98
Dowlatshahi, E. A., Van Der Voort, E. A. M., Arends, L. R. & Nijsten, T. Markers of systemic inflammation in psoriasis: A systematic review and meta-analysis. Br. J. Dermatol. 169, 266–282 (2013).
pubmed: 23550658 doi: 10.1111/bjd.12355
Boehncke, W.-H., Boehncke, S., Tobin, A.-M. & Kirby, B. The ‘psoriatic march’: A concept of how severe psoriasis may drive cardiovascular comorbidity. Exp. Dermatol. 20, 303–307 (2011).
pubmed: 21410760 doi: 10.1111/j.1600-0625.2011.01261.x
Yadav, K., Singh, D. & Singh, M. R. Protein biomarker for psoriasis: A systematic review on their role in the pathomechanism, diagnosis, potential targets and treatment of psoriasis. Int. J. Biol. Macromol. 118, 1796–1810 (2018).
pubmed: 30017989 doi: 10.1016/j.ijbiomac.2018.07.021
Wang, J., Wei, L., Yang, X. & Zhong, J. Roles of growth differentiation factor 15 in atherosclerosis and coronary artery disease. J. Am. Heart Assoc. 8, e012826 (2019).
pubmed: 31432727 pmcid: 6755840 doi: 10.1161/JAHA.119.012826
Taddei, S. & Virdis, A. Growth differentiation factor-15 and cardiovascular dysfunction and disease: Malefactor or innocent bystander? Eur. Heart J. 31, 1168–1171 (2010).
pubmed: 20299701 doi: 10.1093/eurheartj/ehq077
Wollert, K. C. et al. Prognostic value of growth-differentiation factor-15 in patients with non-ST-elevation acute coronary syndrome. Circulation 115, 962–971 (2007).
pubmed: 17283261 doi: 10.1161/CIRCULATIONAHA.106.650846
Khan, S. Q. et al. Growth differentiation factor-15 as a prognostic marker in patients with acute myocardial infarction. Eur. Heart J. 30, 1057–1065 (2009).
pubmed: 19168526 doi: 10.1093/eurheartj/ehn600
Lind, L. et al. Growth-differentiation factor-15 is an independent marker of cardiovascular dysfunction and disease in the elderly: Results from the Prospective Investigation of the Vasculature in Uppsala Seniors (PIVUS) study. Eur. Heart J. 30, 2346–2353 (2009).
pubmed: 19561023 doi: 10.1093/eurheartj/ehp261
Rohatgi, A. et al. Association of growth differentiation factor-15 with coronary atherosclerosis and mortality in a young, multiethnic population: Observations from the dallas heart study. Clin. Chem. 58, 172–182 (2012).
pubmed: 22065155 doi: 10.1373/clinchem.2011.171926
Johnen, H. et al. Increased expression of the TGF-b superfamily cytokine MIC-1/GDF15 protects ApoE−/− mice from the development of atherosclerosis. Cardiovasc. Pathol. 21, 499–505 (2012).
pubmed: 22386250 doi: 10.1016/j.carpath.2012.02.003
Shin, M. Y. et al. Association between growth differentiation factor 15 (GDF15) and cardiovascular risk in patients with newly diagnosed type 2 diabetes mellitus. J. Korean Med. Sci. 31, 1413–1418 (2016).
pubmed: 27510384 pmcid: 4974182 doi: 10.3346/jkms.2016.31.9.1413
Bonaca, M. P. et al. Growth differentiation factor-15 and risk of recurrent events in patients stabilized after acute coronary syndrome: Observations from PROVE IT-TIMI 22. Arterioscler. Thromb. Vasc. Biol. 31, 203–210 (2011).
pubmed: 20966402 doi: 10.1161/ATVBAHA.110.213512
Kim, J. M. et al. Effect of atorvastatin on growth differentiation factor-15 in patients with type 2 diabetes mellitus and dyslipidemia. Diabetes Metab. J. 40, 70–78 (2016).
pubmed: 26616597 pmcid: 4768053 doi: 10.4093/dmj.2016.40.1.70
Antonopoulos, S., Margaritis, M., Lee, R., Channon, K. & Antoniades, C. Statins as anti-inflammatory agents in atherogenesis: Molecular mechanisms and lessons from the recent clinical trials. Curr. Pharm. Des. 18, 1519–1530 (2012).
pubmed: 22364136 pmcid: 3394171 doi: 10.2174/138161212799504803
Al-Mashhadi, R. H. et al. 18Fluorodeoxyglucose accumulation in arterial tissues determined by PET signal analysis. J. Am. Coll. Cardiol. 74, 1220–1232 (2019).
pubmed: 31466620 doi: 10.1016/j.jacc.2019.06.057
Bernardi, S., Bossi, F., Toffoli, B. & Fabris, B. Roles and clinical applications of OPG and TRAIL as biomarkers in cardiovascular disease. BioMed. Res. Int. https://doi.org/10.1155/2016/1752854 (2016).
doi: 10.1155/2016/1752854 pubmed: 27200369 pmcid: 4856888
Amin, T. E. et al. Serum level of receptor activator of nuclear factor kappa-B ligand in patients with psoriasis. Int. J. Dermatol. 55, e227–e233 (2016).
pubmed: 26712216 doi: 10.1111/ijd.13159
Wu, M., Rementer, C. & Giachelli, C. M. Challenges in treatment. Calcif. Tissue Int. 93, 365–373 (2013).
pubmed: 23456027 pmcid: 3714357 doi: 10.1007/s00223-013-9712-z
Zaba, L. C. et al. Identification of TNF-related apoptosis-inducing ligand and other molecules that distinguish inflammatory from resident dendritic cells in patients with psoriasis. J. Allergy Clin. Immunol. 125, 1261 (2010).
pubmed: 20471070 pmcid: 2910451 doi: 10.1016/j.jaci.2010.03.018
Nybo, M. & Rasmussen, L. M. The capability of plasma osteoprotegerin as a predictor of cardiovascular disease: A systematic literature review. Eur. J. Endocrinol. 159, 603–608 (2008).
pubmed: 18697793 doi: 10.1530/EJE-08-0554
Wang, W. M. & Jin, H. Z. Role of neutrophils in psoriasis. J. Immunol. Res. 2020, 18–23 (2020).
doi: 10.1155/2020/3709749
Yurtdaş, M. et al. Neutrophil-to-lymphocyte ratio may predict subclinical atherosclerosis in patients with psoriasis. Echocardiography 31, 1095–1104 (2014).
pubmed: 24447343 doi: 10.1111/echo.12511
Naik, H. B. et al. Severity of psoriasis associates with aortic vascular inflammation detected by FDG PET/CT and neutrophil activation in a prospective observational study. Arterioscler. Thromb. Vasc. Biol. 35, 2667–2676 (2015).
pubmed: 26449753 pmcid: 4662627 doi: 10.1161/ATVBAHA.115.306460
Naruko, T. et al. Neutrophil infiltration of culprit lesions in acute coronary syndromes. Circulation 106, 2894–2900 (2002).
pubmed: 12460868 doi: 10.1161/01.CIR.0000042674.89762.20
Van der Valk, F. M. et al. Thresholds for arterial wall inflammation quantified by 18F-FDG PET imaging: Implications for vascular interventional studies. JACC Cardiovasc. Imaging 9, 1198–1207 (2016).
pubmed: 27639759 pmcid: 5056585 doi: 10.1016/j.jcmg.2016.04.007

Auteurs

Hannah Kaiser (H)

Department of Cardiology, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark. lilian.hannah.kaiser@regionh.dk.
Department of Dermatology and Allergy, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark. lilian.hannah.kaiser@regionh.dk.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark. lilian.hannah.kaiser@regionh.dk.

Xing Wang (X)

Division of Clinical Immunology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Amanda Kvist-Hansen (A)

Department of Cardiology, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.
Department of Dermatology and Allergy, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Martin Krakauer (M)

Department of Clinical Physiology and Nuclear Medicine, Herlev and Gentofte Hospital, Hellerup, Denmark.
Department of Clinical Physiology and Nuclear Medicine, Bispebjerg and Frederiksberg Hospital, University Hospital, Copenhagen, Denmark.

Peter Michael Gørtz (PM)

Department of Clinical Physiology and Nuclear Medicine, Herlev and Gentofte Hospital, Hellerup, Denmark.

Benjamin D McCauley (BD)

Division of Clinical Immunology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Lone Skov (L)

Department of Dermatology and Allergy, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Christine Becker (C)

Division of Clinical Immunology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Peter Riis Hansen (PR)

Department of Cardiology, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

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