Association between psoriasis and coronary calcium score

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Citações na Scopus
39
Tipo de produção
article
Data de publicação
2014
Título da Revista
ISSN da Revista
Título do Volume
Editora
ELSEVIER IRELAND LTD
Citação
ATHEROSCLEROSIS, v.237, n.2, p.847-852, 2014
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Background: Emerging data suggests that chronic inflammatory disease, such as psoriasis, may be associated to coronary artery disease (CAD). Objective: Analyze the association between psoriasis and subclinical atherosclerosis using coronary calcium score (CAC). Methods: We investigated 221 participants with psoriasis and 718 age-and sex-matched controls without prior known CAD. All participants completed a questionnaire and underwent laboratory tests and a CAC exam. Logistic regression models adjusted for Framingham risk score (FRS) and C-reactive protein (hs-CRP) were built. CAC was included in the models as a binary variable with different cut off values. Results: Body-mass index, race, hypertension, HDL, LDL and hs-CRP were significantly associated with psoriasis presence and severity. Psoriasis severity was significantly associated with CAC (p = 0.04), particularly for very high CAC (>400) (p <0.01). The OR for severe psoriasis and CAC >400 was 2.45 (95%CI: 1.26-4.75) in unadjusted models. In a model adjusted for the FRS, this association was no longer significant, but a trend was noted (p = 0.09). No significant changes in the association were noted after the inclusion of hs-CRP in the model. Conclusion: Psoriasis is associated with higher CAC values, mainly in individuals with severe psoriasis. The current findings also suggest the potential involvement of other mechanisms beyond classical cardiovascular risk factors and inflammation in this association.
Palavras-chave
Coronary artery calcium, Cardiovascular disease, Cardiovascular risk factors, Psoriasis, Subclinical atherosclerosis
Referências
  1. AGATSTON AS, 1990, J AM COLL CARDIOL, V15, P827
  2. Antonucci V.A., 2012, J EUR ACAD DERMATOL, V28, P512
  3. Aquino EML, 2012, AM J EPIDEMIOL, V175, P315, DOI 10.1093/aje/kwr294
  4. Armstrong AW, 2012, AM J CARDIOL, V109, P976, DOI 10.1016/j.amjcard.2011.11.025
  5. Armstrong AW, 2013, J HYPERTENS, V31, P433, DOI 10.1097/HJH.0b013e32835bcce1
  6. Atzeni F, 2011, J RHEUMATOL, V38, P1661, DOI 10.3899/jrheum.100893
  7. Balci D.D., 2009, EUR ACAD DERMATOL VE, V23, P1
  8. Coto-Segura P., 2013, BR J DERMATOL, V91
  9. Dowlatshahi EA, 2013, J INVEST DERMATOL, V133, P2347, DOI 10.1038/jid.2013.131
  10. Dowlatshahi E.A., 2013, BR J DERMATOL, V168
  11. Eder L., 2013, ANN RHEUM DIS, V73, P1990
  12. Eder L, 2008, J RHEUMATOL, V35, P877
  13. Enany B., 2012, HERZ, V5, P527
  14. Finlay AY, 2005, BRIT J DERMATOL, V152, P861, DOI 10.1111/j.1365-2133.2005.06502.x
  15. Gaeta M., 2013, INT J CARDIOL
  16. Gelfand JM, 2005, ARCH DERMATOL, V141, P1537, DOI 10.1001/archderm.141.12.1537
  17. Gelfand JM, 2006, JAMA-J AM MED ASSOC, V296, P1735, DOI 10.1001/jama.296.14.1735
  18. Gonzalez-Juanatey C, 2007, ARTHRIT RHEUM-ARTHR, V57, P1074, DOI 10.1002/art.22884
  19. Kaul M.S., 2012, ARTHRIT CARE RES, V65, P266
  20. Kimhi O., 2007, ARTHRITIS RHEUM, V36, P203
  21. Kurd SK, 2009, J AM ACAD DERMATOL, V60, P218, DOI 10.1016/j.jaad.2008.09.022
  22. Ludwig RJ, 2007, BRIT J DERMATOL, V156, P271, DOI 10.1111/j.1365-2133.2006.07562.x
  23. Mehta NN, 2010, EUR HEART J, V31, P1000, DOI 10.1093/eurheartj/ehp567
  24. Patel RV, 2011, J GEN INTERN MED, V26, P1036, DOI 10.1007/s11606-011-1698-5
  25. Pitzalis C, 1998, BRIT J RHEUMATOL, V37, P480
  26. Tam LS, 2008, ARTHRIT RHEUM-ARTHR, V59, P1322, DOI 10.1002/art.24014
  27. The Centers for Disease Control and Prevention, 2004, NAT HLTH NUTR EX SUR
  28. Troitzsch P, 2012, ATHEROSCLEROSIS, V225, P486, DOI 10.1016/j.atherosclerosis.2012.09.026
  29. Warrington KJ, 2005, ARTHRITIS RES THER, V7, pR984, DOI 10.1186/ar1775
  30. Wilson PWF, 1998, CIRCULATION, V97, P1837
  31. Yiu KH, 2013, J INTERN MED, V273, P273, DOI 10.1111/joim.12002