Subclinical right ventricle systolic dysfunction in childhood-onset systemic lupus erythematosus: insights from two-dimensional speckle-tracking echocardiography

Carregando...
Imagem de Miniatura
Citações na Scopus
34
Tipo de produção
article
Data de publicação
2015
Editora
SAGE PUBLICATIONS LTD
Indexadores
Título da Revista
ISSN da Revista
Título do Volume
Autor de Grupo de pesquisa
Editores
Coordenadores
Organizadores
Citação
LUPUS, v.24, n.6, p.613-620, 2015
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Objective The objective of this article is to evaluate right ventricle strain imaging by two-dimensional speckle-tracking (2DST) in childhood-onset systemic lupus erythematosus (c-SLE). Methods Thirty-five c-SLE patients with no signs or symptoms of heart failure and 33 healthy volunteers were evaluated by standard echocardiogram and 2DST. Conventional parameters included tricuspid annular plane systolic excursion (TAPSE), RV tissue-Doppler-derived Tei index and systolic pulmonary artery pressure. Global peak longitudinal systolic strain (PLSS) and strain rate (PLSSR) of RV were obtained by 2DST. Demographic/clinical features, SLEDAI-2K/SLICC/ACR-DI and treatment were also assessed. Results The median current age was similar in patients and controls (14.75 vs. 14.88 years, p=0.62). RV PLSS was significantly reduced in c-SLE (-24.55.09 vs. -27.62 +/- 3.02%, p=0.003). Similar findings were observed after excluding patients with pulmonary hypertension (-24.62 +/- 4.87% vs. -27.62 +/- 3.02%, p=0.0041). RV PLSS was positively correlated with TAPSE (r=+0.49, p=0.0027) and negatively correlated with Tei index (r=-0.34, p=0.04) in c-SLE. RV PLSSR was not different comparing patients and controls (-0.65s(-1)+/- 0.47 vs. -1.87 +/- 0.49s(-1), p=0.07). Further analysis of c-SLE patients revealed higher frequencies of neuropsychiatric manifestations (39% vs. 0%, p=0.007) and antiphospholipid antibodies (55% vs. 18%, p=0.035) in those with RV PLSS-23.7% vs >-23.7%. No differences were evidenced in demographic data, disease activity/damage or treatments (p>0.05). Conclusions The present study, using a new and more sensitive technique, revealed subclinical RV systolic dysfunction in c-SLE patients that may have future prognostic implications. The novel association of asymptomatic RV dysfunction with neuropsychiatric manifestations and antiphospholipid antibodies may suggest common physiopathological pathways.
Palavras-chave
Childhood-onset systemic lupus erythematosus, right ventricle systolic function, speckle-tracking echocardiography, antiphospholipid antibodies, neuropsychiatric manifestations
Referências
  1. [Anonymous], 1999, ARTHRITIS RHEUM, V42, P599
  2. Avcin T, 2008, PEDIATRICS, V122, pE1100, DOI 10.1542/peds.2008-1209
  3. Benseler SM, 2007, LUPUS, V16, P564, DOI 10.1177/0961203307078971
  4. Bleeker GB, 2006, HEART, V92, P19
  5. Bleeker GB, 2006, HEART, V92, pI19, DOI 10.1136/hrt.2005.082503
  6. BRANDT JT, 1995, THROMB HAEMOSTASIS, V74, P1185
  7. Bussadori C, 2009, CARDIOVASC ULTRASOUN, V13, P7
  8. Daniels SR, 2008, PEDIATRICS, V122, P198, DOI 10.1542/peds.2008-1349
  9. Dell'Italia LJ, 2012, CARDIOL CLIN, V30, P167, DOI [10.1016/j.ccl.2012.03.009, 10.1016/j.cc1.2012.03.009]
  10. DEVEREUX RB, 1977, CIRCULATION, V55, P613
  11. ELKON KB, 1984, J IMMUNOL, V132, P2350
  12. Gazarian M, 1998, J PEDIATR-US, V132, P109, DOI 10.1016/S0022-3476(98)70494-9
  13. GHARAVI AE, 1987, ANN RHEUM DIS, V46, P1, DOI 10.1136/ard.46.1.1
  14. Gin PL, 2006, J AM SOC ECHOCARDIOG, V19, P441, DOI 10.1016/j.echo.2005.10.018
  15. Gladman DD, 2002, J RHEUMATOL, V29, P288
  16. Gladman DD, 1997, ARTHRITIS RHEUM-US, V40, P809, DOI 10.1002/art.1780400506
  17. Greene ER, 2012, LUPUS, V21, P380, DOI 10.1177/0961203311428458
  18. Harambat J, 2012, PEDIATR NEPHROL, V27, P363, DOI 10.1007/s00467-011-1939-1
  19. HAYCOCK GB, 1978, J PEDIATR-US, V93, P62, DOI 10.1016/S0022-3476(78)80601-5
  20. Hochberg MC, 1997, ARTHRITIS RHEUM, V40, P1725, DOI 10.1002/art.1780400928
  21. Huang BT, 2014, ECHOCARDIOGR-J CARD, V31, P1085, DOI 10.1111/echo.12515
  22. KURATA N, 1976, ARTHRITIS RHEUM, V19, P574, DOI 10.1002/art.1780190309
  23. Lin CY, 2014, INT J CARDIOL, V176, P847, DOI 10.1016/j.ijcard.2014.08.006
  24. Lopez L, 2010, J AM SOC ECHOCARDIOG, V23, P465, DOI 10.1016/j.echo.2010.03.019
  25. Meris A, 2010, J AM SOC ECHOCARDIOG, V23, P823, DOI 10.1016/j.echo.2010.05.009
  26. Mineo C, 2013, CURR RHEUMATOL REP, V15, DOI 10.1007/s11926-013-0324-4
  27. Mor-Avi V, 2011, EUR J ECHOCARDIOGR, V12, P167, DOI 10.1093/ejechocard/jer021
  28. Motoki H, 2014, J AM SOC ECHOCARDIOG, V27, P726, DOI 10.1016/j.echo.2014.02.007
  29. Muscal E, 2007, AUTOIMMUN REV, V6, P215, DOI 10.1016/j.autrev.2006.08.003
  30. National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents, 2004, PEDIATRICS, V114, P555, DOI 10.1542/PEDS.114.2.S2.555
  31. Paran D, 2007, ANN RHEUM DIS, V66, P506, DOI 10.1136/ard.2005.044073
  32. Petitjean C, 2005, J CARDIOVASC MAGN R, V7, P501, DOI 10.1081/JCMR-200053610
  33. Plazak W, 2011, LUPUS, V20, P936, DOI 10.1177/0961203311399607
  34. Plazak W, 2011, ACTA CARDIOL, V66, P159, DOI 10.2143/AC.66.2.2071246
  35. Rudski LG, 2010, J AM SOC ECHOCARDIOG, V23, P685, DOI 10.1016/j.echo.2010.05.010
  36. Sacre K, 2010, ARTHRITIS RHEUM-US, V62, P2093, DOI 10.1002/art.27488
  37. TEICHHOLZ LE, 1976, AM J CARDIOL, V37, P7, DOI 10.1016/0002-9149(76)90491-4
  38. Tham EB, 2014, J AM SOC ECHOCARDIOG, V27, P314, DOI 10.1016/j.echo.2013.11.012