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Abstract Number: 694

Peripheral Bone Marrow-Derived Endothelial Progenitor Cells  and N-Terminal Probrain Natriuretic Peptide  in Scleroderma Mexican Patients With and Without Diastolic Dysfunction: A Preliminary Report

Jesús Sepúlveda1,2, Olga Vera-Lastra3, Maria Pilar Cruz-Dominguez4, Laura Montiel-Cervantes5, Joaquín Gómez-León6, Luis Robles-Espinoza7, Ramón Lozano-Morales7, Sergio Mendoza-Alvarez1, Rubiraida Molina-Aguilar5, Gabriela Medina8, Jorge Vela-Ojeda9 and Luis J. Jara10, 1Internal Medicine, Instituto Mexicano del Seguro Social, Mexico City, Mexico, 2Unidad de Estudios de Posgrado, Universidad Nacional Autónoma de México, Mexico City, Mexico, 3Internal Medicine, MD, Mexico City, Mexico, 4Division of Research, Hospital de Especialidades Centro Medico Nacional La Raza., Mexico, DF, Mexico, 5Hematology Laboratory, Instituto Mexicano del Seguro Social, Mexico City, Mexico, 6Cardiology Department, Instituto Mexicano del Seguro Social, Mexico City, Mexico, 7Central Laboratory, Instituto Mexicano del Seguro Social, Mexico City, Mexico, 8CMN La Raza IMSS, Seris/Zachila s/n La Raza, Mexico City, Mexico, 9Instituto Mexicano del Seguro Social, Mexico City, Mexico, 10Research and Education, Hospital de Especialidades Centro Medico La Raza, México City, Mexico

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Cardiovascular disease, endothelial cells, measure and scleroderma, NT-proBNP

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Session Information

Title: Systemic Sclerosis, Fibrosing Syndromes, and Raynaud’s - Clinical Aspects and Therapeutics I

Session Type: Abstract Submissions (ACR)

Background/Purpose: Diastolic dysfunction (DD) in systemic sclerosis (SSc) is a marker of increased risk of death. The N-terminal pro-brain natriuretic peptide (NT-proBNP) is a neurohormone released by ventricular and atrial myocytes and cardiac fibroblasts in response to pressure overload. NT-proBNP is highly associated with pulmonary arterial hypertension in SSc and is a potent vasculogenic agent that enhances bone marrow-derived endothelial progenitor cells (EPC) mobilization to cardiac regeneration. Our purpose was to explore the relationship between NT-proBNP  levels and peripheral EPC in SSc patients with and without DD.

Methods: Cross-sectional study in 56 SSc adult patients and 28 matched healthy controls. Exclusion criteria: systolic dysfunction, structural cardiopathy, neoplasms, overlap syndrome, diabetes and hypertension. DD (mild, moderate and severe) was determined according to 2009 EAE/ASE guidelines for the evaluation of diastolic function. EPC were characterized in peripheral blood by flow cytometry according to the expression surface markers CD309, CD34 and CD133 and 7AAD as a viability biomarker. CPE were divided in three phenotypes: 1.CD309+CD34+CD133-,2.CD309+CD133+CD34-, and 3. CD309+CD34+CD133+. Serum levels of NT-proBNP were measured by electroquimioluminiscence. SSc patients were divided according to the severity of DD. Statistical analysis data were expressed in median and range and comparison was made with Wilcoxon, Kruskal Wallis and Pearson correlation tests. P value<0.05 was considered significant.

Results: Results are summarized in Table 1. DD prevalence was 62%. NTproBNP was higher in mild, moderate and severe DD. NT-proBNP showed weak linear relation with CD309+CD34+ EPC cells (R=-0.36, p=0.04)

Table 1

 

Healthy controls

n= 28

SSc without DD

n=21

SSc with DD

n=35

P Value

 

 

Mild

 (n=20)

Moderate or severe

(n=15)

 

NTproBNP (pg/ml)

21

(15-50)

45.01

(17.3-162.6)

112.5

(35.6-617.5)

251.1

(84.95-965.6)

0.0083

EPC subtypes (cells/µl)

 

CD309+CD34+CD133+

1.53

(0.05-5.45)

1.04

(0.07-2.52)

0.47 (0.07-2.91)

0.0007

CD309+CD34+CD133-

0.72

(0.10-3.12)

0.99

(0.16-4.35)

0.90 (0.05-5.51)

0.45

CD309+CD133+CD34-

1.42

(0.32-6.72)

1.19

(0.181-4.68)

1.06 (0.04-3.81)

0.23

 Conclusion: NT–proBNP level is increased in patients with SSc and significantly correlates with severity of DD. On the other hand, the EPC subtype CD309+CD34+CD133+, was significantly diminished in patients with DD compared to patients without DD and healthy controls. These results support the role of NT-proBNP and EPC in the development of cardiac disease in SSc patients. A prospective study is necessary in order to define the prognostic significance of NT-proBNP and EPC alterations in SSc mexican patients.


Disclosure:

J. Sepúlveda,
None;

O. Vera-Lastra,
None;

M. P. Cruz-Dominguez,
None;

L. Montiel-Cervantes,
None;

J. Gómez-León,
None;

L. Robles-Espinoza,
None;

R. Lozano-Morales,
None;

S. Mendoza-Alvarez,
None;

R. Molina-Aguilar,
None;

G. Medina,
None;

J. Vela-Ojeda,
None;

L. J. Jara,
None.

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