Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Monocytes from male patients with ankylosing spondylitis display decreased osteoclastogenesis and decreased RANKL/OPG ratio

Texto completo
Autor(es):
Caparbo, V. F. [1] ; Saad, C. G. S. [1] ; Moraes, J. C. [1] ; de Brum-Fernandes, A. J. [2] ; Pereira, R. M. R. [1]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Hosp Clin HCFMUSP, Rheumatol Div, Bone Metab Lab, Av Dr Arnaldo 455, 3 Andar, Sala 3193, BR-01246903 Sao Paulo, SP - Brazil
[2] Univ Sherbrooke, Fac Med & Sci Sante, Serv Rhumatol, Dept Med, Sherbrooke, PQ - Canada
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: OSTEOPOROSIS INTERNATIONAL; v. 29, n. 11, p. 2565-2573, NOV 2018.
Citações Web of Science: 3
Resumo

aSummaryThe present study investigates the osteoclastogenic capacity of peripheral blood mononuclear cells (PBMCs) in male patients with ankylosing spondylitis (AS). We demonstrated that monocytes from these patients display a lower capacity to generate osteoclasts compared to cells from healthy controls, and osteoclastogenesis was negatively correlated with disease duration.IntroductionAnkylosing spondylitis (AS) is a disease characterized by new bone growth that leads to syndesmophyte formation but AS patients frequently present with low bone mineral density/fractures. Osteoclastogenesis in AS patients is poorly studied and controversial. The aim of this study is to determine if the osteoclastogenic capacity of PBMCs is different in AS patients compared to controls and the relationship between osteoclastogenesis and clinical/laboratory parameters.MethodsPBMCs from 85 male AS patients and 59 controls were tested for CD16+ cells and induced to differentiate into osteoclasts over 3weeks in vitro. Serum levels of RANKL, osteoprotegerin (OPG), C-terminal telopeptide of type I collagen (CTX), and amino-terminal pro-peptide of type I collagen (P1NP) were also evaluated.ResultsPBMCs from AS patients had fewer CD16+ cells and produced fewer osteoclasts compared to controls. Apoptosis occurred less frequently in osteoclasts obtained from AS patients than in osteoclasts from the controls. A lower RANKL/OPG and CTX/P1NP were observed in AS patients compared to controls. AS patients taking NSAIDs presented no difference regarding the number of OCs produced and the percentage of CD16+ cells compared to controls. However, patients taking TNF inhibitors (TNFi) presented lower OC numbers than controls. A negative correlation was demonstrated between the number of osteoclasts generated from PBMCs of AS patients and disease duration.ConclusionMonocytes from male AS patients display a lower capacity to generate osteoclasts in vitro compared to cells from controls. Osteoclastogenesis was negatively correlated with disease duration. This finding supports the idea that osteoclasts play a role in the physiopathology of bone disease in AS patients. (AU)

Processo FAPESP: 11/23781-2 - Papel da osteoclastogênese e ativação dos osteoclastos em pacientes com espondilite anquilosante
Beneficiário:Rosa Maria Rodrigues Pereira
Modalidade de apoio: Auxílio à Pesquisa - Regular