Osteoclastogenesis in Children with 21-Hydroxylase Deficiency on Long-Term Glucocorticoid Therapy: The Role of Receptor Activator of Nuclear Factor-κB Ligand/Osteoprotegerin Imbalance

被引:40
|
作者
Faienza, Maria Felicia [1 ]
Brunetti, Giacomina [2 ]
Colucci, Silvia [2 ]
Piacente, Laura [1 ]
Ciccarelli, Maria [1 ]
Giordani, Lucia [1 ]
Del Vecchio, Giovanni Carlo [1 ]
D'Amore, Massimo [3 ]
Albanese, Livia [3 ]
Cavallo, Luciano [1 ]
Grano, Maria [2 ]
机构
[1] Univ Bari, Dept Biomed Dev Age, Rheumatol Sect, I-70100 Bari, Italy
[2] Univ Bari, Dept Human Anat & Histol, Rheumatol Sect, I-70100 Bari, Italy
[3] Univ Bari, Dept Internal Med & Publ Med, Rheumatol Sect, I-70100 Bari, Italy
关键词
BONE-MINERAL DENSITY; CONGENITAL ADRENAL-HYPERPLASIA; YOUNG-ADULT PATIENTS; T-CELLS; OSTEOPROTEGERIN LIGAND; INDUCED OSTEOPOROSIS; BODY-COMPOSITION; MECHANISMS; RANKL; STIMULATION;
D O I
10.1210/jc.2008-2446
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Children with 21-hydroxylase deficiency (21-OHD) need chronic glucocorticoid (cGC) therapy to replace congenital deficit of cortisol synthesis. cGC therapy is the most frequent and severe form of drug-induced osteoporosis, and different mechanisms have been proposed to explain its pathogenesis. Objective: We investigated the osteoclastogenic potential of peripheral blood mononuclear cells (PBMCs) from 18 children with 21-OHD on cGC therapy and 25 controls who never received GCs. We also evaluated the presence of circulating osteoclast precursors (OCPs) and the role of T cells in osteoclast formation. Results: Spontaneous osteoclastogenesis, without adding macrophage-colony stimulating factor and receptor activator of nuclear factor-kappa B ligand (RANKL), and significantly higher osteoclasts resorption activity occurred in 21-OHD patients. Conversely, macrophage-colony stimulating factor and RANKL were essential to trigger and sustain osteoclastogenesis in controls. Furthermore, in 21-OHD patients, we identified a significant percentage of CD11b-CD51/CD61 and CD51/61-RANK-positive cells, which are OCPs strongly committed. Additionally, we demonstrated a T cell-dependent osteoclastogenesis from 21-OHD patients' PBMCs. T cells from patients expressed high levels of RANKL and low levels of osteoprotegerin (OPG) with respect to controls. Moreover, 21-OHD patients had higher soluble RANKL and lower OPG serum levels compared with controls; thus, soluble RANKL to OPG ratio was significantly higher in patients than controls. Conclusions: The present study showed for the first time a high osteoclastogenic potential of PBMCs from 21-OHD patients on cGC therapy. This spontaneous osteoclastogenesis seems to be supported by both the presence of circulating OCPs and factors released by T cells. (J Clin Endocrinol Metab 94: 2269-2276, 2009)
引用
收藏
页码:2269 / 2276
页数:8
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