Higher Urinary Levels of 8-Hydroxy-2′-deoxyguanosine Are Associated with a Worse RANKL/OPG Ratio in Postmenopausal Women with Osteopenia

被引:18
作者
Cervellati, Carlo [1 ]
Romani, Arianna [1 ]
Cremonini, Eleonora [2 ]
Bergamini, Carlo M. [1 ]
Fila, Enrica [3 ,4 ]
Squerzanti, Monica [1 ]
Greco, Pantaleo [4 ]
Massari, Leo [3 ,5 ]
Bonaccorsi, Gloria [3 ,4 ]
机构
[1] Univ Ferrara, Sect Med Biochem Mol Biol & Genet, Dept Biomed & Specialist Surg Sci, I-44121 Ferrara, Italy
[2] Univ Calif Davis, Dept Nutr, Davis, CA 95616 USA
[3] Univ Ferrara, Menopause & Osteoporosis Ctr, Dept Morphol Surg & Expt Med, I-44124 Ferrara, Italy
[4] Univ Ferrara, Sect Obstet & Gynecol, Dept Morphol Surg & Expt Med, I-44124 Ferrara, Italy
[5] Univ Ferrara, Sect Orthopaed Clin, Dept Morphol Surg & Expt Med, I-44124 Ferrara, Italy
关键词
KAPPA-B LIGAND; BONE-MINERAL DENSITY; OXIDATIVE STRESS; RECEPTOR ACTIVATOR; ESTROGEN-DEFICIENCY; SERUM-LEVELS; OSTEOPOROSIS; OSTEOPROTEGERIN; ANTIOXIDANTS; EXPRESSION;
D O I
10.1155/2016/6038798
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Postmenopausal osteoporosis (PO) is a major public health issue which affects a large fraction of elderly women. Emerging in vitro evidence suggests a central role of oxidative stress (OxS) in postmenopausal osteoporosis (PO) development. Contrariwise, the human studies on this topic are still scarce and inconclusive. In the attempt to address this issue, we sought to determine if OxS, as assessed by 8-hydroxy-2-deoxyguanosine (8-OHdG), may influence the level of receptor activator of nuclear factor-kappa b ligand (RANKL)/osteoprotegerin (OPG) ratio (a central regulator of bone metabolism) in a sample (n = 124), including postmenopausal women with osteoporosis, osteopenia and normal bone mass density (BMD). The most striking result that emerged in our study was the independent and positive (beta = 0.449, p = 0.004, and R-2 = 0.185) association between the OxS marker and RANKL/OPG ratio which was found in osteopenic but not in the other 2 sample groups. If confirmed by longitudinal studies, our findings would suggest that OxS is implicated in the derangement of bone homeostasis which precedes PO development. In line with these considerations, antioxidant treatment of postmenopausal women with moderately low BMD might contribute to preventing PO and related complications.
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页数:8
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