Metabolic syndrome and fragility fracture risk

被引:0
作者
So, Roberta C. O. S. [1 ]
Falchetti, Alberto [1 ,2 ]
机构
[1] San Giuseppe Hosp, Sect Bone & Mineral Dis, Oggebbio, Verbania, Italy
[2] Ist Auxol Italiano IRCCS, Lab Endocrine & Metab Res, Unit Bone Metab Dis & Diabet, Milan, Italy
关键词
Fractures; bone; Metabolic syndrome; Frailty; BONE-MINERAL DENSITY; TYPE-2; DIABETES-MELLITUS; MARROW FAT-CONTENT; OSTEOPOROTIC FRACTURE; VERTEBRAL FRACTURE; ADIPOSE-TISSUE; OLDER-ADULTS; WOMEN; OBESITY; HEALTH;
D O I
10.23736/S2724-606X.20.04689-4
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
INTRODUCTION: The prevalence of metabolic syndrome has been reported to extremely vary depending on the gender, age, and ethnicity studied. Approximately, 25% of the worldwide adult population is affected by metabolic syndrome, indicating it as a significantly important public health challenge. Likewise, fragility fracture represents an important public health issue too, and the lifetime residual risk of its occurrence has been established in 50% in women and 30% in men over 50 years of age, respectively. Dysmobility syndrome summarizes a cluster of co-existing conditions such as osteoporosis, sarcopenia, obesity. Currently, clinical research focuses essentially on the cardiovascular risks associated with metabolic syndrome. Today, it is conceivable to incorporate all these conditions under a generic "disorder of energy metabolism." EVIDENCE ACQUISITION: Animal and human studies suggest metabolic and dysmobility syndromes negatively impact on the risk for fragility fracture, contributing to increase the associated mortality rate. EVIDENCE SYNTHESIS: In recent years, strong correlation between type 2 diabetes, a frequent constitutive part of metabolic syndrome and fragility fracture risk has been reported, but the possible molecular mechanisms by which it can occur are still to be defined. CONCLUSIONS: Only very few human clinical studies faced these aspects, but they lack adequate endpoints for a good clinical practice in these subjects. Much more still needs to be done before appropriate therapeutic diagnostic pathways will be available for these patients at risk of bone and even generalized fragility. Suggestions for a future overall approach by generating global risk score for these conditions are given.
引用
收藏
页码:744 / 753
页数:10
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