In 880 patients treated with antiresorptive agents for a

median of 2.0 (95% CI, 1.0–4.5) years, the incidence of fractures during treatment with antiresorptive agents in a clinical setting is considerably higher than that observed in randomized clinical trials. Moreover, in adjusted analyses, inadequate compliance to treatment and lack of supplementation Angiogenesis inhibitor of calcium and vitamin D were found to be major determinants of this poor response. Calcium and vitamin D supplementation is frequently perceived by patients and sometimes by their physicians as an excessive medication and is easily dismissed to avoid polypharmacy, especially in elderly patients. Lack of motivation is the most common reason for nonadherence to calcium and vitamin D3 supplementation, emphasizing the need for an active role of physicians in prescribing supplements and motivating patients [26]. In conclusion, calcium and vitamin D should be considered

as an essential (but not sufficient) component of the treatment of osteoporosis, although most patients will derive further benefit in terms of fracture prevention from the addition of an antiresorptive or anabolic agent. However, antifracture efficacy with antiresorptive MK-0457 chemical structure or anabolic osteoporosis medications has only been documented in calcium and vitamin D supplemented individuals. The available evidence suggests that, in many patients, combined supplementation with 1,000–1,200 mg of Enzalutamide research buy elemental calcium and 800 IU of vitamin D may be required. Hormone replacement therapy Estrogen deficiency is the most frequent risk factor

for osteoporosis. Although randomized trials provide strong evidence that bone loss can effectively be prevented even with rather small doses of hormone replacement therapy (HRT) and that fracture risk can be reduced with conventional doses, even in postmenopausal women who do not suffer from osteoporosis [27], the consensus has LCL161 ic50 changed since the Women Health Initiative (WHI) studies. These randomized controlled trials evaluated, however, only two regimens of HRT: either the daily dose of 0.625 mg conjugated equine estrogen (CEE) alone in hysterectomized women or CEE combined with medroxyprogesterone acetate in women with an intact uterus. Following the first publications of these studies, HRT is no longer recommended as a first-line therapy for osteoporosis.