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      Bone mineral density and fractures in older men with chronic obstructive pulmonary disease or asthma

      research-article
      1 , 6 , , 2 , 3 , 4 , 5 , for the Osteoporotic Fractures in Men (MrOS) Research Group
      Osteoporosis International
      Springer-Verlag
      Bone loss, Bone mineral density, Elderly, Fractures, Pulmonary disease

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          Abstract

          Summary

          In 5,541 community dwelling men, chronic obstructive pulmonary disease, or asthma was associated with lower bone mineral density (BMD) at the spine and total hip and an increased risk of vertebral and nonvertebral fractures independent of age, body mass index, and smoking. Men prescribed with corticosteroids had the lowest BMD.

          Introduction

          It is unclear whether chronic obstructive pulmonary disease (COPD) is independently associated with BMD and fractures.

          Methods

          In 5,541 men from the Osteoporotic Fractures in Men Study, history of COPD or asthma, current treatment with corticosteroids, BMD, bone loss after 4.5 years and fractures were ascertained.

          Results

          Seven hundred fourteen (13%) men reported COPD or asthma, of which 103 were prescribed an oral steroid and 177 an inhaled steroid. Independent of confounders, men prescribed corticosteroids for COPD or asthma had the lowest BMD and a 2-fold increased risk of vertebral osteoporosis compared to men with no history of COPD or asthma (OR 2.13, 95% CI (confidence interval) 1.15–3.93 oral steroids; OR 2.05, 95% CI 1.27–3.31 inhaled steroids). During follow-up, BMD increased at the spine, but there was no difference in bone loss at the hip. However, men with COPD or asthma had a 2.6- and 1.4-fold increased risk of vertebral and nonvertebral fractures, respectively.

          Conclusion

          Chronic obstructive pulmonary disease or asthma was associated with lower BMD at the spine and hip and increased risk of vertebral and nonvertebral fractures independent of age, clinic site, BMI, and smoking. A history of COPD or asthma may be a useful clinical risk factor to identify patients with osteoporosis.

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          Most cited references22

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          Assessment of fracture risk and its application to screening for postmenopausal osteoporosis. Report of a WHO Study Group.

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            Assessment of fracture risk and its application to screening for postmenopausal osteoporosis: synopsis of a WHO report. WHO Study Group.

            J Kanis (1994)
            The criteria required for an effective screening strategy for osteoporosis are largely met in Caucasian women. The disease is common and readily diagnosed by the measurement of bone mineral with single- or dual-energy absorptiometry. Such measurements have high specificity but lower sensitivity, so that the value of the technique is greater for those identified as being at higher risk. Against this background there is little evidence that osteoporosis can usefully be tackled by a public health policy to influence risk factors such as smoking, exercise and nutrition. This suggests that it is appropriate to consider targetting of treatment with agents affecting bone metabolism to susceptible individuals. Since the main benefits of the use of hormone replacement therapy (HRT) are probably on cardiovascular morbidity, the major role for selective screening is to direct non-HRT interventions. An appropriate time to consider screening and intervention is at the menopause, but screening at later ages is also worthy of consideration. Since the cost of screening is low and that of bone-active drugs is high, the selective use of screening techniques will improve the cost-benefit ratio of intervention.
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              Design and baseline characteristics of the osteoporotic fractures in men (MrOS) study--a large observational study of the determinants of fracture in older men.

              Very little information is available to direct the prevention or management of osteoporosis in men. The Osteoporotic Fractures in Men (MrOS) Study is a prospective cohort study designed to examine the extent to which fracture risk is related to bone mass, bone geometry, lifestyle, anthropometric and neuromuscular measures, and fall propensity, as well as to determine how fractures affect quality of life in men. The study is also designed to understand how osteoporosis is related to prostate disease. At baseline, participants completed questionnaires regarding medical history, medications, physical activity, diet, alcohol intake, and cigarette smoking. Objective measures of anthropometric, neuromuscular, vision, strength, and cognitive variables were obtained. Skeletal assessments included DEXA, calcaneal ultrasound, and vertebral radiographs. Vertebral and proximal femoral QCT was performed on a subset (65%). Serum, urine, and DNA specimens were collected. After the baseline assessments, a questionnaire is mailed to participants every 4 months to ascertain incident falls, fractures, prostate cancer, and deaths. After an average of 4.5 years, participants are scheduled to return for a second comprehensive visit. Men were eligible if > or =65 years. 5995 men enrolled with a mean (+/-SD) age of 73.7 (+/-5.9) years, 11% of which were minorities. Most rated their health as good/excellent. Few were current smokers, although 59% had smoked previously, and 35% reported no alcohol intake, while 47% consumed at least 2 drinks per week. The mean (range) body mass index was 26.9 kg/m2 (17-56). A non-traumatic fracture after age 50 was reported by 17% of the cohort. The MrOS cohort should provide valuable information concerning the determinants of fracture in men and should help set the stage for the development of effective methods to identify those at risk.
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                Author and article information

                Contributors
                +1-212-9324794 , +1-212-9324374 , td2265@columbia.edu.edu
                Journal
                Osteoporos Int
                Osteoporosis International
                Springer-Verlag (London )
                0937-941X
                1433-2965
                9 October 2009
                9 October 2009
                August 2010
                : 21
                : 8
                : 1341-1349
                Affiliations
                [1 ]Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, New York USA
                [2 ]Research Institute, California Pacific Medical Center, San Francisco, California USA
                [3 ]Geriatric Research Education and Clinical Center and Center for Chronic Disease Outcomes Research, Veterans Affairs Medical Center, Department of Medicine, University of Minnesota, Minneapolis, Minnesota USA
                [4 ]Department of Medicine, School of Medicine, University of California San Diego, La Jolla, California USA
                [5 ]Department of Family and Preventive Medicine, School of Medicine, University of California San Diego, La Jolla, California USA
                [6 ]Columbia University, College of Physicians and Surgeons, 5141 Broadway, New York, New York 10035 USA
                Article
                1076
                10.1007/s00198-009-1076-x
                2895883
                19816753
                93481653-fa59-463a-b6dd-597f220d1d64
                © The Author(s) 2009
                History
                : 22 September 2008
                : 26 August 2009
                Categories
                Original Article
                Custom metadata
                © International Osteoporosis Foundation and National Osteoporosis Foundation 2010

                Orthopedics
                bone loss,fractures,elderly,pulmonary disease,bone mineral density
                Orthopedics
                bone loss, fractures, elderly, pulmonary disease, bone mineral density

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