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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns="http://purl.org/rss/1.0/"><channel rdf:about="http://www.clinicaldensitometry.com/?rss=yes"><title>Journal of Clinical Densitometry</title><description>Journal of Clinical Densitometry RSS feed: Current Issue.    The official journal of the  International Society for Clinical Densitometry (ISCD) , 
the  Journal of Clinical Densitometry: Assessment of Skeletal Health  publishes the latest clinical research on the uses of bone 
mass and density measurements in medical practice, as well as state-of-the-art review articles on critical topics. The Journal is committed 
to serving ISCD's mission—the education of heterogenous physician specialties and technologists who are involved in the clinical assessment 
of skeletal health. The focus of JCD is bone mass measurement, including epidemiology of bone mass, how drugs and diseases alter bone 
mass, new techniques and quality assurance in bone mass imaging technologies, and bone mass health/economics.
  
 

Combining high quality 
research and review articles with sound, practice-oriented advice,  JCD  meets the diverse diagnostic and management needs of 
radiologists, endocrinologists, nephrologists, rheumatologists, gynecologists, family physicians, internists, and technologists whose 
patients require diagnostic clinical densitometry for therapeutic management.   </description><link>http://www.clinicaldensitometry.com/?rss=yes</link><dc:publisher>Elsevier Inc.</dc:publisher><dc:language>en</dc:language><dc:rights> © 2012 The International Society for Clinical Densitometry. Published by Elsevier Inc. All rights reserved. </dc:rights><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:issn>1094-6950</prism:issn><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:publicationDate>April 2012</prism:publicationDate><prism:copyright> © 2012 The International Society for Clinical Densitometry. Published by Elsevier Inc. All rights reserved. </prism:copyright><prism:rightsAgent>healthpermissions@elsevier.com</prism:rightsAgent><items><rdf:Seq><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695012000273/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011001934/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011001727/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS109469501100237X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002368/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002320/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002228/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002174/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002162/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002149/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002137/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002125/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011002101/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011001958/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011001946/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011001806/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS109469501100179X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695011001788/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicaldensitometry.com/article/PIIS1094695012000042/abstract?rss=yes"/></rdf:Seq></items></channel><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695012000273/abstract?rss=yes"><title>A Word From the Editor</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695012000273/abstract?rss=yes</link><description>I am delighted to have been appointed Editor-in-Chief of the Journal of Clinical Densitometry (JCD), the official journal of the International Society of Clinical Densitometry (ISCD). The ISCD’s record is outstanding: in less than 20years, it has grown from a small group of dedicated individuals to a major force in the field of skeletal health, currently boasting about 4000 members from more than 60 countries. JCD is the flagship of ISCD, its ambassador to anyone interested in bone diseases, and the common link between its members. JCD offers a forum for the propagation of scientific and cutting-edge research ideas and ensures that readers are kept informed of state-of-the-art management of bone diseases—but its mission is not accomplished yet.</description><dc:title>A Word From the Editor</dc:title><dc:creator>Ronald C. Hamdy</dc:creator><dc:identifier>10.1016/j.jocd.2012.02.012</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-04-01</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-04-01</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Editorials</prism:section><prism:startingPage>129</prism:startingPage><prism:endingPage>129</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011001934/abstract?rss=yes"><title>Commentary on Calcium Supplements and Cardiovascular Events</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011001934/abstract?rss=yes</link><description>We present a commentary from the calcium subcommittee of the Professional Practice Committee of the American Society of Bone and Mineral Research (ASBMR) on the current discussions regarding calcium supplement use and the possible association with increased cardiovascular events. Data from randomized controlled trials (RCTs) and 3 recently published meta-analyses are discussed.</description><dc:title>Commentary on Calcium Supplements and Cardiovascular Events</dc:title><dc:creator>Richard S. Bockman, Carol Zapalowski, Douglas P. Kiel, Robert A. Adler</dc:creator><dc:identifier>10.1016/j.jocd.2011.10.002</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-02-10</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-02-10</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Editorials</prism:section><prism:startingPage>130</prism:startingPage><prism:endingPage>134</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011001727/abstract?rss=yes"><title>Comparison Between Amputation-Induced Demineralization and Age-Related Bone Loss Using Digital X-Ray Radiogrammetry</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011001727/abstract?rss=yes</link><description>Abstract: Digital X-ray radiogrammetry (DXR) is a computer-assisted automatic osteodensitometric tool. This study was performed to compare DXR measurements between bone changes following amputation trauma and age-related bone loss. Thirty-five men, who had undergone finger amputations, received a baseline examination and 2–3 serial measurements. As a second group, 215 males older than 70yr were enrolled. All patients obtained standardized hand radiographs. The following DXR parameters evaluating metacarpals were considered: cortical bone mineral density (DXR-BMD), cortical thickness (DXR-CT), metacarpal index (DXR-MCI), outer bone diameter (width; DXR-W), and inner medullary diameter (DXR-MD). In the amputation group, the DXR parameters showed an accentuated initial decrease between first and second measurements (DRX-BMD −12.7%, DXR-CT −14.2%, DXR-W −8.6%, DXR-MCI −6.1%; p&lt;0.001) followed by a less pronounced reduction between second and third radiographs (DRX-BMD −0.5%, DXR-CT −1.5%, DXR-W −0.1%, DXR-MCI −1.3%). DXR-MD revealed a reduction of −3.6% (p&lt;0.05) between first and second estimates and a non-significant increase (+1.1%) between second and third measurements. When compared with the second and third estimates in the amputation group, men older than 70yr presented lower DXR-BMD, DXR-CT, and DXR-MCI values (p&lt;0.001), but larger metacarpal outer and inner bone diameters (DXR-W and DXR-MD; p&lt;0.001). DXR-MD of the elderly men group was also more extended when compared with the baseline measurements of the amputation cohort (p&lt;0.001). The early accentuated cortical bone loss and particularly the pronounced decrease of the outer bone width seem to be characteristic for amputation-induced osteoporosis, suggesting that this might be a distinct secondary osteoporosis entity. When compared with amputation-associated osteoporosis, where the bone loss occurs to a higher extent in the outer bone diameter than in the medullary cavity, the age-related bone changes lead more to an increase of the medullary diameter than of the outer bone width.</description><dc:title>Comparison Between Amputation-Induced Demineralization and Age-Related Bone Loss Using Digital X-Ray Radiogrammetry</dc:title><dc:creator>Max-Ludwig Schäfer, Joachim Böttcher, Alexander Pfeil, Andreas Hansch, Ansgar Malich, Martin H. Maurer, Florian Streitparth, Rainer Röttgen, Diane M. Renz</dc:creator><dc:identifier>10.1016/j.jocd.2011.08.006</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-04-01</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-04-01</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>135</prism:startingPage><prism:endingPage>145</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS109469501100237X/abstract?rss=yes"><title>DXA Femoral Neck Strength Analysis in Chinese Overweight and Normal Weight Adolescents</title><link>http://www.clinicaldensitometry.com/article/PIIS109469501100237X/abstract?rss=yes</link><description>Abstract: The aim of this study was to compare femoral neck (FN) strength in Chinese overweight adolescents with gender-matched normal weight controls and investigate the relationship of total body soft tissue composition (lean and fat masses) to indices of FN strength. Dual-energy X-ray absorptiometry (DXA) measurements of the proximal femur and total body were made in 65 Chinese overweight adolescents and 89 gender-matched normal weight controls using Lunar Prodigy DXA bone densitometer (GE Healthcare, Madison, WI). FN bone mineral density (BMD), total body lean mass, fat mass, and bone mineral content (BMC) were measured. Using FN BMD values derived from DXA measurements, hip structural analysis (HSA) was performed using Lunar enCORE (GE Healthcare), version 10.5 software. Structural parameters derived by HSA were bone cross-sectional area (CSA), cross-sectional moment of inertia (CSMI), and the section modulus (Z). Data were analyzed by Student’s t-test, Pearson correlation coefficients (r), and one-way analysis of covariance (ANCOVA). Overweight boys and girls had higher body weight, lean mass, fat mass, and body mass index (p&lt;0.001) than normal controls. CSA, CSMI, and Z were higher in overweight groups compared with controls (p&lt;0.05). Lean mass correlated well with all HSA parameters (range of r: 0.501–0.714) for both genders. ANCOVA test showed no significant differences between overweight and normal weight groups regarding HSA variables in both genders after adjustment for lean mass. However, the differences remain significant after adjustment for fat mass in boys but not in girls. This study supports the conclusion that overweight individuals have greater hip neck strength in comparison with normal weight controls in Chinese adolescents. Lean mass is a major determinant for FN strength.</description><dc:title>DXA Femoral Neck Strength Analysis in Chinese Overweight and Normal Weight Adolescents</dc:title><dc:creator>Jian Gong, Yi Xu, Bin Guo, Hao Xu</dc:creator><dc:identifier>10.1016/j.jocd.2011.12.008</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-03-09</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-03-09</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>146</prism:startingPage><prism:endingPage>151</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002368/abstract?rss=yes"><title>Peak Bone Mineral Density and Its Determinants in an Asian Indian Population</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002368/abstract?rss=yes</link><description>Abstract: Data on peak bone mineral density (BMD) and its determinants in Asian Indians are limited. We studied the peak BMD and its determinants in Asian Indians. A total of 1137 young (age: 25–35yr) healthy volunteers of either sex (558 men and 579 women) were recruited for dietary evaluation, analyses of serum calcium, inorganic phosphorus, alkaline phosphatase, 25-hydroxyvitamin D [25(OH)D], and intact parathyroid hormone (iPTH) levels, and measurement of BMD with dual-energy X-ray absorptiometry. In men and women, peak bone mass (PBM) at the femoral neck, femoral trochanter, total femur, and lumbar spine was achieved between 25 and 30yr of age, whereas PBM at the femoral intertrochanter occurred between 30 and 35yr of age. Peak BMD was lower than that of Caucasians by 15.2–21.1% in men and 14.4–20.6% in women. On stepwise multiple regression, height and weight were the most consistent predictors of BMD at all sites in both groups. In men, 25(OH)D positively predicted BMD at the hip, whereas in women, serum iPTH negatively predicted BMD at the femoral trochanter and total femur. The study concluded that Asian Indians have significantly lower peak BMD than Caucasians and that weight and height are the most consistent predictors of BMD at all sites in both men and women.</description><dc:title>Peak Bone Mineral Density and Its Determinants in an Asian Indian Population</dc:title><dc:creator>Vyankatesh K. Shivane, Vijaya Sarathi, Anurag R. Lila, Tushar Bandgar, Shashank R. Joshi, Padmavathy S. Menon, Nalini S. Shah</dc:creator><dc:identifier>10.1016/j.jocd.2011.12.007</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-03-09</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-03-09</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>152</prism:startingPage><prism:endingPage>158</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002320/abstract?rss=yes"><title>Increase in Android Fat Mass With Age in Healthy Women With Normal Body Mass Index</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002320/abstract?rss=yes</link><description>Abstract: Body fat distribution is gender specific: men tend to accumulate adipose tissue in the android region, whereas women tend to do so in the gynoid region. The aim of the study was to assess total fat mass (TFM), android fat (AF), and gynoid fat (GF) mass in a selected group of healthy adult women with normal body mass index (BMI) to evaluate variations in fat distribution. Seventy-seven women (20–69yr of age) with BMI values between ≥18.5 and ≤24.9kg/m2 were included. TMF, AF, GF, and the AF to GF ratio (A:G) were assessed using dual-energy X-ray absorptiometry. Results showed an increase in AF after the fifth decade of life (D), which reached statistical significance in the sixth and seventh decades (p&lt;0.05–0.008), a 33% increase in kg of AF between the fourth and seventh and a 20% increase in A:G between the third and the seventh, with no significant changes in TFM and GF. In normal BMI women, age appears to be associated with changes in fat mass distribution with an increase in AF, which might have potential deleterious health consequences, after the fifth D.</description><dc:title>Increase in Android Fat Mass With Age in Healthy Women With Normal Body Mass Index</dc:title><dc:creator>Silvina R. Mastaglia, Fabiana Solis, Alicia Bagur, Carlos Mautalen, Beatriz Oliveri</dc:creator><dc:identifier>10.1016/j.jocd.2011.12.006</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-03-09</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-03-09</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>159</prism:startingPage><prism:endingPage>164</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002228/abstract?rss=yes"><title>Social Determinants of Bone Densitometry Uptake for Osteoporosis Risk in Patients Aged 50Yr and Older: A Systematic Review</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002228/abstract?rss=yes</link><description>Abstract: The World Health Organization identifies that osteoporosis is one of the leading health problems in the Western world. An increased risk of fragility fracture is observed in more socially disadvantaged individuals in most Western countries. Dual-energy X-ray absorptiometry (DXA) is currently the procedure of choice to diagnose osteoporosis and assess fracture risk. We systematically reviewed the literature regarding social determinants of DXA utilization for osteoporosis detection in patients aged 50yr and older using a computer-aided search of MEDLINE, EMBASE, CINAHL, and PsychINFO from January 1994 to December 2010. Five cross-sectional studies, incorporating 16 separate analyses, were identified for inclusion in this review. The best evidence analysis identified limited evidence for a positive association between either income or education with DXA utilization; furthermore, the best evidence analysis found no evidence for an association between either marital status or working status and DXA utilization. Further research is required to identify whether a relationship exists and elucidate reasons for disparities in DXA utilization between different social groups, such as choice and referral processes, as a necessary precursor in identifying modifiable determinants and appropriate strategies to promote preventive screening to identify fracture risk.</description><dc:title>Social Determinants of Bone Densitometry Uptake for Osteoporosis Risk in Patients Aged 50Yr and Older: A Systematic Review</dc:title><dc:creator>Sharon L. Brennan, Anita E. Wluka, Haslinda Gould, Geoffrey C. Nicholson, William D. Leslie, Peter R. Ebeling, Brian Oldenburg, Mark A. Kotowicz, Julie A. Pasco</dc:creator><dc:identifier>10.1016/j.jocd.2011.12.005</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-02-10</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-02-10</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>165</prism:startingPage><prism:endingPage>175</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002174/abstract?rss=yes"><title>Hip Cortical Thickness Assessment in Postmenopausal Women With Osteoporosis and Strontium Ranelate Effect on Hip Geometry</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002174/abstract?rss=yes</link><description>Abstract: The aims of this study were to assess the relationship between hip geometry and the 5-yr risk of hip fractures in postmenopausal osteoporotic women and the effects of strontium ranelate on these parameters. Using the 5-yr data of a randomized placebo-controlled trial of strontium ranelate (Treatment of Peripheral Osteoporosis Study [TROPOS]), we reanalyzed the hip dual-energy X-ray absorptiometry scans to determine the role of hip geometry in the risk of hip fractures (placebo group, n=636) and to analyze the effects of strontium ranelate (n=483). The outcomes included the hip structure analysis (HSA) parameters: cross-sectional area (CSA), section modulus, cortical thickness, and buckling ratio, measured at femoral neck, intertrochanteric (IT) region, and proximal shaft. The geometric parameters associated with an increased risk of hip fracture over 5yr were IT CSA and femoral shaft cortical thickness independent of age and total-hip bone mineral density (BMD). Using Bonferroni adjustment, IT cortical thickness was associated with the risk of hip fracture. Over 5yr, significant decreases in some femoral dimensions of the placebo group contrast with significant increases in strontium ranelate group after adjustment for age and BMD. Using Bonferroni adjustment, differences between placebo and strontium ranelate groups were no longer significant after adjustment on 5-yr BMD changes. Some HSA parameters have predictive value for hip fracture risk in postmenopausal osteoporotic women. Strontium ranelate improves some HSA parameters, through the BMD increase.</description><dc:title>Hip Cortical Thickness Assessment in Postmenopausal Women With Osteoporosis and Strontium Ranelate Effect on Hip Geometry</dc:title><dc:creator>Karine Briot, Claude Laurent Benhamou, Christian Roux</dc:creator><dc:identifier>10.1016/j.jocd.2011.11.006</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-02-10</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-02-10</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>176</prism:startingPage><prism:endingPage>185</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002162/abstract?rss=yes"><title>Insulin Resistance in Type 2 Diabetes Mellitus May Be Related to Bone Mineral Density</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002162/abstract?rss=yes</link><description>Abstract: The mechanism of bone mineral density (BMD) changes in type 2 diabetes mellitus is not clear. We aimed to investigate the effect of insulin resistance in type 2 diabetics on BMD. Insulin resistance was determined using the homeostasis model assessment index (HOMA-IR). Nineteen type 2 diabetic patients with a HOMA-IR &lt;2.7 (mean age, 51.5±9.6yr; body mass index [BMI], 27.3±5.1kg/m2; duration of diabetes, 10.5±7.3yr) were included in Group A, and 30 BMI- and age-matched type 2 diabetic patients with a HOMA-IR ≥2.7 were included in Group B. The BMD was measured with dual-energy X-ray absorptiometry. Independent t-test was used for statistical analysis. The Group A values for mean fasting glucose and insulin levels were 160.1±77.0mg/dL and 4.79±2.89μU/L, respectively, whereas the Group B values were 195.1±58.9mg/dL (p&gt;0.05) and 19.30±16.89μU/L (p=0.0001). Significantly higher total lumbar vertebra T-score (p=0.02) and total lumbar vertebra BMD in Group A were determined than Group B (p=0.033). The lumbar vertebra total Z-score was significantly lower in Group B (p=0.042). Marked insulin resistance may have a negative effect on BMD in type 2 diabetics, while the presence of hyperinsulinemia may be associated with the low BMD.</description><dc:title>Insulin Resistance in Type 2 Diabetes Mellitus May Be Related to Bone Mineral Density</dc:title><dc:creator>Senay Arikan, Alpaslan Tuzcu, Mithat Bahceci, Sehmuz Ozmen, Deniz Gokalp</dc:creator><dc:identifier>10.1016/j.jocd.2011.11.005</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-02-10</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-02-10</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>186</prism:startingPage><prism:endingPage>190</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002149/abstract?rss=yes"><title>Anthropometric Predictors of Geometric Indices of Hip Bone Strength in a Group of Lebanese Postmenopausal Women</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002149/abstract?rss=yes</link><description>Abstract: The effects of anthropometric characteristics on hip bone strength in postmenopausal women are not completely elucidated. The aim of this study was to investigate the influence of anthropometric characteristics on geometric indices of hip bone strength using the hip structure analysis (HSA) program in a group of Lebanese postmenopausal women. This study included 109 postmenopausal women (aged 64–84yr). Age and years since menopause were recorded. Body composition and bone mineral density were assessed by dual-energy X-ray absorptiometry (DXA). To evaluate hip bone strength, DXA scans were analyzed at the femoral neck (FN), the intertrochanteric (IT), and the femoral shaft (FS) by the HSA program. Cross-sectional area (CSA), an index of axial compression strength, section modulus (Z), an index of bending strength, and buckling ratio (BR), an estimate of cortical stability in buckling, were measured from bone mass profiles. Using univariate analysis, weight, height, body mass index (BMI), lean mass, and fat mass were positively correlated to CSA and Z of the FN, IT, and FS. Weight, BMI, fat mass, and fat mass percentage were negatively correlated to BR of the FN, IT, and FS. Multiple linear regression analysis showed that lean mass was a stronger determinant of FN CSA, FN Z, IT Z, and FS Z than fat mass, whereas fat mass was a stronger determinant of IT CSA, FS CSA, IT BR, and FS BR than lean mass. This study suggests that, in postmenopausal women, fat mass is a strong predictor of hip axial compression strength and cortical stability in buckling, and lean mass is a strong predictor of hip bending strength.</description><dc:title>Anthropometric Predictors of Geometric Indices of Hip Bone Strength in a Group of Lebanese Postmenopausal Women</dc:title><dc:creator>Rawad El Hage, Rafic Baddoura</dc:creator><dc:identifier>10.1016/j.jocd.2011.11.003</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-02-27</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-02-27</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>191</prism:startingPage><prism:endingPage>197</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002137/abstract?rss=yes"><title>Dual-Energy X-Ray Absorptiometry in the Evaluation of Abdominal Aortic Calcifications</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002137/abstract?rss=yes</link><description>Abstract: The objective of this study was to evaluate the diagnostic performance of the new dual-energy X-ray absorptiometry equipment vs digital radiography (DR) in the detection and scoring of abdominal aortic calcifications (AACs). Seventy-five patients with indication for morphometric evaluation of the spine underwent vertebral fracture assessment (VFA) and spinal DR (gold standard). The radiographic and VFA images were analyzed to detect AAC using a previously validated 24-point scale (AAC-24) and a simplified 8-point scale (AAC-8). The evaluation was conducted by 2 expert radiologists and repeated by the more experienced of the 2 after 7d to verify the results. Patients with a score of 5 or more in AAC-24 and 3 or more in AAC-8 were considered at risk for cardiovascular diseases (CVDs). The aorta was not completely visible in 11 VFA and 1 DR images. DR detected AAC in 42 of the 63 patients (66.7%), whereas 15 patients (23.8%) were considered at risk for CVD. The VFA showed sensitivity, specificity, and accuracy in the detection of AAC with values of 78.6%, 85.7%, and 81.0%, respectively, with both AAC-24 and AAC-8; in the identification of patients at risk for CVD, VFA demonstrated sensitivity, specificity, and accuracy, respectively, with values of 86.7%, 100%, and 96.8% using AAC-24 and 86.7%, 93.8%, and 92.1% using AAC-8. In the detection of AAC, intraobserver agreement was superimposable using both the techniques (κ=1.00), whereas in the identification of patients at risk for CVD, kappa values were 0.96 and 0.95 using AAC-24 and 1.00 and 0.96 using AAC-8 for DR and VFA, respectively. Interobserver agreement in the evaluation of the presence/absence of AAC showed a kappa value of 0.76 for DR and 0.71 for VFA, whereas kappa values of 0.91 and 0.87 for DR and 0.85 and 0.83 for VFA were achieved for CVD risk using AAC-24 and AAC-8, respectively. AAC can be easily and accurately diagnosed by VFA with satisfactory accuracy, reproducibility, and repeatability. VFA may be used in the assessment and monitoring of AAC.</description><dc:title>Dual-Energy X-Ray Absorptiometry in the Evaluation of Abdominal Aortic Calcifications</dc:title><dc:creator>Alberto Bazzocchi, Federica Ciccarese, Danila Diano, Paolo Spinnato, Ugo Albisinni, Cristina Rossi, Giuseppe Guglielmi</dc:creator><dc:identifier>10.1016/j.jocd.2011.11.002</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-02-10</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-02-10</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>198</prism:startingPage><prism:endingPage>204</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002125/abstract?rss=yes"><title>Bone Quality and Nutritional Status in Children With Congenital Heart Defects</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002125/abstract?rss=yes</link><description>Abstract: The aim of this study was to evaluate bone quality and nutritional status in children with congenital heart defects (CHDs) using quantitative ultrasound. A cross-sectional study was designed. A population-based sample of 75 children with CHD (age: 0–6yr) from the Department of Pediatric Cardiology at the National Cardiology Institute “Ignacio Chávez” was compared with 106 healthy children during 2009. Weight and height were determined in both groups; bone status was measured at the radius and tibia as speed of sound (SOS). Nutritional status was defined according to the Waterloo and Gómez index. Chi-square test, Student’s t-test, and analysis of variance were used to determine the statistical differences. A linear regression analysis adjusted by age, weight, height, type of CHD, and birth weight was made. Both groups were similar in sex distribution, prematurity, and birth weight. Acyanotic cardiopathy with increased pulmonary flow was the most frequent (61.3%). Prevalence of malnutrition was higher in CHD group compared with healthy children (p&lt;0.001), and radius SOS was lower in children with CHD compared with healthy children (3484±180 vs 3575±159m/s, respectively; 95% confidence interval: 39.8–143; p=0.001). A positive correlation was found between CHD and reduced SOS in the adjusted linear regression model, r2=0.455 (p&lt;0.001). Children with CHD have lower SOS radius values compared with healthy children, suggesting reduced bone quality regardless of the nutritional status.</description><dc:title>Bone Quality and Nutritional Status in Children With Congenital Heart Defects</dc:title><dc:creator>Chico-Barba Laura Gabriela, Vivanco-Muñoz Nalleli, Avilés-Toxqui Dalia Patricia, Tamayo Juan, Rivas-Ruíz Rodolfo, Buendía-Hernández Alfonso, Clark Patricia</dc:creator><dc:identifier>10.1016/j.jocd.2011.11.001</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-03-09</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-03-09</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>205</prism:startingPage><prism:endingPage>210</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011002101/abstract?rss=yes"><title>Evaluation of Bone Mineral Density in Postmenopausal Women in Kuwait</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011002101/abstract?rss=yes</link><description>Abstract: Menopause is the major risk factor for the loss of bone mineral density (BMD) and bone mineral content (BMC) in women. In this study, we determined the prevalence of osteoporosis in postmenopausal women in Kuwait and compared it with that of other Middle East and west countries. Two thousand two hundred ninety-six postmenopausal women ranging in age from 40 to 87yr were included in the study and divided into 4 age groups by decade. We measured body weight, height, body mass index (BMI), BMD, and BMC. The mean age, height, and weight were 59.1+7.9yr, 154.7+6.5cm, and 77.3+14.9kg, respectively. The mean BMI and BMC were 32.4+6.6kg/m2 and 0.9+0.14g/cm2, respectively. The average T-scores for the hip and lumbar spine were −0.280+1.2 and −1.297+1.33, respectively. BMC significantly decreased with age from 0.95 to 0.81g/cm2. Four hundred forty-four (19.3%) were found to have osteoporosis. The incidence of osteoporosis significantly increased from 4.3% to 39.9% with age, which is lower than that reported for Saudi (40%) and Moroccan women (39.6%) and higher than that for US/European (31%) and Lebanese women (11%).</description><dc:title>Evaluation of Bone Mineral Density in Postmenopausal Women in Kuwait</dc:title><dc:creator>Renu Gupta, Osama Al-saeed, Fawaz Azizieh, Abdullatif Albusairi, Pushpak Gupta, Ahmed Mohammed</dc:creator><dc:identifier>10.1016/j.jocd.2011.10.006</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2011-12-12</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2011-12-12</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>211</prism:startingPage><prism:endingPage>216</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011001958/abstract?rss=yes"><title>Association of Bone Mineral Density, Parameters of Bone Turnover, and Body Composition in Patients With Chronic Obstructive Pulmonary Disease</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011001958/abstract?rss=yes</link><description>Abstract: Patients with chronic obstructive pulmonary disease (COPD) often develop osteoporosis. Many hormones regulate bone metabolism and body composition, and some of them are affected in COPD patients vs controls. In 46 COPD patients, we measured hip neck, total hip, lumbar spine, and whole-body T-score with dual-energy X-ray absorptiometry, parameters of body composition (body mass index [BMI], fat mass index [FMI], and fat-free mass index [FFMI]), and adiponectin, leptin, parathormone, osteocalcin, calcitonin, and insulin-like growth factor I (IGF-I) serum levels and correlated them with COPD stage. Our results suggest that total hip bone mineral density (BMD) is affected by FFMI and COPD stage; lumbar spine BMD is affected by FMI and COPD stage; and whole-body BMD is affected by BMI, COPD stage, and leptin. Adiponectin, parathormone, osteocalcin, calcitonin, and IGF-I levels were not significantly correlated to BMD at any of the measured sites. Our findings are in agreement with the current literature in that a decline in lung function is correlated to a decline in BMD.</description><dc:title>Association of Bone Mineral Density, Parameters of Bone Turnover, and Body Composition in Patients With Chronic Obstructive Pulmonary Disease</dc:title><dc:creator>Georgios A. Fountoulis, Markos Minas, Panagiotis Georgoulias, Ioannis V. Fezoulidis, Konstantinos I. Gourgoulianis, Marianna Vlychou</dc:creator><dc:identifier>10.1016/j.jocd.2011.10.004</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2011-12-12</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2011-12-12</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>217</prism:startingPage><prism:endingPage>223</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011001946/abstract?rss=yes"><title>The Frequency of Low Muscle Mass and Its Overlap With Low Bone Mineral Density and Lipodystrophy in Individuals With HIV—A Pilot Study Using DXA Total Body Composition Analysis</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011001946/abstract?rss=yes</link><description>Abstract: As a result of the advances in antiretroviral therapy, the life span of human immunodeficiency virus (HIV)-infected patients has increased dramatically. Attendant to these effects are signs of premature aging with notable changes in the musculoskeletal system. Although changes in bone and fat distribution have been studied extensively, far less is known about changes in muscle. This study examined the extent of low muscle mass (LMM) and its relationship with low bone mineral density (BMD) and lipodystrophy (LD) in HIV-positive males. As such, HIV-positive males on therapy or treatment naive underwent dual-energy X-ray absorptiometry total body composition measurements. Appendicular lean mass/(height)2 and lowest 20% of residuals from regression analysis were used to define LMM. BMD criteria defined osteopenia/osteoporosis, and the percent central fat/percent lower extremity ratio defined LD. Several potential risk factors were assessed through chart review. Sixty-six males (57 with treatment and 9 treatment naive) volunteered. Treated individuals were older than naive (44 vs 34 yr) and had HIV longer (108 vs 14 mo). When definitions for sarcopenia (SP) in elderly individuals were applied, the prevalence of LMM was 21.9% and 18.8% depending on the definition used. Low BMD was present in 68.2% of participants. LD with a cutoff of 1.5 and 1.961 was present in 54.7% and 42.2% of participants, respectively. LMM and LD were negatively associated. In conclusion, this study shows that LMM is common in males with HIV and that SP affecting muscle function could be present in a substantial number of individuals. Future research needs to examine what impact decreased muscle mass and function has on morbidity, physical function, and quality of life in individuals with HIV.</description><dc:title>The Frequency of Low Muscle Mass and Its Overlap With Low Bone Mineral Density and Lipodystrophy in Individuals With HIV—A Pilot Study Using DXA Total Body Composition Analysis</dc:title><dc:creator>Bjoern Buehring, Elizabeth Kirchner, Zhiyuan Sun, Leonard Calabrese</dc:creator><dc:identifier>10.1016/j.jocd.2011.10.003</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2011-12-12</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2011-12-12</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>224</prism:startingPage><prism:endingPage>232</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011001806/abstract?rss=yes"><title>Bone Metabolism in Cholestatic Children Before and After Living-Related Liver Transplantation—a Long-Term Prospective Study</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011001806/abstract?rss=yes</link><description>Abstract: Bone disorders are common in children with end-stage liver diseases, especially those associated with cholestasis. Abnormal hepatocyte function, disordered vitamin D metabolism and calcium-phosphorous homeostasis, malnutrition, and immunosuppressive treatment are potential risk factors of bone tissue pathology before and after transplantation.The aim of the study was to analyze the long-term effect of successful living-related liver transplantation (LRLTx) on skeletal status and bone metabolism in cholestatic children.Eighteen cholestatic children (1.4±0.5yr old; 12 females [F]/6 males [M]) qualified for LRLTx were analyzed; 16 (5F/11M) of them participated in long-term observation (V4). Serum levels of osteocalcin (OC), procollagen type 1 N-terminal propeptide (P1NP), cross-linked telopeptide of type 1 collagen (CTx), insulin-like growth factor I (IGF-I), IGF-I binding protein 3 (IGFBP-3), parathyroid hormone (PTH), 25-hydroxyvitamin D (25(OH)D), and 1,25-dihydroxyvitamin D (1,25(OH)2D) were assayed before (V0) and 6mo (V1), 12mo (V2), 18mo (V3), and 4.4yr (V4) after LRLTx. Total body bone mineral content (TBBMC) and total body bone mineral density (TBBMD) were measured by dual-energy X-ray absorptiometry (DXA) at the same pattern.Before LRLTx, the OC, P1NP, CTx, IGF-I, and IGFBP-3 levels as well as TBBMC and TBBMD were decreased compared with age-matched control group. The mean serum levels of 25(OH)D and 1,25(OH)2D were within reference ranges from V0 to V4. After LRLTx, the OC, P1NP, CTx, IGF-I, and IGFBP-3 as well as TBBMC and TBBMD reached the age-matched reference values. At V4, the level of P1NP decreased below and the PTH increased above the reference range that coincided with reduced Z-scores of both TBBMC (−1.11±1.24) and TBBMD (−1.00±1.19). P1NP and CTx, both measured at V3, correlated with IGF-I at V2 (R=0.86, p=0.014 and R=0.78, p=0.021, respectively) and PTH at V3 for P1NP and V1 for CTx (R=0.64, p=0.048 and R=0.54, p=0.038, respectively). The TBBMC changes between V0 and V4 correlated with IGF-I (R=0.68, p=0.015) and 1,25(OH)2D (R=0.54, p=0.025), both assayed at V1. The change of TBBMC Z-scores between V0 and V4 correlated with P1NP at V1 (R=0.69, p=0.002). The TBBMD changes between V0 and V4 correlated with CTx at V1 (R=0.54, p=0.027) and P1NP change between V0 and V1 (R=0.51, p=0.038).In short-term observation, successful LRLTx led to bone metabolism normalization triggered by probable anabolic action of IGF-I and PTH and manifested by TBBMC and TBBMD increases. In long-term horizon, moderately impaired DXA assessed bone status coincided with disturbances in bone metabolism. Bone metabolism markers, especially P1NP and CTx, appeared to be good predictors of changes in bone status evaluated by DXA.</description><dc:title>Bone Metabolism in Cholestatic Children Before and After Living-Related Liver Transplantation—a Long-Term Prospective Study</dc:title><dc:creator>Edyta Kryskiewicz, Joanna Pawlowska, Pawel Pludowski, Hor Ismail, Elzbieta Karczmarewicz, Mikolaj Teisseyre, Ewa Skorupa, Jozef Ryzko, Piotr Kalicinski, Jerzy Socha, Roman S. Lorenc</dc:creator><dc:identifier>10.1016/j.jocd.2011.09.007</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2011-12-12</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2011-12-12</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>233</prism:startingPage><prism:endingPage>240</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS109469501100179X/abstract?rss=yes"><title>Establishment of Age-Specified Bone Mineral Density Reference Range for Indian Females Using Dual-Energy X-Ray Absorptiometry</title><link>http://www.clinicaldensitometry.com/article/PIIS109469501100179X/abstract?rss=yes</link><description>Abstract: We undertook this study to establish age-specified bone mineral density (BMD) reference range for Indian females using dual-energy X-ray absorptiometry. BMD at multiple skeletal sites was measured in 2034 healthy women aged 18–85yr. The effect of anthropometry and biochemical parameters on BMD was determined. Peak BMD was observed between 30 and 35yr at the hip, lumbar spine, and radius. Significant positive correlation of height and weight with BMD was observed at 33% radius, femur neck, and lumbar spine, whereas significant negative correlation was seen between serum alkaline phosphatase (ALP) and serum parathyroid hormone levels with BMD at aforementioned sites. On multivariate regression analysis, age, weight, and serum ALP were the most consistent contributors to variance in the BMD. Compared with age-matched US females, BMD of lumbar spine was significantly lower for our subjects in all age groups. Prevalence of osteoporosis among women aged older than 50yr was significantly higher based on Caucasian T-scores as opposed to using peak BMD/standard deviation values from the population under review at lumbar spine but not at femoral neck.</description><dc:title>Establishment of Age-Specified Bone Mineral Density Reference Range for Indian Females Using Dual-Energy X-Ray Absorptiometry</dc:title><dc:creator>Raman K. Marwaha, Nikhil Tandon, Parjeet Kaur, Aparna Sastry, Kuntal Bhadra, Archna Narang, Saurav Arora, Kalaivani Mani</dc:creator><dc:identifier>10.1016/j.jocd.2011.09.006</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2011-12-12</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2011-12-12</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>241</prism:startingPage><prism:endingPage>249</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695011001788/abstract?rss=yes"><title>Ethnic Dress, Vitamin D Intake, and Calcaneal Bone Health in Young Women in the United Kingdom</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695011001788/abstract?rss=yes</link><description>Abstract: Clothing styles that conceal skin from ultraviolet sun radiation contribute to vitamin D deficiency, especially in veiled female minorities in high latitudes. This is the first research into possible effects of ethnic dress on the os calcis and the first study outside North Africa and the Middle East to investigate whether discernible differences in bone quality exist between veiled and unveiled women. The limited previous research into clothing habits and bone health has been inconclusive. One hundred eight women aged 18–45yr living in the United Kingdom (around 51° north) were analyzed. Forty-three consistently covered arms, hair, and neck when outdoors, whereas 65 consistently had arms, hair, neck, and possibly legs exposed. The quantitative ultrasound scanning (QUS) measurements at the calcaneus were speed of sound (SOS) and broadband ultrasound attenuation (BUA), which were translated into a single clinical value, stiffness index (SI). Dietary intake of vitamin D and calcium was estimated using a validated food frequency questionnaire, and several other risk factors were assessed. There was no significant difference in SI between veiled and unveiled participants (101.30±1.71 vs 99.98±1.86; p=0.721); SOS and BUA were also not significantly different. However, smoking and long-term use of steroid medication were significant predictors of calcaneal bone quality, confirming existing research. Our analysis suggests that clothing style alone does not lead to appreciable differences in the quality of the os calcis in young women in the United Kingdom as assessed by QUS.</description><dc:title>Ethnic Dress, Vitamin D Intake, and Calcaneal Bone Health in Young Women in the United Kingdom</dc:title><dc:creator>Robert Knoss, Lewis G. Halsey, Sue Reeves</dc:creator><dc:identifier>10.1016/j.jocd.2011.09.005</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2011-12-19</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2011-12-19</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>250</prism:startingPage><prism:endingPage>254</prism:endingPage></item><item rdf:about="http://www.clinicaldensitometry.com/article/PIIS1094695012000042/abstract?rss=yes"><title>Fracture of Vertebral Spine Because of an Unusual Cause of Osteoporosis in a Young Male Patient</title><link>http://www.clinicaldensitometry.com/article/PIIS1094695012000042/abstract?rss=yes</link><description>A 42-yr-old male patient presented to our department with severe back pain, which increased with movement. In his past medical history, there was a caustic esophageal and gastric injury after corrosive substance ingestion 4yr prior for which he underwent esophagectomy and partial gastrectomy. A feeding jejunostomy was inserted postoperatively for his lifelong nutrition. During these 4yr, he was immobile for 18hr per day because of his disability and psychiatric status. Three months ago, he was admitted to another hospital because of back pain. After his biochemical and radiologic evaluation, osteoporosis was detected in the femur and lumbar vertebrae (T-score of the femoral neck was −2.9, and T-scores of the lumbar vertebrae were L1: −4, L2: −4.2, L3: −4.3, and L1–L4: −4.8). A compression fracture was also evident at the level of the 12th thoracic vertebra on plain graphics (), and was confirmed by magnetic resonance imaging. Complete blood count and comprehensive metabolic profile did not reveal any significant abnormality. Serum 25-hydroxy vitamin D was 36ng/mL. Gonadal and anterior hypophyseal hormones showed follicle-stimulating hormone 6.7mIU/mL, luteinizing hormone 3.4mIU/mL, and testosterone 3.4ng/mL. Parathormone was 36pg/mL, and thyroid function tests revealed thyroid stimulating hormone 2mIU/mL, free T3 5pmol/L, and free T4 16pmol/L.</description><dc:title>Fracture of Vertebral Spine Because of an Unusual Cause of Osteoporosis in a Young Male Patient</dc:title><dc:creator>Asena Gökçay Canpolat, Gülay Sain Güven</dc:creator><dc:identifier>10.1016/j.jocd.2012.01.001</dc:identifier><dc:source>Journal of Clinical Densitometry 15, 2 (2012)</dc:source><dc:date>2012-03-09</dc:date><prism:publicationName>Journal of Clinical Densitometry</prism:publicationName><prism:publicationDate>2012-03-09</prism:publicationDate><prism:volume>15</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S1094-6950(12)X0002-7</prism:issueIdentifier><prism:section>Letter to the Editor</prism:section><prism:startingPage>255</prism:startingPage><prism:endingPage>256</prism:endingPage></item></rdf:RDF>
