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  2. Matching Content Categories
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  7. Topics
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We are analyzing https://link.springer.com/article/10.1007/s00198-016-3774-5.

Title:
The time to and determinants of first fractures in boys with Duchenne muscular dystrophy | Osteoporosis International
Description:
Summary Boys with vertebral fractures (VF) identified through routine spine radiographs had milder, less symptomatic, and fewer VF compared to those diagnosed with VF following consultation for back pain. Spontaneous (i.e., medication-unassisted) reshaping of fractured vertebral bodies was absent. Long bone fractures were present even before Duchenne muscular dystrophy (DMD) diagnosis in some boys. Introduction The objective of the study was to determine the time to and characteristics of first fractures in Duchenne muscular dystrophy. Methods This study was a retrospective longitudinal study of 30 boys with DMD <18 years. Boys were classified into four groups according to their first fracture: those with VF identified on routine lateral spine radiographs, those with VF diagnosed following consultation for back pain, those with long bone fractures, and those without fractures. Results Compared to boys diagnosed with VF as their initial fracture following consultation for back pain, those with VF surveillance radiographs had shorter durations of glucocorticoid (GC) therapy at the time of VF diagnosis (median 1.6 versus 5.3 years, p < 0.01), higher areal (mean ± standard deviation −1.4 ± 0.7 versus −3.1 ± 0.8, p = 0.01), and volumetric (−0.3 ± 0.5 versus −2.6 ± 0.8, p < 0.01) lumbar spine bone mineral density Z-scores, as well as fewer VF (median 1.4 versus 5.2 per person, p < 0.01) and a lower median spinal deformity index (median 1.5 versus 9.5, p < 0.01). Vertebral body reshaping following VF was not observed. Ten boys sustained a long bone fracture as their first fracture at a mean age of 8.9 ± 4.0 years; four of these boys later sustained a total of 27 incident VF. Conclusions Routine lateral spine radiographs led to detection of VF in their earlier stages, vertebral body reshaping following VF was absent, and VF were frequent after the first long bone fracture. These results support the inclusion of a lateral spine radiograph starting at the time of GC initiation as part of routine bone health monitoring in DMD.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We don't see any clear sign of profit-making.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com might be cashing in, but we can't detect the method they're using.

Keywords {🔍}

article, google, scholar, pubmed, bone, cas, fractures, dystrophy, duchenne, muscular, vertebral, children, boys, osteoporosis, ward, research, study, ottawa, university, fracture, osteogenesis, imperfecta, treatment, res, miner, pediatric, mcmillan, spine, density, diagnosis, years, mineral, health, child, rauch, int, cheo, department, canada, privacy, cookies, content, time, matzinger, konji, glucocorticoid, therapy, versus, incident, access,

Topics {✒️}

month download article/chapter dual-energy x-ray absorptiometry dxa-derived 3d measurements osteoporosis-related vertebral fractures randomized placebo-controlled study fracture-induced vertebral deformity routine spine radiographs full article pdf bone mineral density spinal deformity index related subjects privacy choices/manage cookies retrospective longitudinal study placebo-controlled trial severe osteogenesis imperfecta inherited neuromuscular diseases cheo research institute disease control duchenne muscular dystrophy fowler wm jr health statistics version decreased bone turnover bone matrix mineralization long bone fractures duchnne muscular dystrophy becker muscular dystrophy long bone fracture randomized controlled study skeletal development grummer-strawn lm fractured vertebral bodies european economic area scope submit manuscript dietary reference intakes body composition measured national observational study de ridder ma conditions privacy policy stanford university press national academies press vf surveillance radiographs prevalent vertebral fractures quality standards subcommittee health research vertebral body reshaping vertebral fracture assessment incident vertebral fractures article log cycle etidronate therapy author information authors

Questions {❓}

  • Nelson DA, Kleerekoper M, Peterson EL (1994) Reversal of vertebral deformities in osteoporosis: measurement error or “rebound”?

Schema {🗺️}

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         headline:The time to and determinants of first fractures in boys with Duchenne muscular dystrophy
         description:Boys with vertebral fractures (VF) identified through routine spine radiographs had milder, less symptomatic, and fewer VF compared to those diagnosed with VF following consultation for back pain. Spontaneous (i.e., medication-unassisted) reshaping of fractured vertebral bodies was absent. Long bone fractures were present even before Duchenne muscular dystrophy (DMD) diagnosis in some boys. The objective of the study was to determine the time to and characteristics of first fractures in Duchenne muscular dystrophy. This study was a retrospective longitudinal study of 30 boys with DMD &lt;18 years. Boys were classified into four groups according to their first fracture: those with VF identified on routine lateral spine radiographs, those with VF diagnosed following consultation for back pain, those with long bone fractures, and those without fractures. Compared to boys diagnosed with VF as their initial fracture following consultation for back pain, those with VF surveillance radiographs had shorter durations of glucocorticoid (GC) therapy at the time of VF diagnosis (median 1.6 versus 5.3 years, p &lt; 0.01), higher areal (mean ± standard deviation −1.4 ± 0.7 versus −3.1 ± 0.8, p = 0.01), and volumetric (−0.3 ± 0.5 versus −2.6 ± 0.8, p &lt; 0.01) lumbar spine bone mineral density Z-scores, as well as fewer VF (median 1.4 versus 5.2 per person, p &lt; 0.01) and a lower median spinal deformity index (median 1.5 versus 9.5, p &lt; 0.01). Vertebral body reshaping following VF was not observed. Ten boys sustained a long bone fracture as their first fracture at a mean age of 8.9 ± 4.0 years; four of these boys later sustained a total of 27 incident VF. Routine lateral spine radiographs led to detection of VF in their earlier stages, vertebral body reshaping following VF was absent, and VF were frequent after the first long bone fracture. These results support the inclusion of a lateral spine radiograph starting at the time of GC initiation as part of routine bone health monitoring in DMD.
         datePublished:2016-10-24T00:00:00Z
         dateModified:2016-10-24T00:00:00Z
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            Duchenne muscular dystrophy
            First fractures
            Glucocorticoids
            Osteoporosis
            Orthopedics
            Endocrinology
            Rheumatology
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      headline:The time to and determinants of first fractures in boys with Duchenne muscular dystrophy
      description:Boys with vertebral fractures (VF) identified through routine spine radiographs had milder, less symptomatic, and fewer VF compared to those diagnosed with VF following consultation for back pain. Spontaneous (i.e., medication-unassisted) reshaping of fractured vertebral bodies was absent. Long bone fractures were present even before Duchenne muscular dystrophy (DMD) diagnosis in some boys. The objective of the study was to determine the time to and characteristics of first fractures in Duchenne muscular dystrophy. This study was a retrospective longitudinal study of 30 boys with DMD &lt;18 years. Boys were classified into four groups according to their first fracture: those with VF identified on routine lateral spine radiographs, those with VF diagnosed following consultation for back pain, those with long bone fractures, and those without fractures. Compared to boys diagnosed with VF as their initial fracture following consultation for back pain, those with VF surveillance radiographs had shorter durations of glucocorticoid (GC) therapy at the time of VF diagnosis (median 1.6 versus 5.3 years, p &lt; 0.01), higher areal (mean ± standard deviation −1.4 ± 0.7 versus −3.1 ± 0.8, p = 0.01), and volumetric (−0.3 ± 0.5 versus −2.6 ± 0.8, p &lt; 0.01) lumbar spine bone mineral density Z-scores, as well as fewer VF (median 1.4 versus 5.2 per person, p &lt; 0.01) and a lower median spinal deformity index (median 1.5 versus 9.5, p &lt; 0.01). Vertebral body reshaping following VF was not observed. Ten boys sustained a long bone fracture as their first fracture at a mean age of 8.9 ± 4.0 years; four of these boys later sustained a total of 27 incident VF. Routine lateral spine radiographs led to detection of VF in their earlier stages, vertebral body reshaping following VF was absent, and VF were frequent after the first long bone fracture. These results support the inclusion of a lateral spine radiograph starting at the time of GC initiation as part of routine bone health monitoring in DMD.
      datePublished:2016-10-24T00:00:00Z
      dateModified:2016-10-24T00:00:00Z
      pageStart:597
      pageEnd:608
      sameAs:https://doi.org/10.1007/s00198-016-3774-5
      keywords:
         Duchenne muscular dystrophy
         First fractures
         Glucocorticoids
         Osteoporosis
         Orthopedics
         Endocrinology
         Rheumatology
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                     type:PostalAddress
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                     name:Department of Pediatrics, and Division of Neurology, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada
                     type:PostalAddress
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            name:G. Karagüzel
            affiliation:
                  name:Karadeniz Technical University School of Medicine
                  address:
                     name:Department of Pediatric Endocrinology, Karadeniz Technical University School of Medicine, Trabzon, Turkey
                     type:PostalAddress
                  type:Organization
            type:Person
            name:C. Goodin
            affiliation:
                  name:Children’s Hospital of Eastern Ontario Research Institute
                  address:
                     name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
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                     name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
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      address:
         name:Department of Pediatrics, and Division of Neurology, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada
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         name:Department of Pediatric Endocrinology, Karadeniz Technical University School of Medicine, Trabzon, Turkey
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         name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
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      name:G. Karagüzel
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            name:Karadeniz Technical University School of Medicine
            address:
               name:Department of Pediatric Endocrinology, Karadeniz Technical University School of Medicine, Trabzon, Turkey
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      name:C. Goodin
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            name:Children’s Hospital of Eastern Ontario Research Institute
            address:
               name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
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      name:J. Wasson
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            name:Children’s Hospital of Eastern Ontario Research Institute
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      name:M. A. Matzinger
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               name:Department of Medical Imaging, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada
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      name:P. DesClouds
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               name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
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            type:Organization
      name:D. Cram
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            address:
               name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
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      name:M. Page
      affiliation:
            name:Children’s Hospital of Eastern Ontario Research Institute
            address:
               name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
               type:PostalAddress
            type:Organization
      name:V. N. Konji
      affiliation:
            name:Children’s Hospital of Eastern Ontario Research Institute
            address:
               name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
               type:PostalAddress
            type:Organization
      name:B. Lentle
      affiliation:
            name:University of British Columbia
            address:
               name:Department of Radiology, University of British Columbia, Vancouver, Canada
               type:PostalAddress
            type:Organization
      name:L. M. Ward
      affiliation:
            name:Children’s Hospital of Eastern Ontario Research Institute
            address:
               name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
               type:PostalAddress
            type:Organization
            name:University of Ottawa
            address:
               name:Department of Pediatrics, and Division of Endocrinology and Metabolism, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
      name:School of Epidemiology, Public Health and Preventive Medicine, University of Ottawa, Ottawa, Canada
      name:Department of Pediatrics, and Division of Neurology, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada
      name:Department of Pediatric Endocrinology, Karadeniz Technical University School of Medicine, Trabzon, Turkey
      name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
      name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
      name:Department of Medical Imaging, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada
      name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
      name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
      name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
      name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
      name:Department of Radiology, University of British Columbia, Vancouver, Canada
      name:Pediatric Bone Health Clinical Research Program, Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada
      name:Department of Pediatrics, and Division of Endocrinology and Metabolism, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada
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