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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
  12. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s001980050236.

Title:
Treatment of Postmenopausal Women with Osteoporosis or Low Bone Density with Raloxifene | Osteoporosis International
Description:
Raloxifene, a selective estrogen receptor modulator (SERM), has been shown to improved bone mineral density (BMD) and serum lipid profiles in healthy postmenopausal women. The objective of this study was to examine the effects of raloxifene on BMD, biochemical markers of bone metabolism and serum lipids in postmenopausal women with low bone density or osteoporosis. This Phase II, multicenter, 24-month, double-masked study assessed the efficacy and safety of raloxifene in 129 postmenopausal women (mean age ± SD: 60.2 ± 6.7 years) with osteoporosis or low bone density (baseline mean lumbar spine BMD T-score: −2.8). Women were randomly assigned to one of three treatment groups: placebo, 60 mg/day raloxifene-HCl (RLX 60) or 150 mg/day raloxifene-HCl (RLX 150) and concomitantly received 1000 mg/day calcium and 300 U/day vitamin D3. At 24 months, BMD was significantly increased in the lumbar spine (+3.2%), femoral neck (+2.1%), trochanter (+2.7%) and total hip (+1.6%) in the RLX 60 group compared with the placebo group (p<0.05). The RLX 150 group had increases in BMD similar to those observed with RLX 60. A greater percentage of raloxifene-treated patients, compared with those receiving placebo, had increased BMD (p<0.05). Serum bone-specific alkaline phosphatase activity, serum osteocalcin, and urinary type I collagen:creatinine ratio were significantly decreased in the RLX-treated groups, compared with the placebo group (p<0.01). RLX 60 treatment significantly decreased serum levels of triglycerides, and total- and LDL-cholesterol levels (p<0.01). The rates of patient discontinuation and adverse events were not significantly different among groups. In this study, raloxifene increased bone density, decreased bone turnover, and improved the serum lipid profile with minimal adverse events, and may be a safe and effective treatment for postmenopausal women with osteoporosis or low bone density.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Social Networks
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  • Insurance

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 7,642,828 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We don’t know how the website earns money.

Not every website is profit-driven; some are created to spread information or serve as an online presence. Websites can be made for many reasons. This could be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

bone, article, raloxifene, osteoporosis, postmenopausal, women, density, treatment, group, bmd, serum, rlx, privacy, cookies, content, low, study, access, information, publish, research, search, placebo, significantly, france, lilly, data, log, journal, meunier, vignot, garnero, month, lumbar, spine, groups, mgday, increased, compared, decreased, discover, springer, optional, personal, parties, policy, find, track, international, cite,

Topics {✒️}

60 mg/day raloxifene-hcl 150 mg/day raloxifene-hcl double-masked study assessed raloxifene/cholecalciferol combination therapy month download article/chapter low bone density decreased bone turnover privacy choices/manage cookies bone turnover markers ldl-cholesterol levels full article pdf /day vitamin d3 serum lipid profiles serum lipid profile raloxifene-treated patients de pathologie osseuse lilly corporate center european economic area scope submit manuscript hĂ´pital edouard herriot investigation des osteoporoses conditions privacy policy serum lipids healthy postmenopausal women accepting optional cookies minimal adverse events main content log rlx-treated groups journal finder publish bone metabolism raloxifene treatment check access instant access significantly decreased rlx 150 group lumbar spine patient discontinuation related subjects article log liu-leage privacy policy personal data serum osteocalcin treatment groups effective treatment books a significantly increased placebo group article cite information

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Treatment of Postmenopausal Women with Osteoporosis or Low Bone Density with Raloxifene
         description: Raloxifene, a selective estrogen receptor modulator (SERM), has been shown to improved bone mineral density (BMD) and serum lipid profiles in healthy postmenopausal women. The objective of this study was to examine the effects of raloxifene on BMD, biochemical markers of bone metabolism and serum lipids in postmenopausal women with low bone density or osteoporosis. This Phase II, multicenter, 24-month, double-masked study assessed the efficacy and safety of raloxifene in 129 postmenopausal women (mean age Âą SD: 60.2 Âą 6.7 years) with osteoporosis or low bone density (baseline mean lumbar spine BMD T-score: −2.8). Women were randomly assigned to one of three treatment groups: placebo, 60 mg/day raloxifene-HCl (RLX 60) or 150 mg/day raloxifene-HCl (RLX 150) and concomitantly received 1000 mg/day calcium and 300 U/day vitamin D3. At 24 months, BMD was significantly increased in the lumbar spine (+3.2%), femoral neck (+2.1%), trochanter (+2.7%) and total hip (+1.6%) in the RLX 60 group compared with the placebo group (p<0.05). The RLX 150 group had increases in BMD similar to those observed with RLX 60. A greater percentage of raloxifene-treated patients, compared with those receiving placebo, had increased BMD (p<0.05). Serum bone-specific alkaline phosphatase activity, serum osteocalcin, and urinary type I collagen:creatinine ratio were significantly decreased in the RLX-treated groups, compared with the placebo group (p<0.01). RLX 60 treatment significantly decreased serum levels of triglycerides, and total- and LDL-cholesterol levels (p<0.01). The rates of patient discontinuation and adverse events were not significantly different among groups. In this study, raloxifene increased bone density, decreased bone turnover, and improved the serum lipid profile with minimal adverse events, and may be a safe and effective treatment for postmenopausal women with osteoporosis or low bone density.
         datePublished:
         dateModified:
         pageStart:330
         pageEnd:336
         sameAs:https://doi.org/10.1007/s001980050236
         keywords:
            Key words:Bone density – Lipids – Menopause – Osteoporosis – Raloxifene
            Orthopedics
            Endocrinology
            Rheumatology
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            name:Osteoporosis International
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                        name:Lilly France (Saint Cloud), Saint Cloud, France;, , FR
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                        name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
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               name:T. Liu
               affiliation:
                     name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA
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                        name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
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      headline:Treatment of Postmenopausal Women with Osteoporosis or Low Bone Density with Raloxifene
      description: Raloxifene, a selective estrogen receptor modulator (SERM), has been shown to improved bone mineral density (BMD) and serum lipid profiles in healthy postmenopausal women. The objective of this study was to examine the effects of raloxifene on BMD, biochemical markers of bone metabolism and serum lipids in postmenopausal women with low bone density or osteoporosis. This Phase II, multicenter, 24-month, double-masked study assessed the efficacy and safety of raloxifene in 129 postmenopausal women (mean age Âą SD: 60.2 Âą 6.7 years) with osteoporosis or low bone density (baseline mean lumbar spine BMD T-score: −2.8). Women were randomly assigned to one of three treatment groups: placebo, 60 mg/day raloxifene-HCl (RLX 60) or 150 mg/day raloxifene-HCl (RLX 150) and concomitantly received 1000 mg/day calcium and 300 U/day vitamin D3. At 24 months, BMD was significantly increased in the lumbar spine (+3.2%), femoral neck (+2.1%), trochanter (+2.7%) and total hip (+1.6%) in the RLX 60 group compared with the placebo group (p<0.05). The RLX 150 group had increases in BMD similar to those observed with RLX 60. A greater percentage of raloxifene-treated patients, compared with those receiving placebo, had increased BMD (p<0.05). Serum bone-specific alkaline phosphatase activity, serum osteocalcin, and urinary type I collagen:creatinine ratio were significantly decreased in the RLX-treated groups, compared with the placebo group (p<0.01). RLX 60 treatment significantly decreased serum levels of triglycerides, and total- and LDL-cholesterol levels (p<0.01). The rates of patient discontinuation and adverse events were not significantly different among groups. In this study, raloxifene increased bone density, decreased bone turnover, and improved the serum lipid profile with minimal adverse events, and may be a safe and effective treatment for postmenopausal women with osteoporosis or low bone density.
      datePublished:
      dateModified:
      pageStart:330
      pageEnd:336
      sameAs:https://doi.org/10.1007/s001980050236
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         Key words:Bone density – Lipids – Menopause – Osteoporosis – Raloxifene
         Orthopedics
         Endocrinology
         Rheumatology
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      isPartOf:
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         issn:
            1433-2965
            0937-941X
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         name:Springer-Verlag London Limited
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            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
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            name:P. J. Meunier
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                  address:
                     name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France, , FR
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                     name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France, , FR
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                  address:
                     name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France, , FR
                     type:PostalAddress
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                  name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France
                  address:
                     name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France, , FR
                     type:PostalAddress
                  type:Organization
            type:Person
            name:E. Paris
            affiliation:
                  name:Centre Lyonnais d’Investigation des Osteoporoses (CLIOS), Lyon, France
                  address:
                     name:Centre Lyonnais d’Investigation des Osteoporoses (CLIOS), Lyon, France, , FR
                     type:PostalAddress
                  type:Organization
            type:Person
            name:S. Liu-Leage
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                  name:Lilly France (Saint Cloud), Saint Cloud, France;
                  address:
                     name:Lilly France (Saint Cloud), Saint Cloud, France;, , FR
                     type:PostalAddress
                  type:Organization
            type:Person
            name:S. Sarkar
            affiliation:
                  name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA
                  address:
                     name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
                     type:PostalAddress
                  type:Organization
            type:Person
            name:T. Liu
            affiliation:
                  name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA
                  address:
                     name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
                     type:PostalAddress
                  type:Organization
            type:Person
            name:M. Wong
            affiliation:
                  name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA
                  address:
                     name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
                     type:PostalAddress
                  type:Organization
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            name:M. W. Draper
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                  name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA
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         name:Centre Lyonnais d’Investigation des Osteoporoses (CLIOS), Lyon, France, , FR
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            name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France
            address:
               name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France, , FR
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      affiliation:
            name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France
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               name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France, , FR
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               name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France, , FR
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            name:Centre Lyonnais d’Investigation des Osteoporoses (CLIOS), Lyon, France
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               name:Centre Lyonnais d’Investigation des Osteoporoses (CLIOS), Lyon, France, , FR
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      name:S. Sarkar
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            name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA
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               name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
               type:PostalAddress
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               name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
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            name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA
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               name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
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      name:Service de Rhumatologie et de Pathologie Osseuse, HĂ´pital Edouard Herriot, Lyon, France, , FR
      name:Centre Lyonnais d’Investigation des Osteoporoses (CLIOS), Lyon, France, , FR
      name:Lilly France (Saint Cloud), Saint Cloud, France;, , FR
      name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
      name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
      name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
      name:Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA, , US
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External Links {🔗}(43)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

3.74s.