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  <controlfield tag="005">20260515163944.0</controlfield>
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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1007/s00198-015-3159-1</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">92302</subfield>
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  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">ART-2015-92302</subfield>
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  <datafield tag="041" ind1=" " ind2=" ">
    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Matute-Llorente, A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-8500-1667</subfield>
  </datafield>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Effect of whole body vibration training on bone mineral density and bone quality in adolescents with Down syndrome: a randomized controlled trial</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2015</subfield>
  </datafield>
  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Summary
Adolescents with Down syndrome (DS) have poorer bone health than their peers without DS. Twenty-five adolescents with DS were randomly assigned to whole-body vibration training (WBV) or control groups. The results indicate that a 20-week WBV might be useful to improve subtotal bone mineral content and density in adolescents with DS.

Introduction
This study aims to determine the effects of 20 weeks of whole body vibration training (WBV) on bone mineral content (BMC), density (BMD), and structure variables in adolescents with Down syndrome (DS).

Methods
This randomized controlled trial of 25 adolescents (12–18 years) with DS (8 females) generated 2 non-equal groups, WBV group (n = 11) and CON group (n = 14). Using an efficacy analysis, the primary outcomes were BMC and BMD by dual-energy X-ray absorptiometry and the secondary were bone structure variables by peripheral quantitative computed tomography. A synchronous vibration platform (PowerPlate®) was used (3/week, 10 repetitions (30–60 s) 1-min rest, frequency of 25–30 Hz, and peak-to-peak displacement of 2 mm (peak acceleration 2.5–3.6 g)).

Results
WBV group improved whole body BMC 2.8 %, 95 % CI [3.5, 2.1], subtotal area, BMC, and BMD by 2.8, 4.8, and 2 %, respectively, 95 % confidence intervals (CIs) [3.4, 2.1], [6.5, 3.1], and [2.8, 1.1], respectively (all, p &lt; 0.05), showing group by time interactions in BMC and BMD (both p &lt; 0.05). Lumbar spine BMC and BMD also increased in the WBV group by 6.6 and 3.3 % both p &lt; 0.05, 95 % CIs [8.6, 4.7], and [4.9, 1.7], respectively. Regarding bone structure, WBV group showed improvements in tibial BMC at 4 % (2.9 %, 95 % CI [3.0, 2.8]) and in volumetric BMD (vBMD), cortical vBMD, and cortical thickness at 66 % of the radius (by 7.0, 2.4, and 10.9 %; 95 % CIs [7.4, 6.7], [2.6, 2.3], and [12.4, 9.3], respectively) (all, p &lt; 0.05).

Conclusions
A 20-week WBV, with this protocol, might be useful to improve subtotal BMC and BMD in adolescents with DS.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/MEC/AP-2012-02854</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN/DEP2009-09183</subfield>
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    <subfield code="9">info:eu-repo/semantics/closedAccess</subfield>
    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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    <subfield code="a">3.445</subfield>
    <subfield code="b">2015</subfield>
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    <subfield code="a">ENDOCRINOLOGY &amp; METABOLISM</subfield>
    <subfield code="b">45 / 131 = 0.344</subfield>
    <subfield code="c">2015</subfield>
    <subfield code="d">Q2</subfield>
    <subfield code="e">T2</subfield>
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  <datafield tag="592" ind1=" " ind2=" ">
    <subfield code="a">1.48</subfield>
    <subfield code="b">2015</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Medicine (miscellaneous)</subfield>
    <subfield code="c">2015</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Endocrinology, Diabetes and Metabolism</subfield>
    <subfield code="c">2015</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">info:eu-repo/semantics/article</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">González-Agüero, A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-1132-5906</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Gómez-Cabello, A.</subfield>
    <subfield code="0">(orcid)0000-0001-6492-2512</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Olmedillas, H.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Vicente-Rodríguez, G.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-4303-4097</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Casajús, J. A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-7215-6931</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1006</subfield>
    <subfield code="2">245</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Fisiatría y Enfermería</subfield>
    <subfield code="c">Área Educación Física y Depor.</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">26, 10 (2015), 2449-2459</subfield>
    <subfield code="p">Osteoporos. int.</subfield>
    <subfield code="t">OSTEOPOROSIS INTERNATIONAL</subfield>
    <subfield code="x">0937-941X</subfield>
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