All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Muscle functions and bone strength are impaired in adolescents with type 1 diabetes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F18%3A10375420" target="_blank" >RIV/00216208:11130/18:10375420 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11320/18:10375420 RIV/00064203:_____/18:10375420

  • Result on the web

    <a href="https://doi.org/10.1016/j.bone.2017.10.005" target="_blank" >https://doi.org/10.1016/j.bone.2017.10.005</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.bone.2017.10.005" target="_blank" >10.1016/j.bone.2017.10.005</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Muscle functions and bone strength are impaired in adolescents with type 1 diabetes

  • Original language description

    Background: Sarcopenia and osteoporosis are among the late complications of type 1 diabetes (T1D) in adults. Whether and to what extent musculoskeletal impairment is present in childhood and adolescence has yet to be determined. The aim of this study was to assess volumetric bone mineral density (BMD) and dynamic muscle function in adolescents with T1D and to assess the clinical and biochemical predictors of their musculoskeletal system. Methods: Ninety-five children and adolescents (59 boys and 36 girls, mean age 16.2 +/- 1.2 years) with T1D were included in this cross-sectional study. Study participants were divided into two groups according to the duration of the disease (&lt;6 years and &gt;9 years, respectively). Volumetric BMD of the non-dominant tibia was assessed using peripheral quantitative computed tomography (pQCT). Dynamic muscle function was evaluated using jumping mechanography. Gender- and height-specific Z-scores were calculated using published reference data. HbA1c was evaluated retrospectively as an average over the past 5 years. Results: Relative muscle power (P-max/mass) and force (F-max/body weight) were significantly decreased in T1D subjects (mean Z-scores -0.4 +/- 1.0; p &lt; 0.001, and -03 +/- 1.1; p &lt; 0.01, respectively). The duration of T1D negatively affected Pmax/mass (p &lt; 0.01) but not Fmax/body weight (p = 0.54). Patients with T1D had also decreased trabecular BMD, the Strength-Strain Index and cortical thickness (mean Z-scores -0.8 +/- 1.3; -0.5 +/- 0.8 and -1.1 0.8, respectively, p &lt; 0.001 for all) whereas cortical BMD was increased when compared to controls (Z-score 12 +/- 0.90, p &lt; 0.001). No association was observed between the HbA1c and 25-hydroxyvitamin D levels and bone or muscle parameters. Conclusion: T1D influences the musculoskeletal system in adolescence. Decreased muscle function could contribute to the osteoporosis reported in adult diabetic patients.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30209 - Paediatrics

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Bone

  • ISSN

    8756-3282

  • e-ISSN

  • Volume of the periodical

    106

  • Issue of the periodical within the volume

    January

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    22-27

  • UT code for WoS article

    000417552200003

  • EID of the result in the Scopus database

    2-s2.0-85030988212