Musculoskeletal system in children and adolescents with inflammatory bowel disease: normal muscle force, decreased trabecular bone mineral density and low prevalence of vertebral fractures
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
Project for conceptual development of research organization 00064203 (Motol University Hospital, Prague)
Ministry of Health (Czech Republic)
136215
Charles University Grant Agency
246216
Charles University Grant Agency
PubMed
28840427
DOI
10.1007/s00431-017-2988-7
PII: 10.1007/s00431-017-2988-7
Knihovny.cz E-zdroje
- Klíčová slova
- Bone strength, Inflammatory bowel disease, Mechanography, Muscle functions, Peripheral quantitative computed tomography, Vitamin D,
- MeSH
- absorpční fotometrie MeSH
- dítě MeSH
- fraktury páteře diagnostické zobrazování epidemiologie etiologie MeSH
- idiopatické střevní záněty komplikace patofyziologie MeSH
- kostní denzita * MeSH
- lidé MeSH
- logistické modely MeSH
- mladiství MeSH
- mladý dospělý MeSH
- prevalence MeSH
- průřezové studie MeSH
- radiografie MeSH
- rizikové faktory MeSH
- svalová síla * MeSH
- trabekulární kostní tkáň patofyziologie MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
UNLABELLED: Low bone mineral density (BMD) and an increased fracture incidence are two extraintestinal complications associated with inflammatory bowel disease (IBD). We aimed to evaluate musculoskeletal traits and assess vertebral fracture (VF) rate in children and adolescents with IBD. Seventy patients with IBD with a median age of 13.8 years were included. The BMD and geometric parameters of the non-dominant tibia were assessed using pQCT. Dynamic muscle functions were evaluated using jumping mechanography. VFs were assessed according to the semiquantitative standardized method by Genant. The muscle functions adjusted for the patients' weight did not differ from the reference population. A low trabecular BMD (Z-score - 1.6; p < 0.001) and cortical thickness (Z-score - 0.7; p < 0.001) were found in children and adolescents with IBD. Conversely, an increased cortical BMD (Z-score 1.1; p < 0.001) was noted. No significant association was found between the 25-OHD serum levels and the bone or muscle measurements. One patient with asymptomatic VF was identified. CONCLUSION: IBD in childhood or adolescents affects bones but not muscles. Bone changes are independent of the 25-OHD serum level. A thoracolumbar spine X-ray should not be routinely recommended in children with IBD. What is Known: • Low bone mineral density and an increased fracture rate are the complications associated with IBD. • Bone strength and structural development is strongly dependent on skeletal muscle stimulation. What is New: • Children with IBD have altered bone density and geometry but normal dynamic muscle functions. • Thoracolumbar spine X-ray should be indicated on an individual basis in children with IBD.
Zobrazit více v PubMed
Gut. 2000 Feb;46(2):176-81 PubMed
Cent Eur J Public Health. 2004 Sep;12 (3):126-30 PubMed
J Clin Endocrinol Metab. 2015 Jul;100(7):2630-9 PubMed
Gut. 1998 Feb;42(2):188-94 PubMed
Arch Dis Child. 1995 Sep;73(3):255-6 PubMed
J Crohns Colitis. 2012 Jul;6(6):665-73 PubMed
J Crohns Colitis. 2014 Feb;8(2):137-46 PubMed
Osteoporos Int. 2010 Feb;21(2):331-7 PubMed
BMC Gastroenterol. 2012 May 14;12:47 PubMed
Osteoporos Int. 1996;6(2):141-8 PubMed
Inflamm Bowel Dis. 2011 May;17(5):1125-30 PubMed
Am J Clin Nutr. 2005 Aug;82(2):413-20 PubMed
J Pediatr Gastroenterol Nutr. 2005 Mar;40(3):295-300 PubMed
J Musculoskelet Neuronal Interact. 2013 Sep;13(3):297-311 PubMed
J Crohns Colitis. 2014 Jul;8(7):626-34 PubMed
Osteoporos Int. 2014 Jul;25(7):1875-83 PubMed
Aliment Pharmacol Ther. 2011 Jun;33(12):1261-72 PubMed
Inflamm Bowel Dis. 2017 Apr;23 (4):514-523 PubMed
Gastroenterology. 1997 May;112(5):1710-3 PubMed
J Pediatr Gastroenterol Nutr. 2006 Oct;43(4):533-5 PubMed
Am J Physiol Gastrointest Liver Physiol. 2007 Jun;292(6):G1793-803 PubMed
Dig Dis Sci. 2014 Aug;59(8):1878-84 PubMed
J Clin Invest. 1998 Jul 15;102(2):274-82 PubMed
J Musculoskelet Neuronal Interact. 2010 Jun;10(2):128-35 PubMed
Gut. 2002 Nov;51(5):654-8 PubMed
J Pediatr Gastroenterol Nutr. 2014 Jun;58(6):795-806 PubMed
Gastroenterology. 2003 Dec;125(6):1591-7 PubMed
Horm Res Paediatr. 2016;85(2):83-106 PubMed
J Pediatr Gastroenterol Nutr. 2011 Jul;53(1):11-25 PubMed
Inflamm Bowel Dis. 2009 Dec;15(12 ):1844-50 PubMed
Eur J Pediatr. 2014 Feb;173(2):141-51 PubMed
Ann Nutr Metab. 2013;63(1-2):10-6 PubMed
J Clin Endocrinol Metab. 2000 Jun;85(6):2122-6 PubMed
J Pediatr Gastroenterol Nutr. 1991 May;12 (4):439-47 PubMed
J Crohns Colitis. 2014 Oct;8(10):1179-207 PubMed
Gastroenterology. 2007 Aug;133(2):423-32 PubMed
Inflamm Bowel Dis. 2010 Feb;16(2):216-25 PubMed
Med Sci Sports Exerc. 2011 Nov;43(11):2102-9 PubMed
J Pediatr Gastroenterol Nutr. 2012 Sep;55(3):340-61 PubMed
Bone. 2015 May;74:160-5 PubMed
Gut Liver. 2014 Sep;8(5):500-7 PubMed
J Bone Miner Res. 1993 Sep;8(9):1137-48 PubMed
Pediatr Res. 2002 Apr;51(4):505-10 PubMed
J Musculoskelet Neuronal Interact. 2010 Dec;10(4):256-66 PubMed
Anat Rec. 1987 Sep;219(1):1-9 PubMed
J Pediatr. 2014 Jun;164(6):1436-43.e1 PubMed
J Clin Densitom. 2008 Apr-Jun;11(2):283-94 PubMed
J Bone Miner Res. 2004 Dec;19(12):1961-8 PubMed
Gastroenterology. 2009 Jan;136(1):123-30 PubMed
Gastroenterology. 2010 Aug;139(2):430-8 PubMed