Pregled bibliografske jedinice broj: 659198
Assessment of bone mass and bone metabolism in children with chronic inflammatory bowel diseases.
Assessment of bone mass and bone metabolism in children with chronic inflammatory bowel diseases. // 6th International Conference on Children's Bone Health, Abstracts / / (ur.).
Rotterdam : Boston (MA) : Taipei: International Conference on Children's Bone Health, 2013. str. P74-70 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 659198 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Assessment of bone mass and bone metabolism in children with chronic inflammatory bowel diseases.
Autori
Kušec, Vesna ; Senečić Čala, Irena
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
6th International Conference on Children's Bone Health, Abstracts
/ - Rotterdam : Boston (MA) : Taipei : International Conference on Children's Bone Health, 2013, P74-70
Skup
6th International Conference on Children's Bone Health
Mjesto i datum
Rotterdam, Nizozemska, 22.06.2013. - 25.06.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
kost; kronične gastrointestinalne bolesti; djeca
(bone; chronic gastrointestinal diseases; children)
Sažetak
Skeletal integrity during childhood may be compromised by diseases interfering with bone metabolism. Chronic inflammatory bowel diseases (CIBD ; Crohn’s disease, ulcerative colitis) in children is a recognized risk of osteoporosis in adulthood. This study was aimed at assessment of bone mass and bone metabolism in children with CIBD at diagnosis and after one year during therapy. Patient population comprised 64 children (boys 23, girls 42) and adolescents aged 14.6+/- 2.7 years (7-20). Dual x-ray densitometry (lumbar spine) and , measurement of 25-OH D and bone markers (osteocalcin, P1CP, CTX, crosslaps urine, osteoprotegerin) by standard methods were performed. No difference between sexes was found. Densitometry z-scores (-0.67+/-1.28 ; range -3.95 to 2.47) indicating decreased bone mass (<-2) were found in 5 patients. At time of diagnosis hypovitaminosis D (<50 nmol/L) was found in 69% of patients. Increased bone markers (as compared to adult reference ranges) were observed in 75% for osteocalcin, 95% for P1CP, 98% for CTX and 45% for crosslaps urine. Osteoprotegerin was similar to normal adult values in 92% of patients. After one year follow-up statistically significant increase was found for osteocalcin (0.002) and P1CP (0.001), and decrease for crosslaps urine (0.0005) and osteoprotegerin (0.03). Hypovitaminosis D was still present in 41% of cases. These results indicate that CIBD in children and adolescents did not considerably impair the skeleton. Increased bone markers probably indicate increased bone turnover characteristic of growth and puberty. The observed changes of bone markers during follow-up probably reflects recovery and continuation of growth processes. Normal osteoprotegerin levels suggest that bone resorption at diagnosis and during monitoring was not predominant. Prevalence of hypovitaminosis D is a serious problem of this disorder, its treatment and prevention should be a measure for preventing osteoporosis risk.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
214-1080229-0163 - Zajednička molekularna osnova etiopatogeneza koštanih poremećaja u ljudi (Kušec, Vesna, MZOS ) ( CroRIS)
Ustanove:
Klinički bolnički centar Zagreb