4.5 Article

Comparison of the Effects of 1,25 Dihydroxyvitamin D and 25 Hydroxyvitamin D on Bone Pathology and Disease Activity in Crohn's Disease Patients

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INFLAMMATORY BOWEL DISEASES
卷 15, 期 11, 页码 1656-1662

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OXFORD UNIV PRESS INC
DOI: 10.1002/ibd.20947

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Crohn's disease; bone metabolism; osteoporosis; vitamin D

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Background: Vitamin D is essential for osteopenia therapy in Crohn's disease (CD). The active form of vitamin-D (aVD) is the 1.25(OH)2D. There are no data available whether aVD or plain vitamin-D (pVD) has any advantage in managing osteoporosis in CD or has tiny effect oil the activity of the disease itself. Our work is a prospective study to compare the effects of aVD and pVD oil bone metabolism and the clinical course of CD. Methods: In all. 37 inactive CD patients were involved in the Study and divided into 2 age-, gender-. and t-score-matched groups. Group A was treated with aVD while group B received pVD. Osteocalcin, beta-CrossLaps, osteoprotegerin, and receptor activator clear factor kappa-B ligand concentrations were estimated at the start of file Study and at 6 weeks and 3 and 12 months. The activity of CD was also measured clinically and by laboratory parameters. Results: At week 6 the Crohn's Disease Activity Index (CDAI) scores and concentration of C-reactive protein decreased (69.44 +/- 58.6 versus 57.0 +/- 54.89 and 15.8 +/- 23.57 mmol/L versus 7.81 +/- 3.91 mmol/L. respectively, P < 0.05) parallel with markers of bone turnover (beta-CrossLaps: 0.46 +/- 0.21 ng/mL versus 0.40 +/- 0.25 ng/mL, and osteocalcin: 32.29 +/- 15.3 ng/mL versus 29.98 +/- 14.14 ng/mL. P < 0.05), however, osteoprotegerin concentration (marker of osteoblast activity) increased (3.96 +/- 2.1 pg/mL versus 4.58 +/- 2.19 pg/mL) in group A, but did not change in group B. Osteocalcin and beta-CrossLaps concentrations changed more significantly by the 3rd month: however. these changes disappeared by the 12th month. Conclusions: According to our study, aVD has it more prominent short-term beneficial effect on bone metabolism and disease activity in CD compared with pVD.

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