@article{3114219, title = "The effect of vitamin K supplementation on biochemical markers of bone formation in children and adolescents with cystic fibrosis", author = "Nicolaidou, Polyxeni and Stavrinadis, Ilias and Loukou, Ioanna and and Papadopoulou, Anna and Georgouli, Helen and Douros, Konstantinos and and Priftis, Kostas N. and Gourgiotis, Dimitrios and Matsinos, Yiannis G. and and Doudounakis, Stavros", journal = "European Journal of Pediatrics", year = "2006", volume = "165", number = "8", pages = "540-545", publisher = "Springer-Verlag", issn = "0340-6199, 1432-1076", doi = "10.1007/s00431-006-0132-1", keywords = "cystic fibrosis; osteopenia; osteoporosis; vitamin D; vitamin K", abstract = "Introductions: Impaired vitamin K status in cystic fibrosis (CF) has been considered as a newly emerged pathogenetic factor for reduced bone mineral density (BMD). Objectives: Our aim was to evaluate the effectiveness of vitamin K supplementation in managing bone formation abnormalities in children and adolescents with CF. materials and methods: The statuses of vitamins K and D in relation to biochemical markers of bone metabolism and BMD were examined in 20 CF children receiving vitamin D supplements but not vitamin K supplements. Laboratory tests were carried out at the beginning of the study period and after 1 year of vitamin K supplementation (10 mg single oral dose/week) and the results were compared; the results were also compared with those of 25 healthy controls. Results and discussions: Ten of the CF patients had BMD z-score <= 2.5 (n=5) or between -1 and -2.5 (n=5). Biochemical tests on patients before vitamin K supplementation revealed that the levels of osteoblastic activity markers, namely, bone alkaline phosphatase (BAP), serum osteocalcin (Gla-OC), serum carboxy-terminal propeptide of type I procollagen (PICP) and serum amino-terminal propeptide of type I procollagen (PINP), were significantly reduced compared with those of the controls. These patients had also lower 25-hydroxy-vitamin D (25(OH)D) and vitamin K serum levels, higher undercaboxylated osteocalcin (Glu-OC) and parathormone (PTH) levels and a higher calcium to creatinine ratio (Ca/Cr) than the controls. Vitamin K intake was associated with an increase in Gla-OC, PINP, PICP levels and a decrease in Glu-OC levels. PTH levels were lower after vitamin K supplementation without any difference in BMD z-scores. Conclusions: Our data indicate that vitamin K supplementation may have a beneficial role in bone health in CF children." }