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. 1994 Aug;55(2):90-3.
doi: 10.1007/BF00297181.

Carboxyterminal propeptide of type I procollagen in osteomalacia

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Carboxyterminal propeptide of type I procollagen in osteomalacia

F Li et al. Calcif Tissue Int. 1994 Aug.

Abstract

Carboxyterminal propeptide of type I procollagen (PICP) was measured in sera from 25 patients with osteomalacia due to privational vitamin D deficiency. The mean value of serum PICP was significantly raised in patients with osteomalacia compared with 40 normal subjects (mean +/- SD, 161 +/- 82 ng/ml and 113 +/- 31 ng/ml, respectively; P = 0.01). The raised serum PICP reflected the accelerated bone turnover in this condition as did the elevated serum total alkaline phosphatase (ALP), but the variation in values of serum PICP noted in individual patients may reflect the different stages of osteomalacia. The normalization of serum PICP and ALP, indicating a healing process of the bone disorder, needed longer time of vitamin D and calcium therapy. In contrast, adjusted serum calcium and inorganic phosphate (IP) responded and normalized rapidly. Serum PICP and total ALP appeared to behave differently in the disease and in its response to vitamin D therapy suggesting that these two markers may represent different functions of osteoblasts in osteomalacia.

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References

    1. J Clin Endocrinol Metab. 1983 May;56(5):1063-7 - PubMed
    1. Baillieres Clin Endocrinol Metab. 1988 Feb;2(1):125-55 - PubMed
    1. J Bone Miner Res. 1987 Oct;2(5):427-36 - PubMed
    1. Metabolism. 1991 Feb;40(2):205-8 - PubMed
    1. J Clin Endocrinol Metab. 1988 May;66(5):951-7 - PubMed