SYSTEMIC GLUCOCORTICOID TREATMENT DECREASES SERUM CONCENTRATIONS OF CARBOXYTERMINAL PROPEPTIDE OF TYPE-I PROCOLLAGEN AND AMINOTERMINAL PROPEPTIDE OF TYPE-III PROCOLLAGEN

被引:63
作者
OIKARINEN, A
AUTIO, P
VUORI, J
VAANANEN, K
RISTELI, L
KIISTALA, U
RISTELI, J
机构
[1] DEACONESS INST OULU,OULU,FINLAND
[2] CENT MIL HOSP,DEPT DERMATOL,HELSINKI,FINLAND
[3] UNIV OULU,DEPT ANAT,SF-90100 OULU 10,FINLAND
[4] UNIV OULU,DEPT MED BIOCHEM,SF-90100 OULU 10,FINLAND
[5] UNIV OULU,DEPT CLIN CHEM,SF-90100 OULU 10,FINLAND
关键词
D O I
10.1111/j.1365-2133.1992.tb07816.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The effect of systemic glucocorticoid treatment on collagen synthesis in patients with various dermatoses was studied by measuring the carboxyterminal propeptide of type I procollagen (PICP) and the aminoterminal propeptide of type III procollagen (PIIINP) in serum. Changes in the propeptide concentrations were compared with those of osteocalcin, which reflects osteoblastic activity, and tartrate resistant acid phosphatase (TRAP), which reflects osteoclastic activity. The treatment caused significant decreases in levels of PICP, PIIINP and osteocalcin of 38, 34 and 49%, respectively (P < 0.001). For TRAP, both increases and decreases were seen. The effects on PICP and PIIINP were evident 2-4 days after the onset of steroid therapy. The decrease in PICP was dose-related (r = 0.470, P < 0.005) but even relatively small doses (0.1 mg of prednisone/kg/1 day) caused a significant reduction in PICP. After cessation of treatment, the levels of PICP returned to the pretreatment level in 1 week. The present study demonstrates that systemic glucocorticoid therapy in humans suppresses the synthesis of type I and III collagens and also non-collagenous bone matrix proteins.
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页码:172 / 178
页数:7
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