Steroid therapy is often administered for patients with nephritic syndrome. It has been reported that long-term steroid therapy could induce osteoporosis. However, there has been no data regarding the effect of short-term steroid therapy on bone turnover. The objective of this study is to investigate the effect of commonly prescribed doses of steroids on bone markers. Ten male patients (mean age: 21 years old, range: 19-28 years old) with a first attack of idiopathic full-blown nephritic syndrome between 1996 and 1997 were enrolled in this study. They all received standard steroid therapy only, and got complete remission. Patients were assessed before inclusion (0: data at entry) and subsequently at 1 month (1: data at 1 month) and 4 month (4: data at 4 month) after steroid therapy. Serum level of albumin (ALB), total cholesterol (T.chol), daily protein loss (DPL), body weight (BW), serum carboxyterminal propeptide of type I procollagen (PICP), pyridinoline cross linked telopeptide domain of type I collagen (ICTP), intact parathyroid hormone (iPHT) and ionized calcium (iCa) all were measured simultaneously. On the other hard, we also congregated nine healthy age matched male as control group (c: data of control group). Data were expressed as mean ± standard error of mean, and were analyzed by one-way ANOVA and Student's t-test. Our results disclosed that a). PICP₀ showed no significant difference compared with PICPс and PICP₄, but had a trend of increment; b). There was no significant difference between ICTP₀ and ICTPс, but ICTP₄ was significantly lower than PICP₀ (5.34±0.39μg/l vs. 7.53±0.69, p<0.05); c). Both of baseline data of iPTH and iCa compared with 4 month after treatment showed no significant difference. We conclude that there is no obvious change in bone formation and bone resorption in young male idiopathic nephritic syndrome before steroid treatment, and steroid effect was major in local hormone, but not systemic hormone after receiving short-term steroids treatment.
Steroid therapy is often administered for patients with nephritic syndrome. It has been reported that long-term steroid therapy could induce osteoporosis. However, there has been no data regarding the effect of short-term steroid therapy on bone turnover. The objective of this study is to investigate the effect of commonly prescribed doses of steroids on bone markers. Ten male patients (mean age: 21 years old, range: 19-28 years old) with a first attack of idiopathic full-blown nephritic syndrome between 1996 and 1997 were enrolled in this study. They all received standard steroid therapy only, and got complete remission. Patients were assessed before inclusion (0: data at entry) and subsequently at 1 month (1: data at 1 month) and 4 month (4: data at 4 month) after steroid therapy. Serum level of albumin (ALB), total cholesterol (T.chol), daily protein loss (DPL), body weight (BW), serum carboxyterminal propeptide of type I procollagen (PICP), pyridinoline cross linked telopeptide domain of type I collagen (ICTP), intact parathyroid hormone (iPHT) and ionized calcium (iCa) all were measured simultaneously. On the other hard, we also congregated nine healthy age matched male as control group (c: data of control group). Data were expressed as mean ± standard error of mean, and were analyzed by one-way ANOVA and Student's t-test. Our results disclosed that a). PICP₀ showed no significant difference compared with PICPс and PICP₄, but had a trend of increment; b). There was no significant difference between ICTP₀ and ICTPс, but ICTP₄ was significantly lower than PICP₀ (5.34±0.39μg/l vs. 7.53±0.69, p<0.05); c). Both of baseline data of iPTH and iCa compared with 4 month after treatment showed no significant difference. We conclude that there is no obvious change in bone formation and bone resorption in young male idiopathic nephritic syndrome before steroid treatment, and steroid effect was major in local hormone, but not systemic hormone after receiving short-term steroids treatment.