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Is significant cystic fibrosis-related liver disease a risk factor in the development of bone mineralization abnormalities?

机译:严重的囊性纤维化相关肝病是骨矿化异常发展的危险因素吗?

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In order to assess the effects of significant cystic fibrosis-related liver disease (CFLD) on bone health, we compared the bone mineral status of older children and adolescents with CFLD to those with cystic fibrosis (CF) alone. Thirteen children (age range, 10-19 years) from our clinical CF services were identified with significant CFLD (9 of these 13 patients had clinical and radiological evidence of portal hypertension). This cohort was then matched by age, gender, and anthropometric measurements with equal numbers of patients with CF alone. All patients had a dual-energy X-ray absorptiometry (DEXA) scan to determine bone mineral content (BMC), bone area (BA), bone mineral density (BMD), and bone mineral apparent density (BMAD) in the region of the lumbar spine. Blood was drawn to determine serum vitamin A, D, E, and K status and liver function tests. The best forced expired volume in 1 sec (FEV1) for each patient in the 12 months around the time of the scan was also documented. Patients with CFLD had slightly worse FEV1 (82 +/- 20% vs. 91 +/- 16%, P = 0.05) and significantly higher alanine aminotransferase (65.5 +/- 35 IU/l vs. 30 +/- 20 IU/l, P = 0.01) than those with CF alone. The mean lumbar spine BA, BMC, BMD, and BMAD were not different between children with CFLD and CF. In conclusion, the presence of significant liver disease in children with CF does not appear to be an additional risk factor for the development of abnormal bone mineralization.
机译:为了评估重大的囊性纤维化相关肝病(CFLD)对骨骼健康的影响,我们比较了CFLD的大龄儿童和青少年与单独患有囊性纤维化(CF)的儿童的骨矿物质状况。我们的临床CF服务中有13名儿童(年龄在10-19岁之间)被确认患有显着CFLD(这13例患者中有9例具有门静脉高压症的临床和影像学证据)。然后将该队列与年龄,性别和人体测量学数据相匹配,仅CF患者的数量就相等。所有患者均进行了双能X线骨密度仪(DEXA)扫描,以确定在该区域的骨矿物质含量(BMC),骨面积(BA),骨矿物质密度(BMD)和骨矿物质表观密度(BMAD)。腰椎。抽血以确定血清维生素A,D,E和K的状态以及肝功能检查。还记录了扫描时间前后12个月内,每个患者在1秒内的最佳强制呼出量(FEV1)。 CFLD患者的FEV1较差(82 +/- 20%vs. 91 +/- 16%,P = 0.05),丙氨酸转氨酶明显较高(65.5 +/- 35 IU / l与30 +/- 20 IU / l l,P = 0.01)比仅使用CF的那些。 CFLD和CF患儿的平均腰椎BA,BMC,BMD和BMAD无差异。总之,CF儿童患上严重的肝病似乎并不是异常骨矿化发展的另一个危险因素。

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