Minarich Laurie A, Kirpich Alexander, Fiske Laurie M, Weinstein David A
Glycogen Storage Disease Program and Division of Pediatric Endocrinology, Department of Pediatrics, University of Florida, Gainesville, Florida, USA.
Genet Med. 2013;14(8):737-741. doi: 10.1038/gim.2012.36. Epub 2012 Apr 5.
Purpose:The aim of this study was to characterize the pathogenesis of low bone mineral density in glycogen storage disease type Ia and Ib.Methods:A retrospective chart review performed at the University of Florida Glycogen Storage Disease Program included patients with glycogen storage disease type Ia and Ib for whom dual-energy X-ray absorptiometry analysis was performed. A Z-score less than -2 SD was considered low. Analysis for association of bone mineral density with age, gender, presence of complications, mean triglyceride and 25-hydroxyvitamin D concentrations, erythrocyte sedimentation rate, duration of granulocyte colony-stimulating factor therapy, and history of corticosteroid use was performed.Results:In glycogen storage disease Ia, 23/42 patients (55%) had low bone mineral density. Low bone mineral density was associated with other disease complications (P = 0.02) and lower mean serum 25-hydroxyvitamin D concentration (P = 0.03). There was a nonsignificant trend toward lower mean triglyceride concentration in the normal bone mineral density group (P = 0.1).In patients with glycogen storage disease type Ib, 8/12 (66.7%) had low bone mineral density. We did not detect an association with duration of granulocyte colony-stimulating factor therapy (P = 0.68), mean triglyceride level (P = 0.267), erythrocyte sedimentation rate (P = 0.3), or 25-hydroxyvitamin D (P = 0.63) concentration, and there was no evidence that corticosteroid therapy was associated with lower bone mineral density (P = 1).Conclusion:In glycogen storage disease type Ia, bone mineral density is associated with other complications and 25-hydroxyvitamin D status. In glycogen storage disease type Ib, bone mineral density was not associated with any covariates analyzed, suggesting multifactorial etiology or reflecting a small sample.Genet Med advance online publication 5 April 2012.
本研究旨在明确Ⅰa型和Ⅰb型糖原贮积病中骨矿物质密度降低的发病机制。
在佛罗里达大学糖原贮积病项目中进行了一项回顾性图表审查,纳入了接受双能X线吸收测定分析的Ⅰa型和Ⅰb型糖原贮积病患者。Z评分小于-2个标准差被视为偏低。对骨矿物质密度与年龄、性别、并发症的存在、平均甘油三酯和25-羟基维生素D浓度、红细胞沉降率、粒细胞集落刺激因子治疗持续时间以及皮质类固醇使用史进行了关联分析。
在Ⅰa型糖原贮积病中,23/42例患者(55%)骨矿物质密度偏低。骨矿物质密度降低与其他疾病并发症相关(P = 0.02),且平均血清25-羟基维生素D浓度较低(P = 0.03)。正常骨矿物质密度组的平均甘油三酯浓度有降低的趋势,但无统计学意义(P = 0.1)。
在Ⅰb型糖原贮积病患者中,8/12例(66.7%)骨矿物质密度偏低。我们未检测到与粒细胞集落刺激因子治疗持续时间(P = 0.68)、平均甘油三酯水平(P = 0.267)、红细胞沉降率(P = 0.3)或25-羟基维生素D浓度(P = 0.63)有关联,且没有证据表明皮质类固醇治疗与较低的骨矿物质密度相关(P = 1)。
在Ⅰa型糖原贮积病中,骨矿物质密度与其他并发症及25-羟基维生素D状态相关。在Ⅰb型糖原贮积病中,骨矿物质密度与所分析的任何协变量均无关联,提示病因是多因素的,或反映了样本量较小。《遗传医学》于2012年4月5日在线优先发表。