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本文引用的文献

1
Natural history of hepatocellular adenoma formation in glycogen storage disease type I.糖原贮积病 I 型中肝细胞腺瘤形成的自然史。
J Pediatr. 2011 Sep;159(3):442-6. doi: 10.1016/j.jpeds.2011.02.031. Epub 2011 Apr 9.
2
Hypovitaminosis D in glycogen storage disease type I.I 型糖原贮积病中的维生素 D 缺乏症。
Mol Genet Metab. 2010 Apr;99(4):434-7. doi: 10.1016/j.ymgme.2009.12.012. Epub 2009 Dec 21.
3
Renal function in glycogen storage disease type I, natural course, and renopreservative effects of ACE inhibition.I 型糖原贮积症的肾功能、自然病程和 ACE 抑制剂的肾脏保护作用。
Clin J Am Soc Nephrol. 2009 Nov;4(11):1741-6. doi: 10.2215/CJN.00050109. Epub 2009 Oct 1.
4
Glucocorticoids act directly on osteoclasts to increase their life span and reduce bone density.糖皮质激素直接作用于破骨细胞,以延长其寿命并降低骨密度。
Endocrinology. 2006 Dec;147(12):5592-9. doi: 10.1210/en.2006-0459. Epub 2006 Aug 24.
5
Bone mineral density and markers of bone turnover in patients with glycogen storage disease types I, III and IX.I型、III型和IX型糖原贮积病患者的骨矿物质密度和骨转换标志物
J Inherit Metab Dis. 2004;27(1):1-9. doi: 10.1023/B:BOLI.0000016632.13234.56.
6
Bone mineral density in children, adolescents and adults with glycogen storage disease type Ia: a cross-sectional and longitudinal study.Ia型糖原贮积病儿童、青少年及成人的骨矿物质密度:一项横断面和纵向研究
J Inherit Metab Dis. 2003;26(4):371-84. doi: 10.1023/a:1025111220095.
7
Glycogen storage diseases.糖原贮积病
Rev Endocr Metab Disord. 2003 Mar;4(1):95-102. doi: 10.1023/a:1021831621210.
8
Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease.生玉米淀粉持续葡萄糖治疗对1a型糖原贮积病长期临床病程的影响。
Eur J Pediatr. 2002 Oct;161 Suppl 1:S35-9. doi: 10.1007/s00431-002-1000-2. Epub 2002 Jul 31.
9
Low bone mass in glycogen storage disease type 1 is associated with reduced muscle force and poor metabolic control.1型糖原贮积病患者的低骨量与肌肉力量降低和代谢控制不佳有关。
J Pediatr. 2002 Sep;141(3):350-6. doi: 10.1067/mpd.2002.126456.
10
Inhibition of osteoblastogenesis and promotion of apoptosis of osteoblasts and osteocytes by glucocorticoids. Potential mechanisms of their deleterious effects on bone.糖皮质激素对成骨细胞生成的抑制作用以及对成骨细胞和骨细胞凋亡的促进作用。其对骨骼产生有害影响的潜在机制。
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Ia型和Ib型糖原贮积病的骨矿物质密度

Bone mineral density in glycogen storage disease type Ia and Ib.

作者信息

Minarich Laurie A, Kirpich Alexander, Fiske Laurie M, Weinstein David A

机构信息

Glycogen Storage Disease Program and Division of Pediatric Endocrinology, Department of Pediatrics, University of Florida, Gainesville, Florida, USA.

出版信息

Genet Med. 2013;14(8):737-741. doi: 10.1038/gim.2012.36. Epub 2012 Apr 5.

DOI:10.1038/gim.2012.36
PMID:22481133
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3884026/
Abstract

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.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。