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本文引用的文献

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Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management.黏多糖贮积症患者的心脏疾病:临床表现、诊断与治疗。
J Inherit Metab Dis. 2011 Dec;34(6):1183-97. doi: 10.1007/s10545-011-9359-8. Epub 2011 Jul 9.
2
Cardiovascular manifestations of mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome).黏多糖贮积症 VI 型(马罗托克斯-拉米综合征)的心血管表现。
Int J Cardiol. 2012 Jun 28;158(1):6-11. doi: 10.1016/j.ijcard.2011.06.097. Epub 2011 Jul 6.
3
Fatal coronary artery disease in an infant with severe mucopolysaccharidosis type I.婴儿重症黏多糖贮积症Ⅰ型合并致死性冠状动脉疾病
Pediatrics. 2011 May;127(5):e1343-6. doi: 10.1542/peds.2009-2047. Epub 2011 Apr 4.
4
Cardiac disease in mucopolysaccharidosis type I attributed to catecholaminergic and hemodynamic deficiencies.黏多糖贮积症 I 型的心脏病变归因于儿茶酚胺能和血液动力学不足。
Am J Physiol Heart Circ Physiol. 2011 Jan;300(1):H356-65. doi: 10.1152/ajpheart.00774.2010. Epub 2010 Nov 12.
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Cyclosporin A and atherosclerosis--cellular pathways in atherogenesis.环孢素 A 与动脉粥样硬化——动脉粥样硬化形成中的细胞途径。
Pharmacol Ther. 2010 Oct;128(1):106-18. doi: 10.1016/j.pharmthera.2010.06.001. Epub 2010 Jun 18.
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Echocardiographic study of paediatric patients with mucopolysaccharidosis.黏多糖贮积症患儿的超声心动图研究
Cardiol Young. 2010 Jun;20(3):254-61. doi: 10.1017/S104795110999062X. Epub 2010 Apr 26.
7
Mortality and cause of death in mucopolysaccharidosis type II-a historical review based on data from the Hunter Outcome Survey (HOS).II型黏多糖贮积症的死亡率和死因——基于亨特结果调查(HOS)数据的历史回顾
J Inherit Metab Dis. 2009 Aug;32(4):534-43. doi: 10.1007/s10545-009-1119-7. Epub 2009 Jul 14.
8
Postmortem studies on a patient with mucopolysaccharidosis type I: histopathological findings after one year of enzyme replacement therapy.Ⅰ 型黏多糖贮积症患者的尸检研究:酶替代治疗一年后的组织病理学发现。
J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S53-7. doi: 10.1007/s10545-009-1057-4. Epub 2009 Mar 27.
9
The natural course and the impact of therapies of cardiac involvement in the mucopolysaccharidoses.黏多糖贮积症中心脏受累的自然病程及治疗影响。
Cardiol Young. 2009 Apr;19(2):170-8. doi: 10.1017/S1047951109003576. Epub 2009 Feb 6.
10
Early increase of carotid intima-media thickness in children with parental history of premature myocardial infarction.有父母早发心肌梗死病史的儿童颈动脉内膜中层厚度早期增加。
Heart. 2009 Apr;95(8):642-5. doi: 10.1136/hrt.2008.142836. Epub 2009 Jan 23.

黏多糖贮积症患者的颈动脉内膜中层厚度增加。

Carotid intima-media thickness is increased in patients with mucopolysaccharidoses.

机构信息

Division of Metabolic Disorders, Pediatric Subspecialty Faculty, CHOC Children's, Orange, CA, USA.

出版信息

Mol Genet Metab. 2011 Dec;104(4):592-6. doi: 10.1016/j.ymgme.2011.09.004. Epub 2011 Sep 10.

DOI:10.1016/j.ymgme.2011.09.004
PMID:21963080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3924772/
Abstract

BACKGROUND

The feasibility of carotid artery intima-media thickness (C-IMT), an established cardiovascular disease marker, as a cardiac risk marker in mucopolysaccharidosis (MPS) patients was explored.

OBJECTIVES

To determine if C-IMT is abnormal in MPS versus unaffected controls, and if C-IMT correlates with coronary artery diameter in MPS.

MATERIAL AND METHODS

Measurements of C-IMT via neck ultrasound and echocardiographic parameters, including coronary artery diameters, were obtained from MPS and control patients, and compared.

RESULTS

Sixteen MPS subjects (6 MPS I, 6 MPS II, 2 MPS III, 1 MPS VI, 1 MPS VII) and sixteen age, ethnicity, and gender-matched controls were enrolled. Median MPS and control subject ages were 8.3±4.5 and 8.6±4.3 years, respectively (p=0.73). Mean MPS and control C-IMTs were 0.54±0.070 and 0.48±0.034 mm (p=0.0029). No differences in left main, left anterior descending, or right coronary artery diameters were seen between MPS and controls. A significant proportion of MPS subjects had mitral insufficiency (14/16; p=0.0002), aortic insufficiency (10/16; p=0.0021), and left ventricular dilatation (7/16, p=0.037) versus controls. C-IMT did not correlate significantly with age, height, weight, coronary measurements, or duration of treatment.

CONCLUSION

C-IMT in MPS patients is increased compared to matched controls, likely reflective of arterial intima-medial glycosaminoglycan accumulation. MPS subjects demonstrated a high percentage of left-sided valvular insufficiency and ventricular dilatation. Additional studies should be performed in MPS patients to determine if C-IMT correlates with arterial elasticity, biomarkers of vascular dysfunction, and higher risk of cardiovascular events.

摘要

背景

颈动脉内膜中层厚度(C-IMT)是一种已确立的心血管疾病标志物,其作为黏多糖贮积症(MPS)患者的心脏风险标志物的可行性已被探索。

目的

确定 C-IMT 在 MPS 患者中是否异常,以及 C-IMT 是否与 MPS 患者的冠状动脉直径相关。

材料和方法

通过颈部超声和超声心动图参数(包括冠状动脉直径)测量 MPS 和对照组患者的 C-IMT,并进行比较。

结果

共纳入 16 名 MPS 患者(6 名 MPS I、6 名 MPS II、2 名 MPS III、1 名 MPS VI、1 名 MPS VII)和 16 名年龄、种族和性别匹配的对照组。MPS 和对照组患者的中位年龄分别为 8.3±4.5 岁和 8.6±4.3 岁(p=0.73)。MPS 和对照组的平均 C-IMT 分别为 0.54±0.070 和 0.48±0.034 mm(p=0.0029)。MPS 和对照组之间左主干、左前降支或右冠状动脉直径无差异。MPS 患者中有相当比例的二尖瓣关闭不全(14/16;p=0.0002)、主动脉瓣关闭不全(10/16;p=0.0021)和左心室扩张(7/16,p=0.037)与对照组相比。C-IMT 与年龄、身高、体重、冠状动脉测量值或治疗持续时间无显著相关性。

结论

与匹配的对照组相比,MPS 患者的 C-IMT 增加,可能反映了动脉内膜中层糖胺聚糖的积累。MPS 患者表现出较高比例的左侧瓣膜关闭不全和心室扩张。应在 MPS 患者中进行更多研究,以确定 C-IMT 是否与动脉弹性、血管功能障碍的生物标志物以及更高的心血管事件风险相关。