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Development of nanoparticle-bound arylsulfatase B for enzyme replacement therapy of mucopolysaccharidosis VI.用于黏多糖贮积症VI酶替代疗法的纳米颗粒结合芳基硫酸酯酶B的研发。
Pharmazie. 2013 Jul;68(7):549-54.
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Growth hormone, gender and face shape in Prader-Willi syndrome.生长激素、性别与普拉德-威利综合征的面型。
Am J Med Genet A. 2013 Oct;161A(10):2453-63. doi: 10.1002/ajmg.a.36100. Epub 2013 Aug 5.
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Objective monitoring of mTOR inhibitor therapy by three-dimensional facial analysis.
Twin Res Hum Genet. 2013 Aug;16(4):840-4. doi: 10.1017/thg.2013.49.
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A Dysmorphometric Analysis to Investigate Facial Phenotypic Signatures as a Foundation for Non-invasive Monitoring of Lysosomal Storage Disorders.一项畸形测量分析,旨在研究面部表型特征作为溶酶体贮积症非侵入性监测基础。
JIMD Rep. 2013;8:31-9. doi: 10.1007/8904_2012_152. Epub 2012 Jun 10.
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Treatment options for lysosomal storage disorders: developing insights.溶酶体贮积症的治疗选择:不断深入的认识。
Expert Opin Pharmacother. 2012 Nov;13(16):2281-99. doi: 10.1517/14656566.2012.729039. Epub 2012 Sep 26.
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Dysmorphometrics: the modelling of morphological abnormalities.畸形测量学:形态异常的建模。
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Stem cell transplantation in inherited metabolic disorders.遗传性代谢疾病的干细胞移植。
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Improved facial outcome assessment using a 3D anthropometric mask.使用 3D 人体测量面具改善面部预后评估。
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利用畸形面部表型特征监测Ⅰ型黏多糖贮积症的治疗

Monitoring of Therapy for Mucopolysaccharidosis Type I Using Dysmorphometric Facial Phenotypic Signatures.

作者信息

Kung Stefanie, Walters Mark, Claes Peter, LeSouef Peter, Goldblatt Jack, Martin Andrew, Balasubramaniam Shanti, Baynam Gareth

机构信息

School of Paediatrics and Child Health, University of Western Australia, D184, Perth, WA, 6840, Australia,

出版信息

JIMD Rep. 2015;22:99-106. doi: 10.1007/8904_2015_417. Epub 2015 Mar 3.

DOI:10.1007/8904_2015_417
PMID:25732999
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4486281/
Abstract

There is a pattern of progressive facial dysmorphology in mucopolysaccharidosis type I (MPS I). Advances in 3D facial imaging have facilitated the development of tools, including dysmorphometrics, to objectively and precisely detect these facial phenotypes. Therefore, we investigated the application of dysmorphometrics as a noninvasive therapy-monitoring tool, by longitudinally scoring facial dysmorphology in a child with MPS I receiving enzyme replacement therapy (ERT) and bone marrow transplantation (BMT). Both dysmorphometric measures showed a decreasing trend, and the greatest differences were found in the severity of facial discordance (Z-RMSE), displaying scores >3 SD higher than the mean at their peak, in comparison to Z-RSD scores that mostly fell within the normative range (maximum; 1.5 SD from the mean). In addition to the general trend of reduced facial dysmorphology with treatment, initial fluctuations were also evident that may have related to transient subcutaneous facial fluctuations, in the context of conditioning for bone marrow transplant. These findings support the potential of our approach as a sensitive, noninvasive, and rapid means of assessing treatment response or failure in clinical trials, and for established therapies, and would be applicable for other inherited disorders of metabolism.

摘要

黏多糖贮积症 I 型(MPS I)存在进行性面部畸形的模式。3D 面部成像技术的进步推动了包括畸形测量学在内的工具的发展,以客观、精确地检测这些面部表型。因此,我们通过对一名接受酶替代疗法(ERT)和骨髓移植(BMT)的 MPS I 患儿的面部畸形进行纵向评分,研究了畸形测量学作为一种非侵入性治疗监测工具的应用。两种畸形测量指标均呈下降趋势,面部不协调严重程度(Z-RMSE)差异最大,其峰值时得分比平均值高 >3 个标准差,而 Z-RSD 得分大多落在正常范围内(最高;比平均值高 1.5 个标准差)。除了治疗后面部畸形减轻的总体趋势外,在骨髓移植预处理的背景下,最初的波动也很明显,这可能与面部皮下短暂波动有关。这些发现支持了我们的方法作为一种敏感、非侵入性且快速的手段在临床试验中评估治疗反应或失败以及既定疗法的潜力,并且适用于其他遗传性代谢紊乱疾病。