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首页> 外文期刊>Journal of Inherited Metabolic Disease >Heparin cofactor II-thrombin complex and dermatan sulphate:chondroitin sulphate ratio are biomarkers of short- and long-term treatment effects in mucopolysaccharide diseases
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Heparin cofactor II-thrombin complex and dermatan sulphate:chondroitin sulphate ratio are biomarkers of short- and long-term treatment effects in mucopolysaccharide diseases

机译:肝素辅因子II-凝血酶复合物和硫酸皮肤素:硫酸软骨素的比率是粘多糖病短期和长期治疗作用的生物标志物

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Early detection of mucopolysaccharidosis (MPS) is an important factor in treatment success; therefore, good disease biomarkers are vital. We evaluate heparin cofactor II-thrombin complex (HCII-T) as a biomarker in serum and dried blood spots (DBS) of MPS patients. Serum HCII-T and urine dermatan sulphate:chondroitin sulphate (DS:CS) ratio are also compared longitudinally against clinical outcomes in MPSI, II and VI patients following treatment. Samples were collected from MPS patients at the Royal Manchester Children’s Hospital. DS:CS ratio was obtained by measuring the area density of spots from 2D electrophoresis of urinary glycosaminoglycans. Serum and DBS HCII-T was measured by sandwich ELISA. Serum HCII-T is elevated approximately 25-fold in MPS diseases that store DS, clearly distinguishing untreated MPSI, II and VI patients from unaffected age-matched controls. Serum HCII-T is also elevated in MPSIII, which leads to storage of heparan sulphate, with an increase of approximately 4-fold over unaffected age-matched controls. Urine DS:CS ratio and serum HCII-T decrease in response to treatment of MPSI, II and VI patients. HCII-T appears to respond rapidly to perturbations in treatment, whilst DS:CS ratio responds more slowly. HCII-T is a suitable biomarker for MPSI, II and VI, and it may also be informative for MPS diseases storing HS alone, such as MPSIII, although the elevation observed is smaller. In treated MPS patients, HCII-T and DS:CS ratio appear to measure short-term and long-term treatment outcomes, respectively. The potential value of HCII-T measurement in DBS for newborn screening of MPS diseases warrants further investigation.
机译:早期发现粘多糖贮积症(MPS)是治疗成功的重要因素。因此,良好的疾病生物标记至关重要。我们评估肝素辅助因子II-凝血酶复合物(HCII-T)作为MPS患者血清和干血斑(DBS)中的生物标志物。还纵向比较了治疗后MPSI,II和VI患者的血清HCII-T和尿硫酸皮肤素:硫酸软骨素(DS:CS)的比率与临床结局。样本是从皇家曼彻斯特儿童医院的MPS患者那里收集的。 DS:CS比是通过测量尿糖胺聚糖的2D电泳的斑点的面积密度而获得的。通过夹心ELISA测定血清和DBS HCII-T。在储存DS的MPS疾病中,血清HCII-T升高约25倍,从而明显地将未治疗的MPSI,II和VI患者与未患病的年龄匹配对照区分开来。 MPSIII中的血清HCII-T也升高,这导致硫酸乙酰肝素的储存,与未受影响的年龄匹配的对照相比增加了约4倍。尿DS:CS比和血清HCII-T随MPSI,II和VI患者的治疗而降低。 HCII-T似乎对治疗中的摄动反应迅速,而DS:CS比则反应较慢。 HCII-T是MPSI,II和VI的合适生物标志物,尽管观察到的升高较小,但它对于单独存储HS的MPS疾病(例如MPSIII)也可能是有益的。在接受治疗的MPS患者中,HCII-T和DS:CS比率似乎分别衡量了短期和长期治疗的结局。在DBS中进行HCII-T测量对MPS疾病的新生儿筛查的潜在价值值得进一步研究。

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