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Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3).使用经过验证的疾病严重程度评分系统(DS3)评估1型戈谢病成人患者的疾病负担和治疗反应。
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Study of enzyme replacement therapy for Gaucher Disease: comparative analysis of clinical and laboratory parameters at diagnosis and after two, five and ten years of treatment.戈谢病酶替代疗法的研究:诊断时以及治疗两年、五年和十年后的临床和实验室参数的对比分析。
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本文引用的文献

1
Risk factors for fractures and avascular osteonecrosis in type 1 Gaucher disease: a study from the International Collaborative Gaucher Group (ICGG) Gaucher Registry.1 型戈谢氏病骨折和缺血性骨坏死的危险因素:国际戈谢氏病协作组(ICGG)戈谢氏病登记处的一项研究。
J Bone Miner Res. 2012 Aug;27(8):1839-48. doi: 10.1002/jbmr.1680.
2
Focal splenic lesions in type I Gaucher disease are associated with poor platelet and splenic response to macrophage-targeted enzyme replacement therapy.I 型戈谢病中的脾脏局灶性病变与血小板和脾脏对巨噬细胞靶向酶替代治疗的反应不良有关。
J Inherit Metab Dis. 2010 Dec;33(6):769-74. doi: 10.1007/s10545-010-9175-6. Epub 2010 Aug 4.
3
Dose-response relationships for enzyme replacement therapy with imiglucerase/alglucerase in patients with Gaucher disease type 1.1型戈谢病患者使用伊米苷酶/阿糖苷酶进行酶替代治疗的剂量-反应关系。
Genet Med. 2009 Feb;11(2):92-100. doi: 10.1097/GIM.0b013e31818e2c19.
4
Dosing enzyme replacement therapy for Gaucher disease: older, but are we wiser?戈谢病的酶替代疗法给药:经验更丰富了,但我们更明智了吗?
Genet Med. 2009 Feb;11(2):90-1. doi: 10.1097/GIM.0b013e3181928f6a.
5
Eight-year clinical outcomes of long-term enzyme replacement therapy for 884 children with Gaucher disease type 1.884例1型戈谢病儿童长期酶替代治疗的八年临床结局
Pediatrics. 2008 Dec;122(6):1182-90. doi: 10.1542/peds.2007-2144.
6
A benchmark analysis of the achievement of therapeutic goals for type 1 Gaucher disease patients treated with imiglucerase.对接受伊米苷酶治疗的1型戈谢病患者治疗目标达成情况的基准分析。
Am J Hematol. 2008 Dec;83(12):890-5. doi: 10.1002/ajh.21280.
7
Therapeutic goals in the treatment of Gaucher disease.戈谢病治疗的治疗目标。
Semin Hematol. 2004 Oct;41(4 Suppl 5):4-14. doi: 10.1053/j.seminhematol.2004.07.009.
8
Introduction. Advances in Gaucher Disease: therapeutic goals and evaluation and monitoring guidelines.引言。戈谢病的进展:治疗目标以及评估与监测指南。
Semin Hematol. 2004 Oct;41(4 Suppl 5):1-3. doi: 10.1053/j.seminhematol.2004.07.008.
9
Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry.1028例1型戈谢病患者接受2至5年酶替代治疗后的疗效:来自戈谢病注册机构的报告
Am J Med. 2002 Aug 1;113(2):112-9. doi: 10.1016/s0002-9343(02)01150-6.
10
Low-dose low-frequency imiglucerase as a starting regimen of enzyme replacement therapy for patients with type I Gaucher disease.低剂量低频伊米苷酶作为Ⅰ型戈谢病患者酶替代治疗的起始方案
QJM. 1998 Jul;91(7):483-8. doi: 10.1093/qjmed/91.7.483.

低剂量伊米苷酶治疗戈谢病实现治疗目标:单中心经验

Achievement of therapeutic goals with low-dose imiglucerase in Gaucher disease: a single-center experience.

作者信息

Tukan Irina, Hadas-Halpern Irith, Altarescu Gheona, Abrahamov Ayala, Elstein Deborah, Zimran Ari

机构信息

Shaare Zedek Medical Center, Affiliated to the Hadassah-Hebrew University School of Medicine, Ein Karem 91031, Israel.

出版信息

Adv Hematol. 2013;2013:151506. doi: 10.1155/2013/151506. Epub 2013 Oct 28.

DOI:10.1155/2013/151506
PMID:24285960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3830843/
Abstract

Gaucher disease, a lysosomal storage disorder, is a multisystem disorder with variable and unpredictable onset and severity. Disease-specific enzyme replacement therapy (ERT) has been shown to reverse or ameliorate disease-specific hepatosplenomegaly and anemia and thrombocytopenia. ERT also impacts bone manifestations, including bone crises, bone pain, and appearance of new osteonecrosis, and improves bone mineral density to varying degrees. The objective of this study was to assess achievement of predefined therapeutic goals based on international registry outcomes for Israeli patients with Gaucher disease receiving imiglucerase for four consecutive years on a low-dose regimen followed in a single center. All data were taken from patient files. The therapeutic goals were taken from standards published in the literature for disease-specific clinical parameters. Among 164 patients at baseline, values for spleen and liver volumes, hemoglobin and platelet counts, and Z-scores for lumbar spine and femoral were significantly different from the goal. After four years ERT, there was a significant improvement (P = 0.000) in each of the therapeutic goal parameters from baseline. 15.2% of these patients achieved all hematology-visceral goals. In children, there was achievement of linear growth and puberty. This survey highlights the good overall response in symptomatic patients receiving low-dose ERT with imiglucerase in Israel.

摘要

戈谢病是一种溶酶体贮积症,是一种多系统疾病,起病和严重程度多变且不可预测。疾病特异性酶替代疗法(ERT)已被证明可逆转或改善疾病特异性肝脾肿大、贫血和血小板减少症。ERT还会影响骨骼表现,包括骨危象、骨痛和新的骨坏死出现,并不同程度地提高骨密度。本研究的目的是根据国际注册结果评估以色列戈谢病患者在单一中心接受低剂量伊米苷酶连续四年治疗后预定治疗目标的达成情况。所有数据均取自患者档案。治疗目标取自文献中公布的疾病特异性临床参数标准。在164例基线患者中,脾脏和肝脏体积、血红蛋白和血小板计数以及腰椎和股骨的Z评分值与目标值有显著差异。ERT治疗四年后,每个治疗目标参数与基线相比均有显著改善(P = 0.000)。这些患者中有15.2%实现了所有血液学 - 内脏目标。在儿童中,实现了线性生长和青春期发育。这项调查突出了以色列接受低剂量伊米苷酶ERT治疗的有症状患者的总体良好反应。