Anderson L J, Henley W, Wyatt K M, Nikolaou V, Hughes D A, Waldek S, Logan S
Institute of Health Research, University of Exeter Medical School, Veysey Building, Salmon Pool Lane, Exeter, Devon, UK, EX2 4SG.
J Inherit Metab Dis. 2014 Nov;37(6):953-60. doi: 10.1007/s10545-014-9680-0. Epub 2014 Feb 11.
To determine the effectiveness of enzyme replacement therapies (ERT) for adults with Gaucher disease (GD).
A longitudinal, multi-centre cohort study, including prospective and retrospective clinical data. Age- and gender-adjusted treatment effects were estimated using generalised linear mixed models. Treated patients contributed data before and during treatment. Untreated patients contributed natural history data.
Consenting adults (N = 150, aged 16 to 83 years) with a diagnosis of GD who attended a specialist treatment centre in England. At recruitment, 131 patients were receiving ERT (mean treatment duration, 10.8 years; range 0-18 years).
Clinical outcomes chosen to reflect disease progression, included platelet count; haemoglobin; absence/presence of bone pain; spleen and liver volumes and AST levels.
One hundred and fifty adults were recruited. Duration of ERT was associated with statistically significant improvements in platelet count (p < 0.001), haemoglobin (p < 0.001), liver and spleen volumes (p < 0.001) and AST levels (p = 0.02).
These data provide further evidence of the long-term effectiveness of ERT in adults with GD.
确定酶替代疗法(ERT)对成年戈谢病(GD)患者的疗效。
一项纵向、多中心队列研究,包括前瞻性和回顾性临床数据。使用广义线性混合模型估计年龄和性别调整后的治疗效果。接受治疗的患者提供治疗前和治疗期间的数据。未接受治疗的患者提供自然病史数据。
150名同意参与研究的成年患者(年龄16至83岁),他们被诊断患有戈谢病,并在英国的一家专科治疗中心就诊。招募时,131名患者正在接受ERT治疗(平均治疗时长为10.8年;范围为0至18年)。
选择反映疾病进展的临床指标,包括血小板计数、血红蛋白、是否存在骨痛、脾脏和肝脏体积以及AST水平。
招募了150名成年患者。ERT治疗时长与血小板计数(p < 0.001)、血红蛋白(p < 0.001)、肝脏和脾脏体积(p < 0.001)以及AST水平(p = 0.02)的统计学显著改善相关。
这些数据进一步证明了ERT对成年戈谢病患者的长期疗效。