Skeletal Manifestations, Bone Pain, and BMD Changes in Albanian Type 1 Gaucher Patients Treated with Taliglucerase Alfa

IF 1.1 Q3 ORTHOPEDICS
V. Velmishi, E. Troja, M. Tanka, D. Bali, E. Dervishi, A. Tako, Laurant Kollcaku, P. Cullufi
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Abstract

Gaucher disease is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunctions in multiple organs. Bone involvement is one of the most prevalent aspects of Gaucher disease. Pain, disability, and reduced quality of life remain the most frequent characteristics of bone involvement in Gaucher patients. Patients and Method. In this study, we will take into consideration data from 24 patients diagnosed with type 1 Gaucher disease. We followed them closely for six years in progress. At baseline, all patients started therapy with taliglucerase alfa at a mean dosage of 45 UI/kg; later, during the study, two of them switched their cure toward velaglucerase alfa. Before baseline evaluations, 12 patients had been treated with imiglucerase at variable duration times. At baseline, we performed an X-ray of long bones and the spine, and each year, different standard assessments were performed, such as bone pain, MRI of the vertebral spine and pelvis, and DEXA for bone density. Four patients left the study for various reasons, two of them at baseline and two others during year 3 (FU3). Results. At baseline, we had 8 children and 16 adults. The average age was 28.7 ± 16.5 SD years. The most frequent skeletal manifestations in our patients were reduction of tibial femoral space (40%), osteonecrosis (36%), and body vertebral reduction (32%). At baseline, 15 patients presented with bone pain to different degrees. Over the years, bone pain in our patients had a gradual improvement. The most dramatic bone pain improvement was seen in a patient who presented bone crises. Another impressive finding was a significant BMD improvement during six years of treatment. Our study showed a significant improvement in BMD comparing FU5 and baseline values (p = 0.0007). Especially children demonstrated a significant improvement in BMD (p = 0.00061) compared to adults (p = 0.3673). Mean BMD change was more indicative in switched patients (p = 0.0142) compared to naïve patients (p = 0.147). Conclusions. Skeletal manifestations are very different in Gaucher type 1 patients. In our study, as a result of long-term evaluations, it was noticed that the most frequent skeletal manifestation was a reduction of tibiofemoral space. Bone pain has gradually improved in all patients. Also, BMD values have been enhanced over six years of treatment, especially in children.
接受 Taliglucerase Alfa 治疗的阿尔巴尼亚 1 型戈谢病患者的骨骼表现、骨痛和 BMD 变化
戈谢病是一种罕见的遗传性溶酶体疾病,导致多器官的脂质积累和功能障碍。骨受累是戈谢病最普遍的方面之一。疼痛、残疾和生活质量下降仍然是戈歇患者骨骼受累最常见的特征。患者和方法。在本研究中,我们将考虑24例诊断为1型戈谢病的患者的数据。我们密切关注了他们六年的进展。在基线时,所有患者开始使用平均剂量为45 iu /kg的taliglucerase α - fa治疗;后来,在研究过程中,其中两人将治疗方法改为velaglucerase α。在基线评估之前,12名患者在不同的持续时间内接受了imiglucerase治疗。在基线,我们对长骨和脊柱进行x光检查,每年进行不同的标准评估,如骨痛,脊柱和骨盆的MRI检查,骨密度的DEXA检查。4名患者因各种原因退出研究,其中2名在基线时,另外2名在第3年(FU3)。结果。在基线时,我们有8名儿童和16名成年人。平均年龄28.7±16.5 SD年。我们患者中最常见的骨骼表现是胫骨股间隙缩小(40%),骨坏死(36%)和椎体缩小(32%)。基线时,15例患者出现不同程度的骨痛。多年来,我们患者的骨痛逐渐得到改善。最显著的骨痛改善见于出现骨危机的患者。另一个令人印象深刻的发现是,在六年的治疗期间,骨密度显著改善。我们的研究显示,比较FU5和基线值,BMD有显著改善(p = 0.0007)。与成人(p = 0.3673)相比,儿童在骨密度方面表现出显著改善(p = 0.00061)。与naïve患者(p = 0.147)相比,切换组患者的平均骨密度变化更具指示性(p = 0.0142)。结论。戈歇1型患者的骨骼表现非常不同。在我们的研究中,作为长期评估的结果,我们注意到最常见的骨骼表现是胫股间隙缩小。所有患者骨痛均逐渐改善。此外,在六年的治疗中,骨密度值也有所提高,尤其是在儿童中。
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
6
审稿时长
20 weeks
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