Wilson's Disease in Oman: A National Cohort Study of Clinical Spectrum, Diagnostic Delay, and Long-Term Outcomes.

IF 2.2 Q2 MEDICINE, GENERAL & INTERNAL
Said A Al-Busafi, Juland N Al Julandani, Zakariya Alismaeili, Juhaina J Al Raisi
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引用次数: 0

Abstract

Background/Objectives: Wilson's disease (WD) is a rare autosomal recessive disorder of copper metabolism that results in hepatic, neurological, and psychiatric manifestations. Despite being described globally, data from the Middle East remains limited. This study presents the first comprehensive national cohort analysis of WD in Oman, examining clinical features, diagnostic challenges, treatment patterns, and long-term outcomes. Methods: A retrospective cohort study was conducted on 36 Omani patients diagnosed with WD between 2013 and 2020 at Sultan Qaboos University Hospital using AASLD diagnostic criteria. Clinical presentation, biochemical parameters, treatment regimens, and progression-free survival were analyzed. Results: The median age at diagnosis was 14.5 years, with a slight female predominance (55.6%). Clinical presentation varied: 25% had hepatic symptoms, 22.2% had mixed hepatic-neurological features, and 16.7% presented with neurological symptoms alone. Asymptomatic cases identified via family screening accounted for 33.3%. Diagnostic delays were most pronounced among patients presenting with neurological symptoms. A positive family history was reported in 88.9% of cases, suggesting strong familial clustering despite a low rate of consanguinity (5.6%). Regional distribution was concentrated in Ash Sharqiyah North and Muscat. Chelation therapy with trientine or penicillamine, often combined with zinc, was the mainstay of treatment. Treatment adherence was significantly associated with improved progression-free survival (p = 0.012). Conclusions: WD in Oman is marked by heterogeneous presentations, frequent diagnostic delays, and strong familial clustering. Early detection through cascade screening and sustained treatment adherence are critical for favorable outcomes. These findings support the need for national screening policies and structured long-term care models for WD in the region.

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阿曼威尔逊氏病:临床谱、诊断延迟和长期结果的国家队列研究。
背景/目的:威尔逊氏病(WD)是一种罕见的铜代谢常染色体隐性遗传病,可导致肝脏、神经系统和精神方面的表现。尽管在全球范围内进行了描述,但来自中东的数据仍然有限。本研究首次对阿曼的WD进行了全面的全国队列分析,考察了临床特征、诊断挑战、治疗模式和长期结果。方法:采用AASLD诊断标准,对2013年至2020年在苏丹卡布斯大学医院诊断为WD的36例阿曼患者进行回顾性队列研究。分析临床表现、生化指标、治疗方案和无进展生存期。结果:中位诊断年龄为14.5岁,女性占55.6%。临床表现各不相同:25%有肝脏症状,22.2%有肝-神经混合特征,16.7%有单独的神经症状。经家庭筛查发现无症状病例占33.3%。诊断延迟在出现神经系统症状的患者中最为明显。88.9%的病例报告有阳性家族史,尽管有较低的血缘关系(5.6%),但有较强的家族聚集性。区域分布集中在Ash Sharqiyah北部和Muscat。用曲恩汀或青霉胺进行螯合治疗,通常与锌结合,是主要的治疗方法。治疗依从性与改善无进展生存期显著相关(p = 0.012)。结论:WD在阿曼的特点是异质的表现,频繁的诊断延迟,和强家族聚类。通过级联筛查的早期发现和持续的治疗依从性对于良好的结果至关重要。这些发现支持在该地区制定国家筛查政策和结构化的WD长期护理模式的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinics and Practice
Clinics and Practice MEDICINE, GENERAL & INTERNAL-
CiteScore
2.60
自引率
4.30%
发文量
91
审稿时长
10 weeks
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