NCT07462026

Exchangeable and Relative Exchangeable Copper as an Alternative to 24-Hour Urinary Copper in Wilson's Disease Monitoring

Comparison of Serum Exchangeable and Relative Exchangeable Copper Levels With Clinical Parameters and Multiparametric Liver MRI Findings in Patients With Wilson's Disease

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 81 (actual)
• Sponsor: Hacettepe University · Academic / Other
• Sex: All
• Age: —
• Healthy volunteers: Accepted

Summary

Serum exchangeable copper (EC) and relative exchangeable copper (REC) are blood tests developed to improve the assessment of copper levels in patients with Wilson's disease. EC measures the fraction of copper in the blood that is not bound to ceruloplasmin and reflects copper accumulation in the body. REC represents the proportion of this exchangeable copper relative to total serum copper. Previous studies have shown that EC and REC are more accurate than traditional copper tests for diagnosing Wilson's disease. This study aimed to evaluate the relationship between EC/REC and routine copper measurements in patients with Wilson's disease during follow-up, to assess their potential value in disease monitoring.

Detailed description

Wilson's disease (WD) is an inherited disorder of copper metabolism caused by mutations in the ATP7B gene and transmitted in an autosomal recessive manner. The disease leads to progressive copper accumulation in multiple organs, particularly the liver and brain, resulting in a wide spectrum of clinical manifestations, including hepatic, neurological, and psychiatric involvement. Accurate monitoring of copper levels is essential for evaluating treatment response and adjusting therapy in patients with WD. In routine clinical practice, copper status is commonly assessed using 24-hour urinary copper excretion and non-ceruloplasmin-bound copper. However, these traditional measurements have important limitations. Collection of 24-hour urine samples is cumbersome and prone to errors, and interpretation may be challenging in patients with renal dysfunction or neurological involvement. Total serum copper reflects both ceruloplasmin-bound and non-ceruloplasmin-bound copper. In WD, despite increased total body copper, serum ceruloplasmin levels are reduced, leading to low ceruloplasmin-bound copper concentrations. As a result, total serum copper measurements may not reliably reflect copper overload. Non-ceruloplasmin-bound copper is calculated indirectly by subtracting ceruloplasmin-bound copper from total serum copper and depends on accurate ceruloplasmin measurement. Immunological assays may overestimate ceruloplasmin levels, resulting in unreliable or even negative calculated values. Serum exchangeable copper (EC) and relative exchangeable copper (REC) have been developed to address these limitations. EC represents the directly measured fraction of serum copper that is not bound to ceruloplasmin and is thought to better reflect bioavailable and tissue copper accumulation. REC is calculated as the ratio of EC to total serum copper. Previous studies have shown that EC and REC are more sensitive and specific than conventional copper tests and have been validated for the diagnosis of WD. However, their role as biomarkers in the follow-up and management of patients with WD has not been fully established. The aim of this study was to evaluate the relationship between EC and REC and routine copper measurements in adult patients with Wilson's disease during follow-up, in order to assess their potential utility in monitoring copper status.

Conditions

• Wilson's Disease

Timeline

• Start date: 2021-01-31
• Primary completion: 2021-09-05
• Completion: 2021-09-05
• First posted: 2026-03-10
• Last updated: 2026-03-10

Locations

1 site across 1 country: Turkey (Türkiye)