ArticlePloS one2018
The optimal threshold of serum ceruloplasmin in the diagnosis of Wilson's disease: A large hospital-based study.
Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.
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Who cites it
11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.
- Biochemical testing for the diagnosis of Wilson's disease: A systematic review.Journal of clinical laboratory analysis · 2022Pooled it
- Biomarkers for diagnosis of Wilson's disease.The Cochrane database of systematic reviews · 2019Pooled it
- A cross-sectional assessment of the diagnostic value of serum ceruloplasmin for Wilson's disease in children.Medicine · 2026Article
- Insights into the coexistence of WilsonLiver research (Beijing, China) · 2025Article
- Functional characterisation of missense ceruloplasmin variants and real-world prevalence assessment of Aceruloplasminemia using population data.EBioMedicine · 2025Article
- Insights Into the Role of Copper in Neurodegenerative Diseases and the Therapeutic Potential of Natural Compounds.Current neuropharmacology · 2024Review
- Monitoring of Copper in Wilson Disease.Diagnostics (Basel, Switzerland) · 2023Review
- Assessment of the diagnostic value of serum ceruloplasmin for Wilson's disease in children.BMC gastroenterology · 2022Article
- Role of serum ceruloplasmin in the diagnosis of Wilson's disease: A large Chinese study.Frontiers in neurology · 2022Article
- Wilson disease: revision of diagnostic criteria in a clinical series with great genetic homogeneity.Journal of gastroenterology · 2021Article
- Characterization of Fibrinogen as a Key Modulator in Patients with Wilson's Diseases with Functional Proteomic Tools.International journal of molecular sciences · 2019Article
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Authors and funding
4 authors at 1 institution in 1 country.
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Abstract
BACKGROUND AND
aimsA ceruloplasmin (CP) concentration <200 mg/L is conventionally considered as one of the major diagnostic criteria for Wilson's disease (WD). However, the diagnostic accuracy of this threshold has never been investigated in a sufficiently large group of patients. This study aims to present the results of serum CP measurements in various patients and to identify the optimal cutoff value of CP for the diagnosis of WD. MATERIALS AND
methodsWe identified patients whose CP levels were evaluated from January 1, 2016 to December 31, 2016 using a laboratory information database. Data related to CP measurement were retrieved. We carefully reviewed patients' electronic medical records to correct errors and to obtain other necessary data. Data related to WD were retrieved from a special document containing medical records of patients with WD, which were created, modified, and maintained by authors.
resultsCP level was determined in 4048 patients (WD, 297; non-WD, 3751). The mean serum CP level in patients with WD was 50.6±44.2 mg/L, which was significantly lower than that in non-WD patients (293.2±117.3 mg/L, p<0.001). Only 1.0% of patients with WD had CP ≥200 mg/L. The sensitivity and specificity of CP for the diagnosis of WD were 99.0 and 80.9%, respectively, for the conventional cutoff value <200 mg/L and 95.6 and 95.5%, respectively, for the cutoff value <150 mg/L; the latter provided a higher diagnostic accuracy for WD. 53.0% of patients with liver failure, 37.7% of patients with nephrotic syndrome, and 23.0% of patients age 1 to 6 months had serum CP <200 mg/L. Patients who were pregnant and those with malignant tumors, and infectious and inflammatory diseases had significantly higher mean serum CP levels.
conclusionThe optimal cutoff value of CP for the diagnosis of WD in China is 150 mg/L, with a sensitivity of 95.6% and specificity of 95.5%, thereby providing the highest diagnostic accuracy for WD.
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