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Non-ceruloplasmin-bound copper in routine clinical practice in different laboratories.
J Trace Elem Med Biol. 2008; 22(1):50-3.JT

Abstract

BACKGROUND

Copper is an essential nutrient but is toxic when the free form is in excess. Wilson's disease (WD) is an autosomal recessive disorder of copper excess. Its diagnosis is a challenge, especially in the absence of obvious neurological changes, or Kayser-Fleischer rings. Non-ceruloplasmin-bound copper is a calculated parameter devised for the investigation of patients who potentially have WD.

METHODS

We compared non-ceruloplasmin-bound copper from three different laboratories. We retrospectively reviewed paired ceruloplasmin and copper data and calculated non-ceruloplasmin-bound copper. Comparative statistics, linear regression, chi-square test and graphical techniques were employed to compare the data.

RESULTS

All three assays had negative results for over 20% of the non-ceruloplasmin-bound copper concentrations; this was not significantly different. However, there were statistically significant differences for the 97.5th percentile. When plotted against the ceruloplasmin and copper concentrations, significant differences existed for both the visual and linear regression data between the three different laboratories.

CONCLUSIONS

Non-ceruloplasmin-bound copper cut-offs may not be transferable between laboratories. Each laboratory should derive its own cut-offs for the 97.5th percentile, as there are differences due to assays, populations or both.

Authors+Show Affiliations

Department of Clinical Biochemistry, The Ipswich Hospital, Ipswich IP4 5PD, UK. ptwomey@nhs.netNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

18319140

Citation

Twomey, Patrick J., et al. "Non-ceruloplasmin-bound Copper in Routine Clinical Practice in Different Laboratories." Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS), vol. 22, no. 1, 2008, pp. 50-3.
Twomey PJ, Viljoen A, Reynolds TM, et al. Non-ceruloplasmin-bound copper in routine clinical practice in different laboratories. J Trace Elem Med Biol. 2008;22(1):50-3.
Twomey, P. J., Viljoen, A., Reynolds, T. M., & Wierzbicki, A. S. (2008). Non-ceruloplasmin-bound copper in routine clinical practice in different laboratories. Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS), 22(1), 50-3. https://doi.org/10.1016/j.jtemb.2007.11.001
Twomey PJ, et al. Non-ceruloplasmin-bound Copper in Routine Clinical Practice in Different Laboratories. J Trace Elem Med Biol. 2008;22(1):50-3. PubMed PMID: 18319140.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Non-ceruloplasmin-bound copper in routine clinical practice in different laboratories. AU - Twomey,Patrick J, AU - Viljoen,Adie, AU - Reynolds,Timothy M, AU - Wierzbicki,Anthony S, Y1 - 2008/02/19/ PY - 2007/10/09/received PY - 2007/11/12/revised PY - 2007/11/15/accepted PY - 2008/3/6/pubmed PY - 2008/8/8/medline PY - 2008/3/6/entrez SP - 50 EP - 3 JF - Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) JO - J Trace Elem Med Biol VL - 22 IS - 1 N2 - BACKGROUND: Copper is an essential nutrient but is toxic when the free form is in excess. Wilson's disease (WD) is an autosomal recessive disorder of copper excess. Its diagnosis is a challenge, especially in the absence of obvious neurological changes, or Kayser-Fleischer rings. Non-ceruloplasmin-bound copper is a calculated parameter devised for the investigation of patients who potentially have WD. METHODS: We compared non-ceruloplasmin-bound copper from three different laboratories. We retrospectively reviewed paired ceruloplasmin and copper data and calculated non-ceruloplasmin-bound copper. Comparative statistics, linear regression, chi-square test and graphical techniques were employed to compare the data. RESULTS: All three assays had negative results for over 20% of the non-ceruloplasmin-bound copper concentrations; this was not significantly different. However, there were statistically significant differences for the 97.5th percentile. When plotted against the ceruloplasmin and copper concentrations, significant differences existed for both the visual and linear regression data between the three different laboratories. CONCLUSIONS: Non-ceruloplasmin-bound copper cut-offs may not be transferable between laboratories. Each laboratory should derive its own cut-offs for the 97.5th percentile, as there are differences due to assays, populations or both. SN - 0946-672X UR - https://www.unboundmedicine.com/medline/citation/18319140/Non_ceruloplasmin_bound_copper_in_routine_clinical_practice_in_different_laboratories_ DB - PRIME DP - Unbound Medicine ER -