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- Publisher Website: 10.1258/acb.2011.011202
- Scopus: eid_2-s2.0-84867118775
- PMID: 22589359
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Article: A spuriously 'normal' haemoglobin A1c result
Title | A spuriously 'normal' haemoglobin A1c result |
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Authors | |
Issue Date | 2012 |
Publisher | Royal Society of Medicine Press Ltd. The Journal's web site is located at http://www.roysocmed.ac.uk/pub/acb.htm |
Citation | Annals of Clinical Biochemistry, 2012, v. 49 n. 4, p. 408-411 How to Cite? |
Abstract | We report a case of spuriously 'normal' haemoglobin A1c (HbA1c) result due to misidentification of HbG Taipei as HbAo by the Variant II built-in retention time algorithm. The defect was circumvented effectively by the implementation of a chromatographic system specific internal quality control mechanism for peak identity verification. HbA1c and estimated average glucose results were corrected from 4.7% to 8.2%, and 4.9 to 10.5 mmol/L, respectively. The results were consistent with the patient's concurrent and previous fasting blood glucose concentrations and existence of diabetes mellitus dermopathy, indicating poor glycaemic control. A review of currently available analytical systems showed that other than mass spectrometry, HbA1c measurements by these systems were generally affected by the presence of haemoglobin variants. The same haemoglobin variant may affect different analytical systems differently, resulting in the deviation of HbA1c results from the true value to different extents. Including the analytical principle of HbA1c measurement in the laboratory report can avoid inappropriate comparison of results obtained by different analytical systems. Moreover, since individual haemoglobinopathy may affect the degree of glucose binding to haemoglobin in a different way, this uncertainty limits the general application of same decision cut-off of established guidelines for glycaemic control monitoring. Adoption of an individualized monitoring system based on the critical difference or reference change value of HbA1c can be considered. |
Description | Case report |
Persistent Identifier | http://hdl.handle.net/10722/160063 |
ISSN | 2023 Impact Factor: 2.1 2023 SCImago Journal Rankings: 0.598 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lo, VMH | en_US |
dc.contributor.author | Ma, ESK | en_US |
dc.contributor.author | Chau, EMC | en_US |
dc.contributor.author | So, JCC | en_US |
dc.date.accessioned | 2012-08-16T06:02:11Z | - |
dc.date.available | 2012-08-16T06:02:11Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Annals of Clinical Biochemistry, 2012, v. 49 n. 4, p. 408-411 | en_US |
dc.identifier.issn | 0004-5632 | - |
dc.identifier.uri | http://hdl.handle.net/10722/160063 | - |
dc.description | Case report | - |
dc.description.abstract | We report a case of spuriously 'normal' haemoglobin A1c (HbA1c) result due to misidentification of HbG Taipei as HbAo by the Variant II built-in retention time algorithm. The defect was circumvented effectively by the implementation of a chromatographic system specific internal quality control mechanism for peak identity verification. HbA1c and estimated average glucose results were corrected from 4.7% to 8.2%, and 4.9 to 10.5 mmol/L, respectively. The results were consistent with the patient's concurrent and previous fasting blood glucose concentrations and existence of diabetes mellitus dermopathy, indicating poor glycaemic control. A review of currently available analytical systems showed that other than mass spectrometry, HbA1c measurements by these systems were generally affected by the presence of haemoglobin variants. The same haemoglobin variant may affect different analytical systems differently, resulting in the deviation of HbA1c results from the true value to different extents. Including the analytical principle of HbA1c measurement in the laboratory report can avoid inappropriate comparison of results obtained by different analytical systems. Moreover, since individual haemoglobinopathy may affect the degree of glucose binding to haemoglobin in a different way, this uncertainty limits the general application of same decision cut-off of established guidelines for glycaemic control monitoring. Adoption of an individualized monitoring system based on the critical difference or reference change value of HbA1c can be considered. | - |
dc.language | eng | en_US |
dc.publisher | Royal Society of Medicine Press Ltd. The Journal's web site is located at http://www.roysocmed.ac.uk/pub/acb.htm | - |
dc.relation.ispartof | Annals of Clinical Biochemistry | en_US |
dc.subject.mesh | Aged | - |
dc.subject.mesh | Hemoglobin A, glycosylated - analysis | - |
dc.subject.mesh | Male | - |
dc.subject.mesh | Reference values | - |
dc.subject.mesh | Sensitivity and specificity | - |
dc.subject.mesh | Animals | - |
dc.subject.mesh | Humans | - |
dc.subject.mesh | Rats | - |
dc.title | A spuriously 'normal' haemoglobin A1c result | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lo, VMH: mhlo@hksh.com | en_US |
dc.identifier.email | Ma, ESK: eskma@hkucc.hku.hk | en_US |
dc.identifier.email | So, JCC: scc@pathology.hku.hk | - |
dc.identifier.authority | So, JCC=rp00391 | en_US |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1258/acb.2011.011202 | - |
dc.identifier.pmid | 22589359 | - |
dc.identifier.scopus | eid_2-s2.0-84867118775 | - |
dc.identifier.hkuros | 205193 | en_US |
dc.identifier.volume | 49 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 408 | en_US |
dc.identifier.epage | 411 | en_US |
dc.identifier.isi | WOS:000307798900017 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 0004-5632 | - |