Identification of a rare compound heterozygous hemoglobin variant β0-thal [β17(A14) Lys>Stop, HBB: c.52A>T] and Hb J-Lome [β59(E3) Lys>Asn, HBB: c.180G>C]. Issue 1 (31st December 2022)
- Record Type:
- Journal Article
- Title:
- Identification of a rare compound heterozygous hemoglobin variant β0-thal [β17(A14) Lys>Stop, HBB: c.52A>T] and Hb J-Lome [β59(E3) Lys>Asn, HBB: c.180G>C]. Issue 1 (31st December 2022)
- Main Title:
- Identification of a rare compound heterozygous hemoglobin variant β0-thal [β17(A14) Lys>Stop, HBB: c.52A>T] and Hb J-Lome [β59(E3) Lys>Asn, HBB: c.180G>C]
- Authors:
- Chen, Zixin
Shao, Limei
Jiang, Mingfeng
Ma, Run
Ping, Hongfen
Wang, Zuo
Ba, Xuejiao
Ma, Bingjie
Zhou, Tao - Abstract:
- ABSTRACT: Background: HbA1c is the validated biomarker for glycemic management in diabetic individuals. Here, we report a compound heterozygote for β 0 -thal and Hb J-Lomeand evaluate its effect on HbA1c measurements. Methods: A 51-year-old female was suspected of harboring a hemoglobin variant following no value of HbA1c levelby Arkray HA-8180 V (48s HbA1c mode), abnormal hematological data, and abnormalhemoglobin analysison capillary electrophoresis (Capillarys 2 Flex Piercing, Hb program). Sanger sequencing of the α and β genes was subsequently performed on the proband.HbA1c was reanalyzed using D10 (Bio-Rad), Capillarys 2 Flex Piercing (Sebia), and Roche Cobas c501 (Roche Diagnostics). Results: Sanger sequencing identified a compound heterozygote for β 0 -thal [β17(A14) Lys > Stop, HBB: c.52A > T] and Hb J-Lome [β59(E3) Lys > Asn, HBB: c.180G > C].HbA1c values determinedby D10, Capillarys 2 Flex Piercing (HbA1c program), and Roche Cobas c501were 2.3%, no HbA1c value, and 5.1 (32 mmol/mol), respectively. During pedigree analysis, the son of the proband was found to have normal blood glucose (5.55 mmol/L), decreased HbA1c (3.6%, 16 mmol/mol)by Arkray HA-8180 V (48s HbA1c mode), an abnormal band on the electrophoretogram of Capillarys2 (Hb program), and the Hb J-Lome mutation in the β globin gene.Subsequently, HbA1c values determinedby D10, Capillarys 2 Flex Piercing (HbA1c program), and Roche Cobas c501 were4.0% (20 mmol/mol), no HbA1c value, and 5.0 (31 mmol/mol),ABSTRACT: Background: HbA1c is the validated biomarker for glycemic management in diabetic individuals. Here, we report a compound heterozygote for β 0 -thal and Hb J-Lomeand evaluate its effect on HbA1c measurements. Methods: A 51-year-old female was suspected of harboring a hemoglobin variant following no value of HbA1c levelby Arkray HA-8180 V (48s HbA1c mode), abnormal hematological data, and abnormalhemoglobin analysison capillary electrophoresis (Capillarys 2 Flex Piercing, Hb program). Sanger sequencing of the α and β genes was subsequently performed on the proband.HbA1c was reanalyzed using D10 (Bio-Rad), Capillarys 2 Flex Piercing (Sebia), and Roche Cobas c501 (Roche Diagnostics). Results: Sanger sequencing identified a compound heterozygote for β 0 -thal [β17(A14) Lys > Stop, HBB: c.52A > T] and Hb J-Lome [β59(E3) Lys > Asn, HBB: c.180G > C].HbA1c values determinedby D10, Capillarys 2 Flex Piercing (HbA1c program), and Roche Cobas c501were 2.3%, no HbA1c value, and 5.1 (32 mmol/mol), respectively. During pedigree analysis, the son of the proband was found to have normal blood glucose (5.55 mmol/L), decreased HbA1c (3.6%, 16 mmol/mol)by Arkray HA-8180 V (48s HbA1c mode), an abnormal band on the electrophoretogram of Capillarys2 (Hb program), and the Hb J-Lome mutation in the β globin gene.Subsequently, HbA1c values determinedby D10, Capillarys 2 Flex Piercing (HbA1c program), and Roche Cobas c501 were4.0% (20 mmol/mol), no HbA1c value, and 5.0 (31 mmol/mol), respectively. Conclusion: Atypically low HbA1c levels or a discrepancy between blood glucose and HbA1c levels should raise concerns about hemoglobin variations. … (more)
- Is Part Of:
- Hematology. Volume 27:Issue 1(2022)
- Journal:
- Hematology
- Issue:
- Volume 27:Issue 1(2022)
- Issue Display:
- Volume 27, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 27
- Issue:
- 1
- Issue Sort Value:
- 2022-0027-0001-0000
- Page Start:
- 946
- Page End:
- 950
- Publication Date:
- 2022-12-31
- Subjects:
- Hb J-Lome -- glycated hemoglobin (Hb) -- hemoglobin variant -- interference
Blood -- Diseases -- Periodicals
Hematology -- Periodicals
Blood -- Transfusion -- Periodicals
616.15005 - Journal URLs:
- http://www.ingentaconnect.com/content/maney/hem ↗
https://www.tandfonline.com/journals/yhem20 ↗
http://maneypublishing.com/ ↗ - DOI:
- 10.1080/16078454.2022.2114672 ↗
- Languages:
- English
- ISSNs:
- 1024-5332
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4291.565000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23884.xml