Eleven Cases of Hb J-Paris-I [ HBA2: c.38C>A (or HBA1)]: A Stable α Chain Variant Elutes in the P3 Window on High-Performance Liquid Chromatography

Hemoglobin. 2021 Sep;45(5):322-324. doi: 10.1080/03630269.2021.2003381. Epub 2021 Nov 16.

Abstract

Hb J-Paris-I [HBA2: c.38C>A (or HBA1)] is a stable fast-moving hemoglobin (Hb) that elutes in the P3 window on high performance liquid chromatography (HPLC). The mutation can happen on either the α1- or α2-globin gene. Codon 12 changes from GCC to GAC to replace the alanine amino acid with aspartic acid. This change is external with no clinical significance. The elution in the P3 wave on HPLC can interfere with the glycated Hb assay by HPLC. In this study, data of 11 cases of Hb J-Paris-I were thoroughly presented. The majority of the cases were of Indian ethnicity. The mean value of Hb J-Paris-I on HPLC was 26.7 ± 2.0%. The retention time (RT) was 1.75 ± 0.03 min. The isoelectric focusing (IEF) mean value was -5.6 (range -6.1 to -4.9). Hb A2 was consistently reduced to 1.8 ± 0.3%. A fraction of 0.8% corresponding to the Hb A2-J-Paris-I (α2J-Paris-Iδ2) is likely to be concealed within the A0 peak of Hb A on HPLC. Interestingly, two cases were associated with two different polymorphisms [HBA2: c.-24C>G or Cap +14 (C>G) and HBA2: c.*136A>G polymorphism] without apparent effect on the variant expression.

Keywords: Cap +14 (C>G); HBA2: c.*136A>G polymorphism; Hb J-Paris-I; hemoglobin (Hb); α Variant.

MeSH terms

  • Chromatography, High Pressure Liquid
  • Genotype
  • Glycated Hemoglobin / genetics
  • Hemoglobin A2 / genetics
  • Hemoglobin J
  • Hemoglobinopathies* / genetics
  • Hemoglobins, Abnormal* / genetics
  • Humans
  • alpha-Globins / genetics
  • alpha-Thalassemia* / genetics

Substances

  • Glycated Hemoglobin A
  • Hemoglobins, Abnormal
  • alpha-Globins
  • Hemoglobin J
  • Hemoglobin A2
  • hemoglobin J-Paris