HbA1c adjusted by erythrocyte creatine is a useful glycemic control indicator in patients with hemolysis.


Journal

Clinical biochemistry
ISSN: 1873-2933
Titre abrégé: Clin Biochem
Pays: United States
ID NLM: 0133660

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 06 05 2019
revised: 01 08 2019
accepted: 02 08 2019
pubmed: 7 8 2019
medline: 22 11 2019
entrez: 7 8 2019
Statut: ppublish

Résumé

HbA1c shows low in patients with hemolysis, whereas glycated albumin (GA) is not affected by hemolysis. Therefore, the GA/HbA1c ratio reflects hemolysis in diabetic patients with hemolysis. Erythrocyte creatine (EC) is an indicator of hemolysis that reflects the mean erythrocyte age. The aim of this study was to examine whether HbA1c adjusted by EC accurately reflected glycemic control in patients with hemolysis. A total of 238 individuals, consisting of 131 diabetic patients and 107 non-diabetic subjects, and consisting of 42 patients with hemolysis, and 196 subjects without hemolysis were selected for the study. HbA1c expressed in the IFCC units (iA1c) as well as in the NGSP units (A1C) were used. From the fact that EC and the GA/iA1c ratio showed a significant positive correlation, a formula for iA1c adjusted by EC (ECadj-iA1c) was created from a regression equation between EC and the GA/iA1c ratio. Significant correlations were observed between the GA/iA1c ratio and various hemolytic indicators but not between the GA/ECadj-iA1c ratio and those hemolytic indicators. The GA/iA1c ratio in individuals with hemolysis was significantly higher than in individuals without hemolysis, while no significant differences were observed in the GA/ECadj-iA1c ratio between the groups. Further, iA1c concentrations in non-diabetic patients with hemolysis were significantly lower than in the non-diabetic subjects without hemolysis, whereas ECadj-iA1c and GA concentrations showed no significant difference between the two groups. These results suggested that ECadj-iA1c accurately reflected glycemic control in patients with hemolysis.

Identifiants

pubmed: 31386833
pii: S0009-9120(19)30482-5
doi: 10.1016/j.clinbiochem.2019.08.004
pii:
doi:

Substances chimiques

Glycated Hemoglobin A 0
Glycation End Products, Advanced 0
Serum Albumin 0
hemoglobin A1c protein, human 0
Creatine MU72812GK0
Glycated Serum Albumin 0

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

77-81

Informations de copyright

Copyright © 2019 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.

Auteurs

Masafumi Koga (M)

Department of Internal Medicine, Hakuhokai Central Hospital, 4-23-1 Higashisonoda-cho, Amagasaki, Hyogo 661-0953, Japan. Electronic address: m-koga@kawanishi-city-hospital.com.

Shinya Inada (S)

Department of Internal Medicine, Kawanishi City Hospital, Hyogo, Japan.

Masaru Shibata (M)

Department of Internal Medicine, Kawanishi City Hospital, Hyogo, Japan.

Hiroko Ijima (H)

Central Laboratory, Jinnouchi Hospital, Kumamoto, Japan.

Hideaki Jinnouchi (H)

Department of Internal Medicine, Jinnouchi Hospital, Kumamoto, Japan.

Yasuhiro Ono (Y)

Department of Internal Medicine, Takagi Hospital, Fukuoka, Japan.

Tsuyoshi Iwasaka (T)

Preventive Medical Center, Takagi Hospital, Fukuoka, Japan.

Shinji Tokuhiro (S)

Department Clinical Laboratory, Kochi Medical School Hospital, Kochi, Japan.

Yoshihisa Matsumura (Y)

Department of Laboratory Medicine, Kochi Medical School, Kochi, Japan.

Hirotaka Matsui (H)

Department of Molecular Laboratory Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Toshika Okumiya (T)

Department of Biomedical Laboratory Sciences, Faculty of Health Sciences, Kumamoto University, Kumamoto, Japan.

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Classifications MeSH