Analysis of five cases showing false-high Hemoglobin A1c due to reduced catalase activity-Reference-Cited by-同舟云学术

Analysis of five cases showing false-high Hemoglobin A1c due to reduced catalase activity

Published:2024 Issue:1 Volume:71 Page:39-44
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Hara Kenji¹,Ujiie Atsushi¹,Suzuki Shiori¹,Okumura Takenori¹,Kubo Mio¹,Shinozaki Hiroyuki¹,Yamauchi Mototaka¹,Tsuchiya Takafumi¹,Takebayashi Kohzo¹,Shimozawa Nobuyuki²,Koga Masafumi³,Hashimoto Koshi¹^ORCID

Affiliation:

1. Department of Diabetes, Endocrinology and Hematology, Dokkyo Medical University Saitama Medical Center, Saitama 343-8555, Japan

2. Division of Genomics Research, Life Science Research Center, Gifu University, Gifu 501-1193, Japan

3. Department of Internal Medicine, Hakuhokai Central Hospital, Hyogo 661-0953, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.jstage.jst.go.jp/article/endocrj/71/1/71_EJ23-0212/_pdf

Reference13 articles.

1. 1 International Expert Committee (2009) International Expert Committee report on the role of the A1C assay in the diagnosis of diabetes. Diabetes Care 32: 1327–1334.

2. 2 Koga M (2014) Glycated albumin; clinical usefulness. Clin Chim Acta 433: 96–104.

3. 3 Goth L, Rass P, Madarasi I (2001) A novel catalase mutation detected by polymerase chain reaction-single strand conformation polymorphism, nucleotide sequencing, and western blot analyses is responsible for the type C of Hungarian acatalasemia. Electrophoresis 22: 49–51.

4. 4 Kishimoto Y, Murakami Y, Hayashi K, Takahara S, Sugimura T, et al. (1992) Detection of a common mutation of the catalase gene in Japanese acatalasemic patients. Hum Genet 88: 487–490.

5. 5 Yamashita T, Mitsui J, Shimozawa N, Takashima S, Umemura H, et al. (2017) Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype. J Neurol Sci 375: 424–429.

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