Home Testing for HbA1c, in addition to the oral glucose tolerance test, in screening for abnormal glucose regulation helps to reveal patients with early β-cell function impairment
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Testing for HbA1c, in addition to the oral glucose tolerance test, in screening for abnormal glucose regulation helps to reveal patients with early β-cell function impairment

  • Yu-Hsuan Li , Wayne Huey-Herng Sheu , Wen-Jane Lee , I-Te Lee , Shih-Yi Lin , Wen-Lieng Lee , Kae-Woei Liang and Jun-Sing Wang EMAIL logo
Published/Copyright: March 29, 2018

Abstract

Background:

The oral glucose tolerance test (OGTT) is recommended to screen for diabetes in patients with coronary artery disease. We hypothesized that testing for glycated hemoglobin (HbA1c), in addition to the OGTT, in screening for abnormal glucose regulation may help to reveal patients with β-cell function impairment.

Methods:

Patients with no history of diabetes who were admitted for coronary angiography were recruited to undergo an OGTT and HbA1c test 2–4 weeks after hospital discharge. β-cell function and insulin resistance were assessed using the homeostasis model assessment (HOMA-β and HOMA-IR, respectively). For patients with normal glucose tolerance (NGT) based on the OGTT, we compared HOMA-β between two subgroups of patients using an HbA1c cutoff of 39 mmol/mol or 42 mmol/mol. For patients with prediabetes based on an OGTT, we compared the HOMA-β between two subgroups of patients using an HbA1c cutoff of 48 mmol/mol.

Results:

A total of 1044 patients were analyzed. In patients with NGT by OGTT (n=432), those with an HbA1c ≥42 mmol/mol had a lower HOMA-β compared to those with an HbA1c <42 mmol/mol (107±82 vs. 132±96, p=0.018). In patients with prediabetes by OGTT (n=423), those with an HbA1c ≥48 mmol/mol had a lower HOMA-β compared to those with an HbA1c <48 mmol/mol (91±52 vs. 120±88, p=0.003). No significant between-group difference in HOMA-IR was noted.

Conclusions:

The use of HbA1c in addition to the OGTT in screening for abnormal glucose regulation helped to reveal patients with early β-cell function impairment.


Corresponding author: Jun-Sing Wang, MD, Division of Endocrinology and Metabolism, Department of Internal Medicine, Taichung Veterans General Hospital, #1650, Sec. 4, Taiwan Boulevard, Taichung 407, Taiwan, Phone: +886-4-23592525/3062, Fax: +886-4-23593662; and Department of Medicine, School of Medicine, National Yang-Ming University, Taipei, Taiwan

Acknowledgments

The authors are grateful to their colleagues at the Taichung Veterans General Hospital Cardiovascular Center for their assistance, and to the study subjects for their participation.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This work was supported by The National Science Council, Taiwan [NSC MOST 104-2314-B-075A-003, 2015]; and Taichung Veterans General Hospital, Taichung, Taiwan [TCVGH-YM1050103, 2016; TCVGH-1053501B, 2016].

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organizations played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2017-09-18
Accepted: 2018-02-01
Published Online: 2018-03-29
Published in Print: 2018-07-26

©2018 Walter de Gruyter GmbH, Berlin/Boston

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