Glucagon Response to Glucose Challenge in Patients with Idiopathic Postprandial Syndrome

Minami Kosuda, Kentaro Watanabe, Masao Koike, Ai Morikawa, Hitoki Saito, Genta Kohno, Hisamitsu Ishihara

研究成果: ジャーナルへの寄稿記事査読

1 被引用数 (Scopus)

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Division of Diabetes and Metabolic Diseases, Department of Internal Medicine, Nihon University School of Medicine, Tokyo, Japan Background: Postprandial syndrome is characterized by hunger, weakness, and anxiety neurosis after meals. Although abnormal glucagon response is a suggested mechanism, inaccuracies in conventional glucagon measurement methods have prevented precise analysis. Recently, a more reliable dual-antibody sandwich enzyme-linked immunosorbent assay for glucagon was developed. Methods: We conducted a 75-g oral glucose tolerance test (OGTT) extending to 4 hours in 14 patients with idiopathic postprandial syndrome. In addition to blood glucose and insulin, glucagon concentra-tion was measured with the novel method and analyzed retrospectively. Results: Median (lower quartile, upper quartile) age and body-mass index were 40 years (30, 49) and 24.9 (23.1, 26.2), respectively. The OGTT revealed that one patient had a diabetic pattern, and two were glucose intolerant. Fasting insulin was 7.6 μU/mL (6.8, 8.8) and reached 73.7 μU/mL (54.3, 82.6) at 30 min. Insulin remained elevated until 180 min. Fasting glucagon was 21.1 pg/mL (16.1, 33.8), reached a nadir of 6.9 (3.5, 10.3) at 60 min, one-third the baseline level, and remained suppressed until 180 min. We observed two types of glucagon dynamics: a lower fasting glucagon with further suppression and a normal or higher fasting glucagon with a subsequent large decrease. Conclusions: These data suggest that glucagon suppression is greater in patients with idiopathic postprandial syndrome than in previously studied healthy subjects. The present data will contribute to our understanding and future research of this syndrome. (J Nippon Med Sch 2022; 89: 102―107).

本文言語英語
ページ(範囲)102-108
ページ数7
ジャーナルJournal of Nippon Medical School
89
1
DOI
出版ステータス出版済み - 2022

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