2011年2月
Influence of plasma glucagon levels on glycemic control in children with type 1 diabetes.
Pediatrics international : official journal of the Japan Pediatric Society
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- 巻
- 53
- 号
- 1
- 開始ページ
- 46
- 終了ページ
- 9
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1111/j.1442-200X.2010.03184.x
- 出版者・発行元
- WILEY-BLACKWELL
OBJECTIVE: The aim of this study was to investigate the association between plasma glucose (PG), HbA1c and plasma glucagons levels in children with type 1 diabetes to determine the influence of plasma glucagon on their glycemic control. METHODS: The study was conducted in 60 Japanese children, aged 13.3 ± 4.6 years, with type 1 diabetes for at least 3 years of diabetes. Most of the subjects had absent pancreatic β-cell function. We compared the glucagon levels among patient groups stratified according to the 2-hour postprandial levels (<50, 50-99, 100-199, 200-299, and ≥ 300 mg/dL), and the HbA1c levels (<7.0, 7.0-7.9, 8.0-8.9, and ≥ 9%). RESULTS: The mean 2-hour postprandial PG, HbA1c and plasma glucagon levels were 174 ± 97 mg/dL, 7.7 ± 1.3% and 84.0 ± 32.6 pg/mL, respectively. The glucagon levels were highly correlated with the PG levels (r=0.553, P<0.0001) and mildly correlated with the HbA1c levels (r=0.301, P=0.0192). Patients with high PG levels had significantly higher levels of glucagon as compared with those with lower PG levels (139.4 ± 47.2, 78.4 ± 17.3, 82.4 ± 21.0, 98.3 ± 29.2 and 93.8 ± 18.3 pg/mL, P=0.0009). On the other hand, there were no significant differences in plasma glucagon levels among patient groups stratified according to HbA1c levels (P=0.1566), however, patients with HbA1c levels ≥ 9% had significantly higher levels of glucagon than those with HbA1c levels < 7% (113.3 ± 53.4 vs 80.8 ± 18.4 pg/mL, P=0.0291). CONCLUSION: These results suggest that patients with high PG are likely to have high concentrations of plasma glucagon, which may aggravate glycemic control progressively, leading to elevation of HbA1c levels.
- リンク情報
- ID情報
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- DOI : 10.1111/j.1442-200X.2010.03184.x
- ISSN : 1328-8067
- PubMed ID : 20557473
- Web of Science ID : WOS:000287662900011