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用于I型糖原贮积病青年患者夜间治疗的玉米淀粉疗法。

Cornstarch regimens for nocturnal treatment of young adults with type I glycogen storage disease.

作者信息

Wolfsdorf J I, Crigler J F

机构信息

Department of Medicine, Children's Hospital, Boston, MA 02115, USA.

出版信息

Am J Clin Nutr. 1997 May;65(5):1507-11. doi: 10.1093/ajcn/65.5.1507.

Abstract

The goal of treatment of type I glycogen storage disease (GSD-I) is to prevent hypoglycemia and its biochemical consequences. In seven patients with GSD-I with a mean age of 19.5 y (range: 18.8-21.7 y), we compared the biochemical effects of isoenergetic amounts of uncooked cornstarch (UCS; 1.76 +/- 0.41 g/kg) given in random order on consecutive nights either as a single dose at 2100 (time 0) or as equally divided doses at 2100 and 0200. Over the 10-h period of observation there were significant regimen-by-time interactions for plasma glucose, serum insulin, and blood lactate concentrations. Mean time-averaged plasma glucose (5.8 +/- 0.5 compared with 4.9 +/- 0.9 mmol/L) and serum insulin (244 +/- 93 compared with 151 +/- 57 pmol/L) concentrations from 0 to 360 min were significantly higher after the single dose; blood lactate and serum fatty acid concentrations were not significantly different. At 360 min, mean plasma glucose (4.8 +/- 1.2 compared with 4.7 +/- 1.6 mmol/L) and serum insulin (138 +/- 76 compared with 136 +/- 116 pmol/L) concentrations were virtually identical. After a single dose, plasma glucose concentrations were > or = 3.9 mmol/L for 7 h in five of seven subjects; three subjects were treated for hypoglycemia after 7-9.5 h. With divided doses, plasma glucose concentrations were > or = 3.9 mmol/L for 9 h in six of seven subjects; hypoglycemia occurred at 6 h in one subject. A single dose (1.76 +/- 0.41 g/kg) of UCS at bedtime maintains plasma glucose concentrations > or = 3.9 mmol/L for > or = 7 h in most young adults with GSD-I.

摘要

I型糖原贮积病(GSD-I)的治疗目标是预防低血糖及其生化后果。在7例平均年龄为19.5岁(范围:18.8 - 21.7岁)的GSD-I患者中,我们比较了连续两个晚上随机给予等能量未煮熟玉米淀粉(UCS;1.76±0.41 g/kg)的生化效应,给药方式为在21:00(时间0)单次给药或在21:00和02:00等量分两次给药。在10小时的观察期内,血浆葡萄糖、血清胰岛素和血乳酸浓度存在显著的给药方案与时间的交互作用。0至360分钟的平均时间加权血浆葡萄糖(分别为5.8±0.5与4.9±0.9 mmol/L)和血清胰岛素(分别为244±93与151±57 pmol/L)浓度在单次给药后显著更高;血乳酸和血清脂肪酸浓度无显著差异。在360分钟时,平均血浆葡萄糖(分别为4.8±1.2与4.7±1.6 mmol/L)和血清胰岛素(分别为138±76与136±116 pmol/L)浓度几乎相同。单次给药后,7名受试者中有5名的血浆葡萄糖浓度在7小时内≥3.9 mmol/L;3名受试者在7 - 9.5小时后因低血糖接受治疗。分两次给药时,7名受试者中有6名的血浆葡萄糖浓度在9小时内≥3.9 mmol/L;1名受试者在6小时时发生低血糖。对于大多数患有GSD-I的年轻成年人,睡前单次给予一剂(1.76±0.41 g/kg)UCS可使血浆葡萄糖浓度≥3.9 mmol/L至少7小时。

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