Greene H L, Slonim A E, O'Neill J A, Burr I M
N Engl J Med. 1976 Feb 19;294(8):423-5. doi: 10.1056/NEJM197602192940805.
The clinical and biochemical abnormalities associated with Type 1 glycogen-storage disease can be reversed by avoidance of hypoglycemia and secondary hormonal flux. Three patients with Type 1 disease were treated with intragastric infusions of a high glucose formula at night with three-hour starch feedings during the day. This regimen stabilized blood glucose levels above 70 mg per deciliter and decreased serum uric acid, triglyceride, lactate and serum oxalacetic transaminase levels, as well as hepatic size, in all patients. Increased linear growth rate (mean 1 cm per month) was associated with a decrease in mean plasma glucagon (from 190 to 40 pg per milliliter) and an increase in mean plasma insulin (from 19 to 43 muU per milliliter, [two patients]). These changes occurred within four weeks of beginning of treatment and continued with home treatment for 13 months. No complications resulted from tube placement daily by the patients. Type 1 disease can be managed by nighttime intragastric feeding and frequent daytime high starch meals.
通过避免低血糖和继发性激素波动,可逆转与1型糖原贮积病相关的临床和生化异常。3例1型疾病患者夜间通过胃内输注高糖配方奶进行治疗,白天每3小时喂食淀粉。该方案使所有患者的血糖水平稳定在每分升70毫克以上,并降低了血清尿酸、甘油三酯、乳酸和血清草酰乙酸转氨酶水平,以及肝脏大小。线性生长速率增加(平均每月1厘米)与平均血浆胰高血糖素降低(从每毫升190皮克降至40皮克)和平均血浆胰岛素增加(从每毫升19微单位增至43微单位,[2例患者])相关。这些变化在治疗开始后的四周内出现,并在家庭治疗13个月后持续存在。患者每日放置胃管未出现并发症。1型疾病可通过夜间胃内喂养和白天频繁食用高淀粉餐进行管理。