Irons M, Levy H L, O'Flynn M E, Stack C V, Langlais P J, Butler I J, Milstien S, Kaufman S
J Pediatr. 1987 Jan;110(1):61-7. doi: 10.1016/s0022-3476(87)80289-5.
We gave folinic acid to three siblings, and to a fourth child, who have or had dihydropteridine reductase (DHPR) deficiency. The youngest began folinic acid therapy in addition to neurotransmitter precursors and a phenylalanine-restricted diet at age 2 months, and at 2 years of age has near normal development without evidence of neurologic impairment. His older brother began similar treatment at 5 1/2 months of age, when early neurologic findings were evident. At age 6 years his mental retardation and neurologic impairment are less severe than reported in most patients with DHPR deficiency. Little improvement occurred in their sister, who first received treatment at 2 years of age, when she already had severe neurologic impairment. An unrelated boy with profound neurologic impairment showed subtle signs of improvement after he began treatment with folinic acid alone at age 9 years. These results provide evidence that folinic acid is important in the treatment of DHPR deficiency and, if begun early in infancy, may prevent irreversible neurologic damage. The mechanism of folinic acid action in DHPR deficiency may be to increase indirectly the synthesis of 5-methyltetrahydrofolate.
我们给了三名患有或曾患二氢蝶啶还原酶(DHPR)缺乏症的兄弟姐妹以及第四名儿童亚叶酸。最小的孩子在2个月大时开始接受亚叶酸治疗,同时补充神经递质前体并采用低苯丙氨酸饮食,2岁时发育接近正常,没有神经功能障碍的迹象。他的哥哥在5个半月大时开始类似治疗,当时已有早期神经学表现。6岁时,他的智力发育迟缓及神经功能障碍程度比大多数DHPR缺乏症患者轻。他们的姐姐2岁时开始接受治疗,当时已有严重神经功能障碍,治疗后几乎没有改善。一名患有严重神经功能障碍的 unrelated 男孩在9岁开始单独使用亚叶酸治疗后,出现了轻微的改善迹象。这些结果表明,亚叶酸在DHPR缺乏症的治疗中很重要,若在婴儿期早期开始使用,可能预防不可逆的神经损伤。亚叶酸在DHPR缺乏症中的作用机制可能是间接增加5-甲基四氢叶酸的合成。