Batshaw M L, Bursilow S W
Pediatr Res. 1978 Mar;12(3):221-4. doi: 10.1203/00006450-197803000-00012.
At 0-3 days of age the plasma ammonium concentration in full term appropriate for gestational age (AGA) infants was (mean +/- SEM) 27.5 +/- 0.5 micron; a value similar to that reported in adults. Ammonium levels in low birthweight AGA and SGA groups were 47.0 +/- 2.0 micron and 45.1 +/- 3.3 micron respectively; significantly elevated (P less than 0.001) as compared to the full term group. These increased ammonium levels persisted at 3-5 weeks of age. Associated with the hyperammonemia was a significant (P less than 0.01) decrease in plasma alpha-ketoglutarate concentration: 11.8 +/- 1.0 micron, in the low birthweight AGA as compared to 20.7 +/- 0.6 micron in the full term AGA infants. There was an inverse linear correlation between plasma concentrations of ammonium and alpha-ketoglutarate r = -0.86, P less than 0.001. Urinary orotate excretion was significantly elevated (P less than 0.05) in low birthweight AGA infants. There was no difference in the plasma concentrations of glutamine, glutamate, or alanine among the various groups. Hyperammonemia was not associated with neurologic dysfunction.
在出生0至3天,足月适于胎龄(AGA)婴儿的血浆铵浓度(均值±标准误)为27.5±0.5微摩尔;该值与成人报道的相似。低出生体重AGA组和小于胎龄儿(SGA)组的铵水平分别为47.0±2.0微摩尔和45.1±3.3微摩尔;与足月组相比显著升高(P<0.001)。这些升高的铵水平在3至5周龄时持续存在。与高氨血症相关的是血浆α-酮戊二酸浓度显著降低(P<0.01):低出生体重AGA组为11.8±1.0微摩尔,而足月AGA婴儿为20.7±0.6微摩尔。血浆铵和α-酮戊二酸浓度之间呈负线性相关,r=-0.86,P<0.001。低出生体重AGA婴儿的尿乳清酸排泄显著升高(P<0.05)。各组间谷氨酰胺、谷氨酸或丙氨酸的血浆浓度无差异。高氨血症与神经功能障碍无关。