David L, Anast C S
J Clin Invest. 1974 Aug;54(2):287-96. doi: 10.1172/JCI107764.
Serum immunoreactive parathyroid hormone (iPTH) and plasma total calcium, ionized calcium, magnesium, and phosphorus levels were determined during the first 9 days of life in 137 normal term infants, 55 "sick" infants, and 43 hypocalcemic (Ca <7.5 mg/100 ml; Ca(++)<4.0 mg/100 ml) infants. In the cord blood, elevated levels of plasma Ca(++) and Ca were observed, while levels of serum iPTH were either undetectable or low. In normal newborns during the first 48 h of life there was a decrease in plasma Ca and Ca(++), while the serum iPTH level in most samples remained undetectable or low; after 48 h there were parallel increases in plasma Ca and Ca(++) and serum iPTH levels. Plasma Mg and P levels increased progressively after birth in normal infants. In the sick infants, plasma Ca, Ca(++) and P levels were significantly lower than in the normal newborns, while no significant differences were found in the plasma Mg levels. The general pattern of serum iPTH levels in the sick infants was similar to that observed in the normal group, though there was a tendency for the increase in serum iPTH to occur earlier and for the iPTH levels to be higher in the sick infants. In the hypocalcemic infants, plasma Mg levels were consistently lower than in the normal infants after 24 h of age, while no significant differences were found in the plasma P levels. Hyperphosphatemia was uncommon and did not appear to be a contributing factor in the pathogenesis of hypocalcemia in most infants. Most of the hypocalcemic infants, including those older than 48 h, had inappropriately low serum iPTH levels. Evidence obtained from these studies indicates that parathyroid secretion is normally low in the early new born period and impaired parathyroid function, characterized by undetectable or low serum iPTH, is present in most infants with neonatal hypocalcemia. Additional unknown factors appear to contribute to the lowering of plasma Ca in the neonatal period. The net effect of unknown plasma hypocalcemic factor(s) on the one hand and parathyroid activity on the other may account for differences in plasma Ca levels observed between normal, sick, and hypocalcemic infants. Depressed plasma Mg is frequently present in hypocalcemic infants. To what degree the hypomagnesemia reflects parathyroid insufficiency or the converse, to what degree parathyroid insufficiency and hypocalcemia are secondary to hypomagnesemia, is uncertain.
对137名足月正常婴儿、55名“患病”婴儿和43名低钙血症(血钙<7.5mg/100ml;离子钙<4.0mg/100ml)婴儿在出生后的前9天测定了血清免疫反应性甲状旁腺激素(iPTH)以及血浆总钙、离子钙、镁和磷水平。在脐血中,观察到血浆离子钙和总钙水平升高,而血清iPTH水平要么检测不到,要么很低。在正常新生儿出生后的头48小时内,血浆总钙和离子钙水平下降,而大多数样本中的血清iPTH水平仍检测不到或很低;48小时后,血浆总钙和离子钙水平以及血清iPTH水平平行升高。正常婴儿出生后血浆镁和磷水平逐渐升高。在患病婴儿中,血浆总钙、离子钙和磷水平显著低于正常新生儿,而血浆镁水平未发现显著差异。患病婴儿血清iPTH水平的总体模式与正常组相似,尽管患病婴儿血清iPTH升高的趋势出现得更早,且iPTH水平更高。在低钙血症婴儿中,24小时龄后血浆镁水平始终低于正常婴儿,而血浆磷水平未发现显著差异。高磷血症并不常见,在大多数婴儿中似乎不是低钙血症发病机制的促成因素。大多数低钙血症婴儿,包括那些年龄超过48小时的婴儿,血清iPTH水平都异常低。这些研究获得的证据表明,新生儿早期甲状旁腺分泌通常较低,大多数新生儿低钙血症婴儿存在以血清iPTH检测不到或低为特征的甲状旁腺功能受损。其他未知因素似乎导致了新生儿期血浆钙的降低。一方面未知血浆低钙因子的净效应,另一方面甲状旁腺活动的净效应,可能解释了正常、患病和低钙血症婴儿之间观察到的血浆钙水平差异。低钙血症婴儿经常出现血浆镁降低。低镁血症在多大程度上反映甲状旁腺功能不全,反之亦然,甲状旁腺功能不全和低钙血症在多大程度上继发于低镁血症,尚不确定。