Mallette L E, Wilson D P, Kirkland J L
Pediatrics. 1983 Jan;71(1):64-9.
The diagnosis of hypoparathyroidism by radioimmunoassay of serum parathyroid hormone (PTH) has been hampered by lack of an assay system sensitive enough to allow discrimination between low and normal values. A new assay for human PTH that has improved sensitivity has been developed. It uses an homologous antiserum (against the human hormone) and uses a carboxy-terminal fragment of bovine PTH as tracer to provide an assay monospecific for the midregion of PTH. Immunoreactive PTH (iPTH) was detectable in 25/27 normal children and borderline detectable in the other two. The pediatric normal range was slightly lower than that previously established in adults. Among patients with secondary hyperparathyroidism and normal renal function, iPTH was 3- to 8-fold elevated in those with rickets, and 1.3- to 2.0-fold above normal in those with more acute forms of hypocalcemia. Twelve patients with hypoparathyroidism were studied. iPTH was undetectable in seven with permanent total hypoparathyroidism, and was borderline detectable in five, including four neonates who proved to have transient hypoparathyroidism. In these four patients, iPTH became detectable as the requirements for supplemental calcium decreased. Measurement of iPTH with an adequately sensitive assay may be useful in the diagnosis and management of pediatric hypocalcemia.
血清甲状旁腺激素(PTH)放射免疫测定法对甲状旁腺功能减退症的诊断一直受到阻碍,因为缺乏一种足够灵敏的检测系统,无法区分低值和正常数值。现已开发出一种灵敏度更高的新型人PTH检测方法。它使用同源抗血清(针对人激素),并使用牛PTH的羧基末端片段作为示踪剂,以提供针对PTH中间区域的特异性检测。在27名正常儿童中,有25名可检测到免疫反应性PTH(iPTH),另外两名勉强可检测到。儿童正常范围略低于先前确定的成人正常范围。在继发性甲状旁腺功能亢进且肾功能正常的患者中,佝偻病患者的iPTH升高3至8倍,更急性低钙血症患者的iPTH高于正常水平1.3至2.0倍。对12名甲状旁腺功能减退症患者进行了研究。7名永久性完全甲状旁腺功能减退症患者检测不到iPTH,5名勉强可检测到,其中包括4名被证明患有暂时性甲状旁腺功能减退症的新生儿。在这4名患者中,随着补充钙需求的减少,iPTH变得可检测到。使用灵敏度足够的检测方法测量iPTH可能有助于小儿低钙血症的诊断和管理。