Yamada K, Tamura Y, Yamamoto M, Kumagai A
Endocrinol Jpn. 1979 Apr;26(2):147-57. doi: 10.1507/endocrj1954.26.147.
A 31-year-old man and a 12-year-old girl were diagnosed as pseudohypoparathyroidism (PHP) Type I because of a failure to respond to the administration of parathyroid hormone (PTH) with increased urinary excretion of phosphate and cyclic adenosine-3', 5'-monophosphate (cAMP). A 22-year-old woman was diagnosed as PHP Type II because there was no increase in the urinary excretion of phosphate despite of a marked increase in urinary cAMP excretion. With the combined calcium-PTH infusion or PTH infusion after vitamin D therapy, renal response was improved in these patients. Also dibutyryl adenosine-3'-5'-cyclic monophosphate (dbcAMP) infusion evoked an increased urinary phosphate excretion in all of the patients. The metabolic defect of our patients with PHP Type I may be caused not by a lack or defective form of PTH-sensitive receptor adenylate cyclase complex but rather by an abnormal conformation in the plasma membrane-associated receptor adenylate cyclase enzyme complex in kidney. In the patient with PHP Type II, as cAMP generation is intact, the metabolic defect might be related to a defect of calcium mobilization in renal tubular cells in response to PTH.
一名31岁男性和一名12岁女孩因对甲状旁腺激素(PTH)给药无反应且尿磷酸盐和环磷酸腺苷(cAMP)排泄增加而被诊断为I型假性甲状旁腺功能减退症(PHP)。一名22岁女性被诊断为II型PHP,因为尽管尿cAMP排泄显著增加,但尿磷酸盐排泄未增加。通过联合钙-PTH输注或维生素D治疗后PTH输注,这些患者的肾脏反应得到改善。此外,二丁酰腺苷-3',5'-环磷酸(dbcAMP)输注在所有患者中均引起尿磷酸盐排泄增加。我们的I型PHP患者的代谢缺陷可能不是由PTH敏感受体腺苷酸环化酶复合物的缺乏或缺陷形式引起的,而是由肾细胞膜相关受体腺苷酸环化酶酶复合物的异常构象引起的。在II型PHP患者中,由于cAMP生成完整,代谢缺陷可能与肾小管细胞对PTH反应的钙动员缺陷有关。