Carroll Ty B, Fisco Amy J H, Auchus Richard J, Kennedy Laurence, Findling James W
Endocrinology Center and Clinics, Medical College of Wisconsin, Milwaukee, Wisconsin.
Division of Endocrinology, Metabolism, and Clinical Nutrition, Medical College of Wisconsin, Milwaukee, Wisconsin Division of Endocrinology, Diabetes and Metabolism, Wheaton Franciscan Medical Group, Racine, Wisconsin.
Endocr Pract. 2014 Jul;20(7):646-9. doi: 10.4158/EP13348.OR.
The use of ovine corticotropin releasing hormone (oCRH) maximizes the diagnostic accuracy of inferior petrosal sinus sampling (IPSS) in patients with adrenocorticotropin hormone (ACTH)-dependent Cushing's syndrome (CS). oCRH is marketed as ACTHrel and, understandably, may be confused with cosyntropin [ACTH (1-24)]. The inadvertent substitution of synthetic ACTH(1-24) for oCRH (ACTHrel) during IPSS may cause unexpected and misleading results. The aim of this report is to raise awareness of the potential confounding results created when synthetic ACTH(1-24) is mistakenly used during IPSS.
We present 3 patients treated at 3 different centers with ACTH-dependent CS in whom ACTH(1-24) was mistakenly substituted for oCRH (ACTHrel) during IPSS.
In all patients, there was an abrupt and unexpected decrease in plasma ACTH in the inferior petrosal sinus (IPS) samples after presumptive stimulation with oCRH. Re-evaluation of the patients' pharmacy records confirmed that synthetic ACTH(1-24) had been used rather than oCRH during each procedure. Because "sandwich" immunometric assays for ACTH measure the entire pool of endogenous ACTH, the administration of synthetic ACTH(1-24) artifactually decreases the endogenous plasma ACTH(1-39) measurement by binding only to the N-terminal antibody raised against ACTH(1-17) and not to the C-terminal antibody raised against ACTH(34-39). This results in a lack of a detectable sandwich complex and explains the apparent reduction in ACTH concentration.
An abrupt decrease in ACTH during IPSS suggests that synthetic ACTH(1-24) rather than oCRH (ACTHrel) has been administered. The labeling of oCRH as ACTHrel poses a potential patient safety problem about which endocrinologists, interventional radiologists, and pharmacists should be aware.
在促肾上腺皮质激素(ACTH)依赖性库欣综合征(CS)患者中,使用羊促肾上腺皮质激素释放激素(oCRH)可使岩下窦采血(IPSS)的诊断准确性最大化。oCRH以ACTHrel的商品名销售,不难理解,它可能会与合成促肾上腺皮质激素[ACTH(1 - 24)]混淆。在IPSS期间无意中用合成ACTH(1 - 24)替代oCRH(ACTHrel)可能会导致意外且具有误导性的结果。本报告的目的是提高对IPSS期间错误使用合成ACTH(1 - 24)可能产生的潜在混淆结果的认识。
我们介绍3例在3个不同中心接受治疗的ACTH依赖性CS患者,他们在IPSS期间ACTH(1 - 24)被错误地替代为oCRH(ACTHrel)。
在所有患者中,在用oCRH进行假定刺激后,岩下窦(IPS)样本中的血浆ACTH出现突然且意外的下降。对患者药房记录的重新评估证实,在每次操作过程中使用的是合成ACTH(1 - 24)而非oCRH。因为用于ACTH的“夹心”免疫测定法测量的是内源性ACTH的总量,合成ACTH(1 - 24)的给药仅与针对ACTH(1 - 17)产生的N端抗体结合,而不与针对ACTH(34 - 39)产生的C端抗体结合,从而人为地降低了内源性血浆ACTH(1 - 39)的测量值。这导致缺乏可检测到的夹心复合物,并解释了ACTH浓度的明显降低。
IPSS期间ACTH突然下降表明使用的是合成ACTH(1 - 24)而非oCRH(ACTHrel)。将oCRH标记为ACTHrel存在潜在的患者安全问题,内分泌学家、介入放射学家和药剂师应予以关注。