Agha Amar, Tomlinson Jeremy W, Clark Penelope M, Holder Geoff, Stewart Paul M
Division of Medical Sciences, University of Birmingham, Queen Elizabeth Hospital, Edgbaston, Birmingham B15 2TH, United Kingdom.
J Clin Endocrinol Metab. 2006 Jan;91(1):43-7. doi: 10.1210/jc.2005-1131. Epub 2005 Oct 25.
The high-dose short Synacthen (corticotropin) test (SST) is widely used to investigate suspected secondary adrenal insufficiency, but concern remains about falsely reassuring results.
Our objective was to evaluate the long-term safety of the SST.
We retrospectively evaluated the clinical outcome in 178 patients who achieved 30-min cortisol values in the lowest 15th percentile of normal healthy responses. Thirty patients were later excluded because of missing case notes (20 patients) or unsubstantiated pituitary pathology (10 patients). The remaining 148 patients were divided into two groups: group 1, patients with cortisol response between the 5th and 15th percentiles of normal response (551-635 nmol/liter, 98 patients); and group 2, patients with borderline response between the 2.5th and 5th percentiles (510-550 nmol/liter, 50 patients). Patients did not receive routine glucocorticoid therapy, but those in group 2 were advised to take hydrocortisone in case of intercurrent illness.
The median follow-up period from the initial SST was 4.2 yr (range, 4 months to 7 yr). A total of 137 patients showed no clinical or biochemical evidence of adrenal insufficiency during follow-up. Of the remaining 11 patients, seven became hypoadrenal after subsequent pituitary surgery or radiotherapy, one patient in group 1 developed adrenal insufficiency at 2 yr, and one patient in group 2 developed adrenal insufficiency at 6 months. The other two patients who were in group 2 had clinical diagnostic uncertainty.
The high-dose SST is safe for the purpose of excluding clinically significant secondary adrenal insufficiency and is indicated as the first line of investigation for this purpose.
高剂量短程辛纳肽(促肾上腺皮质激素)试验(SST)被广泛用于调查疑似继发性肾上腺皮质功能减退,但对于结果可能会产生误导性安慰效应的担忧依然存在。
我们的目的是评估SST的长期安全性。
我们回顾性评估了178例患者的临床结局,这些患者在30分钟时的皮质醇值处于正常健康反应最低的第15百分位数。后来有30例患者因病例记录缺失(20例患者)或垂体病变未经证实(10例患者)而被排除。其余148例患者分为两组:第1组,皮质醇反应处于正常反应第5至15百分位数之间(551 - 635 nmol/升,98例患者);第2组,皮质醇反应处于第2.5至5百分位数之间的临界反应(510 - 550 nmol/升,50例患者)。患者未接受常规糖皮质激素治疗,但第2组患者被建议在并发疾病时服用氢化可的松。
从初次SST开始的中位随访期为4.2年(范围为4个月至7年)。共有137例患者在随访期间未出现肾上腺皮质功能减退的临床或生化证据。其余11例患者中,7例在随后的垂体手术或放疗后出现肾上腺功能减退,第1组中有1例患者在2年时出现肾上腺皮质功能减退,第2组中有1例患者在6个月时出现肾上腺皮质功能减退。第2组中的另外2例患者临床诊断存在不确定性。
高剂量SST对于排除临床上有意义的继发性肾上腺皮质功能减退是安全的,并且为此目的被推荐作为一线检查方法。