Feldman E C, Nelson R W, Feldman M S
Department of Medicine, University of California, Davis 95616, USA.
J Am Vet Med Assoc. 1996 Aug 15;209(4):772-5.
To evaluate low- and high-dose dexamethasone suppression tests for differentiating pituitary dependent hyperadrenocorticism (PDH) from adrenal tumor hyperadrenocorticism (ATH) in dogs.
Prospective study.
181 dogs with PDH and 35 dogs with ATH.
Plasma cortisol concentrations from dogs with naturally developing hyperadrenocorticism were evaluated before, and 4 and 8 hours after administration of standard low- and high-doses of dexamethasone (0.01 mg/kg of body weight, i.v., and 0.1 mg/kg, i.v.; respectively).
In response to the low-dose test, all but 3 dogs had an 8-hours post-dexamethasone plasma cortisol concentration that was consistent with a diagnosis of hyperadrenocorticism, that is, > or = 1.4 micrograms/dl. Criteria used to distinguish PDH from ATH in response to low-dose dexamethasone included a 4-hour post-dexamethasone plasma cortisol concentration < 50% of the basal value or < 1.4 micrograms/dl, or an 8-hours post-dexamethasone plasma cortisol concentration < 50% of the basal concentration. Criteria used to distinguish PDH from ATH in response to high-dose dexamethasone included 4- or 8-hour post-dexamethasone plasma cortisol concentrations < 50% of the basal concentration or < 1.4 micrograms/dl. In response to the low-dose test, 111 dogs met criteria for suppression (each had PDH). In response to the high-dose test, 137 dogs met criteria for suppression (2 had ATH, 135 had PDH). Twenty-six dogs with PDH (12%) had indications of adrenal suppression in response to high-dose but not low-dose testing.
Low-dose dexamethasone test has value as a discrimination test to distinguish dogs with PDH from those with ATH. The high-dose test need only be considered in dogs with hyperadrenocorticism that do not have adrenal suppression in response to the low-dose test.
评估低剂量和高剂量地塞米松抑制试验在区分犬垂体依赖性肾上腺皮质功能亢进(PDH)与肾上腺肿瘤性肾上腺皮质功能亢进(ATH)中的作用。
前瞻性研究。
181只患有PDH的犬和35只患有ATH的犬。
对自然发生肾上腺皮质功能亢进的犬,在静脉注射标准低剂量(0.01mg/kg体重)和高剂量(0.1mg/kg体重)地塞米松之前、之后4小时和8小时,评估血浆皮质醇浓度。
在低剂量试验中,除3只犬外,所有犬地塞米松注射后8小时的血浆皮质醇浓度均符合肾上腺皮质功能亢进的诊断标准,即≥1.4μg/dl。用于区分低剂量地塞米松反应下PDH与ATH的标准包括:地塞米松注射后4小时血浆皮质醇浓度<基础值的50%或<1.4μg/dl,或地塞米松注射后8小时血浆皮质醇浓度<基础浓度的50%。用于区分高剂量地塞米松反应下PDH与ATH的标准包括:地塞米松注射后4小时或8小时血浆皮质醇浓度<基础浓度的50%或<1.4μg/dl。在低剂量试验中,111只犬符合抑制标准(均患有PDH)。在高剂量试验中,137只犬符合抑制标准(2只患有ATH,135只患有PDH)。26只患有PDH的犬(12%)在高剂量而非低剂量试验中有肾上腺抑制的迹象。
低剂量地塞米松试验作为区分患有PDH的犬与患有ATH的犬的鉴别试验具有价值。仅对低剂量试验无肾上腺抑制反应的肾上腺皮质功能亢进犬才需考虑进行高剂量试验。