Stokes F J, Bailey L M, Ganguli A, Davison A S
Department of Clinical Biochemistry and Metabolic Medicine, Royal Liverpool and Broadgreen University Hospitals Trust, Liverpool, UK
Department of Clinical Biochemistry and Metabolic Medicine, Royal Liverpool and Broadgreen University Hospitals Trust, Liverpool, UK.
Ann Clin Biochem. 2014 Jul;51(Pt 4):503-6. doi: 10.1177/0004563213509793. Epub 2013 Oct 22.
Inhaled steroids are widely used for the treatment of asthma. Concerns over adrenal suppression when used at high doses or in combination with drugs such as ritonavir exist, requiring the measurement of serum cortisol. Herein, we investigate the cross-reactivity of the inhaled steroids betamethasone, fluticasone and beclomethasone in the Roche cortisol immunoassay, in addition to five other steroids.
Five replicates were produced from a serum pool for each of the eight steroids at a final concentration of 0.1 and 1 µg/mL. Each steroid was dissolved in 50% methanol, with 50% methanol of the same volume added to the control sample. The cross-reactivity of each steroid in the cortisol assay was calculated.
There was no statistically or clinically significant cross-reactivity in the measurement of cortisol when fluticasone, beclomethasone or betamethasone were spiked at 0.1 and 1.0 µg/mL, except for beclomethasone at a concentration of 1 µg/mL (1490 nmol/L) with a cross-reactivity of 1.6%, which is unlikely to be clinically significant. At both steroid concentrations investigated, prednisolone, 17-hydroxyprogesterone and 11-deoxycortisol exhibited statistically significant cross-reactivities that were greater than the least significant change of the assay (13.1%), whereas dexamethasone and metyrapone did not. Mean inter-assay precision was 1.5% (405-1586 nmol/L).
The cross-reactivity of the inhaled steroids; betamethasone, fluticasone and beclomethasone in the Roche cortisol immunoassay are unlikely to be clinically significant at the concentrations found in patients on therapeutic doses. This will enable confident assessment of adrenal status in patients at risk of adrenal suppression.
吸入性类固醇广泛用于治疗哮喘。人们担心高剂量使用或与利托那韦等药物联合使用时会出现肾上腺抑制,因此需要检测血清皮质醇。在此,我们除了研究其他五种类固醇外,还研究了吸入性类固醇倍他米松、氟替卡松和布地奈德在罗氏皮质醇免疫测定中的交叉反应性。
从混合血清中为八种类固醇中的每一种制备五个复制品,最终浓度为0.1和1μg/mL。每种类固醇都溶解在50%的甲醇中,向对照样品中加入相同体积的50%甲醇。计算每种类固醇在皮质醇测定中的交叉反应性。
当氟替卡松、布地奈德或倍他米松的添加浓度为0.1和1.0μg/mL时,在皮质醇测量中没有统计学或临床意义上的交叉反应性,除了浓度为1μg/mL(1490nmol/L)的布地奈德,其交叉反应性为1.6%,这在临床上不太可能具有显著意义。在所研究的两种类固醇浓度下,泼尼松龙、17-羟孕酮和11-脱氧皮质醇均表现出统计学上显著的交叉反应性,大于该测定的最小显著变化(13.1%),而地塞米松和甲吡酮则没有。批间平均精密度为1.5%(405-1586nmol/L)。
在罗氏皮质醇免疫测定中,吸入性类固醇倍他米松、氟替卡松和布地奈德的交叉反应性在接受治疗剂量的患者中所发现的浓度下不太可能具有临床意义。这将有助于对有肾上腺抑制风险的患者的肾上腺状态进行可靠评估。