Mylonas Panagiotis G, Makri Maria, Georgopoulos Neoklis A, Theodoropoulou Anastasia, Leglise Michel, Vagenakis Apostolos G, Markou Kostas B
Department of Internal Medicine, Division of Endocrinology, University Hospital of Patras Medical School, Patras, Greece.
Steroids. 2006 Mar;71(3):273-6. doi: 10.1016/j.steroids.2005.11.005. Epub 2006 Jan 23.
Steroids determination in saliva offers several advantages. The collection of saliva is a noninvasive, less stressful technique than blood withdrawal and reflects the circulating unbound fractions. The suitability of saliva for 17-hydroxyprogesterone and cortisol determinations has been documented in healthy subjects as well as in diseases like Congenital Adrenal Hyperplasia and Cushing syndrome. The aim of the study was to compare the influence of different collection methods on the results of 17-hydroxyprogesterone measurement in saliva collected by different ways, using commercially available RIAs developed for plasma. 17-hydroxyprogesterone was determined in 64 healthy adult volunteers (30 males, 34 females) in serum (Group SE) and in saliva collected before meals at 8-10 p.m. by directly spitting into a plastic tube (Group SP), using a cotton swab (Group SA) and using a polyester swab Salivette (Group SB). We used a commercially available direct radioimmunoassay without separation technique. The 17-hydroxyprogesterone mean values (ng/ml) were 1.16+/-1.3 (Group SE), 0.056+/-0.046 (Group SP), 0.089+/-0.048 (Group SA) and 0.058+/-0.049 (Group SB). The detection limit was 0.010 ng/ml. The correlations between the values in serum (Group SE) and in saliva were: r=0.77, p<0.05 (Group SP); r=0.62, p<0.05 (Group SA); r=0.70, p<0.05 (Group SB). The saliva values corresponding to the serum cut-off point of 3 ng/ml upper limit of normal values were in ng/ml 0.13 (Group SP), 0.16 (Group SA) and 0.11 (Group SB). In conclusion, 17-hydroxyprogesterone determinations in saliva using commercially available RIAs primarily developed for serum, is a reliable and easy to perform procedure. The three different methods of saliva collection showed 17-hydroxyprogesterone concentrations to have good agreement.
唾液中类固醇的测定具有多个优点。与采血相比,唾液采集是一种非侵入性、压力较小的技术,且能反映循环中的游离部分。在健康受试者以及先天性肾上腺皮质增生症和库欣综合征等疾病中,唾液对17 - 羟孕酮和皮质醇测定的适用性已有文献记载。本研究的目的是使用为血浆开发的市售放射免疫分析(RIA)方法,比较不同采集方法对不同方式收集的唾液中17 - 羟孕酮测量结果的影响。对64名健康成年志愿者(30名男性,34名女性)的血清(SE组)以及晚上8 - 10点饭前直接吐入塑料管(SP组)、使用棉签(SA组)和使用聚酯拭子唾液采集器(Salivette,SB组)收集的唾液中的17 - 羟孕酮进行测定。我们使用了一种市售的无需分离技术的直接放射免疫分析方法。17 - 羟孕酮的平均值(ng/ml)分别为:SE组1.16±1.3,SP组0.056±0.046,SA组0.089±0.048,SB组0.058±0.049。检测限为0.010 ng/ml。血清(SE组)和唾液中值之间的相关性为:r = 0.77,p < 0.05(SP组);r = 0.62,p < 0.05(SA组);r = 0.70,p < 0.05(SB组)。对应血清正常上限3 ng/ml截断点的唾液值(ng/ml)分别为:SP组0.13,SA组0.16,SB组0.11。总之,使用主要为血清开发的市售RIA方法测定唾液中的17 - 羟孕酮是一种可靠且易于操作的程序。三种不同的唾液采集方法显示17 - 羟孕酮浓度具有良好的一致性。