Rosner William, Auchus Richard J, Azziz Ricardo, Sluss Patrick M, Raff Hershel
St. Luke's/Roosevelt Hospital Center, 1000 Tenth Avenue, AJA 403, New York, New York 10019, USA.
J Clin Endocrinol Metab. 2007 Feb;92(2):405-13. doi: 10.1210/jc.2006-1864. Epub 2006 Nov 7.
The objective of the study was to evaluate the current state of clinical assays for total and free testosterone.
The five participants were appointed by the Council of The Endocrine Society and charged with attaining the objective using published data and expert opinion.
Data were gleaned from published sources via online databases (principally PubMed, Ovid MEDLINE, Google Scholar), the College of American Pathologists, and the clinical and laboratory experiences of the participants.
The statement was an effort of the committee and was reviewed in detail by each member. The Council of The Endocrine Society reviewed a late draft and made specific recommendations.
Laboratory proficiency testing should be based on the ability to measure accurately and precisely samples containing known concentrations of testosterone, not only on agreement with others using the same method. When such standardization is in place, normative values for total and free testosterone should be established for both genders and children, taking into account the many variables that influence serum testosterone concentration.
本研究的目的是评估总睾酮和游离睾酮临床检测的现状。
五名参与者由内分泌学会理事会任命,负责利用已发表的数据和专家意见实现该目标。
数据通过在线数据库(主要是PubMed、Ovid MEDLINE、谷歌学术)、美国病理学家学会以及参与者的临床和实验室经验从已发表的资料中收集。
该声明是委员会的成果,并由每位成员进行了详细审查。内分泌学会理事会审查了最终草案并提出了具体建议。
实验室能力验证应基于准确和精确测量含有已知浓度睾酮样本的能力,而不仅仅基于与使用相同方法的其他人的一致性。当建立起这种标准化时,应考虑到影响血清睾酮浓度的诸多变量,为男性、女性和儿童建立总睾酮和游离睾酮的标准值。