New England Research Institutes, Watertown, Massachusetts 02472, USA.
Clin Endocrinol (Oxf). 2007 Dec;67(6):853-62. doi: 10.1111/j.1365-2265.2007.02976.x.
Estimates of intraindividual variation in hormone levels provide the basis for interpreting hormone measurements clinically and for developing eligibility criteria for trials of hormone replacement therapy. However, reliable systematic estimates of such variation are lacking.
To estimate intraindividual variation of serum total, free and bioavailable testosterone (T), dihydrotestosterone (DHT), SHBG, LH, dehydroepiandrosterone (DHEA), dehydroepiandrosterone sulphate (DHEAS), oestrone, oestradiol and cortisol, and the contributions of biological and assay variation to the total.
Paired blood samples were obtained 1-3 days apart at entry and again 3 months and 6 months later (maximum six samples per subject). Each sample consisted of a pool of equal aliquots of two blood draws 20 min apart.
Men aged 30-79 years were randomly selected from the respondents to the Boston Area Community Health Survey, a study of the health of the general population of Boston, MA, USA. Analysis was based on 132 men, including 121 who completed all six visits, 8 who completed the first two visits and 3 who completed the first four visits.
Day-to-day and 3-month (long-term) intraindividual standard deviations, after transforming measurements to logarithms to eliminate the contribution of hormone level to intraindividual variation.
Biological variation generally accounted for more of total intraindividual variation than did assay variation. Day-to-day biological variation accounted for more of the total than did long-term biological variation. Short-term variability was greater in hormones with pulsatile secretion (e.g. LH) than those that exhibit less ultradian variation. Depending on the hormone, the intraindividual standard deviations imply that a clinician can expect to see a difference exceeding 18-28% about half the time when two measurements are made on a subject. The difference will exceed 27-54% about a quarter of the time.
Given the level of intraindividual variability in hormone levels found in this study, one sample is generally not sufficient to characterize an individual's hormone levels but collecting more than three is probably not warranted. This is true for clinical measurements and for hormone measurements used to determine eligibility for a clinical trial of hormone replacement therapy.
激素水平的个体内变异估计为临床解释激素测量值和制定激素替代治疗试验的入选标准提供了基础。然而,目前缺乏可靠的系统变异估计值。
估计血清总、游离和生物可利用睾酮(T)、二氢睾酮(DHT)、性激素结合球蛋白(SHBG)、黄体生成素(LH)、脱氢表雄酮(DHEA)、硫酸脱氢表雄酮(DHEAS)、雌酮、雌二醇和皮质醇的个体内变异,并评估生物学和检测变异对总变异的贡献。
在入组时和 3 个月及 6 个月后(每位受试者最多 6 个样本),每 1-3 天采集一次间隔 20 分钟的两份等量血样,共采集 6 次。
从美国马萨诸塞州波士顿市波士顿地区社区健康调查的应答者中随机选择 30-79 岁男性。该研究是对一般人群健康状况的调查。分析基于 132 名男性,包括 121 名完成全部 6 次访视、8 名完成前 2 次访视和 3 名完成前 4 次访视的男性。
经对数转换消除激素水平对个体内变异的贡献后,测量日内和 3 个月(长期)的个体内标准差。
生物学变异通常比检测变异对总个体内变异的贡献更大。与长期生物学变异相比,测量日内生物学变异对总个体内变异的贡献更大。具有脉冲分泌的激素(如 LH)的短期变异性大于表现出较少超短周期变异的激素。根据激素不同,个体内标准差意味着当对受试者进行两次测量时,约有一半时间可以预期两次测量的差异超过 18-28%。约四分之一的时间,差异将超过 27-54%。
鉴于本研究中发现的激素水平个体内变异性水平,一次采样通常不足以描述个体的激素水平,但采集超过三次可能没有必要。这对于临床测量和用于确定激素替代治疗临床试验入选资格的激素测量均适用。