Pearson J D, Morrell C H, Landis P K, Carter H B, Brant L J
Longitudinal Studies Branch, National Institute on Aging, Baltimore, MD 21224.
Stat Med. 1994;13(5-7):587-601. doi: 10.1002/sim.4780130520.
Although prostate cancer and benign prostatic hyperplasia are major health problems in U.S. men, little is known about the early stages of the natural history of prostate disease. A molecular biomarker called prostate specific antigen (PSA), together with a unique longitudinal bank of frozen serum, now allows a historic prospective study of changes in PSA levels for decades prior to the diagnosis of prostate disease. Linear mixed-effects regression models were used to test whether rates of change in PSA were different in men with and without prostate disease. In addition, since the prostate cancer cases developed their tumours at different (and unknown) times during their periods of follow-up, a piece-wise non-linear mixed-effects regression model was used to estimate the time when rapid increases in PSA were first observable beyond the background level of PSA change. These methods have a wide range of applications in biomedical research utilizing repeated measures data such as pharmacokinetic studies, crossover trials, growth and development studies, aging studies, and disease detection.
尽管前列腺癌和良性前列腺增生是美国男性面临的主要健康问题,但对于前列腺疾病自然史的早期阶段却知之甚少。一种名为前列腺特异性抗原(PSA)的分子生物标志物,连同一组独特的纵向冷冻血清库,现在使得对前列腺疾病诊断前数十年内PSA水平变化进行历史性前瞻性研究成为可能。使用线性混合效应回归模型来检验患有和未患有前列腺疾病的男性中PSA变化率是否不同。此外,由于前列腺癌病例在其随访期间的不同(且未知)时间发生肿瘤,因此使用分段非线性混合效应回归模型来估计首次观察到PSA快速升高超过PSA变化背景水平的时间。这些方法在利用重复测量数据的生物医学研究中具有广泛应用,如药代动力学研究、交叉试验、生长发育研究、衰老研究和疾病检测。