Department of Biostatistics, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
Nucleic Acids Res. 2013 Jul;41(13):e131. doi: 10.1093/nar/gkt370. Epub 2013 May 13.
Recent longitudinal studies of age-dependent leukocyte telomere length (LTL) attrition have reported that variable proportions of individuals experience LTL lengthening. Often, LTL lengthening has been taken at face value, and authors have speculated about the biological causation of this finding. Based on empirical data and theoretical considerations, we show that regardless of the method used to measure telomere length (Southern blot or quantitative polymerase chain reaction-based methods), measurement error of telomere length and duration of follow-up explain almost entirely the absence of age-dependent LTL attrition in longitudinal studies. We find that LTL lengthening is far less frequent in studies with long follow-up periods and those that used a high-precision Southern blot method (as compared with quantitative polymerase chain reaction determination, which is associated with larger laboratory error). We conclude that the LTL lengthening observed in longitudinal studies is predominantly, if not entirely, an artifact of measurement error, which is exacerbated by short follow-up periods. We offer specific suggestions for design of longitudinal studies of LTL attrition to diminish this artifact.
最近的一些关于年龄相关的白细胞端粒长度(LTL)损耗的纵向研究报告称,个体中存在不同比例的 LTL 延长现象。通常,LTL 延长被视为理所当然,作者们推测了这一发现的生物学原因。基于经验数据和理论考虑,我们表明,无论使用何种方法测量端粒长度(Southern blot 或基于定量聚合酶链反应的方法),端粒长度的测量误差和随访时间几乎完全可以解释纵向研究中不存在年龄相关的 LTL 损耗的原因。我们发现,在随访时间较长的研究和使用高精度 Southern blot 方法的研究中(与定量聚合酶链反应测定相比,后者与更大的实验室误差相关),LTL 延长的情况要少得多。我们得出结论,纵向研究中观察到的 LTL 延长主要(如果不是完全)是测量误差的结果,而短的随访时间会加剧这种误差。我们为设计 LTL 损耗的纵向研究提供了具体建议,以减少这种假象。