DST/NRF Centre of Excellence for Biomedical Tuberculosis Research/MRC Centre for Molecular and Cellular Biology, Division of Molecular Biology and Human Genetics, Stellenbosch University, South Africa.
Tuberculosis (Edinb). 2009 May;89(3):238-42. doi: 10.1016/j.tube.2009.01.006. Epub 2009 Feb 26.
Many molecular epidemiological investigations of M. tuberculosis are reported using data collected over relatively short timeframes. We postulated that such studies would tend to under-estimate the amount of disease in a community attributable to ongoing transmission. To test this hypothesis we used 12-year datasets of both real and simulated epidemics with the latter being based on two possible models of transmission. We analysed the effect of viewing the datasets through time windows of varying sizes on the measured degree of strain clustering as an indicator of ongoing transmission. We found that shorter windows significantly under-estimated transmission and that this effect was inversely correlated with the size of a cluster. Accordingly, we recommend that molecular epidemiological studies of M. tuberculosis, for the purposes of estimating transmission, be conducted over a minimum of 3-4 years and that the distribution of cluster size be taken into account in the interpretation of such data.
许多结核分枝杆菌的分子流行病学研究使用相对较短时间内收集的数据进行报告。我们推测,此类研究往往会低估社区中由持续传播引起的疾病负担。为了验证这一假设,我们使用了真实和模拟疫情的 12 年数据集,后者基于两种可能的传播模型。我们分析了通过不同大小的时间窗口查看数据集对衡量正在进行的传播的菌株聚类程度的影响。我们发现较短的窗口会显著低估传播,并且这种影响与聚类的大小成反比。因此,我们建议为了估计传播,结核分枝杆菌的分子流行病学研究应至少进行 3-4 年,并在解释此类数据时考虑聚类大小的分布。