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多发性硬化症发病年龄的预测:方法学陷阱。

Anticipation of age at onset in multiple sclerosis: methodologic pitfalls.

机构信息

Neurology Department, Malmö University Hospital, Sweden.

出版信息

Acta Neurol Scand. 2010 Jun;121(6):426-8. doi: 10.1111/j.1600-0404.2009.01273.x.

Abstract

BACKGROUND/AIM: There are several reports that claim anticipation in complex or polygenic diseases such as multiple sclerosis (MS), Crohn disease or schizophrenia. The aim of the present study was to assess age at onset of MS during the last 60 years in the region of Costa de Ponent (Barcelona, Spain) showing how apparent changes in age at onset between generations can be an artefact of analysis based on cohorts that have not been followed enough time.

METHODS

The study comprised 1100 patients diagnosed of MS. The method used to correct for follow-up time bias involves constructing comparison cohorts that had been observed for the same amount of time. To ensure equal follow-up times, we restricted our analysis to patients whose onset was by 37 years of age (percentile 75) and were at least 37 years old. We analysed differences in age at onset using log-rank test to compare survival curves estimated by Kaplan-Meier method.

RESULTS

Age at onset decreases progressively from older to younger generations. However, when adjustment to equal follow-up time was done, anticipation in age at onset was not found.

CONCLUSION

Anticipation of age at onset is undetectable when adjusted for follow-up time.

摘要

背景/目的:有几项报告声称,在多发性硬化症(MS)、克罗恩病或精神分裂症等复杂或多基因疾病中存在预期现象。本研究的目的是评估过去 60 年来在西班牙蓬特德科斯塔地区(巴塞罗那)MS 的发病年龄,研究表明,基于未随访足够时间的队列进行分析,世代之间发病年龄的明显变化可能是分析的人为因素。

方法

本研究纳入了 1100 名确诊为 MS 的患者。用于纠正随访时间偏倚的方法包括构建观察时间相同的比较队列。为了确保随访时间相等,我们将分析仅限于发病年龄在 37 岁以下(第 75 个百分位数)且至少 37 岁的患者。我们使用对数秩检验分析发病年龄的差异,以比较通过 Kaplan-Meier 方法估计的生存曲线。

结果

发病年龄从老一代到年轻一代逐渐降低。然而,当进行相等随访时间的调整时,并未发现发病年龄的预期提前。

结论

调整随访时间后,无法检测到发病年龄的提前。

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