Glostrup和Framingham前瞻性研究中血总胆固醇和高密度脂蛋白胆固醇和血压的回归稀释偏倚。

Sarah Lewington, Troels Thomsen, Michael Davidsen, Paul Sherliker, Robert Clarke
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引用次数: 0

摘要

背景:在流行病学研究中,某一危险因素测量值的个人内部变异性可能低估了某一危险因素长期或“通常”水平与疾病风险之间的关联——“回归稀释”。回归稀释对高密度脂蛋白(HDL)-胆固醇的重要性以及它与总胆固醇的不同程度尚不清楚。本研究的目的是评估两项前瞻性队列研究中不同随访间隔后hdl -胆固醇、总胆固醇和血压的回归稀释偏倚的程度。方法:利用Glostrup人口研究和NHLBI Framingham心脏研究中基线值和重新调查值在不同时间间隔后的相关性,估计每个危险因素的回归稀释比。在测量间隔固定后,比较每个队列的回归稀释率。结果:Glostrup和Framingham 10年后收缩压的回归稀释比分别为0.51和0.56;舒张压分别为0.52和0.54;总胆固醇为0.68和0.63。在这两项研究中,随着测量间隔的增加,这些危险因素的回归稀释率变得更加极端。在Glostrup中,10年后hdl -胆固醇的回归稀释比为0.72,这表明hdl -胆固醇回归稀释的重要性与总胆固醇相似。结论:未能纠正随着随访时间的延长而增加的回归稀释可能是在不同随访间隔的流行病学研究中对这些危险因素的重要性所获得的一些差异结果的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regression dilution bias in blood total and high-density lipoprotein cholesterol and blood pressure in the Glostrup and Framingham prospective studies.

Background: In epidemiological studies, within-person variability in measured values of a risk factor may underestimate the association between prolonged or 'usual' levels of a risk factor with risk of disease - 'regression dilution'. The importance of regression dilution for high-density lipoprotein (HDL)-cholesterol and the extent to which this may differ from that for total cholesterol is not known. The aim of this study was to assess the magnitude of regression dilution bias for HDL-cholesterol, total cholesterol and blood pressure after varying intervals of follow-up in two prospective cohort studies.

Methods: Regression dilution ratios were estimated for each risk factor using the correlations between baseline and re-survey values in the Glostrup Population Studies and the NHLBI Framingham Heart Study after various time intervals. The regression dilution ratios in each cohort after a fixed interval between measurements were compared.

Results: The regression dilution ratios after 10 years were 0.51 and 0.56 for systolic blood pressure in Glostrup and Framingham, respectively; 0.52 and 0.54 for diastolic blood pressure; and 0.68 and 0.63 for total cholesterol. In both studies, the regression dilution ratios for these risk factors became more extreme with increasing intervals between measurements. The regression dilution ratio for HDL-cholesterol after 10 years in Glostrup was 0.72, which suggests that the importance of regression dilution for HDL-cholesterol was similar to that for total cholesterol.

Conclusion: Failure to correct for increasing regression dilution with longer follow-up may account for some of the discrepant results obtained for the importance of these risk factors in epidemiological studies at varying intervals of follow-up.

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