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Genetic and environmental influences on stability and change in baseline levels of C-reactive protein:A longitudinal twin study

机译:遗传和环境对C反应蛋白基线水平的稳定性和变化的影响:一项纵向双生子研究

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摘要

Background and aims: Cross-sectional twin and family studies report a moderate heritability of baseline levels of C-reactive protein (CRP), ranging from 0.10 to 0.65 for different age ranges. Here, we investigated the stability and relative impact of genetic and environmental factors underlying serum levels of CRP, using a longitudinal classical twin design. Methods: A maximum of 6201 female twins from the TwinsUK registry with up to three CRP measurements (i.e. visit 1 [V1], visit 2 [V2] and visit 3 [V3]) over a 10-year follow-up period were included in this study. Structural equation modeling was applied to dissect the observed phenotypic variance into its genetic and environ-mental components. To estimate the heritability of CRP as well as its genetic and environmental correlations across different time points, a trivariate model was used. Results: Natural log (ln) CRP levels significantly increased from V1 to V2 (p=4.4 × 10−25) and between V1 and V3 (p=1.2 × 10−15), but not between V2 and V3. The median (IQR) follow-up time between V1 and V3 was 9.58 (8.00–10.46) years. Heritability estimates for CRP were around 50% and constant over time (0.46–0.52). Additionally, adjustment for BMI did not meaningfully change the heritability estimates (0.49–0.51). The genetic correlations between visits were significantly smaller than one, ranging from 0.66 to 0.85. Conclusions: The present study provides evidence for stable heritability estimates of CRP of around 50% with advancing age. However, between-visit genetic correlations are significantly lower than 1, indicating emergence of new genetic effects on CRP levels with age.
机译:背景和目的:横断面双胞胎和家族研究报告了C反应蛋白(CRP)基线水平的中等遗传力,不同年龄段的范围为0.10至0.65。在这里,我们使用纵向经典双胞胎设计研究了血清和血清CRP水平的遗传和环境因素的稳定性和相对影响。方法:将包括在TwinsUK注册表中的最多6201例女性双胞胎,在10年的随访期内进行了3次CRP测量(即,访问1 [V1],访问2 [V2]和访问3 [V3])。这项研究。应用结构方程模型将观察到的表型变异分解为遗传和环境成分。为了估计CRP的遗传力以及其在不同时间点的遗传和环境相关性,使用了三变量模型。结果:自然对数(ln)CRP水平从V1显着增加到V2(p = 4.4×10−25),并且在V1和V3之间(p = 1.2×10-15)之间增加,但在V2和V3之间没有增加。 V1和V3之间的中位数(IQR)随访时间为9.58(8.00-10.46)年。 CRP的遗传力估计约为50%,并且随着时间的推移保持恒定(0.46-0.52)。此外,对BMI的调整并没有有意义地改变遗传度估计值(0.49–0.51)。访视之间的遗传相关性显着小于1,介于0.66至0.85之间。结论:本研究为随着年龄的增长稳定的CRP遗传力估计值提供了大约50%的证据。但是,两次访问之间的遗传相关性显着低于1,表明随着年龄的增长,新的遗传效应对CRP水平产生了影响。

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