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Evidence for genetic factors explaining the association between birth weight and low-density lipoprotein cholesterol and possible intrauterine factors influencing the association between birth weight and high-density lipoprotein cholesterol: Analysis in twins

机译:遗传因素的证据解释出生体重与低密度脂蛋白胆固醇之间的关联以及可能的子宫内因素影响出生体重与高密度脂蛋白胆固醇之间的关联:双胞胎分析

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摘要

Recent studies have demonstrated an association between low weight at birth and an atherogenic lipid profile in later life. To examine the influences of intrauterine and genetic factors, we investigated 53 dizygotic and 61 monozygotic adolescent twin pairs. Regression analysis demonstrated that low birth weight was associated with high levels of total cholesterol, low-density lipoprotein (LDL) cholesterol and apolipoprotein B (-0.17 mmol/liter per kg, P = 0.07; -0.18 mmol/liter per kg, P = 0.04; and -0.07 g/liter per kg, P = 0.02, respectively) and with low levels of high-density lipoprotein (HDL) cholesterol (+0.04 mmol/liter per kg, P = 0.1), after adjustment for age, sex, and body mass index. Intrapair differences in birth weight were significantly associated with differences in total cholesterol, LDL cholesterol, and apolipoprotein B in dizygotic twins after adjustment for differences in current body mass index (-0.49 mmol/liter per kg, P = 0.02; -0.51 mmol/liter per kg, P = 0.01; and -0.10 g/liter per kg, P = 0.04, respectively), demonstrating that the larger the difference in birth weight, the higher these risk factors in the twin with the lower birth weight, compared with the cotwin with the higher birth weight. In monozygotic twins, however, the associations between intrapair differences in birth weight and differences in total cholesterol, LDL cholesterol, and apolipoprotein B were in the opposite direction (+0.32 mmol/liter per kg, P = 0.03; +0.23 mmol/liter per kg, P = 0.08; and +0.06 g/liter per kg, P = 0.04, respectively). The association between intrapair differences in birth weight and differences in HDL cholesterol was not significant in dizygotic twins (+0.04 mmol/liter per kg, P = 0.6) and of borderline significance in monozygotic twins (+0.11 mmol/liter per kg, P = 0.05). These data suggest that genetic factors account for the association of low birth weight with high levels of total cholesterol, LDL cholesterol, and apolipoprotein B, whereas intrauterine factors possibly play a role in the association between birth weight and HDL cholesterol.
机译:最近的研究表明,出生时体重轻与以后的生活中致动脉粥样硬化的脂质状况有关。为了检查宫内和遗传因素的影响,我们调查了53对同卵双生和61对同卵双生的青少年双胞胎。回归分析表明,低出生体重与高水平的总胆固醇,低密度脂蛋白(LDL)胆固醇和载脂蛋白B相关(-0.17 mmol / L / kg,P = 0.07; -0.18 mmol / L / kg,P =调整年龄,性别后,高密度脂蛋白(HDL)胆固醇水平较低(+0.04 mmol /升每千克,P = 0.1),而0.04和-0.07克/升每千克,P分别为0.02)和低水平和体重指数。校正当前体重指数的差异(-0.49 mmol / L / kg,P = 0.02; -0.51 mmol / L)后,出生体重的成对内差异与同卵双胞胎的总胆固醇,LDL胆固醇和载脂蛋白B的差异显着相关每公斤,P = 0.01;和-0.10克/升/公斤,P = 0.04),表明出生体重差异越大,与出生体重越低的双胞胎相比,这些危险因素越高出生体重较高的科特温。然而,在单卵双胞胎中,成对体重差异与总胆固醇,LDL胆固醇和载脂蛋白B差异的对之间的关​​系相反(+0.32 mmol / L / kg,P = 0.03; +0.23 mmol / L / kg千克,P = 0.08;和每千克+0.06克/升,P = 0.04)。成对双胞胎中出生体重差异与高密度脂蛋白胆固醇差异之间的相关性不显着(+0.04 mmol / L / kg,P = 0.6),单卵双胞胎(+0.11 mmol / L / kg,P = 0.05)。这些数据表明,遗传因素导致低出生体重与高水平的总胆固醇,LDL胆固醇和载脂蛋白B的关联,而宫内因素可能在出生体重与HDL胆固醇之间的关联中起作用。

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