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Assessment of carotid atherosclerosis in normocholesterolemic individuals with proven mutations in the low-density lipoprotein receptor or apolipoprotein B genes.对低密度脂蛋白受体或载脂蛋白B基因已证实存在突变的正常胆固醇血症个体的颈动脉粥样硬化评估。
Circ Cardiovasc Genet. 2011 Aug 1;4(4):413-7. doi: 10.1161/CIRCGENETICS.110.959239. Epub 2011 Jun 4.
2
Dyslipidemia of mothers with familial hypercholesterolemia deteriorates lipids in adult offspring.家族性高胆固醇血症母亲的血脂异常会使成年后代的血脂恶化。
Arterioscler Thromb Vasc Biol. 2010 Dec;30(12):2673-7. doi: 10.1161/ATVBAHA.110.209064. Epub 2010 Sep 23.
3
Two years after molecular diagnosis of familial hypercholesterolemia: majority on cholesterol-lowering treatment but a minority reaches treatment goal.家族性高胆固醇血症分子诊断两年后:多数患者接受降脂治疗,但只有少数患者达到治疗目标。
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4
Management of fertility in women with familial hypercholesterolaemia: summary of NICE guidance.家族性高胆固醇血症女性的生育管理:英国国家卫生与临床优化研究所指南摘要
BJOG. 2009 Mar;116(4):478-9. doi: 10.1111/j.1471-0528.2008.02084.x.
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Statin treatment in hypercholesterolemic pregnant mice reduces cardiovascular risk factors in their offspring.高胆固醇血症妊娠小鼠接受他汀类药物治疗可降低其后代的心血管危险因素。
Hypertension. 2008 Apr;51(4):939-44. doi: 10.1161/HYPERTENSIONAHA.107.100982. Epub 2008 Feb 19.
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Characterization of a murine model of fetal programming of atherosclerosis.
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Prediction of clinical cardiovascular events with carotid intima-media thickness: a systematic review and meta-analysis.利用颈动脉内膜中层厚度预测临床心血管事件:一项系统评价与荟萃分析。
Circulation. 2007 Jan 30;115(4):459-67. doi: 10.1161/CIRCULATIONAHA.106.628875. Epub 2007 Jan 22.
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Marked changes in plasma lipids and lipoproteins during pregnancy in women with familial hypercholesterolemia.
Atherosclerosis. 2006 Dec;189(2):451-7. doi: 10.1016/j.atherosclerosis.2006.01.002. Epub 2006 Feb 8.
9
Maternal cholesterol in fetal development: transport of cholesterol from the maternal to the fetal circulation.胎儿发育过程中的母体胆固醇:胆固醇从母体循环向胎儿循环的转运。
Am J Clin Nutr. 2005 Dec;82(6):1155-61. doi: 10.1093/ajcn/82.6.1155.
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Update of the molecular basis of familial hypercholesterolemia in The Netherlands.荷兰家族性高胆固醇血症分子基础的更新
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家族性高胆固醇血症的遗传模式和心血管风险标志物。

Inheritance pattern of familial hypercholesterolemia and markers of cardiovascular risk.

机构信息

Academic Medical Center, Amsterdam, The Netherlands.

出版信息

J Lipid Res. 2013 Sep;54(9):2543-9. doi: 10.1194/jlr.M034538. Epub 2013 Jul 5.

DOI:10.1194/jlr.M034538
PMID:23833242
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3735950/
Abstract

Studies in children and adults have resulted in conflicting evidence in the quest for the answer to the hypothesis that offspring from hypercholesterolemic mothers might have an increased cardiovascular risk. Previous studies might have suffered from limitations such as cohort size and clinical sampling bias. We therefore explored this hypothesis in large cohorts of both subjects with familial hypercholesterolemia (FH) and unaffected siblings in a wide age range. In three cohorts (cohort 1: n = 1,988, aged 0-18 years; cohort 2: n = 300, 8-30 years; cohort 3: n = 369, 18-60 years), we measured lipid and lipoproteins as well as carotid intima-media thickness (c-IMT) in offspring from FH mothers versus FH fathers. For LDL cholesterol, triglycerides (TGs), and c-IMT, we performed a pooled analysis. No significant differences could be observed in c-IMT, lipid, or lipoprotein levels from offspring of FH mothers versus FH fathers. Pooled analyses showed no significant differences for either LDL cholesterol [mean difference 0.02 (-0.06,0.11) mmol/l, P = 0.60], TGs [mean difference 0.07 (0.00,0.14) mmol/l, P = 0.08], or c-IMT [mean difference -0.00 (-0.01,0.01) mm, P = 0.86]. Our data do not support the hypothesis that cardiovascular risk markers are different between offspring from FH mothers and FH fathers.

摘要

在探索来自高胆固醇血症母亲的后代是否存在心血管风险增加这一假说的过程中,儿童和成人的研究得出了相互矛盾的证据。先前的研究可能受到队列规模和临床抽样偏差等限制。因此,我们在多个大样本队列中研究了这一假说,这些队列包括家族性高胆固醇血症(FH)患者及其在广泛年龄范围内未受影响的兄弟姐妹。在三个队列中(队列 1:n = 1988,年龄 0-18 岁;队列 2:n = 300,8-30 岁;队列 3:n = 369,18-60 岁),我们测量了 FH 母亲和 FH 父亲的后代的血脂和脂蛋白以及颈动脉内膜中层厚度(c-IMT)。对于 LDL 胆固醇、甘油三酯(TGs)和 c-IMT,我们进行了汇总分析。在 FH 母亲和 FH 父亲的后代中,c-IMT、血脂或脂蛋白水平没有显著差异。汇总分析显示,LDL 胆固醇[平均差异 0.02(-0.06,0.11)mmol/L,P = 0.60]、TGs[平均差异 0.07(0.00,0.14)mmol/L,P = 0.08]或 c-IMT[平均差异-0.00(-0.01,0.01)mm,P = 0.86]的差异均无统计学意义。我们的数据不支持心血管风险标志物在 FH 母亲和 FH 父亲的后代之间存在差异的假说。