Suzuki Keiko, Juo Suh-Hang Hank, Rundek Tanja, Boden-Albala Bernadette, Disla Norbelina, Liu Rui, Park Naeun, Di Tullio Marco R, Sacco Ralph L, Homma Shunichi
Division of Cardiology, Department of Medicine, Columbia University College of Physicians and Surgeons, 630 West 168th Street, New York, NY 10032, USA.
Atherosclerosis. 2008 Mar;197(1):212-6. doi: 10.1016/j.atherosclerosis.2007.03.023. Epub 2007 Apr 25.
Brachial artery flow-mediated dilation (FMD) is a non-invasive measure of endothelial function. Endothelial dysfunction has been associated with traditional vascular risk factors and increased risk of cardiovascular disease. The importance of genetic contribution to FMD and baseline brachial artery diameter has not been shown in Hispanic populations. The purpose of this study was to estimate the heritability of FMD.
Flow mediated dilation and brachial artery diameter were measured in a subset of Caribbean Hispanic families from the ongoing Northern Manhattan Family Study (NOMAFS), which studies the contribution of genetics to stroke and cardiovascular risk factors. The age- and sex-adjusted heritability of FMD was estimated using variance component methods.
The current data include 620 subjects (97 probands and 523 relatives) from 97 families. The age and sex-adjusted heritability of brachial artery diameter was 0.57 (p<0.01). The age- and sex-adjusted heritability of FMD was 0.20 (p=0.01). After additional adjustment for systolic and diastolic blood pressure, body mass index, smoking, lipid, diabetes mellitus, medication, and baseline brachial artery diameter, the heritability of FMD was 0.17 (p=0.01).
We found modest heritability of FMD. FMD might be a reasonable phenotype for further investigation of genetic contribution to atherosclerosis.
肱动脉血流介导的血管舒张功能(FMD)是一种评估内皮功能的非侵入性方法。内皮功能障碍与传统血管危险因素及心血管疾病风险增加相关。在西班牙裔人群中,基因对FMD及肱动脉基线直径的影响尚未见报道。本研究旨在评估FMD的遗传度。
在正在进行的北曼哈顿家族研究(NOMAFS)中的一部分加勒比西班牙裔家庭中测量血流介导的血管舒张功能和肱动脉直径,该研究旨在探讨基因对中风及心血管危险因素的作用。采用方差成分法估计FMD经年龄和性别调整后的遗传度。
当前数据包括来自97个家庭的620名受试者(97名先证者和523名亲属)。肱动脉直径经年龄和性别调整后的遗传度为0.57(p<0.01)。FMD经年龄和性别调整后的遗传度为0.20(p=0.01)。在进一步调整收缩压和舒张压、体重指数、吸烟、血脂、糖尿病、药物治疗及肱动脉基线直径后,FMD的遗传度为0.17(p=0.01)。
我们发现FMD具有适度的遗传度。FMD可能是进一步研究基因对动脉粥样硬化影响的一个合理表型。