National Heart, Lung, and Blood Institute's Framingham Heart Study, 73 Mt, Wayte Avenue, Suite 2, Framingham, Massachusetts 01702, USA.
BMC Med Genet. 2011 Nov 1;12:148. doi: 10.1186/1471-2350-12-148.
Ectopic fat accumulation in the renal sinus is associated with chronic kidney disease and hypertension. The genetic contributions to renal sinus fat accumulation in humans have not been well characterized.
The present analysis consists of participants from the Framingham Offspring and Third Generation who underwent computed tomography; renal sinus fat and visceral adipose tissue (VAT) were quantified. Renal sinus fat was natural log transformed and sex- and cohort-specific residuals were created, adjusted for (1) age, (2) age and body mass index (BMI), and (3) age and VAT. Residuals were pooled and used to calculate heritability using variance-components analysis in SOLAR. A genome-wide association study (GWAS) for renal sinus fat was performed using an additive model with approximately 2.5 million imputed single nucleotide polymorphisms (SNPs). Finally, we identified the associations of renal sinus fat in our GWAS results with validated SNPs for renal function (n=16), BMI (n=32), and waist-to-hip ratio (WHR, n=14), and applied a multi-SNP genetic risk score method to determine if the SNPs for each renal and obesity trait were in aggregate associated with renal sinus fat.
The heritability of renal sinus fat was 39% (p<0.0001); results were not materially different after adjustment for BMI (39%) or VAT (40%). No SNPs reached genome-wide significance in our GWAS. In our candidate gene analysis, we observed nominal, direction consistent associations with renal sinus fat for one SNP associated with renal function (p=0.01), two associated with BMI (p<0.03), and two associated with WHR (p<0.03); however, none remained significant after accounting for multiple testing. Finally, we observed that in aggregate, the 32 SNPs associated with BMI were nominally associated with renal sinus fat (multi-SNP genetic risk score p=0.03).
Renal sinus fat is a heritable trait, even after accounting for generalized and abdominal adiposity. This provides support for further research into the genetic determinants of renal sinus fat. While our study was underpowered to detect genome-wide significant loci, our candidate gene BMI risk score results suggest that variability in renal sinus fat may be associated with SNPs previously known to be associated with generalized adiposity.
肾脏窦脂肪在人体中的积累与慢性肾脏病和高血压有关。但是,人类肾脏窦脂肪积累的遗传贡献尚未得到很好的描述。
本分析包括接受计算机断层扫描的弗雷明汉后代和第三代参与者;定量了肾脏窦脂肪和内脏脂肪组织(VAT)。对肾脏窦脂肪进行自然对数转换,并根据(1)年龄、(2)年龄和体重指数(BMI)以及(3)年龄和 VAT 生成性别和队列特异性残差。将残差汇集在一起,并使用 SOLAR 中的方差成分分析计算遗传性。使用加性模型对肾脏窦脂肪进行全基因组关联研究(GWAS),该模型使用大约 250 万个已导入的单核苷酸多态性(SNP)。最后,我们确定了我们的 GWAS 结果中肾脏窦脂肪与验证过的肾功能(n=16)、BMI(n=32)和腰臀比(WHR,n=14)的 SNP 之间的关联,并应用多 SNP 遗传风险评分方法来确定每个肾脏和肥胖特征的 SNP 是否与肾脏窦脂肪有总体关联。
肾脏窦脂肪的遗传率为 39%(p<0.0001);在调整 BMI(39%)或 VAT(40%)后,结果没有明显差异。我们的 GWAS 中没有 SNP 达到全基因组显著性。在我们的候选基因分析中,我们观察到一个与肾功能相关的 SNP 与肾脏窦脂肪呈名义上一致的方向相关(p=0.01),两个与 BMI 相关的 SNP(p<0.03)和两个与 WHR 相关的 SNP(p<0.03);然而,在考虑到多次检验后,没有一个 SNP 仍然具有统计学意义。最后,我们观察到,总体而言,与 BMI 相关的 32 个 SNP 与肾脏窦脂肪呈名义相关(多 SNP 遗传风险评分 p=0.03)。
即使考虑到全身和腹部肥胖,肾脏窦脂肪也是一种可遗传的特征。这为进一步研究肾脏窦脂肪的遗传决定因素提供了支持。虽然我们的研究没有足够的能力来检测全基因组显著的基因座,但我们的候选基因 BMI 风险评分结果表明,肾脏窦脂肪的变异性可能与先前已知与全身肥胖相关的 SNP 相关。