Wheeler Heather E, Metter E Jeffrey, Tanaka Toshiko, Absher Devin, Higgins John, Zahn Jacob M, Wilhelmy Julie, Davis Ronald W, Singleton Andrew, Myers Richard M, Ferrucci Luigi, Kim Stuart K
Department of Genetics, Stanford University Medical Center, Stanford, California, USA.
PLoS Genet. 2009 Oct;5(10):e1000685. doi: 10.1371/journal.pgen.1000685. Epub 2009 Oct 16.
Kidneys age at different rates, such that some people show little or no effects of aging whereas others show rapid functional decline. We sequentially used transcriptional profiling and expression quantitative trait loci (eQTL) mapping to narrow down which genes to test for association with kidney aging. We first performed whole-genome transcriptional profiling to find 630 genes that change expression with age in the kidney. Using two methods to detect eQTLs, we found 101 of these age-regulated genes contain expression-associated SNPs. We tested the eQTLs for association with kidney aging, measured by glomerular filtration rate (GFR) using combined data from the Baltimore Longitudinal Study of Aging (BLSA) and the InCHIANTI study. We found a SNP association (rs1711437 in MMP20) with kidney aging (uncorrected p = 3.6 x 10(-5), empirical p = 0.01) that explains 1%-2% of the variance in GFR among individuals. The results of this sequential analysis may provide the first evidence for a gene association with kidney aging in humans.
肾脏的衰老速度各不相同,因此有些人几乎没有或完全没有衰老的影响,而另一些人则表现出快速的功能衰退。我们依次使用转录谱分析和表达定量性状位点(eQTL)定位来缩小用于测试与肾脏衰老相关的基因范围。我们首先进行全基因组转录谱分析,以找到630个在肾脏中随年龄变化表达的基因。使用两种方法检测eQTL,我们发现这些年龄调节基因中有101个包含与表达相关的单核苷酸多态性(SNP)。我们使用来自巴尔的摩纵向衰老研究(BLSA)和基安蒂研究(InCHIANTI)的合并数据,通过肾小球滤过率(GFR)来衡量,测试这些eQTL与肾脏衰老的关联。我们发现一个与肾脏衰老相关的SNP(MMP20基因中的rs1711437,未校正p = 3.6 x 10(-5),经验p = 0.01),它解释了个体间GFR变异的1%-2%。这种顺序分析的结果可能为人类中与肾脏衰老相关的基因关联提供了首个证据。