Wattacheril Julia, Lavine Joel E, Chalasani Naga P, Guo Xiuqing, Kwon Soonil, Schwimmer Jeffrey, Molleston Jean P, Loomba Rohit, Brunt Elizabeth M, Chen Yii-Der Ida, Goodarzi Mark O, Taylor Kent D, Yates Katherine P, Tonascia James, Rotter Jerome I
Medicine, Columbia University, New York, NY.
Pediatrics, Columbia University, New York, NY.
J Pediatr. 2017 Nov;190:100-107.e2. doi: 10.1016/j.jpeds.2017.08.004. Epub 2017 Sep 14.
To identify genetic loci associated with features of histologic severity of nonalcoholic fatty liver disease in a cohort of Hispanic boys.
There were 234 eligible Hispanic boys age 2-17 years with clinical, laboratory, and histologic data enrolled in the Nonalcoholic Steatohepatitis Clinical Research Network included in the analysis of 624 297 single nucleotide polymorphisms (SNPs). After the elimination of 4 outliers and 22 boys with cryptic relatedness, association analyses were performed on 208 DNA samples with corresponding liver histology. Logistic regression analyses were carried out for qualitative traits and linear regression analyses were applied for quantitative traits.
The median age and body mass index z-score were 12.0 years (IQR, 11.0-14.0) and 2.4 (IQR, 2.1-2.6), respectively. The nonalcoholic fatty liver disease activity score (scores 1-4 vs 5-8) was associated with SNP rs11166927 on chromosome 8 in the TRAPPC9 region (P = 8.7). Fibrosis stage was associated with SNP rs6128907 on chromosome 20, near actin related protein 5 homolog (p = 9.9). In comparing our results in Hispanic boys with those of previously reported SNPs in adult nonalcoholic steatohepatitis, 2 of 26 susceptibility loci were associated with nonalcoholic fatty liver disease activity score and 2 were associated with fibrosis stage.
In this discovery genome-wide association study, we found significant novel gene effects on histologic traits associated with nonalcoholic fatty liver disease activity score and fibrosis that are distinct from those previously recognized by adult nonalcoholic fatty liver disease genome-wide association studies.
在一组西班牙裔男孩队列中确定与非酒精性脂肪性肝病组织学严重程度特征相关的基因位点。
共有234名年龄在2至17岁之间符合条件的西班牙裔男孩,他们具有临床、实验室和组织学数据,纳入非酒精性脂肪性肝炎临床研究网络,对624297个单核苷酸多态性(SNP)进行分析。在剔除4个异常值和22名有隐性亲缘关系的男孩后,对208份DNA样本及其相应的肝脏组织学进行了关联分析。对定性性状进行逻辑回归分析,对定量性状进行线性回归分析。
年龄中位数和体重指数z评分分别为12.0岁(四分位间距,11.0 - 14.0)和2.4(四分位间距,2.1 - 2.6)。非酒精性脂肪性肝病活动评分(1 - 4分与5 - 8分)与8号染色体TRAPPC9区域的SNP rs11166927相关(P = 8.7)。纤维化阶段与20号染色体上靠近肌动蛋白相关蛋白5同源物的SNP rs6128907相关(P = 9.9)。将我们在西班牙裔男孩中的结果与先前报道的成人非酒精性脂肪性肝炎SNP结果进行比较,26个易感位点中有2个与非酒精性脂肪性肝病活动评分相关,2个与纤维化阶段相关。
在这项全基因组关联研究发现中,我们发现了与非酒精性脂肪性肝病活动评分和纤维化相关的组织学性状有显著的新基因效应,这些效应与先前成人非酒精性脂肪性肝病全基因组关联研究所识别的不同。