Zarrinpar Amir, Gupta Shakti, Maurya Mano R, Subramaniam Shankar, Loomba Rohit
NAFLD Translational Research Unit, University of California, San Diego, La Jolla, California, USA Division of Gastroenterology, Department of Medicine, University of California, San Diego, La Jolla, California, USA.
Department of Bioengineering, San Diego Supercomputer Center, University of California, San Diego, La Jolla, California, USA.
Gut. 2016 Sep;65(9):1546-54. doi: 10.1136/gutjnl-2015-309456. Epub 2015 May 22.
In the setting where two individuals are genetically similar, epigenetic mechanisms could account for discordance in the presence or absence of non-alcoholic fatty liver disease (NAFLD). This study investigated if serum microRNAs (miRs) could explain discordance in NAFLD.
This is a cross-sectional analysis of a prospective cohort study of 40 (n=80) twin-pairs residing in Southern California. All participants underwent a standardised research visit, liver MRI using proton-density fat fraction to quantify fat content and miR profiling of their serum.
Among the 40 twin-pairs, there were 6 concordant for NAFLD, 28 were concordant for non-NAFLD and 6 were discordant for NAFLD. The prevalence of NAFLD was 22.5% (18/80). Within the six discordant twins, a panel of 10 miRs differentiated the twin with NAFLD from the one without. Two of these miRs, miR-331-3p and miR-30c, were also among the 21 miRs that were different between NAFLD and non-NAFLD groups (for miR-331-3p: 7.644±0.091 vs 8.057±0.071, respectively, p=0.004; for miR-30c: 10.013±0.126 vs 10.418±0.086, respectively, p=0.008). Both miRs were highly heritable (35.9% and 10.7%, respectively) and highly correlated with each other (R=0.90, p=2.2×10(-16)) suggesting involvement in a common mechanistic pathway. An interactome analysis of these two miRs showed seven common target genes.
Using a novel human twin-study design, we demonstrate that discordancy in liver fat content between the twins can be explained by miRs, and that they are heritable.
在两个个体基因相似的情况下,表观遗传机制可能解释非酒精性脂肪性肝病(NAFLD)存在与否的不一致性。本研究调查血清微小RNA(miR)是否能解释NAFLD的不一致性。
这是一项对居住在南加州的40对(n = 80)双胞胎进行的前瞻性队列研究的横断面分析。所有参与者都接受了标准化的研究访视、使用质子密度脂肪分数进行肝脏MRI以量化脂肪含量以及血清miR谱分析。
在40对双胞胎中,6对NAFLD情况一致,28对非NAFLD情况一致,6对NAFLD情况不一致。NAFLD的患病率为22.5%(18/80)。在6对不一致的双胞胎中,一组10个miR能够区分患NAFLD的双胞胎和未患NAFLD的双胞胎。这10个miR中的两个,即miR - 331 - 3p和miR - 30c,也在NAFLD组和非NAFLD组之间存在差异的21个miR之中(对于miR - 331 - 3p,分别为7.644±0.091和8.057±0.071,p = 0.004;对于miR - 30c,分别为10.013±0.126和10.418±0.086,p = 0.008)。这两个miR都具有高度遗传性(分别为35.9%和10.7%),并且彼此高度相关(R = 0.90,p = 2.2×10⁻¹⁶),表明它们参与了共同的机制途径。对这两个miR的相互作用组分析显示有7个共同的靶基因。
使用新颖的人类双胞胎研究设计,我们证明双胞胎之间肝脏脂肪含量的不一致性可以由miR解释,并且它们具有遗传性。